ATE537843T1 - Neue kinase-hemmer - Google Patents

Neue kinase-hemmer

Info

Publication number
ATE537843T1
ATE537843T1 AT03765881T AT03765881T ATE537843T1 AT E537843 T1 ATE537843 T1 AT E537843T1 AT 03765881 T AT03765881 T AT 03765881T AT 03765881 T AT03765881 T AT 03765881T AT E537843 T1 ATE537843 T1 AT E537843T1
Authority
AT
Austria
Prior art keywords
kinase inhibitors
new kinase
new
inhibitors
kinase
Prior art date
Application number
AT03765881T
Other languages
German (de)
English (en)
Inventor
Rajeev Bhide
Zhen-Wei Cai
Ligang Qian
Stephanie Barbosa
Louis Lombardo
Jeffrey Robl
Original Assignee
Bristol Myers Squibb Co
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 Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Application granted granted Critical
Publication of ATE537843T1 publication Critical patent/ATE537843T1/de

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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
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
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    • A61P1/04Drugs 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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  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
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  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
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  • Oncology (AREA)
  • Diabetes (AREA)
  • Epidemiology (AREA)
  • Communicable Diseases (AREA)
  • Urology & Nephrology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Hematology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Dermatology (AREA)
  • Obesity (AREA)
  • Molecular Biology (AREA)
  • Endocrinology (AREA)
  • Biotechnology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Psychiatry (AREA)
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AT03765881T 2002-07-19 2003-07-18 Neue kinase-hemmer ATE537843T1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US39725602P 2002-07-19 2002-07-19
US44721303P 2003-02-13 2003-02-13
PCT/US2003/022826 WO2004009784A2 (en) 2002-07-19 2003-07-18 Novel inhibitors of kinases

Publications (1)

Publication Number Publication Date
ATE537843T1 true ATE537843T1 (de) 2012-01-15

Family

ID=30773005

Family Applications (2)

Application Number Title Priority Date Filing Date
AT03765881T ATE537843T1 (de) 2002-07-19 2003-07-18 Neue kinase-hemmer
AT03765754T ATE505471T1 (de) 2002-07-19 2003-07-18 Azaindol-kinaseinhibitoren

Family Applications After (1)

Application Number Title Priority Date Filing Date
AT03765754T ATE505471T1 (de) 2002-07-19 2003-07-18 Azaindol-kinaseinhibitoren

Country Status (32)

Country Link
US (6) US6869952B2 (enExample)
EP (3) EP2280012A3 (enExample)
JP (2) JP4361485B2 (enExample)
KR (1) KR100901939B1 (enExample)
CN (3) CN101880283B (enExample)
AR (1) AR040500A1 (enExample)
AT (2) ATE537843T1 (enExample)
AU (2) AU2003254017A1 (enExample)
BR (2) BRPI0312940B1 (enExample)
CA (2) CA2492804C (enExample)
CO (1) CO5680407A2 (enExample)
CY (1) CY1112628T1 (enExample)
DE (1) DE60336732D1 (enExample)
DK (1) DK1534290T3 (enExample)
ES (1) ES2377963T3 (enExample)
GE (2) GEP20074124B (enExample)
HR (2) HRP20050058A2 (enExample)
IL (3) IL166129A0 (enExample)
IS (2) IS7646A (enExample)
MX (2) MXPA05000716A (enExample)
MY (1) MY134848A (enExample)
NO (2) NO330132B1 (enExample)
NZ (1) NZ537523A (enExample)
PE (1) PE20040680A1 (enExample)
PL (2) PL375352A1 (enExample)
PT (1) PT1534290E (enExample)
RS (2) RS20050041A (enExample)
RU (2) RU2331642C2 (enExample)
SI (1) SI1534290T1 (enExample)
TW (1) TWI329112B (enExample)
UA (1) UA82846C2 (enExample)
WO (2) WO2004009601A1 (enExample)

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US20020058286A1 (en) * 1999-02-24 2002-05-16 Danishefsky Samuel J. Synthesis of epothilones, intermediates thereto and analogues thereof
US6982265B1 (en) * 1999-05-21 2006-01-03 Bristol Myers Squibb Company Pyrrolotriazine inhibitors of kinases
US6867300B2 (en) * 2000-11-17 2005-03-15 Bristol-Myers Squibb Company Methods for the preparation of pyrrolotriazine compounds useful as kinase inhibitors
US6670357B2 (en) * 2000-11-17 2003-12-30 Bristol-Myers Squibb Company Methods of treating p38 kinase-associated conditions and pyrrolotriazine compounds useful as kinase inhibitors
TW200300350A (en) * 2001-11-14 2003-06-01 Bristol Myers Squibb Co C-5 modified indazolylpyrrolotriazines
WO2003091229A1 (en) 2002-04-23 2003-11-06 Bristol-Myers Squibb Company Aryl ketone pyrrolo-triazine compounds useful as kinase inhibitors
NZ536014A (en) * 2002-04-23 2006-12-22 Bristol Myers Squibb Co Pyrrolo-triazine aniline compounds useful as kinase inhibitors for treating inflammatory disorders
TW200401638A (en) * 2002-06-20 2004-02-01 Bristol Myers Squibb Co Heterocyclic inhibitors of kinases
TWI329112B (en) * 2002-07-19 2010-08-21 Bristol Myers Squibb Co Novel inhibitors of kinases
EP1767535B1 (en) * 2002-08-23 2009-12-02 Sloan-Kettering Institute For Cancer Research Synthesis of epothilones, intermediates thereto, analogues and uses thereof
US6921769B2 (en) 2002-08-23 2005-07-26 Sloan-Kettering Institute For Cancer Research Synthesis of epothilones, intermediates thereto and analogues thereof
US7649006B2 (en) 2002-08-23 2010-01-19 Sloan-Kettering Institute For Cancer Research Synthesis of epothilones, intermediates thereto and analogues thereof
TW200420565A (en) 2002-12-13 2004-10-16 Bristol Myers Squibb Co C-6 modified indazolylpyrrolotriazines
CN1771234A (zh) 2003-02-05 2006-05-10 布里斯托尔-迈尔斯斯奎布公司 吡咯并三嗪激酶抑制剂的制备方法
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US7459562B2 (en) * 2004-04-23 2008-12-02 Bristol-Myers Squibb Company Monocyclic heterocycles as kinase inhibitors
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CN1993130B (zh) * 2004-06-28 2010-06-23 布里斯托尔-迈尔斯斯奎布公司 用于制备稠合杂环激酶抑制剂的方法和中间体
US7432373B2 (en) * 2004-06-28 2008-10-07 Bristol-Meyers Squibb Company Processes and intermediates useful for preparing fused heterocyclic kinase inhibitors
US7439246B2 (en) * 2004-06-28 2008-10-21 Bristol-Myers Squibb Company Fused heterocyclic kinase inhibitors
US7253167B2 (en) * 2004-06-30 2007-08-07 Bristol-Myers Squibb Company Tricyclic-heteroaryl compounds useful as kinase inhibitors
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US7102003B2 (en) 2004-07-01 2006-09-05 Bristol-Myers Squibb Company Pyrrolotriazine compounds
SE0401790D0 (sv) * 2004-07-07 2004-07-07 Forskarpatent I Syd Ab Tamoxifen response in pre- and postmenopausal breast cancer patients
US7504521B2 (en) * 2004-08-05 2009-03-17 Bristol-Myers Squibb Co. Methods for the preparation of pyrrolotriazine compounds
TW200618803A (en) 2004-08-12 2006-06-16 Bristol Myers Squibb Co Process for preparing pyrrolotriazine aniline compounds useful as kinase inhibitors
US7151176B2 (en) * 2004-10-21 2006-12-19 Bristol-Myers Squibb Company Pyrrolotriazine compounds
CA2587642C (en) 2004-11-30 2013-04-09 Amgen Inc. Substituted heterocycles and methods of use
DE102004060659A1 (de) 2004-12-15 2006-07-06 Lanxess Deutschland Gmbh Neue substituierte 1H-Pyrrolo[2,3-b]pyridine und deren Herstellung
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