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AR066513A1 - Derivado de quinoxalina composicion farmaceutica que lo comprende y su uso para preparar un medicamento util como inhibidor de la pi3 quinasa - Google Patents

Derivado de quinoxalina composicion farmaceutica que lo comprende y su uso para preparar un medicamento util como inhibidor de la pi3 quinasa

Info

Publication number
AR066513A1
AR066513A1 ARP080101977A ARP080101977A AR066513A1 AR 066513 A1 AR066513 A1 AR 066513A1 AR P080101977 A ARP080101977 A AR P080101977A AR P080101977 A ARP080101977 A AR P080101977A AR 066513 A1 AR066513 A1 AR 066513A1
Authority
AR
Argentina
Prior art keywords
substituted
prepare
formula
quinoxaline
diseases
Prior art date
Application number
ARP080101977A
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English (en)
Original Assignee
Smithkline Beecham Corp
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.)
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Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40002590&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR066513(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Publication of AR066513A1 publication Critical patent/AR066513A1/es

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    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

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  • Health & Medical Sciences (AREA)
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  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
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  • Virology (AREA)
  • Psychology (AREA)
  • Diabetes (AREA)
  • Transplantation (AREA)
  • Endocrinology (AREA)
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Abstract

Un compuesto derivado de quinoxalina de formula (1), en la que: R1 es un sistema de anillos opcionalmente sustituidos seleccionado entre un grupo que consiste en: formula (2), (3), (4), (5), (6), (7) y (8); cada R2, R3 y R4 se seleccionaindependientemente entre: hidrogeno, halogeno, acilo, amino, amino sustituido, arilamino, acilamino, heterocicloalquilamino, alquilo C1-6, alquilo C1-6 sustituido, cicloalquilo C3-7, cicloalquilo C3-7 sustituido, heterocicloalquilo C3-7,heterocicloalquilo C3-7 sustituido, alquilcarboxi, aminoalquilo, arilo, arilo sustituido, heteroarilo, heteroarilo sustituido, arilalquilo, arilalquilo sustituido, arilcicloalquilo, arilcicloalquilo sustituido, heteroarilalquilo, heteroarilalquilosustituido, ciano, hidroxilo, alcoxi, aciloxi y ariloxi; n es 0-2; X es C o N; Y es C, O, N o S; y/o una sal farmacéuticamente aceptable del mismo; con la condicion de que en cada una de las formulas (5) a (8) al menos un Y no sea carbono; con lacondicion adicional de que la formula (8) esté sustituida con al menos un grupo oxo; con la condicion adicional de que R1 no sea imidazolidinadiona, y cuando R1 es 4-piridinilo, R2 no sea arilo sustituido, tienilo o tienilo sustituido. Composicionfarmacéutica que los comprende y su uso para preparar un medicamento util para inhibir una o más fosfatoinosítido 3-quinasas (PI3K) en un ser humano y para tratar una o más patologías seleccionadas entre: trastornos autoinmunes, enfermedadesinflamatorias, enfermedades cardiovasculares, enfermedades neurodegenerativas, alergia, asma, pancreatitis, fallo multiorgánico, enfermedades renales, agregacion plaquetaria, cáncer, motilidad de los espermatozoides, rechazo de trasplantes, rechazode injertos y lesiones pulmonares, mediante la administracion de derivados de quinoxalina. Su uso para preparar un medicamento util para tratar cánceres en coadministracion con al menos un agente antineoplásico.
ARP080101977A 2007-05-10 2008-05-09 Derivado de quinoxalina composicion farmaceutica que lo comprende y su uso para preparar un medicamento util como inhibidor de la pi3 quinasa AR066513A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US91712007P 2007-05-10 2007-05-10

Publications (1)

Publication Number Publication Date
AR066513A1 true AR066513A1 (es) 2009-08-26

Family

ID=40002590

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080101977A AR066513A1 (es) 2007-05-10 2008-05-09 Derivado de quinoxalina composicion farmaceutica que lo comprende y su uso para preparar un medicamento util como inhibidor de la pi3 quinasa

Country Status (8)

Country Link
US (2) US20100234386A1 (es)
EP (1) EP2150255A4 (es)
JP (1) JP2010526823A (es)
AR (1) AR066513A1 (es)
CL (1) CL2008001356A1 (es)
PE (1) PE20090288A1 (es)
TW (1) TW200902008A (es)
WO (1) WO2008141065A1 (es)

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EP2569286B1 (en) 2010-05-12 2014-08-20 Vertex Pharmaceuticals Inc. Compounds useful as inhibitors of atr kinase
EP2569289A1 (en) 2010-05-12 2013-03-20 Vertex Pharmaceuticals Incorporated Pyrazines useful as inhibitors of atr kinase
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WO2011163527A1 (en) 2010-06-23 2011-12-29 Vertex Pharmaceuticals Incorporated Pyrrolo- pyrazine derivatives useful as inhibitors of atr kinase
CA2804173C (en) 2010-07-09 2015-01-13 Pfizer Limited Sulfonamide nav1.7 inhibitors
GB201020179D0 (en) 2010-11-29 2011-01-12 Astex Therapeutics Ltd New compounds
US8754114B2 (en) 2010-12-22 2014-06-17 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
KR20140027974A (ko) 2011-04-05 2014-03-07 버텍스 파마슈티칼스 인코포레이티드 Tra 키나제의 억제제로서 유용한 아미노피라진 화합물
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CN103957917A (zh) 2011-09-30 2014-07-30 沃泰克斯药物股份有限公司 用atr抑制剂治疗胰腺癌和非小细胞肺癌
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KR20140084112A (ko) 2011-09-30 2014-07-04 버텍스 파마슈티칼스 인코포레이티드 Atr 키나제의 억제제로서 유용한 화합물
US8853217B2 (en) 2011-09-30 2014-10-07 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of ATR kinase
EP2751088B1 (en) 2011-09-30 2016-04-13 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of atr kinase
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GB201118675D0 (en) 2011-10-28 2011-12-14 Astex Therapeutics Ltd New compounds
GB201118656D0 (en) 2011-10-28 2011-12-07 Astex Therapeutics Ltd New compounds
WO2013071088A1 (en) 2011-11-09 2013-05-16 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of atr kinase
EP2776419B1 (en) 2011-11-09 2016-05-11 Vertex Pharmaceuticals Incorporated Pyrazine compounds useful as inhibitors of atr kinase
WO2013071094A1 (en) 2011-11-09 2013-05-16 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of atr kinase
EP2776420A1 (en) 2011-11-09 2014-09-17 Vertex Pharmaceuticals Incorporated Pyrazine compounds useful as inhibitors of atr kinase
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