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UY31137A1 - Derivados de quinazolina como inhibidores de la pi3 quinasa - Google Patents

Derivados de quinazolina como inhibidores de la pi3 quinasa

Info

Publication number
UY31137A1
UY31137A1 UY31137A UY31137A UY31137A1 UY 31137 A1 UY31137 A1 UY 31137A1 UY 31137 A UY31137 A UY 31137A UY 31137 A UY31137 A UY 31137A UY 31137 A1 UY31137 A1 UY 31137A1
Authority
UY
Uruguay
Prior art keywords
diseases
quinazoline
derivatives
invented
quinasa
Prior art date
Application number
UY31137A
Other languages
English (en)
Inventor
Stanley Schumidt
Lance H Ridgers
Steven Knight
Michael Darcy
Nicholas D Adams
Joelle Lorraine Burgess
Kenneth A Newlander
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.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40156899&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=UY31137(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 UY31137A1 publication Critical patent/UY31137A1/es

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/535—Heterocyclic 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
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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    • A—HUMAN NECESSITIES
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    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/08—Vasodilators for multiple indications
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/04—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems

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  • Life Sciences & Earth Sciences (AREA)
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  • Neurology (AREA)
  • Heart & Thoracic Surgery (AREA)
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  • Biomedical Technology (AREA)
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  • Hematology (AREA)
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  • Reproductive Health (AREA)
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  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Gynecology & Obstetrics (AREA)
  • Pregnancy & Childbirth (AREA)
  • Vascular Medicine (AREA)
  • Endocrinology (AREA)
  • Dermatology (AREA)

Abstract

Se ha inventado un método para inhibir la actividad/función de quinasas PI3 usando derivados de quinazolina. También se ha inventado un método para tratar una o más patologías seleccionadas entre: trastornos autoinmunes, enfermedades inflamatorias, enfermedades cardiovasculares, enfermedades neurodegenerativas, alergia, asma, pancreatitis, fallo multiorgánico, enfermedades renales, agregación plaquetaria, cáncer, motilidad de los espermatozoides, rechazo de trasplantes, rechazo de injertos y lesiones pulmonares, mediante la administración de derivados de quinazolina.
UY31137A 2007-06-14 2008-06-10 Derivados de quinazolina como inhibidores de la pi3 quinasa UY31137A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US94389907P 2007-06-14 2007-06-14

Publications (1)

Publication Number Publication Date
UY31137A1 true UY31137A1 (es) 2009-01-05

Family

ID=40156899

Family Applications (1)

Application Number Title Priority Date Filing Date
UY31137A UY31137A1 (es) 2007-06-14 2008-06-10 Derivados de quinazolina como inhibidores de la pi3 quinasa

Country Status (9)

Country Link
US (2) US20100179144A1 (es)
EP (1) EP2167092A4 (es)
JP (1) JP2010532320A (es)
AR (1) AR066978A1 (es)
CL (1) CL2008001743A1 (es)
PE (1) PE20090835A1 (es)
TW (1) TW200918068A (es)
UY (1) UY31137A1 (es)
WO (1) WO2008157191A2 (es)

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KR20140084112A (ko) 2011-09-30 2014-07-04 버텍스 파마슈티칼스 인코포레이티드 Ａｔｒ 키나제의 억제제로서 유용한 화합물
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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
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