FR2530632A1
(fr)
|
1982-07-26 |
1984-01-27 |
Bouchara Emile |
Nouveaux derives substitues du 2,5-diamino 1,4-diazole, leurs procedes de preparation et les compositions pharmaceutiques en renfermant
|
US4569933A
(en)
|
1984-04-13 |
1986-02-11 |
Cornu Pierre Jean |
Antihypertensive substituted derivatives of 2,5-diamino 1,4-diazole
|
US5304555A
(en)
|
1987-08-26 |
1994-04-19 |
Mitsui Petrochemical Industries, Ltd. |
Pyrimidines and pharmaceutically acceptable salts thereof useful in treatment of neurological disorders
|
US5210015A
(en)
|
1990-08-06 |
1993-05-11 |
Hoffman-La Roche Inc. |
Homogeneous assay system using the nuclease activity of a nucleic acid polymerase
|
US5521184A
(en)
|
1992-04-03 |
1996-05-28 |
Ciba-Geigy Corporation |
Pyrimidine derivatives and processes for the preparation thereof
|
US5466692A
(en)
|
1993-03-24 |
1995-11-14 |
American Home Products Corporation |
Substituted pyridopyrimidines and antihypertensives
|
US6498163B1
(en)
|
1997-02-05 |
2002-12-24 |
Warner-Lambert Company |
Pyrido[2,3-D]pyrimidines and 4-aminopyrimidines as inhibitors of cellular proliferation
|
WO2000009495A1
(en)
|
1998-08-11 |
2000-02-24 |
Novartis Ag |
Isoquinoline derivatives with angiogenesis inhibiting activity
|
US6559152B2
(en)
|
1998-10-13 |
2003-05-06 |
Dupont Pharmaceuticals Company |
6-substituted pyrazolo[3,4-d]pyrimidin-4-ones useful as cyclin dependent kinase inhibitors
|
WO2000025780A1
(en)
|
1998-10-29 |
2000-05-11 |
Bristol-Myers Squibb Company |
Compounds derived from an amine nucleus that are inhibitors of impdh enzyme
|
US6596747B2
(en)
|
1998-10-29 |
2003-07-22 |
Bristol-Myers Squibb Company |
Compounds derived from an amine nucleus and pharmaceutical compositions comprising same
|
JP2002528533A
(ja)
|
1998-10-29 |
2002-09-03 |
ブリストル−マイヤーズ スクイブ カンパニー |
酵素impdhの新規なインヒビター
|
US6133031A
(en)
|
1999-08-19 |
2000-10-17 |
Isis Pharmaceuticals Inc. |
Antisense inhibition of focal adhesion kinase expression
|
GB9905075D0
(en)
|
1999-03-06 |
1999-04-28 |
Zeneca Ltd |
Chemical compounds
|
US6440959B1
(en)
|
1999-04-21 |
2002-08-27 |
Hoffman-La Roche Inc. |
Pyrazolobenzodiazepines
|
GB9914258D0
(en)
|
1999-06-18 |
1999-08-18 |
Celltech Therapeutics Ltd |
Chemical compounds
|
JP2003531103A
(ja)
|
1999-08-12 |
2003-10-21 |
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 |
c−JUNN−末端キナーゼ(JNK)および他のタンパク質キナーゼの阻害剤
|
MXPA02002559A
(es)
|
1999-09-10 |
2002-07-30 |
Merck & Co Inc |
Inhibidores de tirosina cinasa.
|
JP4794793B2
(ja)
|
1999-12-28 |
2011-10-19 |
ファーマコペイア, インコーポレイテッド |
N−ヘテロ環TNF−α発現阻害剤
|
EP1257546A1
(en)
|
2000-02-17 |
2002-11-20 |
Amgen Inc. |
Kinase inhibitors
|
GB0004890D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
GB2361236B
(en)
|
2000-03-29 |
2002-04-24 |
Cyclacel Ltd |
Pyrimidines useful against proliferative disorders
|
PT1294358E
(pt)
|
2000-06-28 |
2004-12-31 |
Smithkline Beecham Plc |
Processo de moagem por via humida
|
WO2002016348A1
(en)
|
2000-08-09 |
2002-02-28 |
Astrazeneca Ab |
Antiangiogenic bicyclic derivatives
|
GB0021726D0
(en)
|
2000-09-05 |
2000-10-18 |
Astrazeneca Ab |
Chemical compounds
|
WO2002022603A1
(en)
|
2000-09-15 |
2002-03-21 |
Vertex Pharmaceuticals Incorporated |
Pyrazole compounds useful as protein kinase inhibitors
|
ES2324763T3
(es)
|
2000-10-31 |
2009-08-14 |
Aventis Pharmaceuticals Inc. |
Derivados acilo y sulfonilo de 2-(trans-1,4-diaminociclohexil)-purinas 6,9-disustituidas y su uso como agentes antiproliferativos.
|
ES2307667T3
(es)
|
2000-12-05 |
2008-12-01 |
Vertex Pharmaceuticals Incorporated |
Inhibidires de quinasas terminales c-jun(jnk) y otras proteinas quinasas.
|
US7122544B2
(en)
|
2000-12-06 |
2006-10-17 |
Signal Pharmaceuticals, Llc |
Anilinopyrimidine derivatives as IKK inhibitors and compositions and methods related thereto
|
US7429599B2
(en)
|
2000-12-06 |
2008-09-30 |
Signal Pharmaceuticals, Llc |
Methods for treating or preventing an inflammatory or metabolic condition or inhibiting JNK
|
MY130778A
(en)
|
2001-02-09 |
2007-07-31 |
Vertex Pharma |
Heterocyclic inhibitiors of erk2 and uses thereof
|
GB0103926D0
(en)
|
2001-02-17 |
2001-04-04 |
Astrazeneca Ab |
Chemical compounds
|
WO2002070751A1
(en)
|
2001-03-02 |
2002-09-12 |
University Of Pittsburgh Of The Commonwealth System Of Higher Education |
Pcr method
|
EP1372643A1
(en)
|
2001-03-30 |
2004-01-02 |
Smithkline Beecham Corporation |
Pyrazolopyridines, process for their preparation and use as therapeutic compounds
|
US20050107400A1
(en)
|
2001-03-30 |
2005-05-19 |
Boyd Leslie F. |
Use of pyrazolopyridines as therapeutic compounds
|
US6812341B1
(en)
|
2001-05-11 |
2004-11-02 |
Ambion, Inc. |
High efficiency mRNA isolation methods and compositions
|
EP1404669A2
(en)
|
2001-05-16 |
2004-04-07 |
Vertex Pharmaceuticals Incorporated |
Heterocyclic substituted pyrazoles as inhibitors of src and other protein kinases
|
EP1392684B1
(en)
|
2001-06-01 |
2006-09-13 |
Vertex Pharmaceuticals Incorporated |
Thiazole compounds useful as inhibitors of protein kinases
|
EP1397142A4
(en)
|
2001-06-19 |
2004-11-03 |
Bristol Myers Squibb Co |
PYRIMIDINE PHOSPHODIESTERASE (PDE) INHIBITORS 7
|
WO2003011837A1
(en)
|
2001-08-01 |
2003-02-13 |
Merck & Co., Inc. |
Tyrosine kinase inhibitors
|
US20040181066A1
(en)
|
2001-08-01 |
2004-09-16 |
Fraley Mark E. |
Tyrosine kinase inhibitors
|
US6958340B2
(en)
|
2001-08-01 |
2005-10-25 |
Merck & Co., Inc. |
Tyrosine kinase inhibitors
|
CN100391958C
(zh)
|
2001-09-19 |
2008-06-04 |
安万特医药股份有限公司 |
化合物
|
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
|
US7473695B2
(en)
|
2001-10-22 |
2009-01-06 |
Mitsubishi Tanabe Pharma Corporation |
4-imidazolin-2-one compounds
|
US7973031B2
(en)
|
2001-10-30 |
2011-07-05 |
Novartis Ag |
Staurosporine derivatives as inhibitors of FLT3 receptor tyrosine kinase activity
|
JP4488740B2
(ja)
|
2001-11-13 |
2010-06-23 |
ダナ−ファーバー キャンサー インスティテュート,インコーポレイテッド |
免疫細胞活性化を調節する作用剤およびその使用方法
|
WO2003048081A2
(en)
|
2001-12-04 |
2003-06-12 |
Bristol-Myers Squibb Company |
Glycinamides as factor xa inhibitors
|
EP1463730B1
(en)
|
2001-12-17 |
2006-04-19 |
SmithKline Beecham Corporation |
Pyrazolopyridazine derivatives
|
US7550459B2
(en)
|
2001-12-28 |
2009-06-23 |
Acadia Pharmaceuticals, Inc. |
Tetrahydroquinoline analogues as muscarinic agonists
|
BR122016021801B8
(pt)
|
2002-01-22 |
2021-05-25 |
Warner Lambert Co |
compostos 2-(piridin-2-ilamino)-pirido[2,3-d]pirimidin-7-onas
|
CA2486446A1
(en)
|
2002-02-07 |
2003-08-14 |
Neurogen Corporation |
Substituted fused pyrazolecarboxylic acid arylamides and related compounds
|
US7247626B2
(en)
|
2002-03-07 |
2007-07-24 |
Smithkline Beecham Corporation |
Pyrazolopyrimidine derivatives and pharmaceutical compositions containing them
|
JP2005533748A
(ja)
|
2002-03-08 |
2005-11-10 |
シグナル ファーマシューティカルズ,インコーポレイテッド |
増殖性障害および癌を治療、予防、または管理するための併用療法
|
WO2003076437A1
(de)
|
2002-03-11 |
2003-09-18 |
Schering Aktiengesellschaft |
Cdk inhibitorische 2-heteroaryl-pyrimidine, deren herstellung und verwendung als arzneimittel
|
CA2479644A1
(en)
|
2002-04-03 |
2003-10-09 |
F. Hoffmann-La Roche Ag |
Imidazo fused compounds
|
GB0210127D0
(en)
|
2002-05-02 |
2002-06-12 |
Merck Sharp & Dohme |
Therapeutic agents
|
PE20040522A1
(es)
|
2002-05-29 |
2004-09-28 |
Novartis Ag |
Derivados de diarilurea dependientes de la cinasa de proteina
|
GB0215676D0
(en)
|
2002-07-05 |
2002-08-14 |
Novartis Ag |
Organic compounds
|
US7252976B2
(en)
|
2002-08-28 |
2007-08-07 |
Board Of Regents The University Of Texas System |
Quantitative RT-PCR to AC133 to diagnose cancer and monitor angiogenic activity in a cell sample
|
JP2006504755A
(ja)
|
2002-10-15 |
2006-02-09 |
スミスクライン ビーチャム コーポレーション |
Gsk−3阻害薬としてのピリダジン化合物
|
AU2003291310A1
(en)
|
2002-11-06 |
2004-06-03 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds and use thereof
|
CL2003002353A1
(es)
|
2002-11-15 |
2005-02-04 |
Vertex Pharma |
Compuestos derivados de diaminotriazoles, inhibidores d ela proteina quinasa; composicion farmaceutica; procedimiento de preparacion; y su uso del compuesto en el tratamiento de enfermedades de desordenes alergicos, proliferacion, autoinmunes, condic
|
UA80767C2
(en)
|
2002-12-20 |
2007-10-25 |
Pfizer Prod Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
US7098332B2
(en)
|
2002-12-20 |
2006-08-29 |
Hoffmann-La Roche Inc. |
5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones
|
AU2003288675B2
(en)
|
2002-12-23 |
2010-07-22 |
Medimmune Limited |
Antibodies against PD-1 and uses therefor
|
US7144911B2
(en)
|
2002-12-31 |
2006-12-05 |
Deciphera Pharmaceuticals Llc |
Anti-inflammatory medicaments
|
GB0303910D0
(en)
|
2003-02-20 |
2003-03-26 |
Merck Sharp & Dohme |
Therapeutic agents
|
GB0305929D0
(en)
|
2003-03-14 |
2003-04-23 |
Novartis Ag |
Organic compounds
|
CA2523126A1
(en)
|
2003-03-25 |
2004-10-14 |
Vertex Pharmaceuticals Incorporated |
Thiazoles useful as inhibitors of protein kinases
|
JP2006524688A
(ja)
|
2003-03-25 |
2006-11-02 |
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のインヒビターとして有用なチアゾール
|
US20050014753A1
(en)
|
2003-04-04 |
2005-01-20 |
Irm Llc |
Novel compounds and compositions as protein kinase inhibitors
|
EP1611123B8
(en)
|
2003-04-09 |
2013-11-13 |
Exelixis, Inc. |
Tie-2 modulators and methods of use
|
GB0308466D0
(en)
|
2003-04-11 |
2003-05-21 |
Novartis Ag |
Organic compounds
|
EP1628968B1
(en)
|
2003-04-21 |
2011-04-06 |
Mitsubishi Tanabe Pharma Corporation |
4-imidazolin-2-one compounds
|
MXPA05013584A
(es)
|
2003-06-11 |
2006-03-09 |
Sankyo Co |
Compuesto amina terciaria ciclica.
|
PL1635835T3
(pl)
|
2003-06-13 |
2010-06-30 |
Novartis Ag |
Pochodne 2-aminopirymidyny jako inhibitory kinazy RAF
|
GB0315966D0
(en)
|
2003-07-08 |
2003-08-13 |
Cyclacel Ltd |
Compounds
|
JP2007500179A
(ja)
|
2003-07-30 |
2007-01-11 |
サイクラセル・リミテッド |
キナーゼ阻害剤としての2−アミノフェニル−4−フェニルピリミジン
|
US7160888B2
(en)
|
2003-08-22 |
2007-01-09 |
Warner Lambert Company Llc |
[1,8]naphthyridin-2-ones and related compounds for the treatment of schizophrenia
|
EP1663204B1
(en)
|
2003-08-29 |
2014-05-07 |
Exelixis, Inc. |
C-kit modulators and methods of use
|
WO2005065074A2
(en)
|
2003-09-09 |
2005-07-21 |
Temple University Of The Commonwealth System Of Higher Education |
Protection of tissues and cells from cytotoxic effects of ionizing radiation by abl inhibitors
|
AR045944A1
(es)
|
2003-09-24 |
2005-11-16 |
Novartis Ag |
Derivados de isoquinolina 1.4-disustituidas
|
CN1897950A
(zh)
|
2003-10-14 |
2007-01-17 |
惠氏公司 |
稠合芳基和杂芳基衍生物及其使用方法
|
US7169781B2
(en)
|
2003-10-17 |
2007-01-30 |
Hoffmann-La Roche Inc. |
Imidazole derivatives and their use as pharmaceutical agents
|
EP1679309A4
(en)
|
2003-10-24 |
2007-03-28 |
Ono Pharmaceutical Co |
ANTISTRESS MEDICAMENT AND ITS MEDICAL USE
|
JP2007517831A
(ja)
|
2004-01-16 |
2007-07-05 |
ノバルティス アクチエンゲゼルシャフト |
2,4−ジアミノピリミジンおよび心筋再生を誘起するためのその使用
|
DK1713806T3
(da)
|
2004-02-14 |
2013-08-05 |
Irm Llc |
Forbindelser og sammensætninger som proteinkinaseinhibitorer
|
JP2007526906A
(ja)
|
2004-03-05 |
2007-09-20 |
大正製薬株式会社 |
ピロロピリミジン誘導体
|
ES2327940T3
(es)
|
2004-03-09 |
2009-11-05 |
Boehringer Ingelheim Pharmaceuticals Inc. |
3-(4-heterociclil-1,2,3-triazol-1-il)-n-aril-benzamidas en calidad de inhibidores de la produccion de citocinas para el tratamiento de enfermedades inflamatorias cronicas.
|
US7306631B2
(en)
|
2004-03-30 |
2007-12-11 |
The Procter & Gamble Company |
Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof
|
JP4879165B2
(ja)
|
2004-04-20 |
2012-02-22 |
トランス テック ファーマ,インコーポレイテッド |
メラノコルチン受容体の調節因子としての置換チアゾール及びピリミジン誘導体
|
WO2005107760A1
(en)
|
2004-04-30 |
2005-11-17 |
Irm Llc |
Compounds and compositions as inducers of keratinocyte differentiation
|
US7405220B2
(en)
|
2004-06-09 |
2008-07-29 |
Hoffmann-La Roche Inc. |
Pyrazolopyrimidines
|
CA2567662C
(en)
|
2004-06-10 |
2012-11-27 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
US7709645B2
(en)
|
2004-07-27 |
2010-05-04 |
Sgx Pharmaceuticals, Inc. |
Pyrrolo-pyridine kinase modulators
|
EP1786817A1
(de)
|
2004-08-26 |
2007-05-23 |
Boehringer Ingelheim International GmbH |
Pteridinone als plk (polo like kinase) inhibitoren
|
JP4972804B2
(ja)
|
2004-08-31 |
2012-07-11 |
Msd株式会社 |
新規置換イミダゾール誘導体
|
US20060069110A1
(en)
|
2004-09-27 |
2006-03-30 |
Andersen Denise L |
Substituted heterocyclic compounds and methods of use
|
WO2006038001A1
(en)
|
2004-10-06 |
2006-04-13 |
Celltech R & D Limited |
Aminopyrimidine derivatives as jnk inhibitors
|
EP1814856A1
(en)
|
2004-11-12 |
2007-08-08 |
Galapagos N.V. |
Nitrogen heteroaromatic compounds which bind to the active site of protein kinase enzymes
|
EP1885352A2
(en)
|
2004-11-24 |
2008-02-13 |
Novartis AG |
Combinations comprising jak inhibitors and at least one of bcr-abl, flt-3, fak or raf kinase inhibitors
|
JP2006188504A
(ja)
|
2004-12-10 |
2006-07-20 |
Sankyo Co Ltd |
環状3級アミン化合物を含有する医薬組成物
|
EP1831181A2
(en)
|
2004-12-14 |
2007-09-12 |
Vertex Pharmaceuticals Incorporated |
Pyrimidine inhibitors of erk protein kinase and uses thereof
|
JP5132319B2
(ja)
|
2004-12-21 |
2013-01-30 |
スミスクライン ビーチャム コーポレーション |
2−ピリミジニルピラゾロピリジンErbBキナーゼ阻害剤
|
US20060142312A1
(en)
|
2004-12-23 |
2006-06-29 |
Pfizer Inc |
C6-aryl and heteroaryl substituted pyrido[2,3-D] pyrimidin-7-ones
|
ATE519759T1
(de)
|
2004-12-30 |
2011-08-15 |
Exelixis Inc |
Pyrimidinderivate als kinasemodulatoren und anwendungsverfahren
|
CN1939910A
(zh)
|
2004-12-31 |
2007-04-04 |
孙飘扬 |
氨基嘧啶类化合物及其盐和其制备方法与药物用途
|
GB0428514D0
(en)
|
2004-12-31 |
2005-02-09 |
Prosidion Ltd |
Compounds
|
EP1846408B1
(en)
|
2005-01-14 |
2013-03-20 |
Janssen Pharmaceutica NV |
5-membered annelated heterocyclic pyrimidines as kinase inhibitors
|
US20060223807A1
(en)
|
2005-03-29 |
2006-10-05 |
University Of Massachusetts Medical School, A Massachusetts Corporation |
Therapeutic methods for type I diabetes
|
PT2439273T
(pt)
|
2005-05-09 |
2019-05-13 |
Ono Pharmaceutical Co |
Anticorpos monoclonais humanos para morte programada 1 (pd- 1) e métodos para o tratamento de cancro utilizando anticorpos anti-pd-1 isoladamente ou em combinação com outros imunoterapêuticos
|
US8193206B2
(en)
|
2005-06-14 |
2012-06-05 |
Taigen Biotechnology Co., Ltd. |
Pyrimidine compounds
|
MY150958A
(en)
|
2005-06-16 |
2014-03-31 |
Astrazeneca Ab |
Compounds for the treatment of multi-drug resistant bacterial infections
|
AU2006261993B2
(en)
|
2005-06-22 |
2011-11-17 |
Plexxikon, Inc. |
Pyrrolo (2, 3-B) pyridine derivatives as protein kinase inhibitors
|
US7442700B2
(en)
|
2005-07-01 |
2008-10-28 |
Bristol-Myers Squibb Company |
Pyrrolotriazine compounds useful as kinase inhibitors and methods of treating kinase-associated conditions therewith
|
BRPI0613361A2
(pt)
|
2005-07-01 |
2011-01-04 |
Medarex Inc |
anticorpo monoclonal humano isolado, composição, imunoconjugado, molécula biespecìfica, molécula de ácido nucleico isolada, vetor de expressão, célula hospedeira, camundongo transgênico, método para modular uma resposta imune num indivìduo, método para inibir crescimento de células tumorais num indivìduo, método para tratar uma doença infecciosa num indivìduo, método para aumentar uma resposta imune a um antìgeno num indivìduo, método para tratar ou prevenir uma doença inflamatória num indivìduo e método para preparar o anticorpo anti-pd-l1
|
US7309787B2
(en)
|
2005-07-13 |
2007-12-18 |
Allergan, Inc. |
Kinase inhibitors
|
US8003624B2
(en)
|
2005-08-25 |
2011-08-23 |
Schering Corporation |
Functionally selective ALPHA2C adrenoreceptor agonists
|
US7803828B2
(en)
|
2005-08-25 |
2010-09-28 |
Schering-Plough Corporation |
Functionally selective alpha2C adrenoreceptor agonists
|
WO2007030362A1
(en)
|
2005-09-07 |
2007-03-15 |
Laboratoires Serono Sa. |
Ikk inhibitors for the treatment of endometriosis
|
CA2621503C
(en)
|
2005-09-07 |
2014-05-20 |
Rigel Pharmaceuticals, Inc. |
Triazole derivatives useful as axl inhibitors
|
US7705009B2
(en)
|
2005-11-22 |
2010-04-27 |
Hoffman-La Roche Inc. |
4-aminopyrimidine-5-thione derivatives
|
CN101326182B
(zh)
|
2005-12-05 |
2011-09-28 |
史密丝克莱恩比彻姆公司 |
2-嘧啶基吡唑并吡啶ErbB激酶抑制剂
|
TW200804349A
(en)
|
2005-12-23 |
2008-01-16 |
Kalypsys Inc |
Novel substituted pyrimidinyloxy ureas as inhibitors of protein kinases
|
WO2007084314A2
(en)
|
2006-01-12 |
2007-07-26 |
Incyte Corporation |
MODULATORS OF 11-ß HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME
|
JP2009526044A
(ja)
|
2006-02-07 |
2009-07-16 |
アストラゼネカ・アクチエボラーグ |
新規な化合物i
|
JP2007217322A
(ja)
|
2006-02-15 |
2007-08-30 |
Ube Ind Ltd |
慢性閉塞性肺疾患の治療又は予防のための医薬組成物
|
JP2009530261A
(ja)
|
2006-03-16 |
2009-08-27 |
ファイザー・プロダクツ・インク |
ピラゾール化合物
|
WO2007129195A2
(en)
|
2006-05-04 |
2007-11-15 |
Pfizer Products Inc. |
4-pyrimidine-5-amino-pyrazole compounds
|
CN101460175A
(zh)
|
2006-05-15 |
2009-06-17 |
Irm责任有限公司 |
用于fgf受体激酶抑制剂的组合物和方法
|
TW200811169A
(en)
*
|
2006-05-26 |
2008-03-01 |
Astrazeneca Ab |
Chemical compounds
|
JO3235B1
(ar)
|
2006-05-26 |
2018-03-08 |
Astex Therapeutics Ltd |
مركبات بيررولوبيريميدين و استعمالاتها
|
TW200815417A
(en)
|
2006-06-27 |
2008-04-01 |
Astrazeneca Ab |
New compounds II
|
WO2008005538A2
(en)
|
2006-07-05 |
2008-01-10 |
Exelixis, Inc. |
Methods of using igf1r and abl kinase modulators
|
JP5042311B2
(ja)
|
2006-07-20 |
2012-10-03 |
ノバルティス アーゲー |
Cetp阻害剤としてのアミノピペリジン誘導体
|
WO2008039359A2
(en)
|
2006-09-25 |
2008-04-03 |
Janssen Pharmaceutica N.V. |
Bicyclic pyrimidine kinase inhibitors
|
JP2010510971A
(ja)
|
2006-11-27 |
2010-04-08 |
アレス トレーディング ソシエテ アノニム |
多発性骨髄腫の治療
|
BRPI0720588B8
(pt)
|
2006-12-21 |
2021-05-25 |
Nerviano Medical Sciences Srl |
derivados de pirazol-quinazolina substituídos, processo para sua preparação e seu uso como inibidores da quinase
|
DK2170959T3
(da)
|
2007-06-18 |
2014-01-13 |
Merck Sharp & Dohme |
Antistoffer mod human programmeret dødsreceptor pd-1
|
WO2009017954A1
(en)
|
2007-08-01 |
2009-02-05 |
Phenomix Corporation |
Inhibitors of jak2 kinase
|
BRPI0815042A2
(pt)
|
2007-08-01 |
2015-02-10 |
Pfizer |
Compostos de pirazol
|
WO2009034390A1
(en)
|
2007-09-14 |
2009-03-19 |
Arrow Therapeutics Limited |
Heterocyclic derivatives and their use in treating hepatitis c
|
US8314094B2
(en)
|
2007-10-05 |
2012-11-20 |
Msd K.K |
Benzoxazinone derivative
|
GB0719803D0
(en)
|
2007-10-10 |
2007-11-21 |
Cancer Rec Tech Ltd |
Therapeutic compounds and their use
|
WO2009061345A2
(en)
|
2007-11-07 |
2009-05-14 |
Cornell Research Foundation, Inc. |
Targeting cdk4 and cdk6 in cancer therapy
|
CN101910152B
(zh)
|
2007-11-16 |
2014-08-06 |
因塞特公司 |
作为janus激酶抑制剂的4-吡唑基-n-芳基嘧啶-2-胺和4-吡唑基-n-杂芳基嘧啶-2-胺
|
CN101883764B
(zh)
|
2007-12-07 |
2013-11-13 |
诺华股份有限公司 |
吡唑衍生物及其作为细胞周期蛋白依赖性激酶抑制剂的用途
|
WO2009076440A2
(en)
|
2007-12-12 |
2009-06-18 |
E.I. Du Pont De Nemours And Company |
Fungicidal bicyclic pyrazoles
|
US7820665B2
(en)
|
2007-12-19 |
2010-10-26 |
Amgen Inc. |
Imidazopyridazine inhibitors of PI3 kinase for cancer treatment
|
MX2010006457A
(es)
|
2007-12-19 |
2010-07-05 |
Amgen Inc |
Compuestos fusionados de piridina, pirimidina y triazina como inhibidores de ciclo celular.
|
CA2711603A1
(en)
|
2008-01-11 |
2009-07-16 |
The Regents Of The University Of California |
Activators of executioner procaspases 3, 6 and 7
|
JP5328816B2
(ja)
|
2008-02-22 |
2013-10-30 |
エフ.ホフマン−ラ ロシュ アーゲー |
アミロイドβの調節薬
|
EP2262837A4
(en)
|
2008-03-12 |
2011-04-06 |
Merck Sharp & Dohme |
PD-1 BINDING PROTEINS
|
EA201001456A1
(ru)
|
2008-03-21 |
2011-06-30 |
Новартис Аг |
Новые гетероциклические соединения и их применение
|
US8865732B2
(en)
|
2008-03-21 |
2014-10-21 |
Novartis Ag |
Heterocyclic compounds and uses thereof
|
EP2108641A1
(en)
|
2008-04-11 |
2009-10-14 |
Laboratorios Almirall, S.A. |
New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors
|
JPWO2009128520A1
(ja)
|
2008-04-18 |
2011-08-04 |
塩野義製薬株式会社 |
Pi3k阻害活性を有する複素環化合物
|
WO2009152027A1
(en)
|
2008-06-12 |
2009-12-17 |
Merck & Co., Inc. |
5,7-dihydro-6h-pyrrolo[2,3-d]pyrimidin-6-one derivatives for mark inhibition
|
US8338439B2
(en)
|
2008-06-27 |
2012-12-25 |
Celgene Avilomics Research, Inc. |
2,4-disubstituted pyrimidines useful as kinase inhibitors
|
DK2361248T3
(en)
|
2008-06-27 |
2019-01-14 |
Celgene Car Llc |
Heteroberl compounds and uses thereof
|
JP5640005B2
(ja)
|
2008-07-14 |
2014-12-10 |
ギリアード サイエンシーズ, インコーポレイテッド |
Hdacおよび/またはcdk阻害剤としてのイミダゾシルピリジン化合物
|
PL2324008T3
(pl)
|
2008-07-24 |
2012-09-28 |
Nerviano Medical Sciences Srl |
3,4-diarylopirazole jako inhibitory kinazy białkowej
|
MX2011002060A
(es)
|
2008-08-25 |
2011-04-05 |
Irm Llc |
Moduladores de la senda de hedgehog.
|
US20120028940A1
(en)
|
2008-09-16 |
2012-02-02 |
Merck Sharp & Dohme Corp. |
Functionally selective azanitrile alpha-2c adrenoreceptor agonists
|
CN102264762B
(zh)
|
2008-09-26 |
2018-03-27 |
达纳-法伯癌症研究公司 |
人抗pd‑1、pd‑l1和pd‑l2的抗体及其应用
|
US8653097B2
(en)
|
2008-10-17 |
2014-02-18 |
Boehringer Ingelheim International Gmbh |
Tetra-aza-heterocycles as phosphatidylinositol-3-kinases (P13-kinases) inhibitor
|
WO2010046780A2
(en)
|
2008-10-22 |
2010-04-29 |
Institut Pasteur Korea |
Anti viral compounds
|
TW201022267A
(en)
|
2008-10-23 |
2010-06-16 |
Gruenenthal Gmbh |
Substituierte pyrimidin-und triazin-derivate
|
WO2010049731A1
(en)
|
2008-10-29 |
2010-05-06 |
Astrazeneca Ab |
Pyrazolo- and imidazopyridinylpyrimidineamines as igf-1r tyrosine kinase inhibitors
|
NZ593937A
(en)
|
2008-12-08 |
2014-05-30 |
Vm Pharma Llc |
Compositions of protein receptor tyrosine kinase inhibitors
|
PE20141722A1
(es)
|
2008-12-09 |
2014-12-02 |
Genentech Inc |
Anticuerpos anti-pd-l1 y su uso para mejorar la funcion de celulas t
|
JO2885B1
(en)
|
2008-12-22 |
2015-03-15 |
ايلي ليلي اند كومباني |
Protein kinase inhibitors
|
CN101759683B
(zh)
|
2008-12-25 |
2011-12-28 |
哈尔滨誉衡药业股份有限公司 |
二氢化茚酰胺化合物制备方法、包含其的药物组合物、及其作为蛋白激酶抑制剂的应用
|
EP2387572B1
(en)
|
2009-01-15 |
2015-09-16 |
Rigel Pharmaceuticals, Inc. |
Protein kinase c inhibitors and uses thereof
|
MA33071B1
(fr)
|
2009-01-30 |
2012-02-01 |
Takeda Pharmaceutical |
Compose a noyau condenses et son utilisation
|
EP3192811A1
(en)
|
2009-02-09 |
2017-07-19 |
Université d'Aix-Marseille |
Pd-1 antibodies and pd-l1 antibodies and uses thereof
|
WO2010116270A1
(en)
|
2009-04-10 |
2010-10-14 |
Pfizer Inc. |
Ep2/4 agonists
|
EP2440559B1
(en)
|
2009-05-05 |
2018-01-10 |
Dana-Farber Cancer Institute, Inc. |
Egfr inhibitors and methods of treating disorders
|
TW201102387A
(en)
|
2009-06-08 |
2011-01-16 |
Medicinova Inc |
Substituted pyrazolo[1,5-a]pyridine compounds having multi-target activity
|
EP2487175A1
(en)
|
2009-10-06 |
2012-08-15 |
Kyowa Hakko Kirin Co., Ltd. |
Pharmaceutical product containing aromatic heterocyclic compound
|
EP2308866A1
(de)
|
2009-10-09 |
2011-04-13 |
Bayer CropScience AG |
Phenylpyri(mi)dinylpyrazole und ihre Verwendung als Fungizide
|
WO2011050245A1
(en)
|
2009-10-23 |
2011-04-28 |
Yangbo Feng |
Bicyclic heteroaryls as kinase inhibitors
|
WO2011066342A2
(en)
|
2009-11-24 |
2011-06-03 |
Amplimmune, Inc. |
Simultaneous inhibition of pd-l1/pd-l2
|
WO2011075699A2
(en)
|
2009-12-18 |
2011-06-23 |
Sunovion Pharmaceuticals Inc. |
Compounds for treating disorders mediated by metabotropic glutamate receptor 5, and methods of use thereof
|
EP2516423A1
(en)
|
2009-12-21 |
2012-10-31 |
Bayer CropScience AG |
Thienylpyri (mi) dinylazole and their use for controlling phytopathogenic fungi
|
US20130022629A1
(en)
|
2010-01-04 |
2013-01-24 |
Sharpe Arlene H |
Modulators of Immunoinhibitory Receptor PD-1, and Methods of Use Thereof
|
WO2011092293A2
(en)
|
2010-02-01 |
2011-08-04 |
Novartis Ag |
Cyclohexyl amide derivatives as crf receptor antagonists
|
US8486967B2
(en)
|
2010-02-17 |
2013-07-16 |
Hoffmann-La Roche Inc. |
Heteroaryl substituted piperidines
|
UY33227A
(es)
|
2010-02-19 |
2011-09-30 |
Novartis Ag |
Compuestos de pirrolopirimidina como inhibidores de la cdk4/6
|
CA2800327A1
(en)
|
2010-04-13 |
2011-10-20 |
Novartis Ag |
Combination comprising a cyclin dependent kinase 4 or cyclin dependent kinase 6 (cdk4/6) inhibitor and an mtor inhibitor for treating cancer
|
WO2011133728A2
(en)
|
2010-04-23 |
2011-10-27 |
Kineta, Inc. |
Anti-viral compounds
|
JP2013147428A
(ja)
|
2010-04-27 |
2013-08-01 |
Dainippon Sumitomo Pharma Co Ltd |
新規2−ヘテロアリール単環ピリミジン誘導体
|
WO2011141848A1
(en)
|
2010-05-11 |
2011-11-17 |
Pfizer Inc. |
Morpholine compounds as mineralocorticoid receptor antagonists
|
EP2569302A1
(en)
|
2010-05-13 |
2013-03-20 |
Amgen, Inc |
Heteroaryloxyheterocyclyl compounds as pde10 inhibitors
|
WO2011159877A2
(en)
|
2010-06-18 |
2011-12-22 |
The Brigham And Women's Hospital, Inc. |
Bi-specific antibodies against tim-3 and pd-1 for immunotherapy in chronic immune conditions
|
US8907053B2
(en)
|
2010-06-25 |
2014-12-09 |
Aurigene Discovery Technologies Limited |
Immunosuppression modulating compounds
|
US8735386B2
(en)
|
2010-07-23 |
2014-05-27 |
Boehringer Ingelheim International Gmbh |
Aminopyrazoloquinazolines
|
JP5938038B2
(ja)
|
2010-08-03 |
2016-06-22 |
ネルヴィアーノ・メディカル・サイエンシズ・ソチエタ・ア・レスポンサビリタ・リミタータ |
ピラゾロフェニル−ベンゼンスルホンアミド化合物の誘導体及びその抗腫瘍薬としての使用
|
RS55135B1
(sr)
|
2010-10-25 |
2016-12-30 |
G1 Therapeutics Inc |
Cdk inhibitori
|
WO2012062704A1
(en)
|
2010-11-09 |
2012-05-18 |
Cellzome Limited |
Pyridine compounds and aza analogues thereof as tyk2 inhibitors
|
JP2014501246A
(ja)
|
2010-12-17 |
2014-01-20 |
イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー |
殺菌・殺カビ性アゾ環式アミド
|
BR112013020035A2
(pt)
|
2011-02-08 |
2016-07-19 |
Pfizer |
moduladores do receptor do glucagon
|
TWI532742B
(zh)
|
2011-02-28 |
2016-05-11 |
艾伯維有限公司 |
激酶之三環抑制劑
|
CA2830516C
(en)
|
2011-03-23 |
2017-01-24 |
Amgen Inc. |
Fused tricyclic dual inhibitors of cdk 4/6 and flt3
|
WO2012134943A1
(en)
|
2011-03-25 |
2012-10-04 |
Abbott Laboratories |
Trpv1 antagonists
|
AR086992A1
(es)
|
2011-06-20 |
2014-02-05 |
Bayer Ip Gmbh |
Tienilpiri(mi)dinilpirazoles
|
US20130123281A1
(en)
|
2011-11-11 |
2013-05-16 |
Beta Cat Pharmaceuticals, Llc |
Compositions and Methods for Inhibition of TBL-1 Binding to Disease-Associated Molecules
|
US9073935B2
(en)
|
2011-11-11 |
2015-07-07 |
Vanderbilt University |
Substituted benzylspiroindolin-2-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor M1
|
US8697888B2
(en)
|
2012-01-06 |
2014-04-15 |
Vanderbilt University |
Substituted (1-(methylsulfonyl)azetidin-3-yl)(heterocycloalkyl)methanone analogs as antagonists of muscarinic acetylcholine M1 receptors
|
WO2013110585A1
(en)
|
2012-01-23 |
2013-08-01 |
Boehringer Ingelheim International Gmbh |
5, 8 -dihydro- 6h- pyrazolo [3, 4 -h] quinazolines as igf-lr/lr inhibitors
|
RU2548363C2
(ru)
|
2012-01-25 |
2015-04-20 |
Общество с ограниченной ответственностью "Асинэкс Медхим." |
СЕЛЕКТИВНЫЕ ИНГИБИТОРЫ Haspin киназы
|
EP2814486B8
(en)
|
2012-02-17 |
2018-05-23 |
Kineta Viral Hemorrhagic Fever, LLC |
Antiviral drugs for treatment of arenavirus infection
|
TW201348231A
(zh)
|
2012-02-29 |
2013-12-01 |
Amgen Inc |
雜雙環化合物
|
GB201204384D0
(en)
|
2012-03-13 |
2012-04-25 |
Univ Dundee |
Anti-flammatory agents
|
US9096579B2
(en)
|
2012-04-20 |
2015-08-04 |
Boehringer Ingelheim International Gmbh |
Amino-indolyl-substituted imidazolyl-pyrimidines and their use as medicaments
|
SG11201406914XA
(en)
|
2012-05-08 |
2014-11-27 |
Anvyl Llc |
Alpha 7 nicotinic acetylcholine receptor allosteric modulators, their derivatives and uses thereof
|
US20130310340A1
(en)
|
2012-05-16 |
2013-11-21 |
Rigel Pharmaceuticals, Inc. |
Method of treating muscular degradation
|
RU2509770C2
(ru)
|
2012-06-22 |
2014-03-20 |
Общество с ограниченной ответственностью "Молекулярные Технологии" |
Новые химические соединения производные 2,4-диамино-1,3,5-триазина для профилактики и лечения заболеваний человека и животных
|
WO2014020043A1
(en)
|
2012-08-02 |
2014-02-06 |
Bayer Pharma Aktiengesellschaft |
Combinations for the treatment of cancer
|
WO2014028669A1
(en)
|
2012-08-15 |
2014-02-20 |
Biogen Idec Ma Inc. |
Novel compounds for modulation of ror-gamma activity
|
EP2888256A4
(en)
|
2012-08-24 |
2016-02-17 |
Univ Texas |
HETEROCYCLIC HIF ACTIVITY MODULATORS FOR THE TREATMENT OF DISEASES
|
CN104583195B
(zh)
|
2012-09-12 |
2018-08-17 |
山东亨利医药科技有限责任公司 |
作为酪氨酸激酶抑制剂的含氮杂芳环衍生物
|
EP2909195B1
(en)
|
2012-10-16 |
2017-06-14 |
Janssen Sciences Ireland UC |
Rsv antiviral compounds
|
NZ708350A
(en)
|
2012-11-20 |
2016-08-26 |
Merial Inc |
Anthelmintic compounds and compositions and method of using thereof
|
CN103864770B
(zh)
|
2012-12-10 |
2019-06-11 |
江苏先声药业有限公司 |
作为Hedgehog信号传导的嘧啶胺类和吡啶胺类抑制剂
|
CN104968664A
(zh)
|
2012-12-12 |
2015-10-07 |
山东亨利医药科技有限责任公司 |
作为酪氨酸激酶抑制剂的并环化合物
|
US20150353542A1
(en)
|
2013-01-14 |
2015-12-10 |
Amgen Inc. |
Methods of using cell-cycle inhibitors to modulate one or more properties of a cell culture
|
WO2014130241A1
(en)
|
2013-02-20 |
2014-08-28 |
E. I. Du Pont De Nemours And Company |
Fungicidal pyrazoles
|
US20140357636A1
(en)
|
2013-02-21 |
2014-12-04 |
Wayne Rothbaum |
Treatment of Skeletal-Related Disorders
|
KR20150114566A
(ko)
|
2013-03-05 |
2015-10-12 |
에프. 호프만-라 로슈 아게 |
항바이러스 화합물
|
WO2014155300A2
(en)
|
2013-03-28 |
2014-10-02 |
Aurigene Discovery Technologies Limited |
Substitued pyrimidine amine derivatives as tak-1 inhibitors
|
AR096532A1
(es)
|
2013-06-06 |
2016-01-13 |
Chiesi Farm Spa |
Inhibidores de quinasa
|
MX370661B
(es)
|
2013-06-19 |
2019-12-19 |
Hoffmann La Roche |
Derivados de indolin-2-ona o pirrolo-piridin/pirimidin-2-ona.
|
EP3010917B1
(en)
|
2013-06-21 |
2018-01-31 |
Zenith Epigenetics Ltd. |
Novel substituted bicyclic compounds as bromodomain inhibitors
|
WO2015006875A1
(en)
|
2013-07-18 |
2015-01-22 |
Methylgene Inc. |
Process for the preparation of substituted pyrimidines
|
CN104418860B
(zh)
|
2013-08-20 |
2016-09-07 |
中国科学院广州生物医药与健康研究院 |
嘧啶并杂环类化合物及其药用组合物和应用
|
AR093580A1
(es)
|
2013-08-30 |
2015-06-10 |
Ptc Therapeutics Inc |
Inhibidores bmi-1 de pirimidina sustituidos
|
WO2015038417A1
(en)
|
2013-09-10 |
2015-03-19 |
Asana Biosciences, Llc |
Compounds for regulating fak and/or src pathways
|
WO2015047124A1
(ru)
|
2013-09-26 |
2015-04-02 |
Общество с ограниченной ответственностью "Молекулярные Технологии" |
Новые химические соединения производные 2,4-диамино-1,3,5-триазина для профилактики и лечения заболеваний человека и животных
|
WO2015058126A1
(en)
|
2013-10-18 |
2015-04-23 |
Syros Pharmaceuticals, Inc. |
Heteroaromatic compounds useful for the treatment of prolferative diseases
|
US20160264552A1
(en)
|
2013-10-18 |
2016-09-15 |
Syros Pharmaceuticals, Inc. |
Heteromaromatic compounds useful for the treatment of prolferative diseases
|
CA2927920A1
(en)
|
2013-10-18 |
2015-04-23 |
Dana-Farber Cancer Institute, Inc. |
Polycyclic inhibitors of cyclin-dependent kinase 7 (cdk7)
|
US10329270B2
(en)
|
2013-10-21 |
2019-06-25 |
Merck Patent Gmbh |
Heteroaryl compounds as BTK inhibitors and uses thereof
|
GB201321738D0
(en)
|
2013-12-09 |
2014-01-22 |
Ucb Pharma Sa |
Therapeutic Agents
|
GB201321732D0
(en)
|
2013-12-09 |
2014-01-22 |
Ucb Pharma Sa |
Therapeutic agents
|
WO2015095840A1
(en)
|
2013-12-20 |
2015-06-25 |
Biomed Valley Discoveries, Inc. |
Cancer treatments using combinations of cdk and erk inhibitors
|
CN104761544B
(zh)
|
2014-01-03 |
2019-03-15 |
北京轩义医药科技有限公司 |
Egfr酪氨酸激酶的临床重要突变体的选择性抑制剂
|
WO2015106025A1
(en)
|
2014-01-09 |
2015-07-16 |
The J. David Gladstone Institutes, A Testamentary Trust Established Under The Will Of J. David Gladstone |
Substituted benzoxazine and related compounds
|
SG10201809260XA
(en)
|
2014-04-04 |
2018-11-29 |
Syros Pharmaceuticals Inc |
Inhibitors of cyclin-dependent kinase 7 (cdk7)
|
WO2015157556A1
(en)
|
2014-04-09 |
2015-10-15 |
Kadmon Corporation, Llc |
Treatment of gvhd
|
US10017477B2
(en)
|
2014-04-23 |
2018-07-10 |
Dana-Farber Cancer Institute, Inc. |
Janus kinase inhibitors and uses thereof
|
MX2016014555A
(es)
|
2014-05-09 |
2017-05-30 |
Pimera Inc |
Composiciones novedosas, usos y metodos para hacerlas.
|
CN104003988A
(zh)
|
2014-06-05 |
2014-08-27 |
中国药科大学 |
基于3-氨基-β-咔啉及其衍生物的CDK2激酶抑制剂及其制备方法和用途
|
CN105315259B
(zh)
|
2014-07-29 |
2018-03-09 |
上海艾力斯医药科技有限公司 |
吡啶胺基嘧啶衍生物、其制备方法及应用
|
US10844064B2
(en)
|
2014-09-17 |
2020-11-24 |
Cyclerion Therapeutics, Inc. |
sGC stimulators
|
KR20170095814A
(ko)
|
2014-10-06 |
2017-08-23 |
플랫틀리 디스커버리 랩, 엘엘씨 |
트라이아졸로피리딘 화합물 및 낭성 섬유증의 치료 방법
|
WO2016058544A1
(en)
|
2014-10-16 |
2016-04-21 |
Syros Pharmaceuticals, Inc. |
Inhibitors of cyclin-dependent kinase 7 (cdk7)
|
CN104447743B
(zh)
|
2014-11-26 |
2016-03-02 |
苏州明锐医药科技有限公司 |
帕博西尼的制备方法
|
BR112017011669A2
(pt)
|
2014-12-02 |
2018-02-27 |
Bayer Cropscience Aktiengesellschaft |
compostos bicíclicos como agentes de controle de pragas.
|
EP3617205B1
(en)
|
2015-02-20 |
2021-08-04 |
Incyte Corporation |
Bicyclic heterocycles as fgfr inhibitors
|
KR101864426B1
(ko)
|
2015-03-27 |
2018-06-05 |
영진약품 주식회사 |
1,2 나프토퀴논 유도체 및 이의 제조방법
|
WO2016177340A1
(zh)
|
2015-05-05 |
2016-11-10 |
上海海雁医药科技有限公司 |
双环取代的苯磺酰胺衍生物、其制法与医药上的用途
|
JP6664414B2
(ja)
|
2015-05-13 |
2020-03-13 |
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 |
IGF−1R/IR阻害薬としての新規5,8−ジメチル−9−フェニル−5,8−ジヒドロ−6H−ピラゾロ[3,4−h]キナゾリン−2−イル)−(1H−ピラゾール−3−イル)−アミン及び誘導体
|
GB201509893D0
(en)
|
2015-06-08 |
2015-07-22 |
Ucb Biopharma Sprl |
Therapeutic agents
|
WO2017007658A1
(en)
|
2015-07-07 |
2017-01-12 |
Rigel Pharmaceuticals, Inc. |
A combination for immune mediated cancer treatment
|
CN106699785A
(zh)
|
2015-07-13 |
2017-05-24 |
南开大学 |
作为CDK4/6抑制剂的2-(N-氧化吡啶-2基氨基)-吡啶并[2,3-d]嘧啶-7-酮类化合物
|
PE20181151A1
(es)
|
2015-07-30 |
2018-07-17 |
Macrogenics Inc |
Moleculas de union a pd-1 y metodos de uso de las mismas
|
RS62728B1
(sr)
|
2015-08-04 |
2022-01-31 |
Yissum Res Dev Co Of Hebrew Univ Jerusalem Ltd |
Derivat pirazol pirimidina i njegove upotrebe
|
GB201514489D0
(en)
|
2015-08-14 |
2015-09-30 |
Bergen Teknologioverføring As |
Hyperphenylalaninemia
|
US10980755B2
(en)
|
2015-09-10 |
2021-04-20 |
The Regents Of The University Of California |
LRH-1 modulators
|
TW201718581A
(zh)
|
2015-10-19 |
2017-06-01 |
英塞特公司 |
作為免疫調節劑之雜環化合物
|
US10851082B2
(en)
|
2015-10-28 |
2020-12-01 |
Northwestern University |
Substituted aromatic n-heterocyclic compounds as inhibitors of mitogen-activated protein kinase interacting kinase 1 (MNK1) and 2 (MNK2)
|
WO2017075367A1
(en)
|
2015-10-28 |
2017-05-04 |
Northwestern University |
Substituted aromatic n-heterocyclic compounds as inhibitors of mitogen-activated protein kinase interacting kinase 1 (mnk1) and 2 (mnk2)
|
MX2018006207A
(es)
|
2015-11-19 |
2018-09-05 |
Incyte Corp |
Compuestos heterociclicos como inmunomoduladores.
|
US11214565B2
(en)
|
2015-11-20 |
2022-01-04 |
Denali Therapeutics Inc. |
Compound, compositions, and methods
|
WO2017106634A1
(en)
|
2015-12-17 |
2017-06-22 |
Incyte Corporation |
N-phenyl-pyridine-2-carboxamide derivatives and their use as pd-1/pd-l1 protein/protein interaction modulators
|
TWI850624B
(zh)
|
2015-12-22 |
2024-08-01 |
美商英塞特公司 |
作為免疫調節劑之雜環化合物
|
WO2017110863A1
(ja)
|
2015-12-25 |
2017-06-29 |
住友化学株式会社 |
オキサジアゾール化合物及びその用途
|
JP6990657B2
(ja)
|
2016-02-08 |
2022-01-13 |
エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト |
Ddr1阻害剤としてのスピロインドリノン
|
WO2017161028A1
(en)
|
2016-03-16 |
2017-09-21 |
Kura Oncology, Inc. |
Substituted inhibitors of menin-mll and methods of use
|
GB201605126D0
(en)
|
2016-03-24 |
2016-05-11 |
Univ Nottingham |
Inhibitors and their uses
|
WO2017178515A1
(en)
|
2016-04-12 |
2017-10-19 |
Laboratorios Del Dr. Esteve, S.A. |
Piperidinylalkylamide derivatives having multimodal activity against pain
|
US10577360B2
(en)
|
2016-04-12 |
2020-03-03 |
Esteve Pharmaceuticals, S.A. |
Arylamide derivatives having multimodal activity against pain
|
PL3442947T3
(pl)
|
2016-04-15 |
2023-10-02 |
Epizyme, Inc. |
Związki arylowe lub heteroarylowe podstawione aminą jako inhibitory ehmt1 i ehmt2
|
US20170320875A1
(en)
|
2016-05-06 |
2017-11-09 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
US20190345558A1
(en)
|
2016-05-18 |
2019-11-14 |
Université Libre de Bruxelles |
Method for determining sensitivity to a cdk4/6 inhibitor
|
US20170342060A1
(en)
|
2016-05-26 |
2017-11-30 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
MD3472167T2
(ro)
|
2016-06-20 |
2023-02-28 |
Incyte Corp |
Compuși heterociclici ca imunomodulatori
|
EP3858835A1
(en)
|
2016-07-01 |
2021-08-04 |
G1 Therapeutics, Inc. |
Pyrimidine-based antiproliferative agents
|
RU2019103870A
(ru)
|
2016-07-13 |
2020-08-14 |
Сирос Фармасьютикалз, Инк. |
Ингибиторы циклин-зависимой киназы 7 (cdk7)
|
EP3484866B1
(en)
|
2016-07-14 |
2022-09-07 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
ES2876411T3
(es)
|
2016-08-15 |
2021-11-12 |
Pfizer |
Inhibidores de piridopirimdinona CDK2/4/6
|
CN107759587B
(zh)
|
2016-08-19 |
2021-01-26 |
中国医药研究开发中心有限公司 |
[1,2,4]三唑并[1,5-a]吡啶类化合物及其制备方法和医药用途
|
EP3504198B1
(en)
|
2016-08-29 |
2023-01-25 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
CN107793413B
(zh)
|
2016-09-05 |
2021-09-28 |
上海科州药物研发有限公司 |
嘧啶杂环化合物及其制备方法和应用
|
CN107840846B
(zh)
|
2016-09-19 |
2020-11-24 |
郑州泰基鸿诺医药股份有限公司 |
一种含嘧啶环的化合物、egfr抑制剂及其应用
|
US20190255042A1
(en)
|
2016-11-04 |
2019-08-22 |
Impact Therapeutics, Inc |
Application of hedgehog pathway inhibitor in treating fibrosis diseases
|
WO2018086591A1
(zh)
|
2016-11-11 |
2018-05-17 |
上海海雁医药科技有限公司 |
吡啶胺取代的杂三环化合物、其制法与医药上的用途
|
MY197501A
(en)
|
2016-12-22 |
2023-06-19 |
Incyte Corp |
Tetrahydro imidazo[4,5-c]pyridine derivatives as pd-l1 internalization inducers
|
US10308644B2
(en)
|
2016-12-22 |
2019-06-04 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
US20180179201A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
US20180179179A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
WO2018119263A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Heterocyclic compounds derivatives as pd-l1 internalization inducers
|
CA3047991A1
(en)
|
2016-12-22 |
2018-06-28 |
Incyte Corporation |
Bicyclic heteroaromatic compounds as immunomodulators
|
WO2018119395A1
(en)
|
2016-12-23 |
2018-06-28 |
Aquinnah Pharmaceuticals, Inc. |
Compouns, compositions and methods of use
|
WO2018124001A1
(ja)
|
2016-12-27 |
2018-07-05 |
国立研究開発法人理化学研究所 |
Bmpシグナル阻害化合物
|
EP3577116A4
(en)
|
2017-02-01 |
2020-12-02 |
Aucentra Therapeutics Pty Ltd |
DERIVATIVES OF N-CYCLOALKYL / HETEROCYCLOALKYL-4- (IMIDAZO [1,2-A] PYRIDINE) PYRIMIDINE-2-AMINE AS THERAPEUTICS
|
CA3054809A1
(en)
|
2017-02-28 |
2018-09-07 |
The General Hospital Corporation |
Uses of pyrimidopyrimidinones as sik inhibitors
|
US20200113901A1
(en)
|
2017-03-31 |
2020-04-16 |
Epizyme, Inc. |
Methods of using ehmt2 inhibitors
|
JP7175026B2
(ja)
|
2017-04-01 |
2022-11-18 |
晟科薬業(江蘇)有限公司 |
プロテインキナーゼ阻害剤としての1h-イミダゾ[4,5-h]キナゾリン系化合物
|
CA3060416A1
(en)
|
2017-04-21 |
2018-10-25 |
Epizyme, Inc. |
Combination therapies with ehmt2 inhibitors
|
WO2018226976A1
(en)
|
2017-06-08 |
2018-12-13 |
Kura Oncology, Inc. |
Methods and compositions for inhibiting the interaction of menin with mll proteins
|
EA202090955A1
(ru)
|
2017-10-18 |
2020-11-27 |
Эпизайм, Инк. |
Способы применения ингибиторов ehmt2 в лечении или предупреждении нарушений со стороны крови
|
MA50417A
(fr)
|
2017-10-18 |
2020-08-26 |
Epizyme Inc |
Procédés d'utilisation d'inhibiteurs de l'ehmt2 dans le traitement ou la prévention de troubles du sang
|
WO2019191707A1
(en)
|
2018-03-30 |
2019-10-03 |
Incyte Corporation |
Heterocyclic compounds as immunomodulators
|
WO2019200214A1
(en)
|
2018-04-13 |
2019-10-17 |
The Regents Of The University Of Michigan |
Compositions and methods for treating cancer
|
RU2762557C1
(ru)
|
2018-04-26 |
2021-12-21 |
Пфайзер Инк. |
Производные 2-аминопиридина или 2-аминопиримидина в качестве циклинзависимых ингибиторов киназы
|
FI3790877T3
(fi)
|
2018-05-11 |
2023-05-09 |
Incyte Corp |
Tetrahydroimidatso[4,5-c]pyridiinijohdannaisia pd-l1-immunomodulaattoreina
|
US20200095322A1
(en)
|
2018-06-20 |
2020-03-26 |
Incyte Corporation |
Anti-pd-1 antibodies and uses thereof
|
US10894788B2
(en)
|
2018-06-29 |
2021-01-19 |
Kinnate Biopharma Inc. |
Inhibitors of cyclin-dependent kinases
|
US20210220408A1
(en)
|
2018-09-04 |
2021-07-22 |
Magenta Therapeutics Inc. |
Aryl hydrocarbon receptor antagonists and methods of use
|
US11066404B2
(en)
|
2018-10-11 |
2021-07-20 |
Incyte Corporation |
Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
|
WO2020140054A1
(en)
|
2018-12-28 |
2020-07-02 |
Spv Therapeutics Inc. |
Cyclin-dependent kinase inhibitors
|
WO2020168197A1
(en)
|
2019-02-15 |
2020-08-20 |
Incyte Corporation |
Pyrrolo[2,3-d]pyrimidinone compounds as cdk2 inhibitors
|
MA54947A
(fr)
|
2019-02-15 |
2021-12-22 |
Incyte Corp |
Biomarqueurs de kinase 2 dépendant de la cycline et leurs utilisations
|
US11472791B2
(en)
|
2019-03-05 |
2022-10-18 |
Incyte Corporation |
Pyrazolyl pyrimidinylamine compounds as CDK2 inhibitors
|
US11919904B2
(en)
|
2019-03-29 |
2024-03-05 |
Incyte Corporation |
Sulfonylamide compounds as CDK2 inhibitors
|
US11440914B2
(en)
|
2019-05-01 |
2022-09-13 |
Incyte Corporation |
Tricyclic amine compounds as CDK2 inhibitors
|
WO2020223558A1
(en)
|
2019-05-01 |
2020-11-05 |
Incyte Corporation |
Tricyclic amine compounds as cdk2 inhibitors
|
KR20220099970A
(ko)
|
2019-10-11 |
2022-07-14 |
인사이트 코포레이션 |
Cdk2 억제제로서의 이환식 아민
|