IN2014CN04065A - - Google Patents

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Publication number
IN2014CN04065A
IN2014CN04065A IN4065CHN2014A IN2014CN04065A IN 2014CN04065 A IN2014CN04065 A IN 2014CN04065A IN 4065CHN2014 A IN4065CHN2014 A IN 4065CHN2014A IN 2014CN04065 A IN2014CN04065 A IN 2014CN04065A
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India
Prior art keywords
methods
syk kinase
kinase activity
compounds
inhibiting
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Inventor
Yonghong Song
Qing Xu
Zhaozhong J Jia
Brian Kane
Shawn M Bauer
Anjali Pandey
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Portola Pharm Inc
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Publication of IN2014CN04065A publication Critical patent/IN2014CN04065A/en

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    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D241/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D241/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with nitrogen atoms directly attached to ring carbon atoms
    • C07D241/28—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with nitrogen atoms directly attached to ring carbon atoms in which said hetero-bound carbon atoms have double bonds to oxygen, sulfur or nitrogen atoms
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    • 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
    • C07D401/12—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 linked by a chain containing hetero atoms as chain links
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    • 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
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    • C07D403/12—Heterocyclic 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 linked by a chain containing hetero atoms as chain links
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    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems

Abstract

Provided are pyrazine compounds for inhibiting of Syk kinase intermediates used in making such compounds methods for their preparation pharmaceutical compositions thereof methods for inhibition Syk kinase activity and methods for treating conditions mediated at least in part by Syk kinase activity.
IN4065CHN2014 2011-11-23 2012-11-23 IN2014CN04065A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161563466P 2011-11-23 2011-11-23
PCT/US2012/066468 WO2013078466A1 (en) 2011-11-23 2012-11-23 Pyrazine kinase inhibitors

Publications (1)

Publication Number Publication Date
IN2014CN04065A true IN2014CN04065A (en) 2015-09-04

Family

ID=48427516

Family Applications (1)

Application Number Title Priority Date Filing Date
IN4065CHN2014 IN2014CN04065A (en) 2011-11-23 2012-11-23

Country Status (18)

Country Link
US (2) US8877760B2 (en)
EP (1) EP2782579B1 (en)
JP (1) JP6039683B2 (en)
KR (1) KR102019530B1 (en)
CN (1) CN104066431B (en)
AU (1) AU2012340555B2 (en)
BR (1) BR112014012396B1 (en)
CA (2) CA3094793A1 (en)
CL (1) CL2014001346A1 (en)
CO (1) CO6990735A2 (en)
EA (1) EA026939B1 (en)
HK (1) HK1201460A1 (en)
IL (1) IL232701A (en)
IN (1) IN2014CN04065A (en)
MX (1) MX363551B (en)
SG (2) SG11201402570QA (en)
WO (1) WO2013078466A1 (en)
ZA (1) ZA201403651B (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA019973B1 (en) 2008-04-16 2014-07-30 Портола Фармасьютиклз, Инк. INHIBITORS OF Syk PROTEIN KINASES
US8138339B2 (en) 2008-04-16 2012-03-20 Portola Pharmaceuticals, Inc. Inhibitors of protein kinases
CA3094793A1 (en) 2011-11-23 2013-05-30 Portola Pharmaceuticals, Inc. Pyrazine kinase inhibitors
US20130310387A1 (en) 2012-05-16 2013-11-21 Novartis Ag Monocyclic Heteroaryl Cycloalkyldiamine Derivatives
WO2014060371A1 (en) 2012-10-19 2014-04-24 F. Hoffmann-La Roche Ag Inhibitors of syk
KR20160093675A (en) * 2013-12-05 2016-08-08 파마싸이클릭스 엘엘씨 Inhibitors of bruton's tyrosine kinase
EP3116506B1 (en) * 2014-03-13 2019-04-17 Merck Sharp & Dohme Corp. 2-pyrazine carboxamides as spleen tyrosine kinase inhibitors
CZ306322B6 (en) 2014-12-17 2016-11-30 Univerzita Karlova v Praze, Farmaceutická fakulta v Hradci Králové Substituted 2-(2-phenylhydrazinyl)pyrazine, process of its preparation, its use and pharmaceutical composition containing thereof
JP2018522823A (en) * 2015-06-02 2018-08-16 ファーマサイクリックス エルエルシー Inhibitors of Breton-type tyrosine kinase
WO2019237125A1 (en) * 2018-06-08 2019-12-12 The General Hospital Corporation Inhibitors of prolyl-trna-synthetase
CN112047899A (en) * 2020-10-19 2020-12-08 成都睿智化学研究有限公司 Method for synthesizing 3-substituted aminobenzo [ c ] isothiazole derivative
WO2023178094A2 (en) * 2022-03-14 2023-09-21 Purdue Research Foundation Spleen tyrosine kinase inhibitor, composition, and methods of use

Family Cites Families (141)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5728536A (en) 1993-07-29 1998-03-17 St. Jude Children's Research Hospital Jak kinases and regulation of Cytokine signal transduction
US5691364A (en) * 1995-03-10 1997-11-25 Berlex Laboratories, Inc. Benzamidine derivatives and their use as anti-coagulants
US6004981A (en) 1996-03-08 1999-12-21 Berlex Laboratories, Inc. Benzamidine derivatives and their use as anti-coagulants
DK0813525T3 (en) 1995-03-10 2004-02-16 Berlex Lab Benzamidine derivatives, their preparation and use as anticoagulants
US6316635B1 (en) 1995-06-07 2001-11-13 Sugen, Inc. 2-indolinone derivatives as modulators of protein kinase activity
CA2230894A1 (en) 1995-09-01 1997-03-13 Signal Pharmaceuticals, Inc. Pyrimidine carboxamides and related compounds and methods for treating inflammatory conditions
US5811428A (en) 1995-12-18 1998-09-22 Signal Pharmaceuticals, Inc. Pyrimidine carboxamides and related compounds and methods for treating inflammatory conditions
US6696448B2 (en) 1996-06-05 2004-02-24 Sugen, Inc. 3-(piperazinylbenzylidenyl)-2-indolinone compounds and derivatives as protein tyrosine kinase inhibitors
IL128691A (en) 1996-09-12 2007-07-24 Bayer Schering Pharma Ag Benzamidine derivatives substituted by cyclic amino acid and cyclic hydroxy acid derivatives and their use as anti-coagulants
US6008234A (en) 1996-09-12 1999-12-28 Berlex Laboratories, Inc. Benzamidine derivatives substituted by cyclic amino acid and cyclic hydroxy acid derivatives and their use as anti-coagulants
US6004985A (en) 1996-10-09 1999-12-21 Berlex Laboratories, Inc. Thio acid derived monocylic N-heterocyclics as anticoagulants
US6316429B1 (en) 1997-05-07 2001-11-13 Sugen, Inc. Bicyclic protein kinase inhibitors
US6486185B1 (en) 1997-05-07 2002-11-26 Sugen, Inc. 3-heteroarylidene-2-indolinone protein kinase inhibitors
GB9718913D0 (en) 1997-09-05 1997-11-12 Glaxo Group Ltd Substituted oxindole derivatives
US6133305A (en) 1997-09-26 2000-10-17 Sugen, Inc. 3-(substituted)-2-indolinones compounds and use thereof as inhibitors of protein kinase activity
US6686364B2 (en) 1997-12-08 2004-02-03 Berlex Laboratories, Inc. Benzamidine derivatives and their use as anti-coagulants
ES2308821T3 (en) 1997-12-15 2008-12-01 Astellas Pharma Inc. NEW DERIVATIVES OF PIRIMIDIN-5-CARBOXAMIDA.
CA2337999A1 (en) 1998-06-30 2000-01-06 Parker Hughes Institute Method for inhibiting c-jun expression using jak-3 inhibitors
KR20010089171A (en) 1998-08-21 2001-09-29 추후제출 Quinazoline derivatives
US6262088B1 (en) 1998-11-19 2001-07-17 Berlex Laboratories, Inc. Polyhydroxylated monocyclic N-heterocyclic derivatives as anti-coagulants
US6127376A (en) 1998-12-04 2000-10-03 Berlex Laboratories, Inc. Aryl and heterocyclyl substituted pyrimidine derivatives as anti-coagulants
GB9828511D0 (en) 1998-12-24 1999-02-17 Zeneca Ltd Chemical compounds
US6841567B1 (en) 1999-02-12 2005-01-11 Cephalon, Inc. Cyclic substituted fused pyrrolocarbazoles and isoindolones
GB9904995D0 (en) 1999-03-04 1999-04-28 Glaxo Group Ltd Substituted aza-oxindole derivatives
US6624171B1 (en) 1999-03-04 2003-09-23 Smithkline Beecham Corporation Substituted aza-oxindole derivatives
US6080747A (en) 1999-03-05 2000-06-27 Hughes Institute JAK-3 inhibitors for treating allergic disorders
GB9905075D0 (en) 1999-03-06 1999-04-28 Zeneca Ltd Chemical compounds
US7125875B2 (en) 1999-04-15 2006-10-24 Bristol-Myers Squibb Company Cyclic protein tyrosine kinase inhibitors
ES2237430T3 (en) 1999-06-09 2005-08-01 Yamanouchi Pharmaceutical Co. Ltd. NEW CARBOXAMIDE HETEROCICLIC DERIVATIVES.
AU5108000A (en) 1999-06-10 2001-01-02 Yamanouchi Pharmaceutical Co., Ltd. Novel nitrogen-contaiing heterocyclic derivatives or salts thereof
GB9918035D0 (en) 1999-07-30 1999-09-29 Novartis Ag Organic compounds
JP2003518023A (en) 1999-11-30 2003-06-03 パーカー ヒューズ インスティテュート Inhibitors of thrombin-induced platelet aggregation
PL218519B1 (en) 1999-12-10 2014-12-31 Pfizer Prod Inc PYRROLO[2,3−d]PYRIMIDINE COMPOUNDS
ES2245955T3 (en) 1999-12-21 2006-02-01 Sugen, Inc. 7-AZA-INDOLIN-2-ONAS 4-SUBSTITUTES AND THEIR USE AS PROTEIN-KINASE INHIBITORS.
US20020065270A1 (en) 1999-12-28 2002-05-30 Moriarty Kevin Joseph N-heterocyclic inhibitors of TNF-alpha expression
AU2968701A (en) 2000-01-24 2001-07-31 Genzyme Corporation Jak/stat pathway inhibitors and the uses thereof
NZ519726A (en) 2000-01-31 2004-05-28 Pfizer Prod Inc Pyrimidine carboxamides useful as inhibitors of PDE4 isozymes
WO2001056993A2 (en) 2000-02-05 2001-08-09 Vertex Pharmaceuticals Incorporated Pyrazole compositions useful as inhibitors of erk
SK14082001A3 (en) 2000-02-05 2002-03-05 Vertex Pharmaceuticals Incorporated Pyrazole derivatives as inhibitors of erk and pharmaceutical composition containing same
GB0004888D0 (en) 2000-03-01 2000-04-19 Astrazeneca Uk Ltd Chemical compounds
US6525051B2 (en) 2000-03-27 2003-02-25 Schering Aktiengesellschaft N-heterocyclic derivatives as NOS inhibitors
AR028261A1 (en) 2000-03-28 2003-04-30 Wyeth Corp TRICICLIC INHIBITORS OF PROTEIN QUINASA
US6608048B2 (en) 2000-03-28 2003-08-19 Wyeth Holdings Tricyclic protein kinase inhibitors
CA2406562C (en) 2000-05-08 2009-09-15 Janssen Pharmaceutica N.V. Hiv replication inhibiting pyrimidines and triazines
ATE423120T1 (en) 2000-06-26 2009-03-15 Pfizer Prod Inc PYRROLOÄ2,3-DÜPYRIMIDINE COMPOUNDS AS IMMUNOSUPPRESSIVE ACTIVES
GB0016877D0 (en) 2000-07-11 2000-08-30 Astrazeneca Ab Chemical compounds
WO2002043735A1 (en) 2000-11-29 2002-06-06 Parker Hughes Institute Inhibitors of thrombin induced platelet aggregation
US20020115173A1 (en) 2000-12-11 2002-08-22 Children's Medical Center Corporation Short peptides from the 'A-region' of protein kinases which selectively modulate protein kinase activity
JP2004518669A (en) 2000-12-20 2004-06-24 スージェン・インコーポレーテッド 4-Aryl substituted indolinone
SI2311825T1 (en) 2000-12-21 2016-02-29 Novartis Ag Pyrimidineamines as angiogenesis modulators
FR2818642B1 (en) 2000-12-26 2005-07-15 Hoechst Marion Roussel Inc NOVEL DERIVATIVES OF PURINE, PROCESS FOR PREPARING THEM, THEIR USE AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS AND THEIR NEW USE
WO2002060492A1 (en) 2001-01-30 2002-08-08 Cytopia Pty Ltd Methods of inhibiting kinases
AUPR279101A0 (en) 2001-01-30 2001-02-22 Cytopia Pty Ltd Protein kinase signalling
SE0101675D0 (en) 2001-05-11 2001-05-11 Astrazeneca Ab Novel composition
PL367130A1 (en) 2001-05-29 2005-02-21 Schering Aktiengesellschaft Cdk inhibiting pyrimidines, production thereof and their use as medicaments
US7301023B2 (en) 2001-05-31 2007-11-27 Pfizer Inc. Chiral salt resolution
US6825190B2 (en) 2001-06-15 2004-11-30 Vertex Pharmaceuticals Incorporated Protein kinase inhibitors and uses thereof
US6433018B1 (en) 2001-08-31 2002-08-13 The Research Foundation Of State University Of New York Method for reducing hypertrophy and ischemia
AU2002334355A1 (en) 2001-09-06 2003-03-18 Prochon Biotech Ltd. Protein tyrosine kinase inhibitors
BR0212435A (en) 2001-09-10 2004-08-17 Sugen Inc 3- (4,5,6,7-Tetrahydroindol-2-ylmethylidene) -2-indolinone derivatives as kinase inhibitors
WO2003030909A1 (en) 2001-09-25 2003-04-17 Bayer Pharmaceuticals Corporation 2- and 4-aminopyrimidines n-substtituded by a bicyclic ring for use as kinase inhibitors in the treatment of cancer
WO2003031438A1 (en) 2001-10-10 2003-04-17 Sugen, Inc. 3-[4-(substituted heterocyclyl)-pyrrol-2-ylmethylidene]-2-indolinone derivatives as kinase inhibitors
GT200200234A (en) 2001-12-06 2003-06-27 NEW CRYSTAL COMPOUNDS
TWI329105B (en) 2002-02-01 2010-08-21 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds and their uses
US6998391B2 (en) 2002-02-07 2006-02-14 Supergen.Inc. Method for treating diseases associated with abnormal kinase activity
US7459455B2 (en) 2002-02-08 2008-12-02 Smithkline Beecham Corporation Pyrimidine compounds
US7338959B2 (en) 2002-03-01 2008-03-04 Smithkline Beecham Corporation Diamino-pyrimidines and their use as angiogenesis inhibitors
GB0206215D0 (en) 2002-03-15 2002-05-01 Novartis Ag Organic compounds
WO2003095448A1 (en) 2002-05-06 2003-11-20 Bayer Pharmaceuticals Corporation Pyridinyl amino pyrimidine derivatives useful for treating hyper-proliferative disorders
RU2004135386A (en) 2002-05-06 2005-07-20 Вертекс Фармасьютикалз Инкорпорейтед (Us) THIADIAZOLE OR OXADIAZOZOL AND THEIR APPLICATION AS JAK PROTEINKINASE INHIBITORS
PL374023A1 (en) 2002-05-30 2005-09-19 Vertex Pharmaceuticals Incorporated Inhibitors of jak and cdk2 protein kinases
PL374963A1 (en) 2002-06-17 2005-11-14 Smithkline Beecham Corporation Chemical process
ATE530530T1 (en) 2002-06-28 2011-11-15 Astellas Pharma Inc DIAMINOPYRIMIDINE CARBONIC ACID AMIDE DERIVATIVE
ATE451104T1 (en) 2002-07-29 2009-12-15 Rigel Pharmaceuticals Inc METHOD FOR TREATING OR PREVENTING AUTOIMMUNE DISEASES USING 2,4-PYRIMIDINEDIAMINE COMPOUNDS
BR0313397A (en) 2002-08-14 2005-06-28 Vertex Pharmaceuticals Incorpo Protein kinase inhibitors and uses of these
ATE454378T1 (en) 2002-11-01 2010-01-15 Vertex Pharma COMPOUNDS ACTIVE AS INHIBITORS OF JAK AND OTHER PROTEIN KINASES
EP1562938B1 (en) 2002-11-04 2007-08-29 Vertex Pharmaceuticals Incorporated Heteroaryl-pyrimidine derivatives as jak inhibitors
AU2003286895A1 (en) 2002-11-05 2004-06-07 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of jak and other protein kinases
TWI335913B (en) 2002-11-15 2011-01-11 Vertex Pharma Diaminotriazoles useful as inhibitors of protein kinases
RS20050380A (en) 2002-11-21 2007-11-15 Pfizer Products Inc., 3-amino piperidine derivatives and methods of manufacture
MXPA05005576A (en) 2002-11-26 2005-07-27 Pfizer Prod Inc Method of treatment of transplant rejection.
US7226919B2 (en) 2002-12-18 2007-06-05 Vertex Pharmaceuticals Inc. Compositions useful as inhibitors of protein kinases
DE602004021472D1 (en) 2003-02-20 2009-07-23 Smithkline Beecham Corp Pyrimiidinverbindungen
GB0305929D0 (en) 2003-03-14 2003-04-23 Novartis Ag Organic compounds
WO2004092154A1 (en) 2003-04-03 2004-10-28 Vertex Pharmaceuticals Incorporated Compositions useful as inhibitors of protein kinases
US7504396B2 (en) 2003-06-24 2009-03-17 Amgen Inc. Substituted heterocyclic compounds and methods of use
US7504429B2 (en) 2003-07-24 2009-03-17 Merck & Co., Inc. Tyrosine kinase inhibitors
WO2005016893A2 (en) 2003-07-30 2005-02-24 Rigel Pharmaceuticals, Inc. 2,4-pyrimidinediamine compounds for use in the treatment or prevention of autoimmune diseases
AP2006003514A0 (en) 2003-08-14 2006-02-28 Pfizer Piperazine derivatives for the treatment of HIV infections.
MXPA06001759A (en) 2003-08-15 2006-05-12 Novartis Ag 2, 4-pyrimidinediamines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders.
AR045595A1 (en) 2003-09-04 2005-11-02 Vertex Pharma USEFUL COMPOSITIONS AS INHIBITORS OF KINASE PROTEINS
GB0321710D0 (en) 2003-09-16 2003-10-15 Novartis Ag Organic compounds
CN100412066C (en) 2003-09-30 2008-08-20 Irm责任有限公司 Compounds and compositions as protein kinase inhibitors
ES2295924T3 (en) 2003-10-03 2008-04-16 Pfizer, Inc. DERIVATIVES OF TROPANE IMIDAZOPIRINE SUBSTITUTED WITH ANTAGONIST ACTIVITY OF CCR5 RECEPTORS FOR THE TREATMENT OF HIV AND INFLAMMATION.
DE10349423A1 (en) 2003-10-16 2005-06-16 Schering Ag Sulfoximine-substituted parimidines as CDK and / or VEGF inhibitors, their preparation and use as medicaments
EP1704145B1 (en) 2004-01-12 2012-06-13 YM BioSciences Australia Pty Ltd Selective kinase inhibitors
MXPA06011327A (en) 2004-03-30 2006-12-15 Vertex Pharma Azaindoles useful as inhibitors of jak and other protein kinases.
GB0407723D0 (en) 2004-04-05 2004-05-12 Novartis Ag Organic compounds
WO2005122294A1 (en) 2004-06-14 2005-12-22 Nec Corporation Electric device packed in film
CA2579017A1 (en) 2004-09-10 2006-03-16 Altana Pharma Ag Roflumilast and syk inhibitor combination and methods of use thereof
US20080027034A1 (en) 2004-09-10 2008-01-31 Shah Tushar P Ciclesonide and Syk Inhibitor Combination and Method of Use Thereof
ATE540035T1 (en) 2004-11-24 2012-01-15 Rigel Pharmaceuticals Inc SPIRO-2,4-PYRIMIDINEDIAMINE COMPOUNDS AND USES THEREOF
RU2416616C2 (en) 2005-01-19 2011-04-20 Райджел Фармасьютикалз, Инк. Prodrugs of 2,4-pyrimidine diamine compounds and use thereof
US20060270694A1 (en) 2005-05-03 2006-11-30 Rigel Pharmaceuticals, Inc. JAK kinase inhibitors and their uses
EP1948658A1 (en) 2005-10-13 2008-07-30 Glaxo Group Limited Pyrrolopyrimidine derivatives as syk inhibitors
WO2007046112A1 (en) 2005-10-19 2007-04-26 Suven Life Sciences Inc. Arylthioether tryptamine derivatives as functional 5-ht6 ligands
US7601713B2 (en) 2005-12-15 2009-10-13 Rigel Pharmaceuticals, Inc. Kinase inhibitors and their uses
NL2000323C2 (en) 2005-12-20 2007-11-20 Pfizer Ltd Pyrimidine derivatives.
GB0526246D0 (en) 2005-12-22 2006-02-01 Novartis Ag Organic compounds
CA2645958C (en) 2006-03-30 2014-11-04 Tibotec Pharmaceuticals Ltd. Hiv inhibiting 5-amido substituted pyrimidines
US8258129B2 (en) 2006-07-06 2012-09-04 Boehringer Ingelheim International Gmbh 4-heterocycloalkylpyri(mi)dines, process for the preparation thereof and their use as medicaments
US20100010025A1 (en) 2006-07-21 2010-01-14 Norvartis Ag Pyrimidine Derivatives
US20080076800A1 (en) 2006-08-24 2008-03-27 Huang Kenneth H Benzene, Pyridine, and Pyridazine Derivatives
US8148391B2 (en) 2006-10-23 2012-04-03 Cephalon, Inc. Fused bicyclic derivatives of 2,4-diaminopyrimidine as ALK and c-Met inhibitors
US20080139531A1 (en) 2006-12-04 2008-06-12 Alcon Manufacturing Ltd. Use of connective tissue mast cell stabilizers to facilitate ocular surface re-epithelization and wound repair
ES2618057T3 (en) 2006-12-29 2017-06-20 Janssen Sciences Ireland Uc HIV-inhibited 5,6-substituted pyrimidines
CN101679440A (en) 2007-04-02 2010-03-24 帕劳制药股份有限公司 Pyrrolopyrimidine derivatives as jak3 inhibitors
ES2369596T3 (en) 2007-05-04 2011-12-02 Astrazeneca Ab DERIVATIVES OF AMINO-TIAZOLIL-PYRIMIDINE AND ITS USE FOR THE TREATMENT OF CANCER.
EP2157090A4 (en) 2007-06-21 2011-09-07 Taisho Pharmaceutical Co Ltd Pyrazinamide compound
AU2008296545B2 (en) 2007-08-28 2011-09-29 Irm Llc 2 -biphenylamino-4 -aminopyrimidine derivatives as kinase inhibitors
US20100292447A1 (en) 2007-10-12 2010-11-18 Merck Patent Gesellschaft Method and agent for refolding proteins
US20090270418A1 (en) * 2008-01-09 2009-10-29 Marianne Sloss Pyrazole pyrazine amine compounds as kinase inhibitors, compositions thereof and methods of treatment therewith
US20090196973A1 (en) 2008-02-01 2009-08-06 Rich Products Corporation Foam Compositions
EA019973B1 (en) 2008-04-16 2014-07-30 Портола Фармасьютиклз, Инк. INHIBITORS OF Syk PROTEIN KINASES
US8138339B2 (en) 2008-04-16 2012-03-20 Portola Pharmaceuticals, Inc. Inhibitors of protein kinases
KR20100132550A (en) * 2008-04-16 2010-12-17 포톨라 파마슈티컬스, 인코포레이티드 2,6-diamino-pyrimidin-5-yl-carboxamides as syk or jak kinases inhibitors
EA024109B1 (en) * 2008-04-16 2016-08-31 Портола Фармасьютиклз, Инк. Protein kinases inhibitors
WO2009131687A2 (en) 2008-04-22 2009-10-29 Portola Pharmaceuticals, Inc. Inhibitors of protein kinases
EP2331507A2 (en) 2008-09-18 2011-06-15 Astellas Pharma Inc. Heterocyclic carboxamide compounds
EP2361902A4 (en) 2008-11-21 2012-04-25 Astellas Pharma Inc 4,6-diaminonicotinamide compound
CN102227409B (en) 2008-11-28 2014-03-26 兴和株式会社 Pyridine-3-carboxyamide derivative
MX2011007499A (en) 2009-01-13 2011-08-04 Glaxo Group Ltd Pyrimidinecarboxamide derivatives as inhibitors of syk kinase.
TW201040162A (en) 2009-05-06 2010-11-16 Portola Pharm Inc Inhibitors of JAK
CA2760061C (en) * 2009-05-08 2017-02-28 Astellas Pharma Inc. Diamino heterocyclic carboxamide compound
US20130244963A1 (en) 2010-09-30 2013-09-19 Portola Pharmaceuticals, Inc. Combination therapy with 4-(3-(2h-1,2,3-triazol-2-yl)phenylamino)-2-((1r,2s)-2-aminocyclohexylamino)pyrimidine-5-carboxamide
WO2012045010A1 (en) 2010-09-30 2012-04-05 Portola Pharmaceuticals, Inc. Combinations of 4-(3-(2h-1,2,3-triazo-2-yl) phenylamino)-2-((1r,2s)-2-aminocyclohexylamino) pyrimidine-5-carboxamide and fludarabine
JP2014005206A (en) 2010-10-22 2014-01-16 Astellas Pharma Inc Arylamino heterocyclic carboxamide compound
US20130317029A1 (en) 2010-11-01 2013-11-28 Portola Pharmaceuticals, Inc. Oxypyrimidines as syk modulators
US9102625B2 (en) 2010-11-01 2015-08-11 Portola Pharmaceuticals, Inc. Nicotinamides as JAK kinase modulators
CA3094793A1 (en) 2011-11-23 2013-05-30 Portola Pharmaceuticals, Inc. Pyrazine kinase inhibitors
CA2856306A1 (en) 2011-11-23 2013-05-30 Portola Pharmaceuticals, Inc. Selective kinase inhibitors

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