+

WO1999029666A1 - Derives d'arylpiperazine et d'arylpiperidine, leur mise au point et leur utilisation en tant qu'antagonistes des recepteurs de 5-ht1a, 5-ht1b et 5-ht1d combines - Google Patents

Derives d'arylpiperazine et d'arylpiperidine, leur mise au point et leur utilisation en tant qu'antagonistes des recepteurs de 5-ht1a, 5-ht1b et 5-ht1d combines Download PDF

Info

Publication number
WO1999029666A1
WO1999029666A1 PCT/EP1998/007803 EP9807803W WO9929666A1 WO 1999029666 A1 WO1999029666 A1 WO 1999029666A1 EP 9807803 W EP9807803 W EP 9807803W WO 9929666 A1 WO9929666 A1 WO 9929666A1
Authority
WO
WIPO (PCT)
Prior art keywords
formula
compound
methylpiperazin
indoline
group
Prior art date
Application number
PCT/EP1998/007803
Other languages
English (en)
Inventor
Laramie Mary Gaster
Paul Adrian Wyman
Original Assignee
Smithkline Beecham Plc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Smithkline Beecham Plc filed Critical Smithkline Beecham Plc
Publication of WO1999029666A1 publication Critical patent/WO1999029666A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/45—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by at least one doubly—bound oxygen atom, not being part of a —CHO group

Definitions

  • the present invention relates to novel piperazine derivatives, processes for their preparation, and pharmaceutical compositions containing them.
  • WO 95/04729, WO 95/06044 and WO 95/06637 all disclose a series of piperazine derivatives which are said to possess 5HTi£) receptor antagonist activity. These compounds are alleged to be of use in the treatment of various CNS disorders such as depression.
  • EPA 0533266/7/8 disclose a series of benzanilide derivatives which are said to possess 5-HTID receptor antagonist activity.
  • the 5-HTJD receptor was subsequently found to consist of a pair of gene products originally designated 5-HTjj) ⁇ and 5-HTjj) ⁇ receptors which have more recently been reclassified as 5-HTi ) and 5-HT ⁇ g receptors respectively (Hartig, P.R. et al., Trends in Pharmacological Sciences 1992, Vol. 13, page 152, Hartig, P.R. et al., Trends in Pharmacological Sciences, 1996, Vol. 17, page 103).
  • the present invention therefore provides a compound of formula (I) or a salt thereof:
  • the ring A is 5, 6 or 7 -membered carbocyclic ring optionally substituted by one or more C ⁇ _6alkyl groups, fused at the 2,3- or 3,4-positions of the adjacent phenyl ring, the ring A being optionally fused to a further phenyl ring optionally substituted by one or more substituents independently selected from C ⁇ _6alkyl and halo;
  • R 2 is halogen, Cj.galkyl, C3_6cycloalkyl, C3_6cycloalkenyl, C ⁇ alkoxy, C ⁇ galkanoyl, aryl, acyloxy, hydroxy, nitro, trifluoromethyl, cyano, CO2 10 , CON 1°R11, NR1°R11 where R O and Ri 1 are independently hydrogen or
  • L is a group of formula
  • D is nitrogen, carbon or a CH group
  • G is hydrogen or C ⁇ galkyl providing that D is nitrogen or a CH group
  • Rbl forms a group W where W is (CR ⁇ R ⁇ )t where t is
  • X is nitrogen or carbon
  • Rbl and R 2 are independently hydrogen, halogen, hydroxy, Cj. ⁇ alkyl,
  • R c is hydrogen or C 1 _6alkyl; and is a single bond when X is nitrogen or a single or double bond when X is carbon.
  • Cj.galkyl groups whether alone or as part of another group may be straight chain or branched.
  • the term 'acyloxy' is used herein to describe a group -OC(O)C ⁇ _6alkyl.
  • the term 'aryl' is used herein to describe, unless otherwise stated, a group such as phenyl.
  • the term 'halogen' is used herein to describe, unless otherwise stated, a group selected from fluorine, chlorine, bromine or iodine.
  • the ring A is preferably formed from a straight chain alkylene grouping containing 2, 3 or 4 carbon atoms.
  • the ring A is preferably a 5 or 6-membered ring in which the oxo group is advantageously attached to a carbon atom adjacent to the phenyl ring, the ring A being preferably attached to the 3,4-positions of the latter phenyl ring, a is preferably 0 or 1 ;
  • R 2 is preferably halogen for example a chloro group or a Cj. ⁇ alkyl group for example a methyl group;
  • the group L is preferably a group of formula: -
  • Y is preferably -NH
  • D is preferably nitrogen and G is preferably a hydrogen atom or together with Rbl forms a group W, preferably -(CH2)2->
  • Rbl and Rb2 are preferably hydrogen or a halogen atom for example bromine or chlorine, or a C ⁇ . ⁇ a ⁇ koxy group for example methoxy, or Rbl together with G forms the group W referred to above.
  • Rb2 has a para relationship with respect to the group L.
  • X is preferably nitrogen.
  • R c is preferably a C ⁇ _6alkyl group for example methyl.
  • Particularly preferred compounds according to the invention include:-
  • Preferred salts of the compounds of formula (I) are pharmaceutically acceptable salts. These include acid addition salts such as hydrochlorides, hydro bromides, phosphates, acetates, fumarates, maleates, tartrates, citrates, oxalates, methanesulphonates and p- toluenesulphonates.
  • acid addition salts such as hydrochlorides, hydro bromides, phosphates, acetates, fumarates, maleates, tartrates, citrates, oxalates, methanesulphonates and p- toluenesulphonates.
  • R -NC( O) (IV) in which R a is defined in formula (I) or a protected derivative thereof, with a compound of formula (V):
  • R a _ ⁇ _ ( 0) - L 3 (VH) in which R a is as defined in formula (I), and L 3 is an appropriate leaving group, with a compound of formula (V):or
  • L,l and L2 include:-
  • L is COL a and L 2 is NH 2 .
  • Li is NH2 and L2 is COL a in which L a is an appropriate leaving group.
  • L a is an appropriate leaving group.
  • one of Ll and L is an activated carboxyhc acid derivative such as an acyl chloride or acid anhydride, and the other is an amine group.
  • Activated compounds of formulae (II) and (III) can also be prepared by reaction of the corresponding carboxyhc acid with a coupling agent such as dicyclohexylcarbodiimide, carbonyldiimidazole or diphenylphosphorylazide.
  • L.1 or L is a group COL a where L a is halo particularly chloro.
  • reaction in process (b) is conveniently effected in an organic solvent such as dichloromethane.
  • the urea forming agent can be carbonyl diimidazole, triphosgene or phosgene, and carried out in an inert organic solvent such as dimethylformamide, tetrahydrofuran or dichloromethane at ambient or elevated temperature in the presence of a base such as triethylamine or pyridine.
  • the leaving group L 3 may be a halogen e.g. chloro group and the reaction may be carried out in an inert organic solvent such as tetrahydrofuran or dichloromethane at ambient or elevated temperature in the presence of a base such as triethylamine or pyridine.
  • the leaving group L 3 may be a halogen e.g. chloro group and the reaction may be carried out in an inert organic solvent such as tetrahydrofuran or dichloromethane at ambient or elevated temperature in the presence of a base such as triethylamine or pyridine.
  • an inert organic solvent such as tetrahydrofuran or dichloromethane
  • a base such as triethylamine or pyridine.
  • Intermediate compounds of formula (II) to (VET) can be prepared using standard procedures known in the art. It will be appreciated to those skilled in the art that it may be necessary to protect certain reactive substituents during some of the above procedures. Standard protection and deprotection techniques can be used. For example, primary amines can be protected as phthalimide, benzyl, benzyloxycarbonyl or trityl derivatives. These groups can be removed by conventional procedures well known in the art. Carboxyhc acid groups can be protected as esters. Aldehyde or ketone groups can be protected as acetals, ketals, thioacetals or thioketals. Deprotection is achieved using standard conditions.
  • Serotonin receptors have been implicated in pharmacological effects such as mood disorders including depression, seasonal affective disorder and dysthymia, anxiety disorders, including generalised anxiety, panic disorder, agoraphobia, social phobia, obsessive compulsive disorder and post-traumatic stress disorder; memory disorders, including dementia, amnesic disorders and age-associated memory impairment; disorders of eating behaviours, including anorexia nervosa and bulimia nervosa, sleep disorders (including disturbances of Circadian rhythm), motor disorders such as Parkinson's disease, dementia in Parkinson's disease, neuroleptic-induced Parkinsonism and tardive dyskinesias, as well as other psychiatric disorders.
  • mood disorders including depression, seasonal affective disorder and dysthymia
  • anxiety disorders including generalised anxiety, panic disorder, agoraphobia, social phobia, obsessive compulsive disorder and post-traumatic stress disorder
  • memory disorders including dementia, amnesic disorders and age-associated memory impairment
  • disorders of eating behaviours including an
  • Serotonin receptor ligands have been shown to be of use in the treatment of emesis and nausea and may also be of use in endocrine disorders such as hyperlactinaemia, vasospasm (particularly in the cerebral vasculature), cerebellar ataxia and hypertension, as well as disorders of the gastrointestinal tract where changes in motility and secretion are involved. They may also be of use in the treatment of sexual dysfunction and hypothermia.
  • WO 95/31988 refers to the use of a 5-HT ⁇ rj receptor antagonist in conjunction with a 5-HT ⁇ receptor antagonist to treat CNS (central nervous system), endocrine and GI (gastrointestinal) disorders
  • K. Rasmussen Annual Reports in Medicinal Chemistry, (1995) 30, 1) describes the utility of 5-HTJA receptor agonists and partial agonists in the treatment of various CNS disorders
  • P. Trouillas Progress in Brain Research, C.I. de Zeeuw, P. Stara and J. Voogd, Eds. 1997, 144, 589) and G. Maura (J.
  • the present invention also provides a compound of general formula (I) or a physiologically acceptable salt or solvate thereof for use in the treatment of the aforementioned disorders.
  • the invention provides a method of treating the aforementioned disorders which comprises administering an effective amount to a patient in need of such treatment of a compound of general formula (I) or a pharmaceutically acceptable salt or solvate thereof.
  • a compound of general formula (I) or a physiologically acceptable salt or solvate thereof for use in the treatment or prophylaxis of depression.
  • the affinities of the compounds of this invention for the 5HTIA > 5-HTJB nd 5-HTID receptors can be determined by the following radioUgand binding assay.
  • HEK 293 cells expressing 5-HT ⁇ A receptors (4 x 10 7 /ml) are homogenised in Tris buffer and stored in lml aliquots.
  • CHO cells expressing 5-HTJB receptors (4 x 10 7 cells/ml) are homogenised in Tris buffer and stored in 1.5 ml aliquots.
  • CHO cells expressing 5-HTID receptors (0.563 x 10 ⁇ /ml) are homogenised in Tris buffer and stored in 1 ml aliquots.
  • the intrinsic activity of the compounds of this invention can be determined according to the following procedure.
  • HEK293 cell membranes stably expressing human 5-HTj x_ receptors and CHO cell membranes stably expressing human 5-HTJB receptors are homogenised in HEPES/EDTA buffer and stored in 1ml aliquots, and [ 3 5S]GTP ⁇ S binding studies are carried out essentially as described by Lazareno et al., (Life Sci., 1993, 52, 449) with some minor modifications.
  • Membranes from 10 ⁇ cells are pre-incubated at 30°C for 30 min in 20 mM HEPES buffer (pH 7.4) in the presence of MgCl2 (3 mM), NaCl (100 mM), GDP (lO ⁇ M) and ascorbate (0.2 mM), with or without compounds.
  • the reaction is started by the addition of 10 ⁇ l of [ 3 ⁇ S]GTP ⁇ S (100 pM, assay concentration) followed by a further 30 minutes incubation at 30°C.
  • Non-specific binding was determined using non- radiolabelled GTP ⁇ S (20 ⁇ M) added prior to the membranes.
  • the reaction is terminated by rapid filtration through Whatman GF/B grade filters followed by 5 x 1 ml washes with ice cold HEPES (20 mM) /MgCl2 (3 mM) buffer. Radioactivity is measured using liquid scintillation spectrometry. This procedure is hereafter referred to as the [ ⁇ S]GTP ⁇ S functional assay.
  • the compounds of formula (I) show high affinity for the 5HTIA > 5-HTIB and 5-HTjr) receptors. It has been found, using the [ 3 5s]GTP ⁇ S functional assay, that certain compounds of formula (I) show varying levels of intrinsic efficacy, which is defined by a scale ranging from 1.0 to 0 (1 defines the maximum response elicited by the agonist 5-HT, 0 defines antagonism).
  • the difficulties in describing intrinsic activity of drugs acting at G protein coupled receptors is recognised in the art (Hoyer and Boddeke, Trends in Pharmacological Sciences, July 1993, [Vol. 14], page 270-275).
  • the compounds of this invention will be useful antidepressants in vivo. It is believed that the preferred compounds of this invention will display 5HTj A> -HTJB and 5-HTij) antagonist activity in vivo and that such compounds will have a rapid onset of action.
  • a rapid onset of action is particularly advantageous for antidepressant compounds: by 'rapid onset of action' we mean that a therapeutic response is seen within 7 days from first administration of the compound, as opposed to a period of about 21 days or more which is typical of SSRI's, tricyclic antidepressants and buspirone.
  • the present invention also provides a pharmaceutical composition, which comprises a compound of formula (I) or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
  • a pharmaceutical composition of the invention which may be prepared by admixture, suitably at ambient temperature and atmospheric pressure, is usually adapted for oral, parenteral or rectal administration and, as such, may be in the form of tablets, capsules, oral liquid preparations, powders, granules, lozenges, reconstitutable powders, injectable or infusible solutions or suspensions or suppositories. Orally administrable compositions are generally preferred.
  • Tablets and capsules for oral administration may be in unit dose form, and may contain conventional excipients, such as binding agents, fillers, tabletting lubricants, disintegrants and acceptable wetting agents.
  • the tablets may be coated according to methods well known in normal pharmaceutical practice.
  • Oral liquid preparations may be in the form of, for example, aqueous or oily suspension, solutions, emulsions, syrups or elixirs, or may be in the form of a dry product for reconstitution with water or other suitable vehicle before use.
  • Such liquid preparations may contain conventional additives such as suspending agents, emulsifying agents, non-aqueous vehicles (which may include edible oils), preservatives, and, if desired, conventional flavourings or colorants.
  • fluid unit dosage forms are prepared utilising a compound of the invention or pharmaceutically acceptable salt thereof and a sterile vehicle.
  • the compound depending on the vehicle and concentration used, can be either suspended or dissolved in the vehicle.
  • the compound can be dissolved for injection and filter sterilised before filling into a suitable vial or ampoule and sealing.
  • adjuvants such as a local anaesthetic, preservatives and buffering agents are dissolved in the vehicle.
  • the composition can be frozen after filling into the vial and the water removed under vacuum.
  • Parenteral suspensions are prepared in substantially the same manner, except that the compound is suspended in the vehicle instead of being dissolved, and sterilisation cannot be accomplished by filtration.
  • the compound can be sterilised by exposure to ethylene oxide before suspension in a sterile vehicle.
  • a surfactant or wetting agent is included in the composition to facilitate uniform distribution of the compound.
  • the composition may contain from 0.1% to 99% by weight, preferably from 10 to 60% by weight, of the active material, depending on the method of administration.
  • suitable unit doses may be 0.05 to 1000 mg, more suitably 1.0 to 200 mg, and such unit doses may be administered more than once a day, for example two or three a day. Such therapy may extend for a number of weeks or months.
  • Example 3 5-Bromo-6-(4-methylpiperazin-l-yl)-l-[(l-oxoindan-5-yl)aminocarbonyl]indoIine (E3)
  • the title compound was prepared from 5-amino-l-indanone and 5-bromo-6-(4- methylpiperazin-l-yl)indoline (D7) using a similar method to Example 1.
  • the title compound was prepared from 7-amino-l -tetralone (EP 0275131) and 5-bromo-6-(4- methylpiperazin-l-yl)indoline (DI) using a similar method to Example 1. This was isolated as its hydrochloride salt.
  • the title compound was prepared from 7-amino-l -tetralone (EP 0275131) and 5-chloro-6-(4- methylpiperazin-l-yl)indoline (D5) using a similar method to Example 1. This was isolated as its hydrochloride salt.
  • the title compound was prepared from 2-amino-9H-fluoren-9-one and 5-chloro-6-(4- methylpiperazin-l-yl)indoline (D5) using a similar procedure to Example 1, as an orange solid (46%).
  • the title compound was prepared from 3-amino-9H-fluoren-9-one and 5-chloro-6-(4- methylpiperazin-l-yl)indoline (D5) using a similar procedure to Example 1, as a yellow/orange solid (66%).
  • the title compound was prepared from 5-amino-l -tetralone (D9) and 5-chloro-6-(4- methylpiperazin-l-yl)indoline (D5) using a similar method to Example 1, as the hydrochloride salt, a buff solid (30%).
  • the title compound was prepared from 5-amino-l -tetralone (D9) and 5-methoxy-6-(4- methylpiperazin-l-yl)indoline (Intermediate 3 in WO 95/06627) using a similar method to Example 1, as the hydrochloride salt, a buff solid (33%).
  • affinities of the compounds of this invention were determined by methods described above.
  • 5-HT ⁇ A > 5-HT ⁇ B a nd 5-HTID Receptor Binding
  • Examples 1, 2, 3, 4, 9, 10, 11 and 14 had pKi values > 7.5 at 5-HT ⁇ A, 5-HTIB and 5-HTID receptors.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Cette invention a trait à des composés correspondant à la formule (I) ou à l'un de leurs sels ayant une activité pharmacologique, formule dans laquelle Ra représente le groupe (1) dans lequel le noyau A représente un noyau carbocyclique à 5, 6 ou 7 ramifications éventuellement substitué par un ou plusieurs groupes alkyles comportant de 1 à 6 atomes de carbone, avec fusion sur les positions 2,3 ou 3,4 du noyau phényle adjacent, ce noyau A étant éventuellement fusionné à un autre noyau phényle éventuellement substitué par un ou plusieurs substituants sélectionnés, de manière indépendante, entre un alkyle comportant de 1 à 6 atomes de carbone et un halo, R2 représente un halogène, un alkyle comportant de 1 à 6 atomes de carbone, un cycloalkyle comportant de 3 à 6 atomes de carbone, un cycloalcényle comportant de 3 à 6 atomes de carbone, un alcoxy comportant de 1 à 6 atomes de carbone, un alcanoyle comportant de 1 à 6 atomes de carbone, un aryle, un hydroxy, un nitro, un trifluorométhyle, un cyano, CO¿2?R?10, CONR10R11, NR10R11 où R10 et R11¿ représentent, de manière indépendante, un hydrogène ou un alkyle comportant de 1 à 6 atomes de carbone, a valant 0, 1 ou 2, L représente un groupe correspondant à la formule: -Y-C(=O)-DG- ou C(=O)-DG ou -DG-C(=O)-, formule dans laquelle Y représente -NH-, NR5 où R5 représente un alkyle comportant de 1 à 6 atomes de carbone, ou bien Y représente -CH¿2?- ou -O-, D représente un azote, un carbone ou un groupe CH, G représente un hydrogène ou un alkyle comportant de 1 à 6 atomes de carbone, à condition que D représente un azote ou un groupe CH ou bien G et R?11¿ constituent un groupe W dans lequel W représente (CR16R17) où t vaut 2, 3 ou 4 et R?16 et R17¿ représentent, de manière indépendante, un hydrogène ou un alkyle comportant de 1 à 6 atomes de carbone ou bien W représente (CR16R17)u-J où u vaut 0, 1, 2 ou 3 et où J représente un oxygène, un soufre, CR?16=R17, CR16=N, =CR16O, =CR16¿S ou =CR16-NR17, à condition que la valeur de u ne soit pas 0 lorsque J représente un oxygène ou un soufre, X représente un azote ou un carbone, R?b1 et Rb2¿ représentent, de manière indépendante, un hydrogène, un halogène, un hydroxy, un alkyle comportant de 1 à 6 atomes de carbone, un alcényle comportant de 2 à 6 atomes de carbone, un cycloalkyle comportant de 3 à 6 atomes de carbone, un trifluorométhyle, un alcoxy comportant de 1 à 6 atomes de carbone ou bien Rb1 et G forment un groupe W tel que défini ci-dessus, Rc représente un hydrogène ou un alkyle comportant de 1 à 6 atomes de carbone et ........ représente une liaison unique lorsque X représente un azote ou bien une liaison unique ou double lorsque X représente un carbone. Cette invention concerne également des procédés de mise au point de ces composés, des compositions les renfermant et leur utilisation dans le traitement d'affections du système nerveux central.
PCT/EP1998/007803 1997-12-05 1998-12-01 Derives d'arylpiperazine et d'arylpiperidine, leur mise au point et leur utilisation en tant qu'antagonistes des recepteurs de 5-ht1a, 5-ht1b et 5-ht1d combines WO1999029666A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9725931.1A GB9725931D0 (en) 1997-12-05 1997-12-05 Novel compounds
GB9725931.1 1997-12-05

Publications (1)

Publication Number Publication Date
WO1999029666A1 true WO1999029666A1 (fr) 1999-06-17

Family

ID=10823279

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1998/007803 WO1999029666A1 (fr) 1997-12-05 1998-12-01 Derives d'arylpiperazine et d'arylpiperidine, leur mise au point et leur utilisation en tant qu'antagonistes des recepteurs de 5-ht1a, 5-ht1b et 5-ht1d combines

Country Status (2)

Country Link
GB (1) GB9725931D0 (fr)
WO (1) WO1999029666A1 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001023374A1 (fr) * 1999-09-25 2001-04-05 Smithkline Beecham P.L.C. Derives de piperazine utilises en tant qu'antagonistes de 5-ht1b
WO2002074764A2 (fr) * 2001-03-15 2002-09-26 Smithkline Beecham P.L.C. Derives de la piperazine, leur preparation et leurs applications therapeutiques
WO2004110994A1 (fr) * 2003-06-18 2004-12-23 Pfizer Products Inc. Nouveaux lactames de piperazinyl-aryloxy et de piperazinyl-heteroaryloxy-n-aryle
WO2020048043A1 (fr) * 2018-09-06 2020-03-12 中国科学院上海药物研究所 Composé d'aniline pour la prévention ou le traitement d'un trouble mental
WO2020183011A1 (fr) 2019-03-14 2020-09-17 Institut Curie Inhibiteurs de htr1d et leurs utilisations dans le traitement du cancer

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995004729A1 (fr) * 1993-08-06 1995-02-16 Smithkline Beecham Plc Derives amides employes comme antagonistes du recepteur 5ht1d
WO1995006044A1 (fr) * 1993-08-20 1995-03-02 Smithkline Beecham Plc Derives d'amide et d'uree en tant qu'antagonistes du recepteur 5ht1d
WO1995006637A1 (fr) * 1993-09-03 1995-03-09 Smithkline Beecham Plc Nouveaux derives d'indole et d'indoline en tant qu'antagonistes du recepteur de 5ht1d
WO1998047885A1 (fr) * 1997-04-18 1998-10-29 Smithkline Beecham Plc Aryl bicyclique ou noyau heterocyclique bicyclique contenant des composes presentant une activite antagoniste combinee contre les recepteurs 5ht1a, 5ht1b et 5ht1d
WO1998050358A1 (fr) * 1997-04-18 1998-11-12 Smithkline Beecham Plc Derives indoliques a activite de recepteur antagoniste 5ht1a, 5ht1b, 5ht1d

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995004729A1 (fr) * 1993-08-06 1995-02-16 Smithkline Beecham Plc Derives amides employes comme antagonistes du recepteur 5ht1d
WO1995006044A1 (fr) * 1993-08-20 1995-03-02 Smithkline Beecham Plc Derives d'amide et d'uree en tant qu'antagonistes du recepteur 5ht1d
WO1995006637A1 (fr) * 1993-09-03 1995-03-09 Smithkline Beecham Plc Nouveaux derives d'indole et d'indoline en tant qu'antagonistes du recepteur de 5ht1d
WO1998047885A1 (fr) * 1997-04-18 1998-10-29 Smithkline Beecham Plc Aryl bicyclique ou noyau heterocyclique bicyclique contenant des composes presentant une activite antagoniste combinee contre les recepteurs 5ht1a, 5ht1b et 5ht1d
WO1998050358A1 (fr) * 1997-04-18 1998-11-12 Smithkline Beecham Plc Derives indoliques a activite de recepteur antagoniste 5ht1a, 5ht1b, 5ht1d

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
PAUWELS P.J. & PALMIER C.: "Functional effects of the 5-HT1D receptor antagonist GR 127,935 at human 5-HT1D.alpha., 5-HT1D.beta., 5-HT1A and opossum 5-HT1B receptors", EUROPEAN JOURNAL OF PHARMACOLOGY. MOLECULAR PHARMACOLOGY SECTION, vol. 290, no. 2, 1995, pages 95 - 103, XP000612639 *
SCHOEFFTER P. & HOYER D.: "Interaction of arylpiperazines with 5-HT1A, 5-HT1B, 5-HT1C and 5-HT1D receptors: Do discriminatory 5-HT1B receptor ligands exist?", NAUNYN-SCHMIEDEBERG'S ARCHIVES OF PHARMACOLOGY, vol. 339, no. 6, 1 June 1989 (1989-06-01), pages 675 - 683, XP000576360 *
STARKEY S.J. & SKINGLE M.: "5-HT1D as well as 5-HT1A autoreceptors modulate 5-HT release in the guinea-pig dorsal Raphé nucleus", NEUROPHARMACOLOGY, vol. 33, no. 3/4, 1994, pages 393 - 402, XP000654898 *

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001023374A1 (fr) * 1999-09-25 2001-04-05 Smithkline Beecham P.L.C. Derives de piperazine utilises en tant qu'antagonistes de 5-ht1b
US6747030B1 (en) 1999-09-25 2004-06-08 Smithkline Beecham P.L.C. Piperazine derivatives as 5-HT1B antagonists
WO2002074764A2 (fr) * 2001-03-15 2002-09-26 Smithkline Beecham P.L.C. Derives de la piperazine, leur preparation et leurs applications therapeutiques
WO2002074764A3 (fr) * 2001-03-15 2002-11-14 Smithkline Beecham Plc Derives de la piperazine, leur preparation et leurs applications therapeutiques
US7109201B2 (en) 2001-03-15 2006-09-19 Smithkline Beecham Plc Piperazine derivatives, their preparation and uses in therapy
WO2004110994A1 (fr) * 2003-06-18 2004-12-23 Pfizer Products Inc. Nouveaux lactames de piperazinyl-aryloxy et de piperazinyl-heteroaryloxy-n-aryle
US7101885B2 (en) 2003-06-18 2006-09-05 Pfizer Inc Piperazinyl-aryloxy and piperazinyl-heteroaryloxy-n-aryl lactams
WO2020048043A1 (fr) * 2018-09-06 2020-03-12 中国科学院上海药物研究所 Composé d'aniline pour la prévention ou le traitement d'un trouble mental
WO2020183011A1 (fr) 2019-03-14 2020-09-17 Institut Curie Inhibiteurs de htr1d et leurs utilisations dans le traitement du cancer

Also Published As

Publication number Publication date
GB9725931D0 (en) 1998-02-04

Similar Documents

Publication Publication Date Title
US6787535B2 (en) Indole derivatives with 5HT6 receptor affinity
US5750700A (en) Certain 1-substituted aminomethyl imidazole and pyrrole derivatives: novel dopamine receptor subtype specific ligands
AU665207B2 (en) Quinazoline derivatives as acetylcholinesterase inhibitors
AU3036000A (en) Compounds
EP0960110B8 (fr) Derives de pyrazolo[4,3-d]pyrimidine a substitution aryle en position 3; ligands specifiques au recepteur de facteur liberateur de corticotrophine (crf1)
JP2004509894A (ja) 置換アゼピノ［４，５−ｂ］インドリン誘導体
US6391891B1 (en) Bicyclic compounds as ligands for 5-HT1 receptors
WO1999031086A1 (fr) Derives de quinoleinepiperazine et de quinoleinepiperidine, leur preparation et leur utilisation en tant qu'antagonistes combines des recepteurs 5-ht1a, 5-ht1b et 5-ht1d
WO1998047868A1 (fr) Derives d'uree contenant un heterocycle utilises comme antagonistes des recepteurs 5ht1a, 5ht1b et 5ht¿1d?
MXPA05002743A (es) Derivados arilpiperazina de benzodioxanos con heterociclos fusionados antidepresivos.
UA54449C2 (uk) 3-заміщені похідні піридо[4',3':4,5]тієно[2,3-d]піримідину
EP1228043A1 (fr) Derives d'isoquinoline et de quinazoline dotes d'une activite combinee de recepteur 5ht1a, 5ht1b et 5ht1d
WO1999029666A1 (fr) Derives d'arylpiperazine et d'arylpiperidine, leur mise au point et leur utilisation en tant qu'antagonistes des recepteurs de 5-ht1a, 5-ht1b et 5-ht1d combines
US5175158A (en) Condensed diazepinones, processes for preparing them and pharmaceutical compositions containing these compounds
US4273773A (en) Antihypertensive tricyclic isoindole derivatives
BG104151A (bg) 3-ЗАМЕСТЕНИ 3,4,5,7-ТЕТРАХИДРОПИРОЛО [3,4,:4,5] ТИЕНО [2,39г] ПИРИМИДИНОВИ ПРОИЗВОДНИ, ТЯХНОТО ПОЛУЧАВАНЕ И ИЗПОЛЗВАНЕ
EP1233965A1 (fr) Derives d'isoquinoline et de quinazoline destines au traitement des troubles du snc
JPH0733743A (ja) ２−アリール−４−キノリノール誘導体
EP0743946A1 (fr) Indoles condenses a titre d'antagonistes des recepteurs de 5ht 2b?
JP2004529124A (ja) ５−ｈｔ１ｂリガンドとしてのピペラジン誘導体およびその使用
JPS63502032A (ja) 抗精神病薬としての２，３−ジヒドロ−１ｈ−フェナレン−２−アミノ化合物
DK159108B (da) Analogifremgangsmaade til fremstilling af 6-anilino-5,8-quinoxalindioner
US6002005A (en) Certain 1-substituted aminomethyl imidazole and pyrrole derivatives: novel dopamine receptor subtype specific ligands
EP1226120B1 (fr) Utilisation de benz[f]indoles dans le traitement de troubles dus au recepteur 5ht
JP2007523073A (ja) ジウレア誘導体

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): CA JP US

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase

Ref country code: CA

点击 这是indexloc提供的php浏览器服务，不要输入任何密码和下载