HU226413B1
(en)
|
1991-06-25 |
2008-11-28 |
Aventis Pharma Sa |
Novel 16-(nitro-substituted methyl)pregna-1,4-dien-3,20-dion derivatives and process for producing them
|
DE4127404A1
(de)
|
1991-08-19 |
1993-02-25 |
Thomae Gmbh Dr K |
Cyclische iminoderivate, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung
|
US5491234A
(en)
|
1992-03-30 |
1996-02-13 |
Pfizer Inc. |
Pyrimidine derivatives for enhancing antitumor activity
|
AU5438299A
(en)
|
1998-08-29 |
2000-03-21 |
Astrazeneca Ab |
Pyrimidine compounds
|
PT1169038E
(pt)
|
1999-04-15 |
2012-10-26 |
Bristol Myers Squibb Co |
Inibidores cíclicos da proteína tirosina cinase
|
US7125875B2
(en)
|
1999-04-15 |
2006-10-24 |
Bristol-Myers Squibb Company |
Cyclic protein tyrosine kinase inhibitors
|
DE10007411A1
(de)
|
2000-02-18 |
2001-08-23 |
Bayer Ag |
Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften
|
GB0004890D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
AU2006201262B2
(en)
|
2000-09-15 |
2008-09-04 |
Vertex Pharmaceuticals Incorporated |
Pyrazole Compounds Useful As Protein Kinase Inhibitors
|
JP4105948B2
(ja)
|
2000-09-15 |
2008-06-25 |
バーテックス ファーマシューティカルズ インコーポレイテッド |
プロテインキナーゼインヒビターとして有用なピラゾール化合物
|
US6660731B2
(en)
|
2000-09-15 |
2003-12-09 |
Vertex Pharmaceuticals Incorporated |
Pyrazole compounds useful as protein kinase inhibitors
|
US6613776B2
(en)
|
2000-09-15 |
2003-09-02 |
Vertex Pharmaceuticals Incorporated |
Pyrazole compounds useful as protein kinase inhibitors
|
AU2006201265B2
(en)
|
2000-09-15 |
2008-09-04 |
Vertex Pharmaceuticals Incorporated |
Pyrazole Compounds Useful As Protein Kinase Inhibitors
|
AU2006201263B2
(en)
|
2000-09-15 |
2008-10-30 |
Vertex Pharmaceuticals Incorporated |
Pyrazole Compounds Useful As Protein Kinase Inhibitors
|
AU2006201264A1
(en)
|
2000-09-15 |
2006-04-27 |
Vertex Pharmaceuticals Incorporated |
Pyrazole Compounds Useful As Protein Kinase Inhibitors
|
AU2006201230B8
(en)
|
2000-09-15 |
2008-09-25 |
Vertex Pharmaceuticals Incorporated |
Triazole Compounds Useful As Protein Kinase Inhibitors
|
KR100909665B1
(ko)
|
2000-12-21 |
2009-07-29 |
버텍스 파마슈티칼스 인코포레이티드 |
단백질 키나제 억제제로서 유용한 피라졸 화합물 및 이를 포함하는 약제학적 조성물
|
AU2006201229B2
(en)
|
2000-12-21 |
2008-11-20 |
Vertex Pharmaceuticals Incorporated |
Pyrazole Compounds Useful as Protein Kinase Inhibitors
|
CA2433018A1
(en)
|
2000-12-21 |
2002-06-27 |
Joel C. Barrish |
Thiazolyl inhibitors of tec family tyrosine kinases
|
MXPA03005696A
(es)
|
2000-12-21 |
2003-10-06 |
Glaxo Group Ltd |
Pirimidinaminas como moduladores de angiogenesis.
|
US6881737B2
(en)
|
2001-04-11 |
2005-04-19 |
Amgen Inc. |
Substituted triazinyl acrylamide derivatives and methods of use
|
WO2002096888A1
(de)
|
2001-05-29 |
2002-12-05 |
Schering Aktiengesellschaft |
Cdk inhibitorische pyrimidine, deren herstellung und verwendung als arzneimittel
|
US6939874B2
(en)
|
2001-08-22 |
2005-09-06 |
Amgen Inc. |
Substituted pyrimidinyl derivatives and methods of use
|
US7115617B2
(en)
|
2001-08-22 |
2006-10-03 |
Amgen Inc. |
Amino-substituted pyrimidinyl derivatives and methods of use
|
AU2006252047B2
(en)
|
2001-09-14 |
2010-02-11 |
Methylgene Inc. |
Inhibitors of histone deacetylase
|
US7868204B2
(en)
|
2001-09-14 |
2011-01-11 |
Methylgene Inc. |
Inhibitors of histone deacetylase
|
AU2002327627B2
(en)
|
2001-09-14 |
2006-09-14 |
Methylgene Inc. |
Inhibitors of histone deacetylase
|
US6897220B2
(en)
|
2001-09-14 |
2005-05-24 |
Methylgene, Inc. |
Inhibitors of histone deacetylase
|
US7163943B2
(en)
|
2001-09-21 |
2007-01-16 |
Reddy Us Therapeutics, Inc. |
Methods and compositions of novel triazine compounds
|
US7169785B2
(en)
|
2001-09-21 |
2007-01-30 |
Reddy Us Therapeutics, Inc. |
Methods and compositions of novel triazine compounds
|
US7132423B2
(en)
|
2001-09-21 |
2006-11-07 |
Reddy Us Therapeutics, Inc. |
Methods and compositions of novel triazine compounds
|
US7173032B2
(en)
|
2001-09-21 |
2007-02-06 |
Reddy Us Therapeutics, Inc. |
Methods and compositions of novel triazine compounds
|
US7112587B2
(en)
|
2001-09-21 |
2006-09-26 |
Reddy Us Therapeutics, Inc. |
Methods and compositions of novel triazine compounds
|
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
|
WO2003026665A1
(en)
|
2001-09-26 |
2003-04-03 |
Bayer Pharmaceuticals Corporation |
2-phenylamino-4-(5-pyrazolylamino)-pyrimidine derivatives as kinase inhibitors, in particular, src kinase inhibitors
|
WO2003040141A1
(en)
|
2001-09-28 |
2003-05-15 |
Bayer Pharmaceuticals Corporation |
Oxazolyl-phenyl-2,4-diamino-pyrimidine compounds and methods for treating hyperproliferative disorders
|
DE50212771D1
(de)
|
2001-10-17 |
2008-10-23 |
Boehringer Ingelheim Pharma |
Pyrimidinderivate, arzneimittel enthaltend diese verbindungen, deren verwendung und verfahren zu ihrer herstellung
|
NZ531853A
(en)
|
2001-11-01 |
2006-02-24 |
Janssen Pharmaceutica Nv |
Heteroaryl amines as glycogen synthase kinase 3beta inhibitors (gsk3 inhibitors)
|
WO2003037877A1
(en)
|
2001-11-01 |
2003-05-08 |
Janssen Pharmaceutica N.V. |
AMINOBENZAMIDE DERIVATIVES AS GLYCOGEN SYNTHASE KINASE 3β INHIBITORS
|
SE0104140D0
(sv)
|
2001-12-07 |
2001-12-07 |
Astrazeneca Ab |
Novel Compounds
|
AU2003202263A1
(en)
|
2002-01-10 |
2003-07-30 |
Bayer Healthcare Ag |
Roh-kinase inhibitors
|
CA2473910C
(en)
|
2002-01-23 |
2011-03-15 |
Bayer Pharmaceuticals Corporation |
Pyrimidine derivatives as rho-kinase inhibitors
|
TWI329105B
(en)
|
2002-02-01 |
2010-08-21 |
Rigel Pharmaceuticals Inc |
2,4-pyrimidinediamine compounds and their uses
|
JP2005524668A
(ja)
|
2002-03-01 |
2005-08-18 |
スミスクライン ビーチャム コーポレーション |
ジアミノピリミジン類及びそれらの血管新生阻害薬としての使用
|
WO2003078423A1
(en)
|
2002-03-15 |
2003-09-25 |
Vertex Pharmaceuticals, Inc. |
Compositions useful as inhibitors of protein kinases
|
AU2003225800A1
(en)
|
2002-03-15 |
2003-09-29 |
Hayley Binch |
Azolylaminoazine as inhibitors of protein kinases
|
WO2003095448A1
(en)
|
2002-05-06 |
2003-11-20 |
Bayer Pharmaceuticals Corporation |
Pyridinyl amino pyrimidine derivatives useful for treating hyper-proliferative disorders
|
ATE451104T1
(de)
|
2002-07-29 |
2009-12-15 |
Rigel Pharmaceuticals Inc |
Verfahren zur behandlung oder pruvention von autoimmunkrankheiten mit 2,4-pyrimidindiamin- verbindungen
|
CA2488739A1
(en)
|
2002-08-30 |
2004-03-11 |
Eisai Co., Ltd. |
Nitrogen-containing aromatic derivatives
|
TW200501960A
(en)
|
2002-10-02 |
2005-01-16 |
Bristol Myers Squibb Co |
Synergistic kits and compositions for treating cancer
|
US20040209930A1
(en)
|
2002-10-02 |
2004-10-21 |
Carboni Joan M. |
Synergistic methods and compositions for treating cancer
|
AU2003285007A1
(en)
|
2002-10-30 |
2004-06-07 |
Merck & Co., Inc. |
Kinase inhibitors
|
EA200500721A1
(ru)
|
2002-11-28 |
2005-12-29 |
Шеринг Акциенгезельшафт |
Пиримидины, ингибирующие chk, pdk и акт, их получение и применение в качестве лекарственных средств
|
RS20060097A
(en)
|
2002-12-20 |
2008-11-28 |
Pfizer Products Inc., |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
US7109337B2
(en)
|
2002-12-20 |
2006-09-19 |
Pfizer Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
UA80767C2
(en)
|
2002-12-20 |
2007-10-25 |
Pfizer Prod Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
JP4634367B2
(ja)
|
2003-02-20 |
2011-02-16 |
スミスクライン ビーチャム コーポレーション |
ピリミジン化合物
|
GB0305929D0
(en)
|
2003-03-14 |
2003-04-23 |
Novartis Ag |
Organic compounds
|
ATE413404T1
(de)
|
2003-07-16 |
2008-11-15 |
Janssen Pharmaceutica Nv |
Triazolopyrimidin derivate als inhibitoren von glycogen synthase kinase-3
|
AU2004260738B2
(en)
|
2003-07-16 |
2009-07-16 |
Janssen Pharmaceutica N.V. |
Triazolopyrimidine derivatives as glycogen synthase kinase 3 inhibitors
|
PL1656372T3
(pl)
|
2003-07-30 |
2013-08-30 |
Rigel Pharmaceuticals Inc |
Związki 2,4-pirymidynodiaminy do stosowania w leczeniu lub zapobieganiu chorobom autoimmunologicznym
|
EP1663211B1
(en)
|
2003-08-06 |
2010-01-20 |
Vertex Pharmaceuticals Incorporated |
Aminotriazole compounds useful as inhibitors of protein kinases
|
ATE504568T1
(de)
|
2003-08-07 |
2011-04-15 |
Nat Health Research Institutes |
Indol-verbindungen als inhibitoren der tubulin- polymerisation zur behandlung von angiogenesisbezogenen erkrankungen
|
US20050113398A1
(en)
|
2003-08-07 |
2005-05-26 |
Ankush Argade |
2,4-pyrimidinediamine compounds and uses as anti-proliferative agents
|
CA2533320A1
(en)
|
2003-08-15 |
2006-02-24 |
Novartis Ag |
2, 4-pyrimidinediamines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders
|
US7767806B2
(en)
|
2003-09-08 |
2010-08-03 |
Chugai Seiyaku Kabushiki Kaisha |
Hyaluronic acid modification products and drug carriers using them
|
JP4205543B2
(ja)
|
2003-09-09 |
2009-01-07 |
本田技研工業株式会社 |
小型船
|
SG146624A1
(en)
|
2003-09-11 |
2008-10-30 |
Kemia Inc |
Cytokine inhibitors
|
CN100584832C
(zh)
|
2003-09-18 |
2010-01-27 |
诺瓦提斯公司 |
可用于治疗增殖性病症的2,4-二(苯基氨基)嘧啶类
|
TW200526253A
(en)
|
2003-11-14 |
2005-08-16 |
Chugai Pharmaceutical Co Ltd |
Cross-linked polysaccharide microparticles and process for producing the same
|
EP1687297B1
(en)
|
2003-11-24 |
2014-06-18 |
ProMetic BioSciences Inc. |
Triazine dimers for the treatment of autoimmune diseases
|
JP2007514775A
(ja)
|
2003-12-19 |
2007-06-07 |
ライジェル ファーマシューティカルズ, インコーポレイテッド |
1−(2,4−ピリミジンジアミノ)−2−シクロペンタンカルボキサイミド合成中間体の立体異性体および立体異性体混合物
|
US7253204B2
(en)
|
2004-03-26 |
2007-08-07 |
Methylgene Inc. |
Inhibitors of histone deacetylase
|
DE602005024382D1
(de)
|
2004-04-13 |
2010-12-09 |
Astellas Pharma Inc |
Polycyclische pyrimidine als kaliumionenkanal-modulatoren
|
US20050234583A1
(en)
|
2004-04-20 |
2005-10-20 |
Alexander Kantarovich |
Methods and systems for online embridery data processing
|
US20060205945A1
(en)
|
2004-05-14 |
2006-09-14 |
Pfizer Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
BRPI0510963A
(pt)
|
2004-05-14 |
2007-11-20 |
Pfizer Prod Inc |
derivados pirimidina para o tratamento do crescimento anormal de células
|
CA2566531A1
(en)
|
2004-05-18 |
2005-12-15 |
Rigel Pharmaceuticals, Inc. |
Cycloalkyl substituted pyrimidinediamine compounds and their uses
|
WO2006012502A2
(en)
|
2004-07-23 |
2006-02-02 |
Rigel Pharmaceuticals, Inc. |
Formulation of insoluble small molecule therapeutics in lipid-based carriers
|
US7521457B2
(en)
|
2004-08-20 |
2009-04-21 |
Boehringer Ingelheim International Gmbh |
Pyrimidines as PLK inhibitors
|
US20060058525A1
(en)
|
2004-09-01 |
2006-03-16 |
Rajinder Singh |
Synthesis of 2,4-pyrimidinediamine compounds
|
US8143391B2
(en)
|
2004-09-07 |
2012-03-27 |
Chugai Seiyaku Kabushiki Kaisha |
Process for producing water-soluble hyaluronic acid modification
|
US7971443B2
(en)
|
2004-10-28 |
2011-07-05 |
Sharp Kabushiki Kaisha |
Refrigerator
|
GB2420559B
(en)
|
2004-11-15 |
2008-08-06 |
Rigel Pharmaceuticals Inc |
Stereoisomerically enriched 3-aminocarbonyl bicycloheptene pyrimidinediamine compounds and their uses
|
MY169441A
(en)
|
2004-12-08 |
2019-04-11 |
Janssen Pharmaceutica Nv |
2,4, (4,6) pyrimidine derivatives
|
EP1831216A2
(en)
|
2004-12-23 |
2007-09-12 |
Pfizer Products Inc. |
Heteroaromatic derivatives useful as anticancer agents
|
ATE519759T1
(de)
|
2004-12-30 |
2011-08-15 |
Exelixis Inc |
Pyrimidinderivate als kinasemodulatoren und anwendungsverfahren
|
US7884109B2
(en)
|
2005-04-05 |
2011-02-08 |
Wyeth Llc |
Purine and imidazopyridine derivatives for immunosuppression
|
WO2006108103A1
(en)
|
2005-04-05 |
2006-10-12 |
Pharmacopeia, Inc. |
Purine and imidazopyridine derivatives for immunosuppression
|
DE102005016634A1
(de)
|
2005-04-12 |
2006-10-19 |
Merck Patent Gmbh |
Neuartige Aza-Hetercyclen als Kinase-Inhibitoren
|
US8227455B2
(en)
|
2005-04-18 |
2012-07-24 |
Rigel Pharmaceuticals, Inc. |
Methods of treating cell proliferative disorders
|
WO2006124874A2
(en)
|
2005-05-12 |
2006-11-23 |
Kalypsys, Inc. |
Inhibitors of b-raf kinase
|
US20070203161A1
(en)
|
2006-02-24 |
2007-08-30 |
Rigel Pharmaceuticals, Inc. |
Compositions and methods for inhibition of the jak pathway
|
WO2006133426A2
(en)
|
2005-06-08 |
2006-12-14 |
Rigel Pharmaceuticals, Inc. |
Compositions and methods for inhibition of the jak pathway
|
JP2009500426A
(ja)
|
2005-07-08 |
2009-01-08 |
ソシエテ・ドゥ・コンセイユ・ドゥ・ルシェルシュ・エ・ダプリカーション・シャンティフィック・エス・ア・エス |
メラノコルチン受容体のリガンド
|
JP2009501711A
(ja)
|
2005-07-11 |
2009-01-22 |
サノフイ−アベンテイス |
新規2,4−ジアニリノピリミジン誘導体、その調製、医薬、医薬組成物としての、特に、ikk阻害剤としてのそれらの使用
|
WO2007014198A1
(en)
|
2005-07-25 |
2007-02-01 |
Synta Pharmaceuticals Corp. |
1, 2, 3 -triazoles inhibitors of tubulin polymerization for the treatment of poliferative disorders
|
US7486280B2
(en)
|
2005-08-04 |
2009-02-03 |
Uniplas Enterprises Pte, Ltd. |
Contoured capacitive touch control panel
|
KR100674813B1
(ko)
|
2005-08-05 |
2007-01-29 |
일양약품주식회사 |
N-페닐-2-피리미딘-아민 유도체 및 그의 제조방법
|
US20090118310A1
(en)
|
2005-08-09 |
2009-05-07 |
University Of Medicine And Dentistry Of New Jersey |
Activated Cdc42-associated kinase (ACK) as a therapeutic target for Ras-induced cancer
|
WO2007042571A1
(en)
|
2005-10-14 |
2007-04-19 |
Neurosearch A/S |
Novel pyrimidine-2,4-diamine derivatives and their use as modulators of small-conductance calcium-activated potassium channels
|
US8133900B2
(en)
|
2005-11-01 |
2012-03-13 |
Targegen, Inc. |
Use of bi-aryl meta-pyrimidine inhibitors of kinases
|
US7528143B2
(en)
|
2005-11-01 |
2009-05-05 |
Targegen, Inc. |
Bi-aryl meta-pyrimidine inhibitors of kinases
|
US8604042B2
(en)
|
2005-11-01 |
2013-12-10 |
Targegen, Inc. |
Bi-aryl meta-pyrimidine inhibitors of kinases
|
US8246984B2
(en)
|
2005-12-06 |
2012-08-21 |
Rigel Pharmaceuticals, Inc. |
Formulation of insoluble small molecule therapeutics in lipid-based carriers
|
NL2000323C2
(nl)
|
2005-12-20 |
2007-11-20 |
Pfizer Ltd |
Pyrimidine-derivaten.
|
JP4332590B2
(ja)
|
2005-12-21 |
2009-09-16 |
ファイザー・プロダクツ・インク |
異常細胞増殖を治療するためのピリミジン誘導体
|
US20070141684A1
(en)
|
2005-12-21 |
2007-06-21 |
Pfizer Inc |
Preparation of gamma-amino acids having affinity for the alpha-2-delta protein
|
DE102005062742A1
(de)
|
2005-12-22 |
2007-06-28 |
Bayer Schering Pharma Ag |
Sulfoximin substituierte Pyrimidine, Verfahren zu deren Herstellung und ihre Verwendung als Arzneimittel
|
US7962290B1
(en)
|
2006-01-09 |
2011-06-14 |
Rigel Pharmaceuticals, Inc. |
Identification of pharmacophores from co-crystals of spleen tyrosine kinase (SYK) and SYK ligands
|
TW200736232A
(en)
|
2006-01-26 |
2007-10-01 |
Astrazeneca Ab |
Pyrimidine derivatives
|
WO2007089768A2
(en)
|
2006-01-30 |
2007-08-09 |
Exelixis, Inc. |
4-aryl-2-amino-pyrimidines or 4-aryl-2-aminoalkyl-pyrimidines as jak-2 modulators and pharmaceutical compositions containing them
|
ES2622493T3
(es)
|
2006-02-24 |
2017-07-06 |
Rigel Pharmaceuticals, Inc. |
Composiciones y métodos para la inhibición de la ruta de JAK
|
CA2648170A1
(en)
|
2006-04-10 |
2007-10-18 |
Boehringer Ingelheim International Gmbh |
2, 4-diaminopyrimidine derivatives and their use for the treatment of cancer
|
CN101058561B
(zh)
|
2006-04-19 |
2011-01-26 |
苏州爱斯鹏药物研发有限责任公司 |
用于抑制蛋白激酶的二苯脲衍生物及其组合物和用途
|
AU2007245223C1
(en)
|
2006-04-26 |
2010-07-15 |
Ito En, Ltd. |
Fat absorption inhibitor
|
WO2007130933A2
(en)
|
2006-05-01 |
2007-11-15 |
Jeffrey W Bezanson |
Apparatuses, methods and systems for vector operations and storage in matrix models
|
JP5437061B2
(ja)
|
2006-05-26 |
2014-03-12 |
アッヴィ・インコーポレイテッド |
ポロ様キナーゼの阻害薬
|
US7460807B2
(en)
|
2006-05-31 |
2008-12-02 |
Kabushiki Kaisha Toshiba |
Image forming apparatus and method of controlling the apparatus
|
US20070293494A1
(en)
|
2006-06-15 |
2007-12-20 |
Djung Jane F |
2-Anilino-4-(Heterocyclic) Amino-Pyrimidines
|
TW200817391A
(en)
|
2006-06-30 |
2008-04-16 |
Astrazeneca Ab |
Novel compounds
|
EP2043651A2
(en)
|
2006-07-05 |
2009-04-08 |
Exelixis, Inc. |
Methods of using igf1r and abl kinase modulators
|
US8008307B2
(en)
|
2006-08-08 |
2011-08-30 |
Millennium Pharmaceuticals, Inc. |
Heteroaryl compounds useful as inhibitors of E1 activating enzymes
|
DE102006041382A1
(de)
|
2006-08-29 |
2008-03-20 |
Bayer Schering Pharma Ag |
Carbamoyl-Sulfoximide als Proteinkinaseinhibitoren
|
MX2009004019A
(es)
|
2006-10-19 |
2009-06-19 |
Signal Pharm Llc |
Compuestos heteroarilo, composiciones de los mismos, y uso de los mismos como inhibidores de proteina cinasa.
|
US20080119496A1
(en)
|
2006-11-16 |
2008-05-22 |
Pharmacopeia Drug Discovery, Inc. |
7-Substituted Purine Derivatives for Immunosuppression
|
SI2091918T1
(sl)
|
2006-12-08 |
2015-01-30 |
Irm Llc |
Spojine in sestavki kot inhibitorji protein-kinaze
|
ES2699585T3
(es)
|
2006-12-15 |
2019-02-11 |
Nantbio Inc |
Derivados de triazina y sus aplicaciones terapéuticas
|
WO2008082537A2
(en)
|
2006-12-19 |
2008-07-10 |
The General Hospital Corporation |
Compounds for modulating integrin cd11b/cd18
|
CN101563327A
(zh)
|
2006-12-19 |
2009-10-21 |
健泰科生物技术公司 |
嘧啶类激酶抑制剂
|
EP2134713A2
(en)
|
2006-12-20 |
2009-12-23 |
Schering Corporation |
Novel jnk inhibitors
|
EP1939185A1
(de)
|
2006-12-20 |
2008-07-02 |
Bayer Schering Pharma Aktiengesellschaft |
Neuartige Hetaryl-Phenylendiamin-Pyrimidine als Proteinkinaseinhibitoren zur Behandlung von Krebs
|
FR2911138B1
(fr)
|
2007-01-05 |
2009-02-20 |
Sanofi Aventis Sa |
Nouveaux derives de n, n'-2,4-dianilinopyrimidines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
|
US20080214558A1
(en)
|
2007-03-01 |
2008-09-04 |
Supergen, Inc. |
Pyrimidine-2,4-diamine derivatives and their use as jak2 kinase inhibitors
|
CA2681015C
(en)
|
2007-03-16 |
2016-06-21 |
The Scripps Research Institute |
Inhibitors of focal adhesion kinase
|
US7947698B2
(en)
|
2007-03-23 |
2011-05-24 |
Rigel Pharmaceuticals, Inc. |
Compositions and methods for inhibition of the JAK pathway
|
US7834024B2
(en)
|
2007-03-26 |
2010-11-16 |
Rigel Pharmaceuticals, Inc. |
Compositions and methods for inhibition of the JAK pathway
|
WO2008124085A2
(en)
|
2007-04-03 |
2008-10-16 |
Exelixis, Inc. |
Methods of using combinations of mek and jak-2 inhibitors
|
PL2154967T3
(pl)
|
2007-04-16 |
2014-08-29 |
Hutchison Medipharma Entpr Ltd |
Pochodne pirymidyny
|
CN101289444B
(zh)
|
2007-04-16 |
2012-01-04 |
和记黄埔医药(上海)有限公司 |
一种嘧啶衍生物及其医药用途
|
CN103951658B
(zh)
|
2007-04-18 |
2017-10-13 |
辉瑞产品公司 |
用于治疗异常细胞生长的磺酰胺衍生物
|
CL2008001626A1
(es)
|
2007-06-05 |
2009-06-05 |
Takeda Pharmaceuticals Co |
Compuestos derivados de heterociclos fusionados, agente farmaceutico que los comprende y su uso en la profilaxis y tratamiento del cancer.
|
EP2014657A1
(de)
|
2007-06-21 |
2009-01-14 |
Bayer Schering Pharma Aktiengesellschaft |
Diaminopyrimidine als Modulatoren des EP2-Rezeptors
|
US20090012045A1
(en)
|
2007-06-26 |
2009-01-08 |
Rigel Pharmaceuticals, Inc. |
Methods of Treating Cell Proliferative Disorders
|
WO2009010789A2
(en)
|
2007-07-16 |
2009-01-22 |
Astrazeneca Ab |
Pyrimidine derivatives 934
|
WO2009017838A2
(en)
|
2007-08-01 |
2009-02-05 |
Exelixis, Inc. |
Combinations of jak-2 inhibitors and other agents
|
FR2919869B1
(fr)
|
2007-08-09 |
2009-09-25 |
Sanofi Aventis Sa |
Nouveaux derives de n, n'-2,4-dianilinopyrimidines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
|
KR101174201B1
(ko)
|
2007-08-28 |
2012-08-16 |
아이알엠 엘엘씨 |
키나제 억제제로서의 2-비페닐아미노-4-아미노피리미딘 유도체
|
EP2184285B1
(en)
|
2007-08-29 |
2015-11-04 |
Takeda Pharmaceutical Company Limited |
Heterocyclic compound and use thereof
|
US7989465B2
(en)
|
2007-10-19 |
2011-08-02 |
Avila Therapeutics, Inc. |
4,6-disubstituted pyrimidines useful as kinase inhibitors
|
AU2008314632B2
(en)
|
2007-10-19 |
2015-05-28 |
Celgene Avilomics Research, Inc. |
Heteroaryl compounds and uses thereof
|
WO2009063240A1
(en)
|
2007-11-16 |
2009-05-22 |
Arrow Therapeutics Limited |
2,4-diaminopyrimidine derivatives useful as inhibitors of aurora kinase
|
ES2734288T3
(es)
|
2007-11-28 |
2019-12-05 |
Dana Farber Cancer Inst Inc |
Inhibidores de miristato de moléculas pequeñas de Bcr-abl y métodos de uso
|
US20090142832A1
(en)
|
2007-11-29 |
2009-06-04 |
James Dalton |
Indoles, Derivatives, and Analogs Thereof and Uses Therefor
|
JP2011505407A
(ja)
*
|
2007-12-03 |
2011-02-24 |
ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング |
過剰な又は異常な細胞増殖を特徴とする疾患を治療するためのジアミノピリジン
|
SI2252300T1
(sl)
|
2008-02-22 |
2017-04-26 |
Rigel Pharmaceuticals, Inc. |
Uporaba 2,4-pirimidindiaminov za zdravljenje ateroskleroze
|
CA2717529A1
(en)
|
2008-03-11 |
2009-09-17 |
Cellzome Limited |
Sulfonamides as zap-70 inhibitors
|
CA2726508C
(en)
|
2008-06-17 |
2016-06-07 |
Astrazeneca Ab |
Pyridine compounds
|
US8445505B2
(en)
|
2008-06-25 |
2013-05-21 |
Irm Llc |
Pyrimidine derivatives as kinase inhibitors
|
UY31929A
(es)
|
2008-06-25 |
2010-01-05 |
Irm Llc |
Compuestos y composiciones como inhibidores de cinasa
|
SG10201510696RA
(en)
|
2008-06-27 |
2016-01-28 |
Celgene Avilomics Res Inc |
Heteroaryl compounds and uses thereof
|
US8338439B2
(en)
|
2008-06-27 |
2012-12-25 |
Celgene Avilomics Research, Inc. |
2,4-disubstituted pyrimidines useful as kinase inhibitors
|
CN101684098A
(zh)
|
2008-09-24 |
2010-03-31 |
中国科学院上海药物研究所 |
一类5-脂氧酶抑制剂及其制备方法、药物组合物和应用
|
DE102008058501B4
(de)
*
|
2008-11-21 |
2011-11-10 |
Eisenmann Ag |
Verfahren zum Betreiben einer Anlage zur Herstellung von Bioethanol
|
EP2241555A1
(en)
*
|
2009-04-14 |
2010-10-20 |
Universita' Degli Studi Di Milano |
New RAC1 inhibitors as potential pharmacological agents for heart failure treatment
|
EP2552211A4
(en)
|
2010-03-26 |
2013-10-23 |
Glaxo Group Ltd |
INDAZOLYL-PYRIMIDINE AS KINASEHEMMER
|
US20130023534A1
(en)
|
2010-03-26 |
2013-01-24 |
Casillas Linda N |
Pyrazolyl-pyrimidines as kinase inhibitors
|
KR20130031296A
(ko)
*
|
2010-05-21 |
2013-03-28 |
케밀리아 에이비 |
신규한 피리미딘 유도체
|
JP2012209902A
(ja)
|
2011-03-30 |
2012-10-25 |
Semiconductor Components Industries Llc |
入出力回路
|
EP2877464B1
(en)
*
|
2012-07-24 |
2016-08-24 |
Boehringer Ingelheim International GmbH |
N-cyclopropyl-n-piperidinyl-amide derivatives and their use as gpr119 modulators
|