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PE20081679A1 - Compuestos del inhibidor de fosfoinositida 3-cinasa y metodos de uso - Google Patents

Compuestos del inhibidor de fosfoinositida 3-cinasa y metodos de uso

Info

Publication number
PE20081679A1
PE20081679A1 PE2007001726A PE2007001726A PE20081679A1 PE 20081679 A1 PE20081679 A1 PE 20081679A1 PE 2007001726 A PE2007001726 A PE 2007001726A PE 2007001726 A PE2007001726 A PE 2007001726A PE 20081679 A1 PE20081679 A1 PE 20081679A1
Authority
PE
Peru
Prior art keywords
aril
alkyl
phosphoinositide
methods
kinase inhibitor
Prior art date
Application number
PE2007001726A
Other languages
English (en)
Inventor
Tracy Bayliss
Irina Chuckowree
Adrian FOLKES
Sally Jane Oxenford
Nan Chi Wan
Georgette Castanedo
Richard Goldsmith
Janet Gunzner
Tim Heffron
Simon Mathieu
Alan Olivero
Daniel P Sutherlin
Bing-Yan Zhu
Steven Staben
Original Assignee
Hoffmann La Roche
Genentech Inc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39188533&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20081679(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche, Genentech Inc filed Critical Hoffmann La Roche
Publication of PE20081679A1 publication Critical patent/PE20081679A1/es

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • A61P31/12Antivirals
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    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
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    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
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Abstract

SE REFIERE A UN COMPUESTO DE FORMULA Ic, Id, DONDE X ES O, S; R1 ES A; R2 ES H, F, Cl, ARIL C6-C20, ENTRE OTROS; R3 ES PIRIDILO, ISOXAZOLIL, PIRIMIDINIL, TETRAZOLIL, ENTRE OTROS; R4 Y R5 SON JUNTO AL ATOMO DE N ADYANCENTE PIRROLIDINA, MORFOLINA, DIAZEPAN, 2,5-DIAZABICICLO[2,2,1]-HEPTANO, ENTRE OTROS; R30 ES H, ALQUIL C1-C6; mor ES UN GRUPO MORFOLINO SUSTITUIDO CON UNO O MAS Cl, I, C(ALQUIL C1-C6), -C(=O)NR12(CR14R15)mNR10R11, ENTRE OTROS; R10, R11 Y R12 SON H, ALQUENIL C2-C8, CARBOCICLIL C3-C12, ARIL C6-C20, ENTRE OTROS; R14 Y R15 SON H, ALQUIL C1-C12 O -(CH2)n-ARIL; m ES 0-1. SON COMPUESTOS SELECCIONADOS: 1-(4-((2-(2-AMINOPIRIMIDIN-5-IL)-4-MORFOLINOTIENO[3,2-d]PIRIMIDIN-6-IL)METIL)PIPERAZIN-1-IL)-2-(METILSULFONIL)ETANONA; 2-AMINO-1-(4-((2-(2-AMINOPIRIMIDIN-5-IL)-4-MORFOLINOTIENO[3,2-d]PIRIMIDIN-6-IL)METIL)PIPERAZIN-1-IL)ETANONA; ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO DE PREPARACION, COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON MODULADORES DE LA ACTIVIDAD CINASA, TAL COMO PI3K, UTIL EN EL TRATAMIENTO DE DESORDENES HIPERPROLIFERATIVOS COMO EL CANCER
PE2007001726A 2006-12-07 2007-12-05 Compuestos del inhibidor de fosfoinositida 3-cinasa y metodos de uso PE20081679A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US87344806P 2006-12-07 2006-12-07
US97725707P 2007-10-03 2007-10-03

Publications (1)

Publication Number Publication Date
PE20081679A1 true PE20081679A1 (es) 2008-12-18

Family

ID=39188533

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2007001726A PE20081679A1 (es) 2006-12-07 2007-12-05 Compuestos del inhibidor de fosfoinositida 3-cinasa y metodos de uso

Country Status (22)

Country Link
US (3) US7888352B2 (es)
EP (2) EP2518074B1 (es)
JP (1) JP5284977B2 (es)
KR (1) KR101460816B1 (es)
AR (1) AR064155A1 (es)
AU (1) AU2007329352B2 (es)
BR (1) BRPI0717923A2 (es)
CA (1) CA2671782C (es)
CL (1) CL2007003520A1 (es)
CO (1) CO6190615A2 (es)
CR (1) CR10915A (es)
EC (1) ECSP099496A (es)
ES (1) ES2544082T3 (es)
MA (1) MA31146B1 (es)
MX (1) MX2009005950A (es)
MY (1) MY180595A (es)
NO (1) NO20092566L (es)
NZ (1) NZ578162A (es)
PE (1) PE20081679A1 (es)
RU (1) RU2468027C2 (es)
TW (1) TWI499420B (es)
WO (1) WO2008070740A1 (es)

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