WO2001064197A2 - Farnesyl protein transferase inhibitor combinations with anti-tumor anthracycline derivatives - Google Patents
Farnesyl protein transferase inhibitor combinations with anti-tumor anthracycline derivatives Download PDFInfo
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- WO2001064197A2 WO2001064197A2 PCT/EP2001/002166 EP0102166W WO0164197A2 WO 2001064197 A2 WO2001064197 A2 WO 2001064197A2 EP 0102166 W EP0102166 W EP 0102166W WO 0164197 A2 WO0164197 A2 WO 0164197A2
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- Prior art keywords
- 6alkyl
- alkyl
- hydrogen
- 6alkyloxy
- formula
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- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
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- A61K31/7034—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
- A61K31/704—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
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- A—HUMAN NECESSITIES
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- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- the present invention is concerned with combinations of a farnesyl transferase inhibitor and an anti-tumor anthracychne derivative for inhibiting the growth of tumor cells, and useful in the treatment of cancer.
- Oncogenes frequently encode protein components of signal transduction pathways which lead to stimulation of cell growth and mitogenesis.
- Oncogene expression in cultured cells leads to cellular transformation, characterized by the ability of cells to grow in soft agar and the growth of cells as dense foci lacking the contact inhibition exhibited by non-transformed cells. Mutation and/or overexpression of certain oncogenes is frequently associated with human cancer.
- a particular group of oncogenes is known as ras which have been identified in mammals, birds, insects, mollusks, plants, fungi and yeasts.
- the family of mammalian ras oncogenes consists of three major members ("isoforms") : H-ras, K-ras and N-ras oncogenes. These ras oncogenes code for highly related proteins generically known as p21 ra5 .
- the mutant or oncogenic forms of p21 ra ' s will provide a signal for the transformation and uncontrolled growth of malignant tumor cells.
- the precursor of the p21 ra ' s oncoprotein must undergo an enzymatically catalyzed farnesylation of the cysteine residue located in a carboxyl- terminal tetrapeptide.
- farnesyl transferase inhibitors can be very useful as anticancer agents for tumors in which ras contributes to transformation.
- WO-97/21701 describes the preparation, formulation and pharmaceutical properties of farnesyl protein transferase inhibiting (imidazoly-5-yl)methyl-2-quinolinone derivatives of formulas (I), (II) and (HI), as well as intermediates of formula (II) and (IE) that are metabolized in vivo to the compounds of formula (I).
- the compounds of formulas (I), (II) and (HI) are represented by
- R 9 is hydroxy, Ci-6alkyl, Ci-6alkyloxy, amino, Ci-8alkylamino or Ci-8alkylamino substituted with Ci_6alkyloxycarbonyl;
- R , R3 and R*6 each independently are hydrogen, hydroxy, halo, cyano, C ⁇ _6alkyl, C ⁇ _6alkyloxy, hydroxyCi-6alkyloxy, C ⁇ _6alkyloxyCi-6alkyloxy, aminoCi-6alkyl- oxy, mono- or di(C ⁇ _6alkyl)aminoCi-6alkyloxy, Ar 1 , Ar ⁇ Ci- ⁇ alkyl, Ar ⁇ oxy,
- Ar ⁇ Ci-galkyloxy, hydroxycarbonyl, Ci-6alkyloxycarbonyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, 4,4-dimethyloxazolyl; or when on adjacent positions R ⁇ and R ⁇ taken together may form a bivalent radical of formula -O-CH2-O- (a-1),
- R4 and R ⁇ each independently are hydrogen, halo, Ar , C ⁇ _6alkyl, hydroxyCi-galkyl, Ci-6alkyloxyC ⁇ _6alkyl, C ⁇ _6alkyloxy, C ⁇ _6alkylthio, amino, hydroxycarbonyl, Ci - ⁇ alkyloxycarbonyl, Ci-6alkylS(O)Ci-6alkyl or Ci-6alkylS(O)2Ci -6alkyl; R6 and R ⁇ each independently are hydrogen, halo, cyano, Ci ⁇ alkyl, Ci- ⁇ alkyloxy,
- Ar 2 oxy, trihalomethyl, Ci-6alkylth ⁇ o, di(C ⁇ _6alkyl)amino, or when on adjacent positions R ⁇ and R ⁇ taken together may form a bivalent radical of formula
- R ⁇ is hydrogen, C ⁇ _6alkyl, cyano, hydroxycarbonyl, C ⁇ _6alkyloxycarbonyl,
- R 0 is hydrogen, Ci-6alkyl, Ci-6alkylcarbonyl, Ar 1 , Ar 2 Ci-6alkyl, Ci-6alkyloxycarbonylCi-6alkyl, or a radical or formula -Alk 2 -ORl3 or -Alk -NR 14 R 15 ;
- RU is hydrogen, C ⁇ _i2alkyl, Ar* or Ar 2 C ⁇ _6alkyl;
- Rl3 i hydrogen, C ⁇ _6alkyl, Ci-6alkylcarbonyl, hydroxy-
- R 14 is hydrogen, Ci_6alkyl, Ar 1 or Ar 2 Ci-6alkyl;
- R 14 is hydrogen, Ci_6alkyl, Ar 1 or Ar 2 Ci-6alkyl;
- Rl5 is hydrogen, C ⁇ _6alkyl, C ⁇ _6alkylcarbonyl, Ar or Ar 2 C ⁇ _6alkyl;
- Rl7 is hydrogen, halo, cyano, Ci-6alkyl, C ⁇ _6alkyloxycarbonyl, Arl;
- R 1 ⁇ is hydrogen, C ⁇ _6alkyl, Ci-6alkyloxy or halo;
- Ar 9 is hydrogen or Ci-6alkyl
- Ar ⁇ is phenyl or phenyl substituted with Ci-6alkyl, hydroxy, amino, C ⁇ _6alkyloxy or halo
- Ar 2 is phenyl or phenyl substituted with Ci-6alkyl, hydroxy, amino, C ⁇ _6alkyloxy or halo.
- WO-97/16443 concerns the preparation, formulation and pharmaceutical properties of farnesyl protein transferase inhibiting compounds of formula (IV), as well as intermediates of formula (V) and (VI) that are metabolized in vivo to the compounds of formula (IV).
- the compounds of formulas (IV), (V) and (VI) are represented by
- R 9 is hydroxy, Ci-6alkyl, C ⁇ _6alkyloxy, amino, Ci-8alkylamino or Ci-8alkylamino substituted with C ⁇ _6alkyloxycarbonyl;
- R 2 and R 3 each independently are hydrogen, hydroxy, halo, cyano, Ci-6alkyl, Ci-6alkyloxy, hydroxyC ⁇ _6alkyloxy, C ⁇ _6alkyloxyCi-6alkyloxy, amino- C ⁇ _6alkyloxy, mono- or di(Ci-6alkyl)aminoCi-6alkyloxy, Ar 1 , Ar 2 C ⁇ _6alkyl, Ar 2 oxy, Ar 2 C ⁇ _6alkyloxy, hydroxycarbonyl, C ⁇ _6alkyloxycarbonyl, trihalomethyl, trihalomethoxy, C2-6alkenyl; or when on adjacent positions R 2 and R 3 taken together may form a bivalent radical of formula
- R 4 and R 5 each independently are hydrogen, Ar 1 , C ⁇ -6 alkyl, C ⁇ - alkyloxyC ⁇ _ 6 alkyl, C 1-6 alkyloxy, C 1- alkylthio, amino, hydroxycarbonyl, C ⁇ -6 alkyloxycarbonyl,
- R6 and R ⁇ each independently are hydrogen, halo, cyano, C ⁇ _6alkyl, C ⁇ _6alkyloxy or
- Ar 2 oxy; R& is hydrogen, Ci-6alkyl, cyano, hydroxycarbonyl, Ci-6alkyloxycarbonyl, C ⁇ _6alkyl- carbonylC ⁇ _6alkyl, cyanoC ⁇ _6alkyl, Ci-6alkyloxycarbonylCi-6alkyl, hydroxy- carbonylCi- ⁇ alkyl, hydroxyCi-6alkyl, aminoC ⁇ _6alkyl, mono- or di(C ⁇ _6alkyl)- aminoCi-6alkyl, haloCi-6alkyl, Ci-6alkyloxyCi-6alkyl, aminocarbonylCi-6alkyl, Ar 1 , Ar 2 Ci-6alkyloxyCi-6alkyl, Ci-6alkylthioCi-6alkyl; R ⁇ is hydrogen, Ci-6alkyl, Ci-6alkyloxy or halo; R 1 is hydrogen or Ci-6alkyl;
- Ar 1 is phenyl or phenyl substituted with C ⁇ _6alkyl, hydroxy, amino, - ⁇ alkyloxy or halo
- Ar 2 is phenyl or phenyl substituted with C ⁇ _6alkyl, hydroxy, amino, C ⁇ _6alkyloxy or halo.
- WO-98/40383 concerns the preparation, formulation and pharmaceutical properties of farnesyl protein transferase inhibiting compounds of formula (VH)
- X is oxygen or sulfur
- R 1 and R 2 each independently are hydrogen, hydroxy, halo, cyano, Ci-6alkyl, trihalomethyl, trihalomethoxy, C2-6 a lkenyl, C ⁇ _6alkyloxy, hydroxyCi-6alkyloxy, C ⁇ _6alkyloxyCi-6alkyloxy, Ci- ⁇ alkyloxycarbonyl, aminoCi-6alkyloxy, mono- or di(Ci-6alkyl)aminoC ⁇ _-6alkyloxy, Ar 2 , Ar 2 -Ci-6alkyl, Ar 2 -oxy, Ar 2 -C ⁇ _6alkyloxy; or when on adjacent positions R and R 2 taken together may form a bivalent radical of formula
- R 3 and R 4 each independently are hydrogen, halo, cyano, Ci-6alkyl, Ci-6alkyloxy, Ar ⁇ -oxy, C ⁇ _6alkylthio, di(Ci-6alkyl)amino, trihalomethyl, trihalomethoxy, or when on adjacent positions R 3 and R 4 taken together may form a bivalent radical of formula
- R5 is a radical of formula
- R 13 is hydrogen, halo, Ar 4 , C ⁇ _6alkyl, hydroxyCi-6alkyl, C ⁇ _6alkyloxy- C ⁇ _6alkyl, Ci-6alkyloxy, C ⁇ _6alkylthio, amino, C ⁇ _6alkyloxy- carbonyl, Ci-6alkylS(O)Ci-6alkyl or Ci-6alkylS(O)2C ⁇ _6alkyl;
- R 14 is hydrogen, C ⁇ _6alkyl or di(C ⁇ _4alkyl)aminosulfonyl;
- R6 is hydrogen, hydroxy, halo, Ci-6alkyl, cyano, haloC ⁇ _6alkyl, hydroxyCi_6alkyl, cyanoC ⁇ _6alkyl, aminoCi- ⁇ alkyl, C ⁇ _6alkyloxyCi-6alkyl, C ⁇ _-6alkylthioCi-6alkyl, aminocarbonylCi_6alkyl,
- Ci-6alkyloxycarbonylC ⁇ _6alkyl or a radical of formula -Alk-OR 1 ⁇ or -Alk-NR ⁇ R 12 ;
- R8 is hydrogen, C ⁇ _6alkyl, Ar or Ar ⁇ -Ci- ⁇ alkyl;
- R 9 is hydrogen, Ci-6alkyl, C ⁇ _6alkylcarbonyl, Ci-6alkyloxycarbonyl, C ⁇ _6alkylaminocarbonyl, Ar ⁇ , Ar ⁇ -Ci- ⁇ alkyl, C ⁇ _6alkylcarbonyl- Ci-6alkyl, Ar ⁇ -carbonyl, Ar ⁇ -Ci- ⁇ alkylcarbonyl, aminocarbonyl- carbonyl, Ci-6alkyloxyCi-6alkylcarbonyl, hydroxy, Ci-6alkyloxy, aminocarbonyl, di(Ci-6alkyl)aminoCi-6alkylcarbonyl, amino,
- Ci-6alkylamino Ci- ⁇ alkylcarbonylamino, or a radical or formula -Alk-OR 10 or -Alk-NR 1 iR 12 ; wherein Alk is C ⁇ _6alkanediyl;
- R ⁇ is hydrogen, Ci- ⁇ alkyl, Ci-6alkylcarbonyl, hydroxyCi-6alkyl, Ar 9 or Ar 9 -C ⁇ _6alkyl;
- R 1 is hydrogen, C ⁇ -6alkyl, C ⁇ _6alkylcarbonyl, Ar 1 ⁇ or
- R 2 is hydrogen, Ci_6alkyl, Ar 11 or Ar ⁇ -Ci- ⁇ alkyl
- Ar 1 to Ar are each independently selected from phenyl; or phenyl substituted with halo, C ⁇ _6alkyl, Ci- ⁇ alkyloxy or trifluoromethyl.
- WO-98/49157 concerns the preparation, formulation and pharmaceutical properties of farnesyl protein transferase inhibiting compounds of formula (VEH)
- R 1 and R 2 each independently are hydrogen, hydroxy, halo, cyano, C ⁇ _6alkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, C ⁇ _6alkyloxy, hydroxyC ⁇ _6alkyloxy,
- R3 and R 4 each independently are hydrogen, halo, cyano, Ci-6alkyl, Ci-6alkyloxy, A ⁇ oxy, C ⁇ _6alkylthio, di(Ci-6alkyl)amino, trihalomethyl or trihalomethoxy;
- R5 is hydrogen, halo, Ci-6alkyl, cyano, haloCi-6alkyl, hydroxyCi-6alkyl, cyanoCi-6alkyl, aminoC ⁇ _6alkyl, Ci-6alkyloxyCi-6alkyl, C i - alkylthioC l - ⁇ alkyl , aminocarbonylC i -6alkyl, C i _6alkyloxycarbonylC i -6alkyl, C i _6alkylcarbonyl-C i -6alkyl , Ci-6alkyloxycarbonyl, mono- or di(Ci-6alkyl)aminoCi-6alkyl, Ar 1 ,
- R 1 ⁇ is hydrogen, C ⁇ _6alkyl, C ⁇ _6alkylcarbonyl, Ar 1 , A ⁇ C ⁇ . ⁇ kyl,
- Ci-6alkyloxycarbonylCi-6alkyl or a radical of formula -Alk-OR 13 or -Alk-NR 14 R 15 ;
- R 1 1 is hydrogen, Ci-6alkyl, Ar 1 or A ⁇ Ci- ⁇ lkyl;
- R 12 is hydrogen, C ⁇ _6alkyl, Ci- ⁇ alkylcarbonyl, C ⁇ _6alkyloxycarbonyl, C ⁇ _6alkylaminocarbonyl, Ar 1 , A ⁇ Ci- ⁇ alkyl, Ci-6alkylcarbonyl-
- C ⁇ _6alkyl Aricarbonyl, AriCi- ⁇ alkylcarbonyl, aminocarbonyl- carbonyl, Ci-6alkyloxyC ⁇ _6alkylcarbonyl, hydroxy, Ci-6alkyloxy, aminocarbonyl, di(Ci-6alkyl)aminoCi-6alkylcarbonyl, amino, Ci-6alkylamino, Ci-6alkylcarbonylamino, or a radical or formula -Alk-OR 13 or -Alk-NR 14 R 15 ; wherein Alk is Ci- ⁇ alkanediyl;
- R 13 is hydrogen, C ⁇ _6alkyl, Ci-6alkylcarbonyl, hydroxy-
- R 14 is hydrogen, Ci-6alkyl, Ar 1 or AriCi- ⁇ alkyl
- R 1 ⁇ is hydrogen, Ci-6alkyl, C ⁇ _6alkylcarbonyl, Ar 1 or AriCi- ⁇ alkyl;
- R ⁇ is a radical of formula
- R ⁇ is hydrogen, halo, Ar 1 , C ⁇ _6alkyl, hydroxyC ⁇ _6alkyl, Ci-6alkyloxy- Ci-6alkyl, Ci-6alkyloxy, Ci-6alkylthio, amino, C ⁇ _6alkyloxycarbonyl, C ⁇ _6alkylthioCi-6alkyl,
- Ar 1 is phenyl; or phenyl substituted with 1 or 2 substituents each independently selected from halo, Ci-6alkyl, Ci-6alkyloxy or trifluoromethyl;
- Ar 2 is phenyl; or phenyl substituted with 1 or 2 substituents each independently selected from halo, C ⁇ _6alkyl, Ci- ⁇ alkyloxy or trifluoromethyl; and
- Het 1 is pyridinyl; pyridinyl substituted with 1 or 2 substituents each independently selected from halo, Ci- ⁇ alkyl, Ci-6alkyloxy or trifluoromethyl.
- each R 6 , R 7 and R 8 are independently hydrogen, C ⁇ -4 alkyl, hydroxy, C ⁇ -4 alkyloxy, aryloxy, C 1- alkyloxycarbonyl, hydroxyC ⁇ -4 alkyl, C 1-4 alkyloxy- C ⁇ - alkyl, mono- or di(C 1-4 alkyl)aminoC 1-4 alkyl, cyano, amino, thio, d. 4 alkyl- thio, arylthio or aryl; >Y'-Y 2 - is a trivalent radical of formula >CH-CHR 9 - (y-1),
- each R 9 independently is hydrogen, halo, halocarbonyl, aminocarbonyl, hydroxyC 1-4 alkyl, cyano, carboxyl, C ⁇ -4 alkyl, C ⁇ -4 alkyloxy, mono- or di(C ⁇ -4 alkyl)amino, mono- or di(C ⁇ - alkyl)aminoC 1-4 alkyl, aryl; r and s are each independently 0, 1, 2, 3, 4 or 5; t is O, 1, 2 or 3; each R 1 and R 2 are independently hydroxy, halo, cyano, Ci-6alkyl, trihalomethyl, trihalomethoxy, C 2-6 alkenyl, C ⁇ -6 alkyloxy, hydroxyd- ⁇ alkyloxy, C 1-6 alkylthio, C ⁇ ⁇ alkyloxyCu ⁇ alkyloxy, C 1-6 alkyloxycarbonyl, aminoC ⁇ alkyloxy, mono- or di(C 1-6
- R 3 is hydrogen, halo, C ⁇ -6 alkyl, cyano, haloC 1-6 alkyl, hydroxyC 1-6 alkyl, cyanod. alkyl, aminoC 1- alkyl, Ci- ⁇ alkyloxyd- ⁇ alkyl, C ⁇ -6 alkylthioC ⁇ -6 alkyl, aminocarbonylC 1-6 alkyl, hydroxycarbonyl, hydroxycarbonylC 1-6 alkyl, C 1 _ 6 alkyloxycarbonylC !
- R 10 is hydrogen, C ⁇ -6 alkyl, C ⁇ _ 6 alkylcarbonyl, aryl, arylC ⁇ - alkyl,
- R 11 is hydrogen, C ⁇ -6 alkyl, aryl or arylC ⁇ -6 alkyl
- R 12 is hydrogen, C]. 6 alkyl, aryl, hydroxy, amino, C ⁇ - alkyloxy,
- alkyloxyd. 6 alkylcarbonyl mono- or di(C 1-6 alkyl)aminocarbonyl wherein the alkyl moiety may optionally be substituted by one or more substituents independently selected from aryl or C 1-3 alkyloxycarbonyl, aminocarbonylcarbonyl, mono- or di(C 1-6 alkyl)aminoCi -6 alkylcarbonyl, or a radical or formula -Alk-OR 13 or -Alk-NR 1 R 15 ; wherein Alk is C ⁇ _ 6 alkanediyl;
- R 13 is hydrogen, C ⁇ -6 alkyl, C 1- alkylcarbonyl, hydroxyd ⁇ alkyl, aryl or arylC ⁇ -6 alkyl;
- R 14 is hydrogen, C 1-6 alkyl, aryl or arylC 1-6 alkyl
- R 15 is hydrogen, C 1- alkyl, C 1-6 alkylcarbonyl, aryl or arylC]. 6 alkyl
- R 4 is a radical of formula wherein R 16 is hydrogen, halo, aryl, C ⁇ . alkyl, hydroxyC ⁇ . 6 alkyl, C ⁇ - 6 alkyloxyC ⁇ . 6 alkyl, C]. 6 alkyloxy, C ⁇ -6 alkylthio, amino, mono- or di(C ⁇ -4 alkyl)amino, hydroxycarbonyl, C ⁇ -6 alkyloxycarbonyl, C ⁇ -6alkylthioC ⁇ _ 6 alkyl, C 1-6 alkylS(O)C ⁇ . 6 alkyl or C ⁇ -6 alkylS(O) 2 C ⁇ _ 6 alkyl;
- R 16 may also be bound to one of the nitrogen atoms in the imidazole ring of formula (c-1) or (c-2), in which case the meaning of R 16 when bound to the nitrogen is limited to hydrogen, aryl, C 1-6 alkyl, hydroxyd ⁇ alkyl, C 1-6 alkyloxyC 1-6 alkyl, C 1-6 alkyloxycarbonyl, C ]-6 alkylS(O)C ⁇ .6alkyl or C ⁇ . 6 alkylS(O) 2 C ⁇ -6 alkyl;
- R 17 is hydrogen, C 1- alkyl, C ⁇ . 6 alkyloxyd. 6 alkyl, arylC ⁇ _ 6 alkyl, trifluoromethyl or di(C ⁇ - alkyl)aminosulfonyl; R 5 is C]. 6 alkyl , C 1-6 alkyloxy or halo; aryl is phenyl, naphthalenyl or phenyl substituted with 1 or more substituents each independently selected from halo, C 1-6 alkyl, d_ 6 alkyloxy or trifluoromethyl.
- Anthracychne derivatives are important anti-tumor agents and comprise antibiotics obtained from the fungus Strep, Promotionicus var. caesius and their derivatives, characterised by having a tetracycline ring structure with an unusual sugar, daunosamine, attached by a glycosidic linkage.
- daunorubicin which has the chemical name 7-(3-amino-2,3,6- trideoxy-L-lyxohexosyloxy)-9-acetyl-7,8,9,10-tetrahydro-6,9,l l-trihydroxy-4-methoxy- 5,12-naphthacenequinone
- doxorubicin which has the chemical name 10-[(3-amino- 2,3,6-trideoxy-alphaL-lyxohexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,l l-trihydroxy- 8-(hydroxylacetyl)-l-methoxy-5,12-naphthacenedione
- idarubicin which has the chemical name 9-acetyl-7-[(3-amino-2,3,6-trideoxy-alphaL-lyxohexopyranosyl)oxy]
- Daunorubicin and idarubicin have been used primarily for the treatment of acute leukaemias whereas doxorubicin displays broader activity against human neoplasms, including a variety of solid tumors particularly breast cancer.
- anthracychne derivatives generally display a serious cardiomyopathy at higher doses, which limits the doses at which these compounds can be administered.
- R 9 is hydroxy, Ci-6alkyl, Ci- ⁇ alkyloxy, amino, Ci -Salkylamino or Ci-8alkylamino substituted with Ci-6alkyloxycarbonyl;
- R 2 , R 3 and R 1 ⁇ each independently are hydrogen, hydroxy, halo, cyano, Ci-6alkyl, C ⁇ _6alkyloxy, hydroxyC ⁇ _6alkyloxy, Ci-6alkyloxyCi-6alkyloxy, aminoCi- ⁇ alkyloxy, mono- or di(C ⁇ _6alkyl)aminoCi-6alkyloxy, Ar 1 , Ar 2 C ⁇ _6alkyl, Ar 2 oxy, Ar 2 Ci-6alkyloxy, hydroxycarbonyl,
- R 4 and R ⁇ each independently are hydrogen, halo, Ar 1 , C ⁇ _6alkyl, hydroxyCi-6alkyl, Ci-6alkyloxyCi-6alkyl , Ci-6alkyloxy, C ⁇ _6alkylthio, amino, hydroxycarbonyl, Ci _6alkyloxycarbonyl, C ⁇ _6alkylS(O)Ci-6alkyl or Ci-6alkylS(O)2Ci-6alkyl; R6 and R ⁇ each independently are hydrogen, halo, cyano, C ⁇ _6alkyl, C ⁇ _6alkyloxy, Ar 2 oxy, trihalomethyl, C ⁇ _6alkylthio, di(Ci-6alkyl)amino, or when on adjacent positions R ⁇ and R ⁇ taken together may form a bivalent radical of formula
- R8 is hydrogen, Ci-6alkyl, cyano, hydroxycarbonyl, Ci-6alkyloxycarbonyl, Ci- 6 alkyl- carbonylCi- ⁇ alkyl, cyanoC ⁇ _6alkyl, Ci-6alkyloxycarbonylCi-6alkyl, carboxy- Ci-6alkyl, hydroxyCi-6alkyl, aminoCi-6alkyl, mono- or di(C ⁇ _6alkyl)amino- Ci-6alkyl, imidazolyl, haloCi-6alkyl, Ci-6alkyloxyCi-6alkyl, aminocarbonyl- C ⁇ _6alkyl, or a radical of formula -O-RiO ( -1),
- R ⁇ is hydrogen, C ⁇ _6alkyl, Ci- ⁇ alkylcarbonyl, Ar 1 , Ar 2 Ci-6alkyl,
- Ci-6alkyloxycarbonylC ⁇ _6alkyl or a radical or formula -Alk 2 -OR 1 3 or -Alk 2 -NRl4Rl5 ;
- R ⁇ is hydrogen, C ⁇ _i2alkyl, Ar 1 or Ar Ci-6alkyl;
- R 2 is hydrogen, C ⁇ _6alkyl, Ci-i6alkylcarbonyl, Ci-6alkyloxycarbonyl,
- Ci-6alkylaminocarbonyl Ar 1 , Ar 2 C ⁇ _6alkyl, Ci-6alkylcarbonyl- C ⁇ _6alkyl, a natural amino acid, A ⁇ carbonyl, Ar 2 Ci-6alkylcarbonyl, aminocarbonylcarbonyl, C ⁇ _6alkyloxyC ⁇ _6alkylcarbonyl, hydroxy, C ⁇ _6alkyloxy, aminocarbonyl, d ⁇ (Ci-6alkyl)am ⁇ noCi-6alkylcarbonyl, amino, Ci-6alkylam ⁇ no, Ci- ⁇ alkylcarbonylamino, or a radical or formula -Alk 2 -OR 13 or -Alk ⁇ NR ⁇ R ⁇ , wherein Alk 2 is Ci-6alkaned ⁇ yl,
- R 13 ts hydrogen, C ⁇ _6alkyl, Ci-6alkylcarbonyl, hydroxy-
- Ci-6alkyl, Ar 1 or Ar 2 Ci-6alkyl, R 14 is hydrogen, Ci-6alkyl, Ar 1 or Ar 2 C ⁇ _ 6 alkyl, R ⁇ is hydrogen, Ci-6alkyl, C ⁇ _6alkylcarbonyl, Ar 1 or
- Ci_6alkyl R ⁇ is hydrogen, halo, cyano, C ⁇ _6alkyl, Ci-6alkyloxycarbonyl, Ar 1 , R ⁇ ts hydrogen, C ⁇ _6alkyl, C ⁇ _6alkyloxy or halo, R 19 is hydrogen or C ⁇ _ 6 alkyl, Ar 1 is phenyl or phenyl substituted with C ⁇ _6alkyl, hydroxy, ammo, Ci-6alkyloxy or halo, and Ar 2 is phenyl or phenyl substituted with Ci- alkyl, hydroxy, ammo, C ⁇ _6alkyloxy or halo
- combinations are hereinafter referred to as combinations according to the invention. These combinations may provide a synergistic effect whereby they demonstrate an advantageous therapeutic effect which is greater than that which would have been expected from the effects of the individual components of the combinations
- R 4 or R ⁇ may also be bound to one of the nitrogen atoms in the lmidazole nng In that case the hydrogen on the nitrogen is replaced by R 4 or R ⁇ and the meaning of R 4 and R ⁇ when bound to the nitrogen is limited to hydrogen, Ar 1 , Ci-6alkyl, hydroxyC ⁇ _6alkyl, Ci-6alkyloxyCi-6alkyl, C ⁇ _6alkyloxycarbonyl, Ci-6alkylS(O)Ci-6alkyl, Ci-6alkylS(O)2Ci-6alkyl
- substituent R 18 is situated on the 5 or 7 position of the qumolmone moiety and substituent R 19 is situated on the 8 position when R 18 is on the 7-pos ⁇ t ⁇ on
- Still another group of interesting compounds are those compounds of formula (I) wherein R 3 is hydrogen or halo; and R 2 is halo, Ci-6alkyl, C2-6alkenyl, C ⁇ _6alkyloxy, trihalomethoxy or hydroxyCi-6alkyloxy.
- a further group of interesting compounds are those compounds of formula (I) wherein R 2 and R 3 are on adjacent positions and taken together to form a bivalent radical of formula (a-1), (a-2) or (a-3).
- a still further group of interesting compounds are those compounds of formula (I) wherein R ⁇ is hydrogen and R 4 is hydrogen or Ci-6alkyl.
- a particular group of compounds are those compounds of formula (I) wherein R° is hydrogen, hydroxy, haloCi-6alkyl, hydroxyCi- ⁇ alkyl, cyanoC ⁇ _6alkyl, Ci-6alkyloxy- carbonylC ⁇ _6alkyl, imidazolyl, or a radical of formula -NR 1 !R 1 wherein R 1 ! ⁇ is hydrogen or Ci-i2alkyl and R 12 is hydrogen, C ⁇ _6alkyl, Ci-6alkyloxy, hydroxy, Ci-6alkyloxyCi-6alkylcarbonyl, or a radical of formula -Alk 2 -OR 1 3 wherein R 13 is hydrogen or C ⁇ _6alkyl.
- X'-X 2 -X 3 is a trivalent radical of formula (x-1), (x-2), (x-3), (x-4) or (x-9) wherein each R 6 independently is hydrogen, C 1-4 alkyl, C ⁇ -4 alkyloxycarbonyl, amino or aryl and R 7 is hydrogen;
- R 1 is halo, C ⁇ -6 alkyl or two R 1 substituents ortho to one another on the phenyl ring may independently form together a bivalent radical of formula (a-1);
- R 3 is halo or a radical of formula (b-1) or (b-3) wherein
- R 10 is hydrogen or a radical of formula -Alk-OR 13 .
- R 1 1 is hydrogen;
- R 12 is hydrogen, C ⁇ . 6 alkyl, d.6alkylcarbonyl, hydroxy, C ⁇ -6alkyloxy or mono- or di(C 1-6 alkyl)aminoC ⁇ -6 alkylcarbonyl;
- Alk is C 1-6 alkanediyl and R 13 is hydrogen;
- R 4 is a radical of formula (c-1) or (c-2) wherein
- R 16 is hydrogen, halo or mono- or di(C ⁇ -4 alkyl)amino
- R 17 is hydrogen or C 1-6 alkyl
- • aryl is phenyl.
- X -X -X is a trivalent radical of formula (x-2), (x-3) or (x-4), >Y1-Y2 is a trivalent radical of formula (y-2), (y-3) or (y-4), r and s are 1, t is 0, R 1 is halo, preferably chloro, and most preferably 3-chloro or R 1 is C ⁇ -4 alkyl, preferably 3-methyl, R 2 is halo, preferably chloro, and most preferably 4-chloro, R 3 is a radical of formula (b-1) or (b-3), R 4 is a radical of formula (c-2), R 6 is C 1- alkyl, R 9 is hydrogen, R 10 and R 11 are hydrogen and R 12 is hydrogen or hydroxy.
- the most preferred compounds of formula (IX) are 7-[(4-fluorophenyl)(lH-imidazol-l-yl)methyl]-5-phenylimidazo[l,2-a]quinoline; ⁇ -(4-chlorophenyl)- ⁇ -(l-methyl-lH-imidazol-5-yl)-5-phenylimidazo[l,2-a]quinoline-
- Ci-6alkyl defines straight and branched chained saturated hydrocarbon radicals having from 1 to 6 carbon atoms such as, for example, methyl, ethyl, propyl, butyl, pentyl, hexyl and the like;
- Ci-8alkyl encompasses the straight and branched chained saturated hydrocarbon radicals as defined in Ci- ⁇ alkyl as well as the higher homologues thereof containing 7 or 8 carbon atoms such as, for example heptyl or octyl;
- Ci-I2alkyl again encompasses Ci-8alkyl and the higher homologues thereof containing 9 to 12 carbon atoms, such as, for example, nonyl, decyl, undecyl, dodecyl;
- C ⁇ _i6alkyl again encompasses Ci-i2alkyl and the higher homologues thereof containing 13 to
- S(O) refers to a sulfoxide
- S(O)2 to a sulfon.
- natural amino acid refers to a natural amino acid that is bound via a covalent amide linkage formed by loss of a molecule of water between the carboxyl group of the amino acid and the amino group of the remainder of the molecule.
- Examples of natural amino acids are glycine, alanine, valine, leucine, isoleucine, methionine, proline, phenylanaline, tryptophan, serine, threonine, cysteine, tyrosine, asparagine, glutamine, aspartic acid, glutamic acid, lysine, arginine, histidine.
- the pharmaceutically acceptable acid or base addition salts as mentioned hereinabove are meant to comprise the therapeutically active non-toxic acid and non-toxic base addition salt forms which the compounds of formulas (I), (Et), (IE), (IV), (V), (VI), (V ⁇ ), (Nm) or (IX) are able to form.
- the compounds of formulas (I), (II), (HI), (IV), (V), (VI), (VII), (V ⁇ i) or (IX) which have basic properties can be converted in their pharmaceutically acceptable acid addition salts by treating said base form with an appropriate acid.
- Appropriate acids comprise, for example, inorganic acids such as hydrohalic acids, e.g.
- hydrochloric or hydrobromic acid sulfuric; nitric; phosphoric and the like acids; or organic acids such as, for example, acetic, propanoic, hydroxyacetic, lactic, pyruvic, oxalic, malonic, succinic (i.e. butanedioic acid), maleic, fumaric, malic, tartaric, citric, methanesulfonic, ethanesulfonic, benzenesulfonic, p-toluenesulfonic, cyclamic, salicylic, p-aminosalicylic, pamoic and the like acids.
- succinic i.e. butanedioic acid
- maleic fumaric, malic, tartaric, citric, methanesulfonic, ethanesulfonic, benzenesulfonic, p-toluenesulfonic, cyclamic, salicylic, p-aminosal
- the compounds of formulae (I), (II), (HI), (IV), (V), (VI), (VII), (VDI) or (IX) which have acidic properties may be converted in their pharmaceutically acceptable base addition salts by treating said acid form with a suitable organic or inorganic base.
- Appropriate base salt forms comprise, for example, the ammonium salts, the alkali and earth alkaline metal salts, e.g. the lithium, sodium, potassium, magnesium, calcium salts and the like, salts with organic bases, e.g. the benzathine, N-methyl-D-glucamine, hydrabamine salts, and salts with amino acids such as, for example, arginine, lysine and the like.
- acid or base addition salt also comprise the hydrates and the solvent addition forms which the compounds of formulae (I), (II), (m), (IV), (V), (VI), (VII), (VIII) or (IX) are able to form.
- Examples of such forms are e.g. hydrates, alcoholates and the like.
- stereochemically isomeric forms of compounds of formulae (I), (II), (III), (IV), (V), (VI), (VH), (VIE) or (IX), as used hereinbefore, defines all possible compounds made up of the same atoms bonded by the same sequence of bonds but having different three-dimensional structures which are not interchangeable, which the compounds of formulae (I), (II), (L ⁇ ), (TV), (V), (VI), (VII), (VIH) or (IX) may possess.
- the chemical designation of a compound encompasses the mixture of all possible stereochemically isomeric forms which said compound may possess. Said mixture may contain all diastereomers and/or enantiomers of the basic molecular structure of said compound.
- Preferred anti-tumor anthracychne derivatives for use in accordance with the invention include daunorubicin, doxorubicin and idarubicin referred to above.
- Daunorubicin is commercially available for example as the hydrochloride salt from Bedford Laboratories under the trade name Cerubidine, and may be prepared for example as described in patent specification No. 4020270, or by processes analogous thereto.
- Doxorubicin is commercially available for example as the hydrochloride salt from Astra, and may be prepared for example as described in U.S. patent specification No. 3803124 or by processes analogous thereto.
- Idarubicin is commercially available for example as the hydrochloride salt from Pharmacia & Upjohn under the trade name Idamycin, and may be prepared for example as described in U.S. patent specification No. 4046878 or by processes analogous thereto Other anti-tumor anthracychne derivatives may be prepared in conventional manner for example by processes analogous to those described above for daunorubicin, doxorubicin and idarubicin.
- the present invention also relates to combinations according to the invention for use in medical therapy for example for inhibiting the growth of tumor cells.
- the present invention also relates to the use of combinations according to the invention for the preparation of a pharmaceutical composition for inhibiting the growth of tumor cells.
- the present invention also relates to a method of inhibiting the growth of tumor cells in a human subject which comprises administering to the subject an effective amount of a combination according to the invention.
- This invention further provides a method for inhibiting the abnormal growth of cells, including transformed cells, by administering an effective amount of a combination according to the invention.
- Abnormal growth of cells refers to cell growth independent of normal regulatory mechanisms (e.g. loss of contact inhibition). This includes the abnormal growth of : (1) tumor cells (tumors) expressing an activated ras oncogene; (2) tumor cells in which the ras protein is activated as a result of oncogenic mutation of another gene; (3) benign and malignant cells of other proliferative diseases in which aberrant ras activation occurs.
- ras oncogenes not only contribute to the growth of of tumors in vivo by a direct effect on tumor cell growth but also indirectly, i.e. by facilitating tumor-induced angiogenesis (Rak. J. et al, Cancer Research, 55, 4575-4580, 1995).
- pharmacologically targetting mutant ras oncogenes could conceivably suppress solid tumor growth in vivo, in part, by inhibiting tumor-induced angiogenesis.
- This invention also provides a method for inhibiting tumor growth by administering an effective amount of a combination according to the present invention, to a subject, e.g. a mammal (and more particularly a human) in need of such treatment.
- this invention provides a method for inhibiting the growth of tumors expressing an activated ras oncogene by the administration of an effective amount of combination according to the present invention.
- tumors which may be inhibited include, but are not limited to, lung cancer (e.g. adenocarcinoma and including non- small celll lung cancer), pancreatic cancers (e.g. pancreatic carcinoma such as, for example exocrine pancreatic carcinoma), colon cancers (e.g.
- colorectal carcinomas such as, for example, colon adenocarcinoma and colon adenoma
- hematopoietic tumors of lymphoid lineage e.g. acute lymphocytic leukemia, B-cell lymphoma, Burkitt's lymphoma
- myeloid leukemias for example, acute myelogenous leukemia (AML)
- thyroid follicular cancer myelodysplastic syndrome (MDS)
- tumors of mesenchymal origin e.g. fibrosarcomas and rhabdomyosarcomas
- melanomas teratocarcinomas
- neuroblastomas gliomas
- gliomas benign tumor of the skin
- breast carcinoma e.g. advanced breast cancer
- kidney carninoma ovary carcinoma
- bladder carcinoma e.g. advanced breast cancer
- This invention also provides a method for inhibiting proliferative diseases, both benign and malignant, wherein ras proteins are aberrantly activated as a result of oncogenic mutation in genes, i.e. the ras gene itself is not activated by mutation to an oncogenic mutation to an oncogenic form, with said inhibition being accomplished by the administration of an effective amount of a combination according to the invention, to a subject in need of such a treatment.
- the benign proliferative disorder neurofibromatosis, or tumors in which ras is activated due to mutation or overexpression of tyrosine kinase oncogenes may be inhibited by the combinations according to the invention.
- the anti-tumor anthracychne derivative and the farnesyl transferase inhibitor may be administered simultaneously (e.g. in separate or unitary compositions) or sequentially in either order. In the latter case, the two compounds will be administered within a period and in an amount and manner that is sufficient to ensure that an advantageous or synergistic effect is achieved.
- the preferred method and order of administration and the respective dosage amounts and regimes for each component of the combination will depend on the particular anti-tumor anthracychne derivative and farnesyl transferase inhibitor being administered, their route of administration, the particular tumor being treated and the particular host being treated.
- the optimum method and order of administration and the dosage amounts and regime can be readily determined by those skilled in the art using conventional methods and in view of the information set out herein.
- the farnesyl transferase inhibitor is advantageously administered in an effective amount of from 0.0001 mg/kg to 100 mg/kg body weight, and in particular from 0.001 mg/kg to 10 mg/kg body weight. More particularly, for an adult patient, the dosage is conveniently in the range of 50 to 500mg bid, advantageously 100 to 400 mg bid and particularly 300mg bid.
- the anti-tumor anthracychne derivative is advantageously administered in a dosage of 10 to 75 mg per square meter (mg/m ) of body surface area, for example 15 to 60 mg/m 2 , particularly for doxorubicin in a dosage of about 40 to 75 mg/m 2 , for daunorubicin in a dosage of about 25 to 45mg/m 2 , and for idarubicin in a dosage of about 10 to 15 mg/m 2 per course of treatment.
- These dosages may be administered for example once, twice or more per course of treatment, which may be repeated for example every 7,14,21 or 28 days.
- the components of the combinations according to the invention i.e. the anti-tumor anthracychne derivative and the farnesyl transferase inhibitor may be formulated into various pharmaceutical forms for administration purposes.
- the components may formulated separately in individual pharmaceutical compositions or in a unitary pharmaceutical composition containing both components.
- Farnesyl protein transferase inhibitors can be prepared and formulated into pharmaceutical compositions by methods known in the art and in particular according to the methods described in the published patent specifications mentioned herein and incorporated by reference; for the compounds of formulae (I), (II) and (HI) suitable examples can be found in WO-97/21701.
- the present invention therefore also relates to a pharmaceutical composition
- a pharmaceutical composition comprising an anti-tumor anthracychne derivative and a farnesyl tranferase inhibitor of formula (I) together with one or more pharmaceutical carriers.
- an effective amount of a particular compound, in base or acid addition salt form, as the active ingredient is combined in intimate admixture with a pharmaceutically acceptable carrier, which carrier may take a wide variety of forms depending on the form of preparation desired for administration.
- a pharmaceutically acceptable carrier which carrier may take a wide variety of forms depending on the form of preparation desired for administration.
- These pharmaceutical compositions are desirably in unitary dosage form suitable, preferably, for administration orally, rectally, percutaneously, or by parenteral injection.
- any of the usual pharmaceutical media may be employed, such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as suspensions, syrups, elixirs and solutions; or solid carriers such as starches, sugars, kaolin, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules and tablets. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit form, in which case solid pharmaceutical carriers are obviously employed.
- the carrier will usually comprise sterile water, at least in large part, though other ingredients, to aid solubility for example, may be included.
- Injectable solutions may be prepared in which the carrier comprises saline solution, glucose solution or a mixture of saline and glucose solution. Injectable suspensions may also be prepared in which case appropriate liquid carriers, suspending agents and the like may be employed.
- the carrier optionally comprises a penetration enhancing agent and/or a suitable wetting agent, optionally combined with suitable additives of any nature in minor proportions, which additives do not cause a significant deleterious effect to the skin. Said additives may facilitate the administration to the skin and/or may be helpful for preparing the desired compositions.
- These compositions may be administered in various ways, e.g., as a transdermal patch, as a spot-on, as an ointment.
- Dosage unit form as used in the specification and claims herein refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier.
- dosage unit forms are tablets (including scored or coated tablets), capsules, pills, powder packets, wafers, injectable solutions or suspensions, teaspoonfuls, tablespoonfuls and the like, and segregated multiples thereof.
- each component of the combination may be administered as two, three, four or more sub-doses at appropriate intervals throughout the course of treatment
- Said sub-doses may be formulated as unit dosage forms, for example, in each case containing independently 0.01 to 500 mg, for example 0.1 to 200 mg and in particular 1 to lOOmg of each active ingredient per unit dosage form.
- the combinations according to the invention may be tested for their efficacy in inhibiting tumor growth using conventional assays described in the literature for example the HTB177 lung carcinoma described by Liu M et al, Cancer Research, Vol. 58, No.21, 1 November 1998, pages 4947-4956, and the anti-mitotic assay described by Moasser M et al, Proc. Natl. Acad. Sci. USA, Vol. 95, pages 1369-1374, February 1998.
- Other in vitro and in vivo models for determining ant-tumor effects of combinations and possible synergy of the combinations according to the invention are described in WO 98/54966 and WO 98/32114.
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Abstract
The present invention is concerned with combinations of a farnesyl transferase inhibitor and an anthracycline derivative for inhibiting the growth of tumor cells and useful in the treatment of cancer.
Description
FARNESYL PROTEIN TRANSFERASE INHIBITOR COMBINATIONS WITH ANTI-TUMOR ANTHRACYCLINE DERIVATIVES
The present invention is concerned with combinations of a farnesyl transferase inhibitor and an anti-tumor anthracychne derivative for inhibiting the growth of tumor cells, and useful in the treatment of cancer.
Oncogenes frequently encode protein components of signal transduction pathways which lead to stimulation of cell growth and mitogenesis. Oncogene expression in cultured cells leads to cellular transformation, characterized by the ability of cells to grow in soft agar and the growth of cells as dense foci lacking the contact inhibition exhibited by non-transformed cells. Mutation and/or overexpression of certain oncogenes is frequently associated with human cancer. A particular group of oncogenes is known as ras which have been identified in mammals, birds, insects, mollusks, plants, fungi and yeasts. The family of mammalian ras oncogenes consists of three major members ("isoforms") : H-ras, K-ras and N-ras oncogenes. These ras oncogenes code for highly related proteins generically known as p21ra5. Once attached to plasma membranes, the mutant or oncogenic forms of p21ra's will provide a signal for the transformation and uncontrolled growth of malignant tumor cells. To acquire this transforming potential, the precursor of the p21ra's oncoprotein must undergo an enzymatically catalyzed farnesylation of the cysteine residue located in a carboxyl- terminal tetrapeptide. Therefore, inhibitors of the enzyme that catalyzes this modification, farnesyl protein transferase, will prevent the membrane attachment of p21r ,s and block the aberrant growth of ras-transformed tumors. Hence, it is generally accepted in the art that farnesyl transferase inhibitors can be very useful as anticancer agents for tumors in which ras contributes to transformation.
Since mutated, oncogenic forms of ras are frequently found in many human cancers, most notably in more than 50 % of colon and pancreatic carcinomas (Kohl et al., Science, vol 260, 1834 - 1837, 1993), it has been suggested that farnesyl tranferase inhibitors can be very useful against these types of cancer. Following further investigations, it has been found that a farnesyl transferase inhibitor is capable of demonstrating antiproliferative effects in vitro and antitumor effects in vivo in a variety of human tumor cell lines with and without ras gene mutations
WO-97/21701 describes the preparation, formulation and pharmaceutical properties of farnesyl protein transferase inhibiting (imidazoly-5-yl)methyl-2-quinolinone derivatives
of formulas (I), (II) and (HI), as well as intermediates of formula (II) and (IE) that are metabolized in vivo to the compounds of formula (I). The compounds of formulas (I), (II) and (HI) are represented by
(I) (II)
(in) the pharmaceutically acceptable acid or base addition salts and the stereochemically isomeric forms thereof, wherein the dotted line represents an optional bond; X is oxygen or sulfur;
R! is hydrogen, Cι_i2alkyl, Ar , Ar^Ci-όalkyl, quinolinylCi-6alkyl, pyridylCi-6alkyl, hydroxyCi-6alkyl, Cι_6alkyloxyCi-6alkyl, mono- or di(Ci-6alkyl)aminoCi-6alkyl, aminoCi-6alkyl, or a radical of formula -Alk!-C(=O)-R9, -Alk!-S(O)-R9 or -Alk1-S(O)2-R9, wherein Alk^ is Ci-βalkanediyl,
R9 is hydroxy, Ci-6alkyl, Ci-6alkyloxy, amino, Ci-8alkylamino or Ci-8alkylamino substituted with Ci_6alkyloxycarbonyl;
R , R3 and R*6 each independently are hydrogen, hydroxy, halo, cyano, Cι_6alkyl, Cι_6alkyloxy, hydroxyCi-6alkyloxy, Cι_6alkyloxyCi-6alkyloxy, aminoCi-6alkyl- oxy, mono- or di(Cι_6alkyl)aminoCi-6alkyloxy, Ar1, Ar^Ci-βalkyl, Ar^oxy,
Ar^Ci-galkyloxy, hydroxycarbonyl, Ci-6alkyloxycarbonyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, 4,4-dimethyloxazolyl; or when on adjacent positions R^ and R^ taken together may form a bivalent radical of formula
-O-CH2-O- (a-1),
-O-CH2-CH2-O- (a-2),
-O-CH=CH- (a-3),
-O-CH2-CH2- (a-4), -O-CH2-CH2-CH2- (a-5), or
-CH=CH-CH=CH- (a-6); R4 and R^ each independently are hydrogen, halo, Ar , Cι_6alkyl, hydroxyCi-galkyl, Ci-6alkyloxyCι_6alkyl, Cι_6alkyloxy, Cι_6alkylthio, amino, hydroxycarbonyl, Ci -όalkyloxycarbonyl, Ci-6alkylS(O)Ci-6alkyl or Ci-6alkylS(O)2Ci -6alkyl; R6 and R^ each independently are hydrogen, halo, cyano, Ci^alkyl, Ci-βalkyloxy,
Ar2oxy, trihalomethyl, Ci-6alkylthιo, di(Cι_6alkyl)amino, or when on adjacent positions R^ and R^ taken together may form a bivalent radical of formula
-O-CH2-O- (c-1), or -CH=CH-CH=CH- (c-2);
R^ is hydrogen, Cι_6alkyl, cyano, hydroxycarbonyl, Cι_6alkyloxycarbonyl,
C 1 -όalkylcarbonylC 1 -6alkyl, cyanoC 1 __6alkyl, C 1 _6alkyloxycarbonylC 1 _6alkyl, carboxyCι_6alkyl, hydroxyCι_6alkyl, aminoCi-6alkyl, mono- or di(Cι_6alkyl)- aminoCi-6alkyl, imidazolyl, haloCi-6alkyl, Cι_6alkyloxyCi-6alkyl, aminocarbonylCi-6alkyl, or a radical of formula
_O-Rl0 (b-1),
_S-Rl0 (b-2),
_N_R11R12 (b-3), wherein R 0 is hydrogen, Ci-6alkyl, Ci-6alkylcarbonyl, Ar1, Ar2Ci-6alkyl, Ci-6alkyloxycarbonylCi-6alkyl, or a radical or formula -Alk2-ORl3 or -Alk -NR14R15;
RU is hydrogen, Cι_i2alkyl, Ar* or Ar2Cι_6alkyl;
Rl2 1S hydrogen, Ci-6alkyl, Cι_i6alkylcarbonyl, Cι_6alkyloxycarbonyl, Ci-6alkylaminocarbonyl, AJI , Ar2Ci-6alkyl, Cι_6alkylcarbonyl- Ci-6alkyl, a natural amino acid, Arlcarbonyl, Ar2Ci-6alkylcarbonyl, aminocarbonylcarbonyl, Ci-6alkyloxyCi-6alkylcarbonyl, hydroxy, Cι_6alkyloxy, aminocarbonyl, di(Cι_6alkyl)aminoCi-6alkylcarbonyl, amino, Ci-6alkylamino, Ci-6alkylcarbonylamino, or a radical or formula -Alk2-OR13 or -Alk -NR14R15; wherein Alk2 is Ci-6alkanediyl;
Rl3 is hydrogen, Cι_6alkyl, Ci-6alkylcarbonyl, hydroxy-
Cι_6alkyl, Ar1 or Ar2Ci-6alkyl; R14 is hydrogen, Ci_6alkyl, Ar1 or Ar2Ci-6alkyl;
Rl5 is hydrogen, Cι_6alkyl, Cι_6alkylcarbonyl, Ar or Ar2Cι_6alkyl; Rl7 is hydrogen, halo, cyano, Ci-6alkyl, Cι_6alkyloxycarbonyl, Arl; R1^ is hydrogen, Cι_6alkyl, Ci-6alkyloxy or halo; R!9 is hydrogen or Ci-6alkyl; Ar^ is phenyl or phenyl substituted with Ci-6alkyl, hydroxy, amino, Cι_6alkyloxy or halo; and Ar2 is phenyl or phenyl substituted with Ci-6alkyl, hydroxy, amino, Cι_6alkyloxy or halo.
WO-97/16443 concerns the preparation, formulation and pharmaceutical properties of farnesyl protein transferase inhibiting compounds of formula (IV), as well as intermediates of formula (V) and (VI) that are metabolized in vivo to the compounds of formula (IV). The compounds of formulas (IV), (V) and (VI) are represented by
(IV) (V)
(VI) the pharmaceutically acceptable acid or base addition salts and the stereochemically isomeric forms thereof, wherein the dotted line represents an optional bond; X is oxygen or sulfur;
R1 is hydrogen, Ci-i2alkyl, Ar1, Ar Ci-6alkyl, quinolinylCi-6alkyl, pyridyl- Ci-6alkyl, hydroxyCi-6alkyl, Ci-6alkyloxyCι_6alkyl, mono- or di(Cι_6alkyl)-
aminoCι_6alkyl, aminoCi-6alkyl, or a radical of formula -Alk!-C(=O)-R9, -Alk!-S(O)-R9 or -Alk1-S(O)2-R9, wherein Alk1 is Ci-βalkanediyl,
R9 is hydroxy, Ci-6alkyl, Cι_6alkyloxy, amino, Ci-8alkylamino or Ci-8alkylamino substituted with Cι_6alkyloxycarbonyl;
R2 and R3 each independently are hydrogen, hydroxy, halo, cyano, Ci-6alkyl, Ci-6alkyloxy, hydroxyCι_6alkyloxy, Cι_6alkyloxyCi-6alkyloxy, amino- Cι_6alkyloxy, mono- or di(Ci-6alkyl)aminoCi-6alkyloxy, Ar1, Ar2Cι_6alkyl, Ar2oxy, Ar2Cι_6alkyloxy, hydroxycarbonyl, Cι_6alkyloxycarbonyl, trihalomethyl, trihalomethoxy, C2-6alkenyl; or when on adjacent positions R2 and R3 taken together may form a bivalent radical of formula
-O-CH2-O- (a-1),
-O-CH2-CH2-O- (a-2), -O-CH=CH- (a-3),
-O-CH2-CH2- (a-4),
-O-CH2-CH2-CH2- (a-5), or -CH=CH-CH=CH- (a-6); R4 and R5 each independently are hydrogen, Ar1, Cι-6alkyl, Cι- alkyloxyCι_6alkyl, C1-6alkyloxy, C1- alkylthio, amino, hydroxycarbonyl, Cι-6alkyloxycarbonyl,
Cι-6alkylS(O)C1-6alkyl or C1-6alkylS(O)2C1-6alkyl; R6 and R^ each independently are hydrogen, halo, cyano, Cι_6alkyl, Cι_6alkyloxy or
Ar2oxy; R& is hydrogen, Ci-6alkyl, cyano, hydroxycarbonyl, Ci-6alkyloxycarbonyl, Cι_6alkyl- carbonylCι_6alkyl, cyanoCι_6alkyl, Ci-6alkyloxycarbonylCi-6alkyl, hydroxy- carbonylCi-βalkyl, hydroxyCi-6alkyl, aminoCι_6alkyl, mono- or di(Cι_6alkyl)- aminoCi-6alkyl, haloCi-6alkyl, Ci-6alkyloxyCi-6alkyl, aminocarbonylCi-6alkyl, Ar1, Ar2Ci-6alkyloxyCi-6alkyl, Ci-6alkylthioCi-6alkyl; R ^ is hydrogen, Ci-6alkyl, Ci-6alkyloxy or halo; R 1 is hydrogen or Ci-6alkyl;
Ar1 is phenyl or phenyl substituted with Cι_6alkyl, hydroxy, amino, -όalkyloxy or halo; Ar2 is phenyl or phenyl substituted with Cι_6alkyl, hydroxy, amino, Cι_6alkyloxy or halo.
WO-98/40383 concerns the preparation, formulation and pharmaceutical properties of farnesyl protein transferase inhibiting compounds of formula (VH)
the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof, wherein
the dotted line represents an optional bond; X is oxygen or sulfur; -A- is a bivalent radical of formula -CH=CH- (a-1), -CH2-S- (a-6), -CH2-CH2- (a-2), -CH2-CH2-S- (a-7),
-CH2-CH2-CH2- (a-3), -CH=N- (a-8), -CH2-O- (a-4), -N=N- (a-9), or
-CH2-CH2-O- (a-5), -CO-NH- (a-10); wherein optionally one hydrogen atom may be replaced by Ci-4alkyl or Ar1; R1 and R2 each independently are hydrogen, hydroxy, halo, cyano, Ci-6alkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, Cι_6alkyloxy, hydroxyCi-6alkyloxy, Cι_6alkyloxyCi-6alkyloxy, Ci-βalkyloxycarbonyl, aminoCi-6alkyloxy, mono- or di(Ci-6alkyl)aminoCι_-6alkyloxy, Ar2, Ar2-Ci-6alkyl, Ar2-oxy, Ar2-Cι_6alkyloxy; or when on adjacent positions R and R2 taken together may form a bivalent radical of formula
-O-CH2-O- (b-1),
-O-CH2-CH2-O- (b-2),
-O-CH=CH- (b-3),
-O-CH2-CH2- (b-4), -O-CH2-CH2-CH2- (b-5), or
-CH=CH-CH=CH- (b-6);
R3 and R4 each independently are hydrogen, halo, cyano, Ci-6alkyl, Ci-6alkyloxy, Ar^-oxy, Cι_6alkylthio, di(Ci-6alkyl)amino, trihalomethyl, trihalomethoxy, or when on adjacent positions R3 and R4 taken together may form a bivalent radical of formula
-O-CH2-O- (c-1),
-O-CH2-CH2-O- (c-2), or
-CH=CH-CH=CH- (c-3);
R5 is a radical of formula
C i -6alkyloxycarbonylC i _6alkyl, C i -6alkylcarbonyl-C i -6alkyl , Ci-6alkyloxycarbonyl, mono- or di(Ci-6alkyl)aminoCi-6alkyl, Ar\ Ar5-Cι_6alkyloxyCi-6alkyl; or a radical of formula -O-R7 (e-1), -S-R7 (e-2),
-N-R8R9 (e-3), wherein
Ci-6alkyloxycarbonylCι_6alkyl, or a radical of formula -Alk-OR1^ or -Alk-NR^R12; R8 is hydrogen, Cι_6alkyl, Ar or Ar^-Ci-όalkyl;
R9 is hydrogen, Ci-6alkyl, Cι_6alkylcarbonyl, Ci-6alkyloxycarbonyl, Cι_6alkylaminocarbonyl, Ar^, Ar^-Ci-όalkyl, Cι_6alkylcarbonyl- Ci-6alkyl, Ar^-carbonyl, Ar^-Ci-όalkylcarbonyl, aminocarbonyl- carbonyl, Ci-6alkyloxyCi-6alkylcarbonyl, hydroxy, Ci-6alkyloxy, aminocarbonyl, di(Ci-6alkyl)aminoCi-6alkylcarbonyl, amino,
Ci-6alkylamino, Ci-βalkylcarbonylamino, or a radical or formula -Alk-OR10 or -Alk-NR1 iR12; wherein Alk is Cι_6alkanediyl;
R ^ is hydrogen, Ci-βalkyl, Ci-6alkylcarbonyl, hydroxyCi-6alkyl, Ar9 or Ar9-Cι_6alkyl;
R1 is hydrogen, Cχ-6alkyl, Cι_6alkylcarbonyl, Ar1^ or
Ar10-Cι_6alkyl;
R 2 is hydrogen, Ci_6alkyl, Ar11 or Ar^-Ci-όalkyl; and
Ar1 to Ar are each independently selected from phenyl; or phenyl substituted with halo, Cι_6alkyl, Ci-βalkyloxy or trifluoromethyl.
WO-98/49157 concerns the preparation, formulation and pharmaceutical properties of farnesyl protein transferase inhibiting compounds of formula (VEH)
R1 and R2 each independently are hydrogen, hydroxy, halo, cyano, Cι_6alkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, Cι_6alkyloxy, hydroxyCι_6alkyloxy,
Ci-6alkyloxyCι_6alkyloxy, Ci-6alkyloxycarbonyl, aminoCι_6alkyloxy, mono- or di(Ci-6alkyl)aminoCi-6alkyloxy, Ar1, A^Ci- alkyl, A^oxy or AriCi-όalkyloxy; R3 and R4 each independently are hydrogen, halo, cyano, Ci-6alkyl, Ci-6alkyloxy, A^oxy, Cι_6alkylthio, di(Ci-6alkyl)amino, trihalomethyl or trihalomethoxy;
R5 is hydrogen, halo, Ci-6alkyl, cyano, haloCi-6alkyl, hydroxyCi-6alkyl, cyanoCi-6alkyl, aminoCι_6alkyl, Ci-6alkyloxyCi-6alkyl, C i - alkylthioC l -βalkyl , aminocarbonylC i -6alkyl, C i _6alkyloxycarbonylC i -6alkyl, C i _6alkylcarbonyl-C i -6alkyl , Ci-6alkyloxycarbonyl, mono- or di(Ci-6alkyl)aminoCi-6alkyl, Ar1,
Ar^i-όalkyloxyCi-όalkyl; or a radical of formula _O-Rl0 (a-1),
_S.RlO (a-2),
-N-Rl lRl2 (a-3), wherein R1^ is hydrogen, Cι_6alkyl, Cι_6alkylcarbonyl, Ar1, Aτ^C\.β∑άkyl,
Ci-6alkyloxycarbonylCi-6alkyl, or a radical of formula -Alk-OR13 or -Alk-NR14R15; R1 1 is hydrogen, Ci-6alkyl, Ar1 or A^Ci-ό lkyl; R12 is hydrogen, Cι_6alkyl, Ci-βalkylcarbonyl, Cι_6alkyloxycarbonyl, Cι_6alkylaminocarbonyl, Ar1, A^Ci-όalkyl, Ci-6alkylcarbonyl-
Cι_6alkyl, Aricarbonyl, AriCi-όalkylcarbonyl, aminocarbonyl-
carbonyl, Ci-6alkyloxyCι_6alkylcarbonyl, hydroxy, Ci-6alkyloxy, aminocarbonyl, di(Ci-6alkyl)aminoCi-6alkylcarbonyl, amino, Ci-6alkylamino, Ci-6alkylcarbonylamino, or a radical or formula -Alk-OR13 or -Alk-NR14R15; wherein Alk is Ci-βalkanediyl;
R13 is hydrogen, Cι_6alkyl, Ci-6alkylcarbonyl, hydroxy-
Ci_6alkyl, Ar1 or AriCi-όalkyl;
R14 is hydrogen, Ci-6alkyl, Ar1 or AriCi-όalkyl;
R1^ is hydrogen, Ci-6alkyl, Cι_6alkylcarbonyl, Ar1 or AriCi-όalkyl;
R^ is a radical of formula
Ci-6alkylS(O)Ci-6alkyl or Ci-6alkylS(O)2Ci -6alkyl; R^is hydrogen, Ci-6alkyl or di(Cι_4alkyl)aminosulfonyl; R7 is hydrogen or Cι_6alkyl provided that the dotted line does not represent a bond; R8 is hydrogen, Ci-6alkyl or Ar2CH2 or Het1CH2; R9 is hydrogen, Ci-6alkyl , Cχ-6alkyloxy or halo; or
R8 and R9 taken together to form a bivalent radical of formula -CH=CH- (c-1),
-CH2-CH2- (c-2),
-CH2-CH2-CH2- (c-3), -CH2-O- (c-4), or
-CH2-CH2-O- (c-5);
Ar1 is phenyl; or phenyl substituted with 1 or 2 substituents each independently selected from halo, Ci-6alkyl, Ci-6alkyloxy or trifluoromethyl;
Ar2 is phenyl; or phenyl substituted with 1 or 2 substituents each independently selected from halo, Cι_6alkyl, Ci-βalkyloxy or trifluoromethyl; and
Het1 is pyridinyl; pyridinyl substituted with 1 or 2 substituents each independently selected from halo, Ci-βalkyl, Ci-6alkyloxy or trifluoromethyl.
WO-00/39082 concerns the preparation, formulation and pharmaceutical properties of farnesyl protein transferase inhibiting compounds of formula (IX)
or the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof, wherein =X1-X2-X3- is a trivalent radical of formula
=N-CR6=CR7- (x-1), =CR6-CR7=CR8- (x-6),
N-N=CR - ( (xx--22)),, =CR6-N=CR7- (x-7),
N-NH-C(=O)- (x-3), =CR -NH-C(=O)- (x-8), or
:N-N=N- (χ-4), =CR6-N=N- (x-9);
:N-CR6=N- (x-5), wherein each R6, R7 and R8 are independently hydrogen, Cι-4alkyl, hydroxy, Cι-4alkyloxy, aryloxy, C1- alkyloxycarbonyl, hydroxyCι-4alkyl, C1-4alkyloxy- Cι- alkyl, mono- or di(C1-4alkyl)aminoC1-4alkyl, cyano, amino, thio, d.4alkyl- thio, arylthio or aryl; >Y'-Y2- is a trivalent radical of formula >CH-CHR9- (y-1),
>C=N- (y-2),
>CH-NR9- (y-3),or
>C=CR9- (y-4); wherein each R9 independently is hydrogen, halo, halocarbonyl, aminocarbonyl, hydroxyC1-4alkyl, cyano, carboxyl, Cι-4alkyl, Cι-4alkyloxy,
mono- or di(Cι-4alkyl)amino, mono- or di(Cι- alkyl)aminoC1-4alkyl, aryl; r and s are each independently 0, 1, 2, 3, 4 or 5; t is O, 1, 2 or 3; each R1 and R2 are independently hydroxy, halo, cyano, Ci-6alkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, Cι-6alkyloxy, hydroxyd-όalkyloxy, C1-6alkylthio, C^όalkyloxyCuόalkyloxy, C1-6alkyloxycarbonyl, aminoC^alkyloxy, mono- or di(C1-6alkyl)amino, mono- or di(C1- alkyl)aminoC].6alkyloxy, aryl, arylCι-6alkyl, aryloxy or arylC1- alkyloxy, hydroxycarbonyl, C1-6alkyloxycarbonyl, aminocarbonyl, aminoC1-6alkyl, mono- or di(C1- alkyl)aminocarbonyl, mono- or di(Cι-6alkyl)aminoC1-6alkyl; or
two R or R substituents adjacent to one another on the phenyl ring may independently form together a bivalent radical of formula
-O-CH2-O- (a-1),
-O-CH2-CH2-O- (a-2), -O=CH=CH- (a-3),
-O-CH2-CH2- (a-4),
-O-CH2-CH2- CH2- (a-5), or -CH=CH-CH=CH- (a-6); R3 is hydrogen, halo, Cι-6alkyl, cyano, haloC1-6alkyl, hydroxyC1-6alkyl, cyanod. alkyl, aminoC1- alkyl, Ci-όalkyloxyd-όalkyl, Cι-6alkylthioCι-6alkyl, aminocarbonylC1-6alkyl, hydroxycarbonyl, hydroxycarbonylC1-6alkyl, C 1 _6alkyloxycarbonylC ! -6alkyl , C 1 - alkylcarbonylC 1-6alkyl, C 1 - alkyloxycarbonyl, aryl, arylCι_6alkyloxyCι_6alkyl, mono- or di(Cι.6alkyl)aminoCι.6alkyl; or a radical of formula -O-R10 (b-D,
-S-R10 (b-2),
-NRnR12 (b-3), wherein R10 is hydrogen, Cι-6alkyl, Cι_6alkylcarbonyl, aryl, arylCι- alkyl,
Cι-6alkyloxycarbonylCι.6alkyl, or a radical of formula -Alk-OR13 or -Alk-NRI4R15;
R11 is hydrogen, Cι-6alkyl, aryl or arylCι-6alkyl;
R12 is hydrogen, C].6alkyl, aryl, hydroxy, amino, Cι- alkyloxy,
Cι-6alkylcarbonylC1-6alkyl, arylC1-6alkyl, Ci-όalkylcarbonylamino, mono- or di(C1-6alkyl)amino, Cι-6alkylcarbonyl, aminocarbonyl, arylcarbonyl, haloC1-6alkylcarbonyl, arylCι-6alkylcarbonyl, C1-6alkyloxycarbonyl,
Cι.6alkyloxyd.6alkylcarbonyl, mono- or di(C1-6alkyl)aminocarbonyl wherein the alkyl moiety may optionally be substituted by one or more substituents independently selected from aryl or C1-3alkyloxycarbonyl, aminocarbonylcarbonyl, mono- or di(C1-6alkyl)aminoCi-6alkylcarbonyl, or a radical or formula -Alk-OR13 or -Alk-NR1 R15; wherein Alk is Cι_6alkanediyl;
R13 is hydrogen, Cι-6alkyl, C1- alkylcarbonyl, hydroxyd^alkyl, aryl or arylCι-6alkyl;
R14 is hydrogen, C1-6alkyl, aryl or arylC1-6alkyl; R15 is hydrogen, C1- alkyl, C1-6alkylcarbonyl, aryl or arylC].6alkyl;
R4 is a radical of formula
wherein R16 is hydrogen, halo, aryl, Cι. alkyl, hydroxyCι.6alkyl, Cι-6alkyloxyCι.6alkyl, C].6alkyloxy, Cι-6alkylthio, amino, mono- or di(Cι-4alkyl)amino, hydroxycarbonyl, Cι-6alkyloxycarbonyl, Cι-6alkylthioCι_6alkyl, C1-6alkylS(O)Cι.6alkyl or Cι-6alkylS(O)2Cι_6alkyl;
R16 may also be bound to one of the nitrogen atoms in the imidazole ring of formula (c-1) or (c-2), in which case the meaning of R16 when bound to the nitrogen is limited to hydrogen, aryl, C1-6alkyl, hydroxyd^alkyl, C1-6alkyloxyC1-6alkyl, C1-6alkyloxycarbonyl, C]-6alkylS(O)Cι.6alkyl or Cι.6alkylS(O)2Cι-6alkyl;
R17 is hydrogen, C1- alkyl, Cι.6alkyloxyd.6alkyl, arylCι_6alkyl, trifluoromethyl or di(Cι- alkyl)aminosulfonyl; R5 is C].6alkyl , C1-6alkyloxy or halo; aryl is phenyl, naphthalenyl or phenyl substituted with 1 or more substituents each independently selected from halo, C1-6alkyl, d_6alkyloxy or trifluoromethyl.
Anthracychne derivatives are important anti-tumor agents and comprise antibiotics obtained from the fungus Strep, peuticus var. caesius and their derivatives, characterised by having a tetracycline ring structure with an unusual sugar, daunosamine, attached by a glycosidic linkage. Among these compounds, the most widely used include daunorubicin, which has the chemical name 7-(3-amino-2,3,6- trideoxy-L-lyxohexosyloxy)-9-acetyl-7,8,9,10-tetrahydro-6,9,l l-trihydroxy-4-methoxy- 5,12-naphthacenequinone, doxorubicin, which has the chemical name 10-[(3-amino- 2,3,6-trideoxy-alphaL-lyxohexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,l l-trihydroxy- 8-(hydroxylacetyl)-l-methoxy-5,12-naphthacenedione, and idarubicin, which has the chemical name 9-acetyl-7-[(3-amino-2,3,6-trideoxy-alphaL-lyxohexopyranosyl)oxy]- 7,8,9, 10-tetrahydro-6,9, 1 l-trihydroxy-5,12-naphthacenedione. Daunorubicin and idarubicin have been used primarily for the treatment of acute leukaemias whereas doxorubicin displays broader activity against human neoplasms, including a variety of solid tumors particularly breast cancer. However, anthracychne derivatives generally display a serious cardiomyopathy at higher doses, which limits the doses at which these compounds can be administered.
There is therefore a need to increase the inhibitory efficacy of anti-tumor anthracychne derivatives against tumor growth and also to provide a means for the use of lower dosages of anti-tumor anthracychne derivatives to reduce the potential of adverse toxic
side effects to the patient.
It is an object of the invention to provide a therapeutic combination of an anti-tumor anthracychne derivative and a farnesyl transferase inhibitor of the type described above which has an advantageous inhibitory effect against tumor cell growth, in comparison with the respective effects shown by the individual components of the combination.
According to the invention therefore we provide a combination of an anti-tumor anthracychne derivative and a farnesyl transferase inhibitor of formula (I), (II), (III), (IV), (V), (VI), (Vπ), (VIE) or (IX) above, in particular a compound of formula (I), (II) or (HI):
(D (ID
(πi) the pharmaceutically acceptable acid or base addition salts and the stereochemically isomeric forms thereof, wherein the dotted line represents an optional bond; X is oxygen or sulfur;
R is hydrogen, Ci-i2alkyl, Ar1, Ar2Cι_6alkyl, quinolinylCi-6alkyl, pyridyl- Ci-6alkyl, hydroxyCi-6alkyl, Ci-6alkyloxyCi-6alkyl, mono- or di(Ci-6alkyl)aminoCi-6alkyl, aminoCi-βalkyl, or a radical of formula -Alk1-C(=O)-R9, -Alk1-S(O)-R9 or -Alk1-S(O)2-R9, wherein Alk1 is Ci-6alkanediyl,
R9 is hydroxy, Ci-6alkyl, Ci-βalkyloxy, amino, Ci -Salkylamino or
Ci-8alkylamino substituted with Ci-6alkyloxycarbonyl; R2, R3 and R1^ each independently are hydrogen, hydroxy, halo, cyano, Ci-6alkyl, Cι_6alkyloxy, hydroxyCι_6alkyloxy, Ci-6alkyloxyCi-6alkyloxy, aminoCi-όalkyloxy, mono- or di(Cι_6alkyl)aminoCi-6alkyloxy, Ar1, Ar2Cι_6alkyl, Ar2oxy, Ar2Ci-6alkyloxy, hydroxycarbonyl,
Cι_6alkyloxycarbonyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, 4,4- dimethyloxazolyl; or when on adjacent positions R2 and R3 taken together may form a bivalent radical of formula -O-CH2-O- (a-1),
-O-CH2-CH2-O- (a-2),
-O-CH=CH- (a-3),
-O-CH2-CH2- (a-4),
-O-CH2-CH2-CH2- (a-5), or -CH=CH-CH=CH- (a-6);
R4 and R^ each independently are hydrogen, halo, Ar1, Cι_6alkyl, hydroxyCi-6alkyl, Ci-6alkyloxyCi-6alkyl , Ci-6alkyloxy, Cι_6alkylthio, amino, hydroxycarbonyl, Ci _6alkyloxycarbonyl, Cι _6alkylS(O)Ci-6alkyl or Ci-6alkylS(O)2Ci-6alkyl; R6 and R^ each independently are hydrogen, halo, cyano, Cι_6alkyl, Cι_6alkyloxy, Ar2oxy, trihalomethyl, Cι_6alkylthio, di(Ci-6alkyl)amino, or when on adjacent positions R^ and R^ taken together may form a bivalent radical of formula
-O-CH2-O- (c-1), or
-CH=CH-CH=CH- (c-2); R8 is hydrogen, Ci-6alkyl, cyano, hydroxycarbonyl, Ci-6alkyloxycarbonyl, Ci-6alkyl- carbonylCi-όalkyl, cyanoCι_6alkyl, Ci-6alkyloxycarbonylCi-6alkyl, carboxy- Ci-6alkyl, hydroxyCi-6alkyl, aminoCi-6alkyl, mono- or di(Cι_6alkyl)amino- Ci-6alkyl, imidazolyl, haloCi-6alkyl, Ci-6alkyloxyCi-6alkyl, aminocarbonyl- Cι_6alkyl, or a radical of formula -O-RiO ( -1),
-S-RlO (b-2),
.N.R11R12 (b-3), wherein R^is hydrogen, Cι_6alkyl, Ci-βalkylcarbonyl, Ar1, Ar2Ci-6alkyl,
Ci-6alkyloxycarbonylCι_6alkyl, or a radical or formula -Alk2-OR13 or -Alk2-NRl4Rl5;
R^ is hydrogen, Cι_i2alkyl, Ar1 or Ar Ci-6alkyl;
R 2is hydrogen, Cι_6alkyl, Ci-i6alkylcarbonyl, Ci-6alkyloxycarbonyl,
Ci-6alkylaminocarbonyl, Ar1, Ar2Cι_6alkyl, Ci-6alkylcarbonyl-
Cι_6alkyl, a natural amino acid, A^carbonyl, Ar2Ci-6alkylcarbonyl, aminocarbonylcarbonyl, Cι_6alkyloxyCι_6alkylcarbonyl, hydroxy, Cι_6alkyloxy, aminocarbonyl, dι(Ci-6alkyl)amιnoCi-6alkylcarbonyl, amino, Ci-6alkylamιno, Ci-βalkylcarbonylamino, or a radical or formula -Alk2-OR13 or -Alk^NR^R^, wherein Alk2 is Ci-6alkanedιyl,
R13 ts hydrogen, Cι_6alkyl, Ci-6alkylcarbonyl, hydroxy-
Ci-6alkyl, Ar1 or Ar2Ci-6alkyl, R14 is hydrogen, Ci-6alkyl, Ar1 or Ar2Cι_6alkyl, R ^ is hydrogen, Ci-6alkyl, Cι_6alkylcarbonyl, Ar1 or
Ar2Ci_6alkyl, R^is hydrogen, halo, cyano, Cι_6alkyl, Ci-6alkyloxycarbonyl, Ar1, R^ts hydrogen, Cι_6alkyl, Cι_6alkyloxy or halo, R19 is hydrogen or Cι_6alkyl, Ar1 is phenyl or phenyl substituted with Cι_6alkyl, hydroxy, ammo, Ci-6alkyloxy or halo, and Ar2 is phenyl or phenyl substituted with Ci- alkyl, hydroxy, ammo, Cι_6alkyloxy or halo
The above descπbed combinations are hereinafter referred to as combinations according to the invention. These combinations may provide a synergistic effect whereby they demonstrate an advantageous therapeutic effect which is greater than that which would have been expected from the effects of the individual components of the combinations
In Formulas (I), (II) and (EH), R4 or R^ may also be bound to one of the nitrogen atoms in the lmidazole nng In that case the hydrogen on the nitrogen is replaced by R4 or R^ and the meaning of R4 and R^ when bound to the nitrogen is limited to hydrogen, Ar1, Ci-6alkyl, hydroxyCι_6alkyl, Ci-6alkyloxyCi-6alkyl, Cι_6alkyloxycarbonyl, Ci-6alkylS(O)Ci-6alkyl, Ci-6alkylS(O)2Ci-6alkyl
Preferably the substituent R18 is situated on the 5 or 7 position of the qumolmone moiety and substituent R19 is situated on the 8 position when R18 is on the 7-posιtιon
Interesting compounds are these compounds of formula (I) wherein X is oxygen
Also interesting compounds are these compounds of formula (I) wherein the dotted line
represents a bond, so as to form a double bond.
Another group of interesting compounds are those compounds of formula (I) wherein R1 is hydrogen, Ci-βalkyl, Ci-6alkyloxyCi-6alkyl, di(Ci-6alkyl)aminoCi-6alkyl, or a radical of formula -Alk1-C(=O)-R9, wherein Alk1 is methylene and R9 is Cι_8alkyl- amino substituted with Ci-6alkyloxycarbonyl.
Still another group of interesting compounds are those compounds of formula (I) wherein R3 is hydrogen or halo; and R2 is halo, Ci-6alkyl, C2-6alkenyl, Cι_6alkyloxy, trihalomethoxy or hydroxyCi-6alkyloxy.
A further group of interesting compounds are those compounds of formula (I) wherein R2 and R3 are on adjacent positions and taken together to form a bivalent radical of formula (a-1), (a-2) or (a-3).
A still further group of interesting compounds are those compounds of formula (I) wherein R^ is hydrogen and R4 is hydrogen or Ci-6alkyl.
Yet another group of interesting compounds are those compounds of formula (I) wherein R^ is hydrogen; and R^ is Ci-6alkyl or halo, preferably chloro, especially
4-chloro.
A particular group of compounds are those compounds of formula (I) wherein R° is hydrogen, hydroxy, haloCi-6alkyl, hydroxyCi-βalkyl, cyanoCι_6alkyl, Ci-6alkyloxy- carbonylCι_6alkyl, imidazolyl, or a radical of formula -NR1 !R1 wherein R1 !■ is hydrogen or Ci-i2alkyl and R12 is hydrogen, Cι_6alkyl, Ci-6alkyloxy, hydroxy, Ci-6alkyloxyCi-6alkylcarbonyl, or a radical of formula -Alk2-OR13 wherein R13 is hydrogen or Cι_6alkyl.
Preferred compounds are those compounds wherein R is hydrogen, Ci-6alkyl, Cι_6alkyloxyCi-6alkyl, di(Ci-6alkyl)aminoCi-6alkyl, or a radical of formula -Alk1-C(=O)-R9, wherein Alk1 is methylene and R9 is Ci-8alkylamino substituted with Ci_6alkyloxycarbonyl; R2 is halo, Ci-6alkyl, C2-6alkenyl, Ci-βalkyloxy, trihalomethoxy, hydroxyCι_6alkyloxy or Ar1; R3 is hydrogen; R4 is methyl bound to the nitrogen in 3-position of the imidazole; R^ is hydrogen; R" is chloro; R^ is hydrogen; R8 is hydrogen, hydroxy, haloCi-όalkyl, hydroxyCi-6alkyl, cyanoCι_6alkyl, Ci-6alkyloxycarbonylCi-6alkyl, imidazolyl, or a radical of formula -NR1 !R12
wherein R1 * is hydrogen or Ci-I2alkyl and R12 is hydrogen, Ci-6alkyl, Ci-6alkyloxy, Ci-6alkyloxyCi-6alkylcarbonyl, or a radical of formula -Alk2-OR13 wherein R13 is Cι_6alkyl; R17 is hydrogen and R 8 is hydrogen.
Most preferred compounds are
4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(l-methyl-lH-imidazol-5-yl)methyl]- l-methyl-2(lH)-quinolinone,
6-[amino(4-chlorophenyl)-l-methyl-lH-imidazol-5-ylmethyl]-4-(3-chlorophenyl)-
1 -methyl-2( 1 H)-quinolinone; 6-[(4-chlorophenyl)hydroxy(l-methyl-lH-imidazol-5-yl)methyl]-4-(3-ethoxyphenyl)-
1 -methyl-2( 1 H)-quinolinone;
6- [(4-chlorophenyl)( 1 -methyl- 1 H-imidazol-5-yl)methyl] -4-(3 -ethoxyphenyl)- 1 -methyl -
2( 1 H)-quinolinone monohydrochloride.monohydrate ;
6-[amino(4-chlorophenyl)(l-methyl-lH-imidazol-5-yl)methyl]-4-(3-ethoxyphenyl)- l-methyl-2(lH)-quinolinone,
6-amino(4-chlorophenyl)(l-methyl-lH-imidazol-5-yl)methyl]-l-methyl-4-(3-propyl- phenyl)-2(lH)-quinolinone; a stereoisomeric form thereof or a pharmaceutically acceptable acid or base addition salt; and
(+)-6-[amino(4-chlorophenyl)(l-methyl-lH-imidazol-5-yl)methyl]-4-(3-chlorophenyl)- l-methyl-2(lH)-quinolinone (Compound 75 in Table 1 of the Experimental part of
WO-97/21701) ; or a pharmaceutically acceptable acid addition salt thereof. The latter compound is especially preferred.
Further preferred embodiments of the present invention include compounds of formula (IX) wherein one or more of the following restrictions apply:
• =X'-X2-X3 is a trivalent radical of formula (x-1), (x-2), (x-3), (x-4) or (x-9) wherein each R6 independently is hydrogen, C1-4alkyl, Cι-4alkyloxycarbonyl, amino or aryl and R7 is hydrogen;
• >Y1-Y2- is a trivalent radical of formula (y-1), (y-2), (y-3), or (y-4) wherein each R9 independently is hydrogen, halo, carboxyl,
or Cj-4alkyloxycarbonyl;
• r is O, 1 or 2;
• s is O or 1;
• t is O;
• R1 is halo, Cι-6alkyl or two R1 substituents ortho to one another on the phenyl ring may independently form together a bivalent radical of formula (a-1);
• R2 is halo;
• R3 is halo or a radical of formula (b-1) or (b-3) wherein
R10 is hydrogen or a radical of formula -Alk-OR13.
R1 1 is hydrogen;
R12 is hydrogen, Cι.6alkyl, d.6alkylcarbonyl, hydroxy, Cι-6alkyloxy or mono- or di(C1-6alkyl)aminoCι-6alkylcarbonyl; Alk is C1-6alkanediyl and R13 is hydrogen; • R4 is a radical of formula (c-1) or (c-2) wherein
R16 is hydrogen, halo or mono- or di(Cι-4alkyl)amino; R17 is hydrogen or C1-6alkyl; • aryl is phenyl.
A particular group of compounds consists of those compounds of formula (IX) wherein =X'-X2-X3 is a trivalent radical of formula (x-1), (x-2), (x-3), (x-4) or (x-9), >Y1-Y2 is a trivalent radical of formula (y-2), (y-3) or (y-4), r is 0 or 1, s is 1, t is 0, R1 is halo, C(ι-4)alkyl or forms a bivalent radical of formula (a-1), R2 is halo or C1-4alkyl, R3 is hydrogen or a radical of formula (b-1) or (b-3), R4 is a radical of formula (c-1) or (c-2), R6 is hydrogen, C1-4alkyl or phenyl, R7 is hydrogen, R9 is hydrogen or
R10 is hydrogen or -Alk-OR13, R11 is hydrogen and R12 is hydrogen or Cι.6alkylcarbonyl and R13 is hydrogen;
Preferred compounds are those compounds of formula (IX) wherein =X -X -X is a trivalent radical of formula (x-1) or (x-4), >Y1-Y2 is a trivalent radical of formula (y- 4), r is 0 or 1, s is 1, t is 0, R1 is halo, preferably chloro and most preferably 3-chloro, R2 is halo, preferably 4-chloro or 4-fluoro, R3 is hydrogen or a radical of formula (b-1) or (b-3), R4 is a radical of formula (c-1) or (c-2), R6 is hydrogen, R7 is hydrogen, R9 is hydrogen, R10 is hydrogen, R11 is hydrogen and R12 is hydrogen;
Other preferred compounds are those compounds of formula (IX) wherein =X -X -X is a trivalent radical of formula (x-2), (x-3) or (x-4), >Y1-Y2 is a trivalent radical of formula (y-2), (y-3) or (y-4), r and s are 1, t is 0, R1 is halo, preferably chloro, and most preferably 3-chloro or R1 is Cι-4alkyl, preferably 3-methyl, R2 is halo, preferably chloro, and most preferably 4-chloro, R3 is a radical of formula (b-1) or (b-3), R4 is a radical of formula (c-2), R6 is C1- alkyl, R9 is hydrogen, R10 and R11 are hydrogen and R12 is hydrogen or hydroxy.
The most preferred compounds of formula (IX) are 7-[(4-fluorophenyl)(lH-imidazol-l-yl)methyl]-5-phenylimidazo[l,2-a]quinoline; α-(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)-5-phenylimidazo[l,2-a]quinoline-
7-methanol;
5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)-imidazo-
[ 1 ,2-a]quinoline-7-methanol ;
5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)imidazo-
[ 1 ,2-a]quinoline-7-methanamine;
5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)tetrazolo- [l,5-a]quinoline-7-methanamine;
5-(3-chlorophenyl)- -(4-chlorophenyl)-l-methyl-α-(l-methyl-lH-imidazol-5-yl)- l,2,4-triazolo[4,3-a]quinoline-7-methanol;
5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)tetrazolo-
[l,5-a]quinoline-7-methanamine; 5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)tetrazolo-
[ 1 ,5-a]quinazoline-7-methanol ;
5-(3-chlorophenyl)-α-(4-chlorophenyl)-4,5-dihydro-α-(l-methyl-lH-imidazol-
5-yl)tetrazolo[l,5-a]quinazoline-7-methanol;
5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(l-methyl-lH-imidazol-5-yl)tetrazolo- [l,5-a]quinazoline-7-methanamine;
5-(3-chlorophenyl)-α-(4-chlorophenyl)-N-hydroxy-α-(l-methyl-lH-imidazol-5-yl)- tetrahydro[l,5-a]quinoline-7-methanamine; α-(4-chlorophenyl)-α-(l -methyl- lH-imidazol-5-yl)-5-(3-methylphenyl)tetrazolo-
[l,5-a]quinoline-7-methanamine; the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof.
5-(3-chlorophenyl)-α-(4-chlorophenyl)- -(l-methyl-lH-imidazol-5-yl)tetrazolo- [l,5-a]quinazoline-7-methanamine, especially the (-) enantiomer, and its pharmaceutically acceptable acid addition salts are especially preferred.
As used in the foregoing definitions and hereinafter halo defines fluoro, chloro, bromo and iodo; Ci-6alkyl defines straight and branched chained saturated hydrocarbon radicals having from 1 to 6 carbon atoms such as, for example, methyl, ethyl, propyl, butyl, pentyl, hexyl and the like; Ci-8alkyl encompasses the straight and branched chained saturated hydrocarbon radicals as defined in Ci-βalkyl as well as the higher homologues thereof containing 7 or 8 carbon atoms such as, for example heptyl or octyl; Ci-I2alkyl again encompasses Ci-8alkyl and the higher homologues thereof containing 9 to 12 carbon atoms, such as, for example, nonyl, decyl, undecyl, dodecyl; Cι_i6alkyl again encompasses Ci-i2alkyl and the higher homologues thereof containing 13 to 16 carbon atoms, such as, for example, tridecyl, tetradecyl, pentedecyl and hexadecyl; C2-6alkenyl defines straight and branched chain hydrocarbon radicals containing one double bond and having from 2 to 6 carbon atoms such as, for example, ethenyl, 2-propenyl, 3-butenyl, 2-pentenyl, 3-pentenyl, 3-methyl-2-butenyl, and the
like; Ci-βalkanediyl defines bivalent straight and branched chained saturated hydrocarbon radicals having from 1 to 6 carbon atoms, such as, for example, methylene, 1,2-ethanediyl, 1,3-propanediyl, 1,4-butanediyl, 1,5-pentanediyl, 1,6-hexanediyl and the branched isomers thereof. The term "C(=O)" refers to a carbonyl group, "S(O)" refers to a sulfoxide and "S(O)2" to a sulfon. The term "natural amino acid" refers to a natural amino acid that is bound via a covalent amide linkage formed by loss of a molecule of water between the carboxyl group of the amino acid and the amino group of the remainder of the molecule. Examples of natural amino acids are glycine, alanine, valine, leucine, isoleucine, methionine, proline, phenylanaline, tryptophan, serine, threonine, cysteine, tyrosine, asparagine, glutamine, aspartic acid, glutamic acid, lysine, arginine, histidine.
The pharmaceutically acceptable acid or base addition salts as mentioned hereinabove are meant to comprise the therapeutically active non-toxic acid and non-toxic base addition salt forms which the compounds of formulas (I), (Et), (IE), (IV), (V), (VI), (Vπ), (Nm) or (IX) are able to form. The compounds of formulas (I), (II), (HI), (IV), (V), (VI), (VII), (Vπi) or (IX) which have basic properties can be converted in their pharmaceutically acceptable acid addition salts by treating said base form with an appropriate acid. Appropriate acids comprise, for example, inorganic acids such as hydrohalic acids, e.g. hydrochloric or hydrobromic acid; sulfuric; nitric; phosphoric and the like acids; or organic acids such as, for example, acetic, propanoic, hydroxyacetic, lactic, pyruvic, oxalic, malonic, succinic (i.e. butanedioic acid), maleic, fumaric, malic, tartaric, citric, methanesulfonic, ethanesulfonic, benzenesulfonic, p-toluenesulfonic, cyclamic, salicylic, p-aminosalicylic, pamoic and the like acids.
The compounds of formulae (I), (II), (HI), (IV), (V), (VI), (VII), (VDI) or (IX) which have acidic properties may be converted in their pharmaceutically acceptable base addition salts by treating said acid form with a suitable organic or inorganic base. Appropriate base salt forms comprise, for example, the ammonium salts, the alkali and earth alkaline metal salts, e.g. the lithium, sodium, potassium, magnesium, calcium salts and the like, salts with organic bases, e.g. the benzathine, N-methyl-D-glucamine, hydrabamine salts, and salts with amino acids such as, for example, arginine, lysine and the like.
The terms acid or base addition salt also comprise the hydrates and the solvent addition forms which the compounds of formulae (I), (II), (m), (IV), (V), (VI), (VII), (VIII) or (IX) are able to form. Examples of such forms are e.g. hydrates, alcoholates and the like.
The term stereochemically isomeric forms of compounds of formulae (I), (II), (III), (IV), (V), (VI), (VH), (VIE) or (IX), as used hereinbefore, defines all possible compounds made up of the same atoms bonded by the same sequence of bonds but having different three-dimensional structures which are not interchangeable, which the compounds of formulae (I), (II), (Lϋ), (TV), (V), (VI), (VII), (VIH) or (IX) may possess. Unless otherwise mentioned or indicated, the chemical designation of a compound encompasses the mixture of all possible stereochemically isomeric forms which said compound may possess. Said mixture may contain all diastereomers and/or enantiomers of the basic molecular structure of said compound. All stereochemically isomeric forms of the compounds of formulae (I), (II), (HI), (IV), (V), (VI), (VII), (VIE) or (IX) both in pure form or in admixture with each other are intended to be embraced within the scope of the present invention.
Some of the compounds of formulae (I), (II), (IE), (IV), (V), (VI), (VH), (Vm) or (IX) may also exist in their tautomeric forms. Such forms although not explicitly indicated in the above formula are intended to be included within the scope of the present invention.
Whenever used hereinafter, the term "compounds of formulae (I), (II), (JH), (TV), (V), (VI), (VII), (VDI) or (IX)" is meant to include also the pharmaceutically acceptable acid or base addition salts and all stereoisomeric forms.
Preferred anti-tumor anthracychne derivatives for use in accordance with the invention include daunorubicin, doxorubicin and idarubicin referred to above. Daunorubicin is commercially available for example as the hydrochloride salt from Bedford Laboratories under the trade name Cerubidine, and may be prepared for example as described in patent specification No. 4020270, or by processes analogous thereto. Doxorubicin is commercially available for example as the hydrochloride salt from Astra, and may be prepared for example as described in U.S. patent specification No. 3803124 or by processes analogous thereto. Idarubicin is commercially available for example as the hydrochloride salt from Pharmacia & Upjohn under the trade name Idamycin, and may be prepared for example as described in U.S. patent specification No. 4046878 or by processes analogous thereto Other anti-tumor anthracychne derivatives may be prepared in conventional manner for example by processes analogous to those described above for daunorubicin, doxorubicin and idarubicin.
The present invention also relates to combinations according to the invention for use in medical therapy for example for inhibiting the growth of tumor cells.
The present invention also relates to the use of combinations according to the invention for the preparation of a pharmaceutical composition for inhibiting the growth of tumor cells.
The present invention also relates to a method of inhibiting the growth of tumor cells in a human subject which comprises administering to the subject an effective amount of a combination according to the invention.
This invention further provides a method for inhibiting the abnormal growth of cells, including transformed cells, by administering an effective amount of a combination according to the invention. Abnormal growth of cells refers to cell growth independent of normal regulatory mechanisms (e.g. loss of contact inhibition). This includes the abnormal growth of : (1) tumor cells (tumors) expressing an activated ras oncogene; (2) tumor cells in which the ras protein is activated as a result of oncogenic mutation of another gene; (3) benign and malignant cells of other proliferative diseases in which aberrant ras activation occurs. Furthermore, it has been suggested in literature that ras oncogenes not only contribute to the growth of of tumors in vivo by a direct effect on tumor cell growth but also indirectly, i.e. by facilitating tumor-induced angiogenesis (Rak. J. et al, Cancer Research, 55, 4575-4580, 1995). Hence, pharmacologically targetting mutant ras oncogenes could conceivably suppress solid tumor growth in vivo, in part, by inhibiting tumor-induced angiogenesis.
This invention also provides a method for inhibiting tumor growth by administering an effective amount of a combination according to the present invention, to a subject, e.g. a mammal (and more particularly a human) in need of such treatment. In particular, this invention provides a method for inhibiting the growth of tumors expressing an activated ras oncogene by the administration of an effective amount of combination according to the present invention. Examples of tumors which may be inhibited include, but are not limited to, lung cancer (e.g. adenocarcinoma and including non- small celll lung cancer), pancreatic cancers (e.g. pancreatic carcinoma such as, for example exocrine pancreatic carcinoma), colon cancers (e.g. colorectal carcinomas, such as, for example, colon adenocarcinoma and colon adenoma), hematopoietic tumors of lymphoid lineage (e.g. acute lymphocytic leukemia, B-cell lymphoma, Burkitt's lymphoma), myeloid leukemias (for example, acute myelogenous leukemia (AML)), thyroid follicular cancer, myelodysplastic syndrome (MDS), tumors of
mesenchymal origin (e.g. fibrosarcomas and rhabdomyosarcomas), melanomas, teratocarcinomas, neuroblastomas, gliomas, benign tumor of the skin (e.g. keratoacanthomas), breast carcinoma (e.g. advanced breast cancer), kidney carninoma, ovary carcinoma, bladder carcinoma and epidermal carcinoma.
This invention also provides a method for inhibiting proliferative diseases, both benign and malignant, wherein ras proteins are aberrantly activated as a result of oncogenic mutation in genes, i.e. the ras gene itself is not activated by mutation to an oncogenic mutation to an oncogenic form, with said inhibition being accomplished by the administration of an effective amount of a combination according to the invention, to a subject in need of such a treatment. For example, the benign proliferative disorder neurofibromatosis, or tumors in which ras is activated due to mutation or overexpression of tyrosine kinase oncogenes may be inhibited by the combinations according to the invention.
The anti-tumor anthracychne derivative and the farnesyl transferase inhibitor may be administered simultaneously (e.g. in separate or unitary compositions) or sequentially in either order. In the latter case, the two compounds will be administered within a period and in an amount and manner that is sufficient to ensure that an advantageous or synergistic effect is achieved. It will be appreciated that the preferred method and order of administration and the respective dosage amounts and regimes for each component of the combination will depend on the particular anti-tumor anthracychne derivative and farnesyl transferase inhibitor being administered, their route of administration, the particular tumor being treated and the particular host being treated. The optimum method and order of administration and the dosage amounts and regime can be readily determined by those skilled in the art using conventional methods and in view of the information set out herein.
The farnesyl transferase inhibitor is advantageously administered in an effective amount of from 0.0001 mg/kg to 100 mg/kg body weight, and in particular from 0.001 mg/kg to 10 mg/kg body weight. More particularly, for an adult patient, the dosage is conveniently in the range of 50 to 500mg bid, advantageously 100 to 400 mg bid and particularly 300mg bid.
The anti-tumor anthracychne derivative is advantageously administered in a dosage of 10 to 75 mg per square meter (mg/m ) of body surface area, for example 15 to 60 mg/m2, particularly for doxorubicin in a dosage of about 40 to 75 mg/m2, for daunorubicin in a dosage of about 25 to 45mg/m2 , and for idarubicin in a dosage of
about 10 to 15 mg/m2 per course of treatment. These dosages may be administered for example once, twice or more per course of treatment, which may be repeated for example every 7,14,21 or 28 days.
It is especially preferred to administer the farnesyl tranferase inhibitor at a dosage of 100 or 200mg bid for 7, 14, 21 or 28 days with a dosage of the anti-tumor anthracychne derivative in the ranges indicated above.
In view of their useful pharmacological properties, the components of the combinations according to the invention, i.e. the anti-tumor anthracychne derivative and the farnesyl transferase inhibitor may be formulated into various pharmaceutical forms for administration purposes. The components may formulated separately in individual pharmaceutical compositions or in a unitary pharmaceutical composition containing both components. Farnesyl protein transferase inhibitors can be prepared and formulated into pharmaceutical compositions by methods known in the art and in particular according to the methods described in the published patent specifications mentioned herein and incorporated by reference; for the compounds of formulae (I), (II) and (HI) suitable examples can be found in WO-97/21701. Compounds of formulae (IV), (V), and (VI) can be prepared and formulated using methods described in WO 97/16443, compounds of formulae (VII) and (VET) according to methods described in WO 98/40383 and WO 98/49157 and compounds of formula (IX) according to methods described in WO 00/39082 respectively.
The present invention therefore also relates to a pharmaceutical composition comprising an anti-tumor anthracychne derivative and a farnesyl tranferase inhibitor of formula (I) together with one or more pharmaceutical carriers. To prepare pharmaceutical compositions for use in accordance with the invention, an effective amount of a particular compound, in base or acid addition salt form, as the active ingredient is combined in intimate admixture with a pharmaceutically acceptable carrier, which carrier may take a wide variety of forms depending on the form of preparation desired for administration. These pharmaceutical compositions are desirably in unitary dosage form suitable, preferably, for administration orally, rectally, percutaneously, or by parenteral injection. For example, in preparing the compositions in oral dosage form, any of the usual pharmaceutical media may be employed, such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as suspensions, syrups, elixirs and solutions; or solid carriers such as starches, sugars, kaolin, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules and tablets. Because of their ease in administration,
tablets and capsules represent the most advantageous oral dosage unit form, in which case solid pharmaceutical carriers are obviously employed. For parenteral compositions, the carrier will usually comprise sterile water, at least in large part, though other ingredients, to aid solubility for example, may be included. Injectable solutions, for example, may be prepared in which the carrier comprises saline solution, glucose solution or a mixture of saline and glucose solution. Injectable suspensions may also be prepared in which case appropriate liquid carriers, suspending agents and the like may be employed. In the compositions suitable for percutaneous administration, the carrier optionally comprises a penetration enhancing agent and/or a suitable wetting agent, optionally combined with suitable additives of any nature in minor proportions, which additives do not cause a significant deleterious effect to the skin. Said additives may facilitate the administration to the skin and/or may be helpful for preparing the desired compositions. These compositions may be administered in various ways, e.g., as a transdermal patch, as a spot-on, as an ointment.
It is especially advantageous to formulate the aforementioned pharmaceutical compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used in the specification and claims herein refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. Examples of such dosage unit forms are tablets (including scored or coated tablets), capsules, pills, powder packets, wafers, injectable solutions or suspensions, teaspoonfuls, tablespoonfuls and the like, and segregated multiples thereof.
It may be appropriate to administer the required dose of each component of the combination as two, three, four or more sub-doses at appropriate intervals throughout the course of treatment Said sub-doses may be formulated as unit dosage forms, for example, in each case containing independently 0.01 to 500 mg, for example 0.1 to 200 mg and in particular 1 to lOOmg of each active ingredient per unit dosage form.
Experimental Testing of Combinations for Inhibition of Tumor Growth
The combinations according to the invention may be tested for their efficacy in inhibiting tumor growth using conventional assays described in the literature for example the HTB177 lung carcinoma described by Liu M et al, Cancer Research, Vol. 58, No.21, 1 November 1998, pages 4947-4956, and the anti-mitotic assay described by Moasser M et al, Proc. Natl. Acad. Sci. USA, Vol. 95, pages 1369-1374, February
1998. Other in vitro and in vivo models for determining ant-tumor effects of combinations and possible synergy of the combinations according to the invention are described in WO 98/54966 and WO 98/32114. Clinical models for determining the efficacy and possible synergism for combination therapy in the clinic are generally described in Cancer: Principles and Practice of Oncology, Fifth Edition, edited by Vincent T DeVita, Jr., Samuel Hellman, Steven A. Rosenberg, Lippincott-Raven, Philadelphia, 1997, especially Chapter 17, pages 342-346.
Claims
1. A combination of an anti-tumor anthracyline derivative and a farnesyl transferase inhibitor selected from compounds of formulae (I), (II), (IE), (IV), (V), (VI), (VE), (VIE) and (IX) below:
(I) (ID
(III) the pharmaceutically acceptable acid or base addition salts and the stereochemically isomeric forms thereof, wherein the dotted line represents an optional bond; X is oxygen or sulfur;
R1 is hydrogen, Ci-i2alkyl, Ar1, Ar2Ci-6alkyl, quinolinylCi-6alkyl, pyridylCi-6alkyl, hydroxyCi-βalkyl, Ci-galkyloxyCi-όalkyl, mono- or di (C i -6alkyl)aminoC i -6alkyl, aminoC i _6alkyl , or a radical of formula -Alk1-C(=O)-R9, -Alki-S^-R9 or -Alk1-S(O)2-R9, wherein Alk1 is Ci-6alkanediyl,
R9 is hydroxy, Ci-6alkyl, Ci-6alkyloxy, amino, Ci-8alkylamino or Ci-8alkylamino substituted with Ci-6alkyloxycarbonyl; R2, R3 and R1^ each independently are hydrogen, hydroxy, halo, cyano, Cι_6alkyl, Ci-6alkyloxy, hydroxyCι_6alkyloxy, Ci-6alkyloxyCi-6alkyloxy, aminoCi-6alkyloxy, mono- or di(Ci-6alkyl)aminoCi_6alkyloxy, Ar1,
Ar2Ci-6alkyl, Ar oxy, Ar2Ci-6alkyloxy, hydroxycarbonyl, Ci_6alkyloxycarbonyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, 4,4- dimethyloxazolyl; or when on adjacent positions R2 and R3 taken together may form a bivalent radical of formula -O-CH2-O- (a-1),
-O-CH2-CH2-O- (a-2),
-O-CH=CH- (a-3),
-O-CH2-CH2- (a-4),
-O-CH2-CH2-CH2- (a-5), or -CH=CH-CH=CH- (a-6);
R4 and R^ each independently are hydrogen, halo, Ar1, Cι_6alkyl, hydroxyCι_6alkyl, Cι_6alkyloxyCi-6alkyl, Ci-galkyloxy, Ci-βalkylthio, amino, hydroxycarbonyl, Cι_6alkyloxycarbonyl, Ci -6alkylS(O)Ci-6alkyl or Ci-6alkylS(O)2Cι_6alkyl; R6 and R7 each independently are hydrogen, halo, cyano, Ci-6alkyl, Cι_6alkyloxy, Ar2oxy, trihalomethyl, Ci-6alkylthio, di(Ci_6alkyl)amino, or when on adjacent positions R" and R*7 taken together may form a bivalent radical of formula
-O-CH2-O- (c-1), or
-CH=CH-CH=CH- (c-2); R8 is hydrogen, Cι_6alkyl, cyano, hydroxycarbonyl, Cι_6alkyloxycarbonyl,
C 1.βalkylcarbonylC 1 _6alkyl, cyanoC i-βalkyl, C 1 -6alkyloxycarbonylC 1 -6alkyl, carboxyCι_6alkyl, hydroxyCι_6alkyl, aminoCi-όalkyl, mono- or di(Cι_6alkyl)- aminoCi-galkyl, imidazolyl, haloCι_6alkyl, Cι_6alkyloxyCi-6alkyl, aminocarbonylCi-6alkyl, or a radical of formula -O-RiO (b-1),
-S-RlO (b-2),
-N-R HR12 (b-3), wherein R1^ is hydrogen, Ci-βalkyl, Cι_6alkylcarbonyl, Ar1, Ar2Cι_6alkyl,
Ci-6alkyloxycarbonylCi-6alkyl, or a radical or formula -Alk2-OR 3 or -Alk2-NR14R15;
R1 ! is hydrogen, Cι_i2alkyl, Ar1 or Ar2Cι_6alkyl; R12 is hydrogen, Cι_6alkyl, Ci-i6alkylcarbonyl, Ci-βalkyloxycarbonyl, Ci-6alkylaminocarbonyl, Ar1, Ar2Cι_.6alkyl, Ci-6alkylcarbonyl- Cι_6alkyl, a natural amino acid, A^carbonyl, Ar2Ci-6alkylcarbonyl, aminocarbonylcarbonyl, Ci-όalkyloxyCi-βalkylcarbonyl, hydroxy,
Ci-6alkyloxy, aminocarbonyl, di(Cι_6alkyl)aminoCi-6alkylcarbonyl, amino, Ci-6alkylamino, Ci-βalkylcarbonylamino, or a radical or formula -Alk2-OR13 or -Alk2-NR14R15; wherein Alk2 is Ci-6alkanediyl;
R13 is hydrogen, Ci-βalkyl, Ci _6alkylcarbonyl, hydroxyCi-6alkyl, Ar1 or Ar2Cι_6alkyl; R14 is hydrogen, Cι_6alkyl, Ar1 or Ar2Ci-6alkyl;
R1^ is hydrogen, Ci-βalkyl, Cι_6alkylcarbonyl, Ar1 or Ar2Ci_6alkyl; R17 is hydrogen, halo, cyano, Cι_6alkyl, Ci-6alkyloxycarbonyl, Ar1; R1^ is hydrogen, Cι_6alkyl, Ci-6alkyloxy or halo; R 9 is hydrogen or Cι_6alkyl; Ar1 is phenyl or phenyl substituted with Ci-6alkyl, hydroxy, amino, Cχ_6alkyloxy or halo; and Ar2 is phenyl or phenyl substituted with Ci-6alkyl, hydroxy, amino, Cι_6alkyloxy or halo.
(IV) (V)
(VI) the pharmaceutically acceptable acid or base addition salts and the stereochemically isomeric forms thereof, wherein the dotted line represents an optional bond; X is oxygen or sulfur;
R1 is hydrogen, Cι_i2alkyl, Ar1, Ar Ci-6alkyl, quinolinylCι_6alkyl, pyridyl- Cι_6alkyl, hydroxyCi-6alkyl, Ci-6alkyloxyCi-6alkyl, mono- or di(Cι_6alkyl)aminoCi-6alkyl, aminoCι_6alkyl, or a radical of formula -Alk1-C(=O)-R9, -Alki-StOj-R9 or -Alk1-S(O)2-R9, wherein Alk1 is Ci-6alkanediyl,
R9 is hydroxy, Cμόalkyl, Ci-βalkyloxy, amino, Ci-salkylamino or C i -8alkylamino substituted with C i .βalkyloxycarbonyl;
R2 and R3 each independently are hydrogen, hydroxy, halo, cyano, Cι_6alkyl, Ci-6alkyloxy, hydroxyCi-βalkyloxy, Ci-βalkyloxyCi-όalkyloxy, amino- Ci-6alkyloxy, mono- or di(Ci-6alkyl)aminoCi-6alkyloxy, Ar1, Ar2Ci-6alkyl, Ar2oxy, Ar2Cι_6alkyloxy, hydroxycarbonyl, Cι_6alkyloxycarbonyl, trihalomethyl, trihalomethoxy, C2-6alkenyl; or when on adjacent positions R2 and R3 taken together may form a bivalent radical of formula
-O-CH2-O- (a-1),
-O-CH2-CH2-O- (a-2), -O-CH=CH- (a-3),
-O-CH2-CH2- (a-4),
-O-CH2-CH2-CH2- (a-5), or -CH=CH-CH=CH- (a-6); R4 and R5 each independently are hydrogen, Ar1, Cι-6alkyl, C1-6alkyloxyC1-6alkyl, 
C1-6alkylthio, amino, hydroxycarbonyl, Cι-6alkyloxycarbonyl,
Cι.6alkylS(O)Cι.6alkyl or C1-6alkylS(O)2C1-6alkyl; R^ and R7 each independently are hydrogen, halo, cyano, Ci-6alkyl, Cι_6alkyloxy or
Ar2oxy; R^ is hydrogen, Cι_6alkyl, cyano, hydroxycarbonyl, Ci-όalkyloxycarbonyl, Ci-6alkyl- carbonylCi-βalkyl, cyanoCi-6alkyl, Cι_6alkyloxycarbonylCi-6alkyl, hydroxy- carbonylCi-βalkyl, hydroxyCi-6alkyl, aminoCi-όalkyl, mono- or di(Ci-6alkyl)- aminoCi-6alkyl, haloCi-6alkyl, Ci-6alkyloxyCi-6alkyl, aminocarbonylCi-6alkyl, Ar1, Ar2Ci-6alkyloxyCi-6alkyl, Ci-6alkylthioCι_6alkyl; R ^ is hydrogen, Cι_6alkyl, Ci-6alkyloxy or halo; R1 ! is hydrogen or Cι_6alkyl;
Ar1 is phenyl or phenyl substituted with Ci-6alkyl,hydroxy,amino,Cι_6alkyloxy or halo; Ar2 is phenyl or phenyl substituted with Ci-βalkyl, hydroxy, amino, Cι_6alkyloxy or halo. 
the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof, wherein the dotted line represents an optional bond; X is oxygen or sulfur; -A- is a bivalent radical of formula
-CH=CH- (a-1), -CH2-S- (a-6),
-CH2-CH2- (a-2), -CH2-CH2-S- (a-7),
-CH2-CH2-CH2- (a-3), -CH=N- (a-8),
--CCHH22--OO-- ((aa--44)),, -N=N- (a-9), or
-CH2-CH2-O- (a-5), -CO-NH- (a-10); wherein optionally one hydrogen atom may be replaced by Ci-4alkyl or Ar1; R and R2 each independently are hydrogen, hydroxy, halo, cyano, Ci -6alkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, Ci-galkyloxy, hydroxyCi- 6alkyloxy, Cι_6alkyloxyCi-6alkyloxy, Ci-βalkyloxycarbonyl, aminoCi-6alkyloxy, mono- or di(Ci-6alkyl)aminoCi-6alkyloxy, Ar2, Ar2-Ci-6alkyl, Ar2-oxy, Ar2-Cι_6alkyloxy; or when on adjacent positions R1 and R2 taken together may form a bivalent radical of formula -O-CH2-O- (b-1), -O-CH2-CH2-O- (b-2),
-O-CH=CH- (b-3),
-O-CH2-CH2- (b-4),
-O-CH2-CH2-CH2- (b-5), or -CH=CH-CH=CH- (b-6); R3 and R4 each independently are hydrogen, halo, cyano, Cι_6alkyl, Cι_6alkyloxy, Ar3-oxy, Ci-6alkylthio, di(Ci-6alkyl)amino, trihalomethyl, trihalomethoxy, or when on adjacent positions R3 and R4 taken together may form a bivalent radical of formula
-O-CH2-O- (c-1), -O-CH2-CH2-O- (c-2), or
-CH=CH-CH=CH- (c-3); R^ is a radical of formula 
wherein R1^ is hydrogen, halo, Ar4, Cι_6alkyl, hydroxyCi-6alkyl, Ci-6alkyloxy- Cι_6alkyl, Ci-6alkyloxy, Cι_6alkylthιo, amino, Ci-6alkyloxycarbonyl, Ci-6alkylS(O)Cι_6alkyl or Ci-6alkylS(O)2Ci -6alkyl; R14ιs hydrogen, Ci-βalkyl or di(Ci-4alkyl)ammosulfonyl; R^ IS hydrogen, hydroxy, halo, Ci-6alkyl, cyano, haloCi-βalkyl, hydroxyCi-βalkyl, cyanoCι_6alkyl, amιnoCι_6alkyl, Ci-6alkyloxyCι_6alkyl,
Ci-6alkylthιoCi-6alkyl, ammocarbonylCι_6alkyl,
C i-6alkyloxycarbonylC i -6alkyl, C i -6alkylcarbonyl-C i _6alkyl,
Ci-6alkyloxycarbonyl, mono- or dι(Ci-6alkyl)ammoCi-6alkyl, Ar^,
Ar5-Ci-6alkyloxyCι_6alkyl; or a radical of formula
-O-R7 (e-1),
-S-R7 (e-2),
-N-RδR9 (e-3), wherein R7 is hydrogen, Ci-6alkyl, Ci-6alkylcarbonyl, Ar^, Ar^-Ci-όalkyl, Ci-6alkyloxycarbonylCι_6alkyl, or a radical of formula -Alk-OR10 or
-Alk-NR^R12;
R8 is hydrogen, Cι_6alkyl, Ar7 or Ar7-Cι_6alkyl; R9 is hydrogen, Cι_6aιkyl, Ci-6alkylcarbonyl, Cι_6alkyloxycarbonyl,
Ci-6alkylamιnocarbonyl, Ar^, Ar^-Cι_6alkyl, Cι_6alkylcarbonyl-
Cι_6alkyl, Ar^-carbonyl, Ar^-Ci-όalkylcarbonyl, aminocarbonyl- carbonyl, Ci-βalkyloxyCi-βalkylcarbonyl, hydroxy, Ci-6alkyloxy, aminocarbonyl, dι(Ci-6alkyl)amιnoCi-6alkylcarbonyl, ammo,
Ci-6alkylamιno, Cι_6alkylcarbonylamιno, or a radical or formula -
Alk-OR10 or -Alk-NR1 iR12; wherein Alk is Ci-6alkanediyl;
R10 is hydrogen, Ci-6alkyl, Cι_6alkylcarbonyl, hydroxyCi-6alkyl,
Ar9 or Ar9-Ci_6alkyl;
R11 is hydrogen, Cχ-6alkyl, Ci-βalkylcarbonyl, Ar10 or
AriO-Ci-βalkyl;
R12 is hydrogen, Cι_6alkyl, Ar1 1 or Ar^-Ci-όalkyl; and
Ar1 to Ar11 are each independently selected from phenyl; or phenyl substituted with halo, Ci-6alkyl, Ci-6alkyloxy or trifluoromethyl. 
the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof, wherein the dotted line represents an optional bond; X is oxygen or sulfur;
R1 and R2 each independently are hydrogen, hydroxy, halo, cyano, Cι_6alkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, Ci-6alkyloxy, hydroxyCi-βalkyloxy, Cι_6alkyloxyCi-6alkyloxy, Cι_6alkyloxycarbonyl, aminoCi-όalkyloxy, mono- or di(Ci-6alkyl)aminoCι_6alkyloxy, Ar1, Ar^Ci-όalkyl, Ar^xy or AriCi-όalkyloxy; R3 and R4 each independently are hydrogen, halo, cyano, Ci-6alkyl, Ci-βalkyloxy, Ci-6alkylthio, di(Ci-6alkyl)amino, trihalomethyl or trihalomethoxy; R5 is hydrogen, halo, Ci-6alkyl, cyano, haloCi-βalkyl, hydroxyCi-βalkyl, cyanoCι_6alkyl, aminoCi-6alkyl, Ci-6alkyloxyCι_6alkyl, Ci-6alkylthioCi-6alkyl, aminocarbonylCi-όalkyl, Ci-6alkyloxycarbonylCι_6alkyl, Cι_6alkylcarbonyl- Cι_6alkyl, Ci-6alkyloxycarbonyl, mono- or di(Ci-6alkyl)aminoCi-6alkyl, Ar1,
Ar^i-όalkyloxyCi-όalkyl; or a radical of formula _O-Rl0 (a-1),
_S_R10 (a-2),
-N-RiiR12 (a-3), wherein R10 is hydrogen, Cι_6alkyl, Ci-6alkylcarbonyl, Ar1, Ar^i-όalkyl,
Ci-6alkyloxycarbonylCi-6alkyl, or a radical of formula -Alk-OR13 or
-Alk-NR14R15; R1 i is hydrogen, Ci-6alkyl, Ar1 or AriCi-όalkyl; R12 is hydrogen, Ci-6alkyl, Cι_6alkylcarbonyl, Cι_6alkyloxycarbonyl, Cι_6alkylaminocarbonyl, Ar1, AriCi-βalkyl, Cι_6alkylcarbonyl-
Ci-6alkyl, A^carbonyl, A^Ci-όalkylcarbonyl, aminocarbonyl- carbonyl,
Cι_6alkyloxyCi-6alkylcarbonyl, hydroxy, Ci-6alkyloxy, aminocarbonyl, di(Ci-6alkyl)aminoCι___6alkylcarbonyl, amino, Ci-galkylamino, Ci-6alkylcarbonylamino, or a radical or formula -Alk-OR13 or -Alk-NR14R15; wherein Alk is Cι_6alkanediyl; Rl3 is hydrogen, Cι_6alkyl, Ci-6alkylcarbonyl, hydroxy- Ci-6alkyl, Ar1 or 
R14 is hydrogen, Ci-6alkyl, Ar1 or A^Ci-όalkyl; Rl5 is hydrogen, Ci-6alkyl, Ci-6alkylcarbonyl, Ar1 or AriCi-όalkyl;
R" is a radical of formula
-N (b-1), // ^_R16
(b-2).
NT
R R 17 wherein
R^is hydrogen, halo, Ar1, Cι_6alkyl, hydroxyCi-όalkyl, Ci-6alkyloxyCi-6alkyl, Ci-6alkyloxy, Ci-6alkylthio, amino, Ci-6alkyloxycarbonyl, Cι_6alkylthioCi-6alkyl, Ci-6alkylS(0)Cι_6alkyl or Cι_6alkyl- S(O)2Cι_6alkyl; R1^ is hydrogen, Cι_6alkyl or di(Ci-4alkyl)aminosulfonyl; R7 is hydrogen or Cι_6alkyl provided that the dotted line does not represent a bond; R8 is hydrogen, Ci-6alkyl or Ar CH2 or Het1CH2; R9 is hydrogen, Cι_6alkyl , Ci-6alkyloxy or halo; or
R8 and R9 taken together to form a bivalent radical of formula -CH=CH- (c-1),
-CH2-CH2- (c-2),
-CH2-CH2-CH2- (c-3),
-CH2-O- (c-4), or -CH2-CH2-O- (c-5);
Ar1 is phenyl; or phenyl substituted with 1 or 2 substituents each independently selected from halo, Cι_6alkyl, Ci-6alkyloxy or trifluoromethyl;
Ar2 is phenyl; or phenyl substituted with 1 or 2 substituents each independently selected from halo, Ci-6alkyl, Ci-6alkyloxy or trifluoromethyl; and
Het1 is pyridinyl; pyridinyl substituted with 1 or 2 substituents each independently selected from halo, Cι_6alkyl, Ci-6alkyloxy or trifluoromethyl
and 
or the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof, wherein =X'-X2-X3- is a trivalent radical of formula =N-CR6=CR7- (x-1), =CR6-CR7=CR8- (x-6),
=N-N=CR6- (x-2), =CR6-N=CR7- (x-7),
=N-NH-C(=O)- (x-3), =CR6-NH-C(=O)- (x-8), or
=N-N=N- (x-4), =CR6-N=N- (x-9);
=N-CR6=N- (x-5), wherein each R6, R7 and R8 are independently hydrogen, Cι_ alkyl, hydroxy,
Cι-4alkyloxy, aryloxy, Cι- alkyloxycarbonyl, hydroxyCι-4alkyl, Cι-4alkyloxyCι. alkyl, mono- or di(C1- alkyl)aminoC1-4alkyl, cyano, amino, thio, Cj- alkylthio, arylthio or aryl;
>Y*-Y2- is a trivalent radical of formula
>CH-CHR9- (y-i),
>C=N- (y-2),
>CH-NR9- (y-3),or
>C=CR9- (y-4); wherein each R9 independently is hydrogen, halo, halocarbonyl, aminocarbonyl, hydroxyC]_ alkyl, cyano, carboxyl, C1-4alkyl, Cι_4alkyloxy, C]- alkyloxyCι_ alkyl,
C].4alkyloxycarbonyl, mono- or di(Cι.4alkyl)amino, mono- or di(Cι-4alkyl)aminoCι- alkyl, aryl; r and s are each independently 0, 1, 2, 3, 4 or 5; t is 0, 1, 2 or 3; each R1 and R2 are independently hydroxy, halo, cyano, Ci-6alkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, C1-6alkyloxy, hydroxyC1- alkyloxy, C1- alkylthio, Cι_ alkyloxyCι-6alkyloxy, C1-6alkyloxycarbonyl, aminoCι.6alkyloxy, mono- or di(Cι-6alkyl)amino, mono- or di(Cι-6alkyl)aminoC1-6alkyloxy, aryl, arylCι-6alkyl, aryloxy or arylCι_6alkyloxy, hydroxycarbonyl, Cι_ alkyloxycarbonyl, aminocarbonyl, aminoCι.6alkyl, mono- or di(Cι-6alkyl)aminocarbonyl, mono- or di(Cι.6alkyl)aminoC]-6alkyl; or two R1 or R2 substituents adjacent to one another on the phenyl ring may independently form together a bivalent radical of formula
-O-CH2-O- (a-χ)'
-O-CH2-CH2-O- (a-2),
-O=CH=CH- (a-3), -O-CH2-CH2- (a-4),
-O-CH2-CH2- CH2- (a-5), or
-CH=CH-CH=CH- (a-6);
R3 is hydrogen, halo, C1- alkyl, cyano, haloCι-6alkyl, hydroxyC1-6alkyl, cyanoCι„6alkyl, aminoCι-6alkyl, Cι.6alkyloxyCι_6alkyl, C1- alkylthioC1-6alkyl, aminocarbonyl Cι- alkyl, hydroxycarbonyl, hydroxycarbonylCι_ alkyl,
C 1 - alkyloxycarbonylC ] -6alkyl , C 1 ^alkylcarbonylC 1 -6alkyl, C 1. alkyloxycarbonyl , aryl, arylC].6alkyloxyCi-6alkyl, mono- or di(C].6alkyl)aminoCι.6alkyl; or a radical of formula
-O-R10 (b-1), -S-R10 G>-2),
-NRnR12 (b-3), wherein
R10 is hydrogen, d^alkyl, Cι-6alkylcarbonyl, aryl, arylC1-6alkyl, Cι_6alkyloxy- carbonyld.6alkyl, or a radical of formula -Alk-OR13 or -Alk-NR14R15; R11 is hydrogen, d.6alkyl, aryl or arylCi-6alkyl;
R12 is hydrogen, C1-6alkyl, aryl, hydroxy, amino, Cι_6alkyloxy, Cι_6alkylcarbonyl- C1- alkyl, arylC1-6alkyl, Cι-6alkylcarbonylamino, mono- or di(Cι_6alkyl)amino, C1-6alkylcarbonyl, aminocarbonyl, arylcarbonyl, haloC1- alkylcarbonyl, arylC -6alkylcarbonyl , C 1 _6alkyloxycarbonyl, C 1 _6alkyloxyC 1 -6alkylcarbonyl , mono- or di(Cι.6alkyl)aminocarbonyl wherein the alkyl moiety may optionally be substituted by one or more substituents independently selected from aryl or C1-3alkyloxycarbonyl, aminocarbonylcarbonyl, mono- or di(d-6alkyl)aminoC1..6alkylcarbonyl, or a radical or formula -Alk-OR13 or -Alk-NR14R15; wherein Alk is C1-6alkanediyl;
R13 is hydrogen, C1-6alkyl, C1-6alkylcarbonyl, hydroxyCι_6alkyl, aryl or arylC1- alkyl;
R14 is hydrogen, Cι-6alkyl, aryl or arylC1-6alkyl; R15 is hydrogen, Cι-6alkyl, Cι-6alkylcarbonyl, aryl or arylCι-6alkyl; R4 is a radical of formula
Cι.6alkyloxyCι-6alkyl, Cι-6alkyloxy, d-6alkylthio, amino, mono- or di(Cι_ alkyl)amino, hydroxycarbonyl, d.6alkyloxycarbonyl, Cι-6alkylthioCι-6alkyl, d.6alkylS(O)C,.6alkyl or Cι.6alkylS(O)2C,.6alkyl; R16 may also be bound to one of the nitrogen atoms in the imidazole ring of formula (c-1) or (c-2), in which case the meaning of R16 when bound to the nitrogen is limited to hydrogen, aryl, C1-6alkyl, hydroxyC1-6alkyl, Cι-6alkyl- oxyCι_6alkyl, 
Cι.6alkylS(O)d.6alkyl or C1.6alkylS(O)2C,.6alkyl; R17 is hydrogen, d^alkyl, Cι-6alkyloxyCι.6alkyl, arylCι-6alkyl, trifluoromethyl or di(C alkyl)aminosulfonyl; R is Cι-6alkyl , Cj.6alkyloxy or halo; aryl is phenyl, naphthalenyl or phenyl substituted with 1 or more substituents each independently selected from halo, Cι_6alkyl, Cι-6alkyloxy or trifluoromethyl .
2. A combination as claimed in claim 1 wherein the farnesyl protein transferase inhibitor is a compound of formula (I) wherein X is oxygen and the dotted line represents a bond.
3. A combination as claimed in claim 1 or claim 2 wherein the farnesyl protein transferase inhibitor is a compound of formula (I) wherein R1 is hydrogen, Ci-6alkyl, Ci-6alkyloxyCi-6alkyl or mono- or di(Cι_6alkyl)aminoCι_6alkyl and wherein R3 is hydrogen and R2 is halo, Ci-βalkyl, C2-6alkenyl, Ci _6alkyloxy, trihalomethoxy or hydroxyCi-6alkyloxy.
4. A combination as claimed in any of the preceding claims wherein the farnesyl protein transferase inhibitor is a compound of formula (I) wherein R8 is hydrogen, hydroxy, haloCι_6alkyl, hydroxyCι_6alkyl, cyanoCi-βalkyl,
Ci-6alkyloxycarbonylCi-6alkyl, imidazolyl, or a radical of formula -NR^R12 wherein R is hydrogen or Ci-i2alkyl and R12 is hydrogen, Ci-6alkyl,
Ci-6alkyloxy, Ci_6alkyloxyCi-6alkylcarbonyl, hydroxy, or a radical of formula -Alk2-OR13 wherein R13 is hydrogen or Cι_6alkyl.
5. A combination as claimed in claim 1 wherein the farnesyl transferase inhibitor is selected from:
4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(l-methyl-lH-imidazol-5-yl)- methyl]- 1 -methyl-2( lH)-quinolinone, 6-[amino(4-chlorophenyl)-l-methyl-lH-imidazol-5-ylmethyl]-4-(3-chlorophenyl)- l-methyl-2(lH)-quinolinone;
6-[(4-chlorophenyl)hydroxy(l-methyl-lH-imidazol-5-yl)methyl]-4-(3-ethoxy- phenyl)-l-methyl-2(lH)-quinolinone;
6-[(4-chlorophenyl)(l-methyl-lH-imidazol-5-yl)methyl]-4-(3-ethoxyphenyl)-l- methyl-2(lH)-quinolinone monohydrochloride.monohydrate;
6-[amino(4-chlorophenyl)(l-methyl-lH-imidazol-5-yl)methyl]-4-(3-ethoxyphenyl)- l-methyl-2(lH)-quinolinone, and
6-amino(4-chlorophenyl)(l -methyl- lH-imidazol-5-yl)methyl]-l -methyl -4-(3- propylphenyl)-2(lH)-quinolinone; a stereoisomeric form thereof or a pharmaceutically acceptable acid or base addition salts thereof.
6. A combination as claimed in claim 1 wherein the farnesyl transferase inhibitor is (+)-6-[amino(4-chlorophenyl)(l-methyl-lH-imidazol-5-yl)methyl]-4-(3-chloro- phenyl)-l-methyl-2(lH)-quinolinone; or a pharmaceutically acceptable acid addition salt thereof.
7. A combination as claimed in claim 1 wherein the farnesyl protein transferase inhibitor is a compound of formula (IX) wherein =X'-X2-X3 is a trivalent radical of formula (x-2), (x-3) or (x-4), >Y1-Y2 is a trivalent radical of formula (y-2), (y-3) or (y-4), r and s are 1, t is 0, R1 is halo, preferably chloro, and most preferably 3- chloro or R1 is C1-4alkyl, preferably 3-methyl, R2 is halo, preferably chloro, and most preferably 4-chloro, R3 is a radical of formula (b-1) or (b-3), R4 is a radical of formula (c-2), R6 is C1-4alkyl, R9 is hydrogen, R10 and R11 are hydrogen and R12 is hydrogen or hydroxy.
. A combination as claimed in claim 1 wherein the farnesyl protein transferase inhibitor is 5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(l-methyl-lH-imidazoI-5- yl)tetrazolo[l,5-a]quinazoline-7-methanamine or a pharmaceutically acceptable acid addition salt thereof.
9. A combination as claimed in any of the preceding claims in which the anti-tumor anthracyline derivative is daunorubicin, doxorubicin or idarubicin.
10. A combination as claimed in any of the preceding claims in the form of a pharmaceutical composition comprising an anti-tumor anthracychne derivative and a farnesyl transferase inhibitor selected from compounds of formulae (I), (E), (El), (IV), (V), (VI), (VE), (VIE) and (IX) (as defined in claim 1) together with one or more pharmaceutical carriers.
11. A combination as claimed in any of the preceding claims for use in medical therapy.
12. A combination as claimed in claim 11 for inhibiting the growth of tumor cells.
13. Use of a combination as claimed in any of claims 1 to 12 in the manufacture of a pharmaceutical composition for inhibiting the growth of tumor cells.
14. A method of inhibiting the growth of tumor cells in a human subject which comprises administering to the subject an effective amount of a combination as claimed in any of claims 1 to 12.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01917033A EP1267872A2 (en) | 2000-02-29 | 2001-02-26 | Farnesyl protein transferase inhibitor combinations with anti-tumor anthracycline derivatives |
| CA002397253A CA2397253A1 (en) | 2000-02-29 | 2001-02-26 | Farnesyl protein transferase inhibitor combinations with anti-tumor anthracycline derivatives |
| AU2001244167A AU2001244167A1 (en) | 2000-02-29 | 2001-02-26 | Farnesyl protein transferase inhibitor combinations with anti-tumor anthracycline derivatives |
| JP2001563094A JP2003525237A (en) | 2000-02-29 | 2001-02-26 | Farnesyl protein transferase inhibitor combinations with antitumor anthracycline derivatives |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP00200696 | 2000-02-29 | ||
| EP00200696.3 | 2000-02-29 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2001064197A2 true WO2001064197A2 (en) | 2001-09-07 |
| WO2001064197A3 WO2001064197A3 (en) | 2002-03-21 |
Family
ID=8171115
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2001/002166 WO2001064197A2 (en) | 2000-02-29 | 2001-02-26 | Farnesyl protein transferase inhibitor combinations with anti-tumor anthracycline derivatives |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1267872A2 (en) |
| JP (1) | JP2003525237A (en) |
| AU (1) | AU2001244167A1 (en) |
| CA (1) | CA2397253A1 (en) |
| WO (1) | WO2001064197A2 (en) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004028541A2 (en) * | 2002-09-27 | 2004-04-08 | Societe De Conseils De Recherches Et D'applications Scientifiques, S.A.S. | Composition for the treatment of nasopharyngeal carcinoma and use thereof |
| WO2007075923A2 (en) | 2005-12-23 | 2007-07-05 | Link Medicine Corporation | Treatment of synucleinopathies |
| US7576215B2 (en) | 2003-12-12 | 2009-08-18 | Wyeth | Quinolines and pharmaceutical compositions thereof |
| US9221804B2 (en) | 2013-10-15 | 2015-12-29 | Janssen Pharmaceutica Nv | Secondary alcohol quinolinyl modulators of RORγt |
| US9284308B2 (en) | 2013-10-15 | 2016-03-15 | Janssen Pharmaceutica Nv | Methylene linked quinolinyl modulators of RORγt |
| US9290476B2 (en) | 2012-10-16 | 2016-03-22 | Janssen Pharmaceutica Nv | Methylene linked quinolinyl modulators of RORγt |
| US9303015B2 (en) | 2012-10-16 | 2016-04-05 | Janssen Pharmaceutica Nv | Heteroaryl linked quinolinyl modulators of RORγt |
| US9309222B2 (en) | 2012-10-16 | 2016-04-12 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
| US9328095B2 (en) | 2013-10-15 | 2016-05-03 | Janssen Pharmaceutica Nv | Heteroaryl linked quinolinyl modulators of RORgammat |
| US9346782B2 (en) | 2013-10-15 | 2016-05-24 | Janssen Pharmaceutica Nv | Alkyl linked quinolinyl modulators of RORγt |
| US9403816B2 (en) | 2013-10-15 | 2016-08-02 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
| US9624225B2 (en) | 2013-10-15 | 2017-04-18 | Janssen Pharmaceutica Nv | Quinolinyl modulators of RORγt |
| US10555941B2 (en) | 2013-10-15 | 2020-02-11 | Janssen Pharmaceutica Nv | Alkyl linked quinolinyl modulators of RORγt |
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2001
- 2001-02-26 WO PCT/EP2001/002166 patent/WO2001064197A2/en not_active Application Discontinuation
- 2001-02-26 AU AU2001244167A patent/AU2001244167A1/en not_active Abandoned
- 2001-02-26 EP EP01917033A patent/EP1267872A2/en not_active Withdrawn
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Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004028541A2 (en) * | 2002-09-27 | 2004-04-08 | Societe De Conseils De Recherches Et D'applications Scientifiques, S.A.S. | Composition for the treatment of nasopharyngeal carcinoma and use thereof |
| WO2004028541A3 (en) * | 2002-09-27 | 2004-07-01 | Sod Conseils Rech Applic | Composition for the treatment of nasopharyngeal carcinoma and use thereof |
| US7576215B2 (en) | 2003-12-12 | 2009-08-18 | Wyeth | Quinolines and pharmaceutical compositions thereof |
| WO2007075923A2 (en) | 2005-12-23 | 2007-07-05 | Link Medicine Corporation | Treatment of synucleinopathies |
| EP2545919A1 (en) | 2005-12-23 | 2013-01-16 | Link Medicine Corporation | Treatment of synucleinopathies |
| US9303015B2 (en) | 2012-10-16 | 2016-04-05 | Janssen Pharmaceutica Nv | Heteroaryl linked quinolinyl modulators of RORγt |
| US9290476B2 (en) | 2012-10-16 | 2016-03-22 | Janssen Pharmaceutica Nv | Methylene linked quinolinyl modulators of RORγt |
| US9309222B2 (en) | 2012-10-16 | 2016-04-12 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
| US9284308B2 (en) | 2013-10-15 | 2016-03-15 | Janssen Pharmaceutica Nv | Methylene linked quinolinyl modulators of RORγt |
| US9221804B2 (en) | 2013-10-15 | 2015-12-29 | Janssen Pharmaceutica Nv | Secondary alcohol quinolinyl modulators of RORγt |
| US9328095B2 (en) | 2013-10-15 | 2016-05-03 | Janssen Pharmaceutica Nv | Heteroaryl linked quinolinyl modulators of RORgammat |
| US9346782B2 (en) | 2013-10-15 | 2016-05-24 | Janssen Pharmaceutica Nv | Alkyl linked quinolinyl modulators of RORγt |
| US9403816B2 (en) | 2013-10-15 | 2016-08-02 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
| US9624225B2 (en) | 2013-10-15 | 2017-04-18 | Janssen Pharmaceutica Nv | Quinolinyl modulators of RORγt |
| US10201546B2 (en) | 2013-10-15 | 2019-02-12 | Janssen Pharmaceutica Nv | Quinolinyl modulators of RORγt |
| US10369146B2 (en) | 2013-10-15 | 2019-08-06 | Janssen Pharmaceutica Nv | Phenyl linked quinolinyl modulators of RORγt |
| US10555941B2 (en) | 2013-10-15 | 2020-02-11 | Janssen Pharmaceutica Nv | Alkyl linked quinolinyl modulators of RORγt |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2001244167A1 (en) | 2001-09-12 |
| JP2003525237A (en) | 2003-08-26 |
| WO2001064197A3 (en) | 2002-03-21 |
| CA2397253A1 (en) | 2001-09-07 |
| EP1267872A2 (en) | 2003-01-02 |
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