JPH0314566A
(ja)
|
1989-06-09 |
1991-01-23 |
Sankyo Co Ltd |
ベンズイミダゾール誘導体
|
US5244912A
(en)
|
1991-03-28 |
1993-09-14 |
Eli Lilly And Company |
6-heterocyclic-4-amino-1,3,4,5-tetrahydrobenz(cd)indoles and pharmaceutical use thereof
|
FR2710915B1
(fr)
|
1993-10-04 |
1995-11-24 |
Synthelabo |
Dérivés de pipéridine, leur préparation et leur utilisation en thérapeutique.
|
FR2731708B1
(fr)
*
|
1995-03-13 |
1997-04-30 |
Synthelabo |
Derives de piperidine, leur procede de preparation et leur application en therapeutique
|
FR2747678B1
(fr)
|
1996-04-22 |
1998-05-22 |
Synthelabo |
Composes derives d'imidazobenzoxazine, leurs procedes de preparation et leurs utilisations en therapeutique
|
FR2753196B1
(fr)
*
|
1996-09-12 |
1998-10-23 |
Synthelabo |
Derives d'indazole tricyclique, leur preparation et leur application en therapeutique
|
ES2253370T3
(es)
|
2000-04-21 |
2006-06-01 |
PHARMACIA & UPJOHN COMPANY LLC |
Cabergolina para el tratamiento del sindrome de fibromialgia y de fatiga cronica.
|
MXPA03000051A
(es)
|
2000-06-28 |
2003-08-19 |
Smithkline Beecham Plc |
Procedimiento de molido en humedo.
|
US6919334B2
(en)
|
2002-09-12 |
2005-07-19 |
Wyeth |
Antidepressant azaheterocyclymethyl derivatives of 4,5-dihydroimidazo[1,4,5-de][1,4]benzoxazine
|
KR100772297B1
(ko)
|
2002-11-22 |
2007-11-02 |
니뽄 다바코 산교 가부시키가이샤 |
융합 비시클릭 질소-함유 헤테로사이클
|
EP1462103A1
(en)
|
2003-03-25 |
2004-09-29 |
Faust Pharmaceuticals |
NO donors, combination products and uses as modulators of neurotransmitter release
|
WO2005080334A1
(ja)
|
2004-02-23 |
2005-09-01 |
Dainippon Sumitomo Pharma Co., Ltd. |
新規へテロ環化合物
|
EP2522670A1
(en)
|
2004-04-07 |
2012-11-14 |
Takeda Pharmaceutical Company Limited |
Heterocyclic CRF receptor antagonists
|
DE102005011058A1
(de)
|
2005-03-10 |
2006-09-14 |
Merck Patent Gmbh |
Substituierte Tetrahydro-pyrrolo-chinolinderivate
|
WO2006124874A2
(en)
|
2005-05-12 |
2006-11-23 |
Kalypsys, Inc. |
Inhibitors of b-raf kinase
|
EP1912989A2
(en)
|
2005-08-05 |
2008-04-23 |
AstraZeneca AB |
Tricyclic benzimidazoles and their use as metabotropic glutamate receptor modulators
|
EP2147310A4
(en)
|
2007-04-27 |
2010-09-08 |
Univ Rochester |
COMPOSITIONS AND METHODS FOR INHIBITING G PROTEIN SIGNALING
|
US9603848B2
(en)
|
2007-06-08 |
2017-03-28 |
Senomyx, Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
US8633186B2
(en)
|
2007-06-08 |
2014-01-21 |
Senomyx Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
US7928111B2
(en)
|
2007-06-08 |
2011-04-19 |
Senomyx, Inc. |
Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
|
WO2009020559A2
(en)
|
2007-08-03 |
2009-02-12 |
The J. David Gladstone Institutes |
Agents that inhibit p-tefb interactions and methods of use thereof
|
US8476260B2
(en)
|
2007-12-28 |
2013-07-02 |
Mitsubishi Tanabe Pharma Corporation |
Antitumor agent
|
DE102008052618A1
(de)
|
2008-10-21 |
2010-04-22 |
Henkel Ag & Co. Kgaa |
Tricyclische Aldehyde und C,H-acide Verbindungen
|
JP5730281B2
(ja)
|
2009-03-27 |
2015-06-10 |
武田薬品工業株式会社 |
ポリ(adp−リボース)ポリメラーゼ(parp)阻害剤
|
TW201103941A
(en)
|
2009-06-10 |
2011-02-01 |
Janssen Pharmaceutica Nv |
Benzimidazole derivatives useful as TRPM8 channel modulators
|
TW201105681A
(en)
|
2009-06-10 |
2011-02-16 |
Janssen Pharmaceutica Nv |
Benzimidazole derivatives useful as TRPM8 channel modulators
|
WO2011024987A1
(ja)
|
2009-08-31 |
2011-03-03 |
塩野義製薬株式会社 |
芳香族縮合へテロ環誘導体およびそれらを含有する医薬組成物
|
GB0919431D0
(en)
|
2009-11-05 |
2009-12-23 |
Glaxosmithkline Llc |
Novel compounds
|
EP2496945B1
(en)
|
2009-11-05 |
2015-04-01 |
GlaxoSmithKline LLC |
Novel process
|
GB0919423D0
(en)
|
2009-11-05 |
2009-12-23 |
Glaxosmithkline Llc |
Novel compounds
|
GB0919426D0
(en)
|
2009-11-05 |
2009-12-23 |
Glaxosmithkline Llc |
Novel compounds
|
ES2564318T3
(es)
|
2009-11-05 |
2016-03-21 |
Glaxosmithkline Llc |
Inhibidor de bromodominio de benzodiazepina
|
PE20121181A1
(es)
|
2009-11-05 |
2012-09-13 |
Glaxosmithkline Llc |
Inhibidor de bromodominio de benzodiazepina
|
GB0919432D0
(en)
|
2009-11-05 |
2009-12-23 |
Glaxosmithkline Llc |
Use
|
GB0919434D0
(en)
|
2009-11-05 |
2009-12-23 |
Glaxosmithkline Llc |
Novel compounds
|
CA2812043A1
(en)
|
2010-04-23 |
2011-10-27 |
Kineta, Inc. |
Pyrimidinedione anti-viral compounds
|
WO2011143657A1
(en)
|
2010-05-14 |
2011-11-17 |
Dana-Farber Cancer Institute, Inc. |
Male contraceptive compositions and methods of use
|
WO2011143651A1
(en)
|
2010-05-14 |
2011-11-17 |
Dana-Farber Cancer Institute, Inc. |
Compositions and methods for modulating metabolism
|
HUE031073T2
(en)
|
2010-05-14 |
2017-06-28 |
Dana Farber Cancer Inst Inc |
Thieno triazolo-diazepine compounds for the treatment of neoplasia
|
JP5935030B2
(ja)
|
2010-05-14 |
2016-06-15 |
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 |
白血病を治療するための組成物および方法
|
US9085582B2
(en)
|
2010-06-22 |
2015-07-21 |
Glaxosmithkline Llc |
Benzotriazolodiazepine compounds inhibitors of bromodomains
|
WO2012075456A1
(en)
|
2010-12-02 |
2012-06-07 |
Constellation Pharmaceuticals |
Bromodomain inhibitors and uses thereof
|
AR084070A1
(es)
|
2010-12-02 |
2013-04-17 |
Constellation Pharmaceuticals Inc |
Inhibidores del bromodominio y usos de los mismos
|
JP5766820B2
(ja)
|
2011-02-09 |
2015-08-19 |
エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft |
Pi3キナーゼ阻害剤としての複素環化合物
|
CA2828212A1
(en)
|
2011-02-23 |
2012-08-30 |
Shiraz Mujtaba |
Inhibitors of bromodomains as modulators of gene expression
|
GB201106750D0
(en)
|
2011-04-21 |
2011-06-01 |
Glaxosmithkline Llc |
Novel compounds
|
GB201106799D0
(en)
|
2011-04-21 |
2011-06-01 |
Glaxosmithkline Llc |
Novel compounds
|
GB201106743D0
(en)
|
2011-04-21 |
2011-06-01 |
Glaxosmithkline Llc |
Novel compounds
|
US9422292B2
(en)
|
2011-05-04 |
2016-08-23 |
Constellation Pharmaceuticals, Inc. |
Bromodomain inhibitors and uses thereof
|
GB201107325D0
(en)
|
2011-05-04 |
2011-06-15 |
Glaxosmithkline Llc |
Novel compounds
|
EP2721031B1
(en)
|
2011-06-17 |
2016-01-20 |
Constellation Pharmaceuticals, Inc. |
Bromodomain inhibitors and uses thereof
|
WO2012178208A2
(en)
|
2011-06-24 |
2012-12-27 |
The Trustees Of The Stevens Institute Of Technology |
Selective inhibitors of histone deacetylase isoform 6 and methods thereof
|
JP2013010719A
(ja)
|
2011-06-30 |
2013-01-17 |
Dainippon Sumitomo Pharma Co Ltd |
ベンズイミダゾロンおよびオキシインドール誘導体ならびにそれらの医薬用途
|
WO2013019710A1
(en)
|
2011-07-29 |
2013-02-07 |
The Children's Hospital Of Philadelphia |
Compositions and methods for the treatment of hiv
|
GB201114103D0
(en)
|
2011-08-17 |
2011-09-28 |
Glaxosmithkline Llc |
Novel compounds
|
WO2013027168A1
(en)
|
2011-08-22 |
2013-02-28 |
Pfizer Inc. |
Novel heterocyclic compounds as bromodomain inhibitors
|
WO2013033269A1
(en)
|
2011-08-29 |
2013-03-07 |
Coferon, Inc. |
Bioorthogonal monomers capable of dimerizing and targeting bromodomains and methods of using same
|
WO2013033270A2
(en)
|
2011-08-29 |
2013-03-07 |
Coferon, Inc. |
Bromodomain ligands capable of dimerizing in an aqueous solution, and methods of using same
|
TWI583680B
(zh)
|
2011-08-31 |
2017-05-21 |
大塚製藥股份有限公司 |
喹啉酮化合物
|
DE102011082013A1
(de)
|
2011-09-01 |
2013-03-07 |
Bayer Pharma AG |
6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine
|
ES2632443T3
(es)
|
2011-09-22 |
2017-09-13 |
Viiv Healthcare Uk Limited |
Compuestos de pirrolopiridinona y procedimientos de tratamiento del VIH
|
WO2013044511A1
(zh)
|
2011-09-30 |
2013-04-04 |
沈阳蓝桑医药生物技术研发有限公司 |
含有瑞利格内酯的药物组合物及其应用
|
CN103945848B
(zh)
|
2011-11-01 |
2016-09-07 |
雷斯韦洛吉克斯公司 |
被取代的喹唑啉酮的口服即释制剂
|
WO2013097052A1
(en)
|
2011-12-30 |
2013-07-04 |
Abbott Laboratories |
Bromodomain inhibitors
|
WO2013148197A1
(en)
|
2012-03-28 |
2013-10-03 |
The J. David Gladstone Institutes |
Compositions and methods for reactivating latent immunodeficiency virus
|
US20130281399A1
(en)
|
2012-04-19 |
2013-10-24 |
Rvx Therapeutics Inc. |
Treatment of diseases by epigenetic regulation
|
US20130281397A1
(en)
|
2012-04-19 |
2013-10-24 |
Rvx Therapeutics Inc. |
Treatment of diseases by epigenetic regulation
|
US20130281398A1
(en)
|
2012-04-19 |
2013-10-24 |
Rvx Therapeutics Inc. |
Treatment of diseases by epigenetic regulation
|
US20130281396A1
(en)
|
2012-04-19 |
2013-10-24 |
Rvx Therapeutics Inc. |
Treatment of diseases by epigenetic regulation
|
JP5989229B2
(ja)
|
2012-04-20 |
2016-09-07 |
アッヴィ・インコーポレイテッド |
イソインドロン誘導体
|
WO2013184878A1
(en)
|
2012-06-06 |
2013-12-12 |
Constellation Pharmaceuticals, Inc. |
Benzo [b] isoxazoloazepine bromodomain inhibitors and uses thereof
|
TWI602820B
(zh)
|
2012-06-06 |
2017-10-21 |
星宿藥物公司 |
溴域抑制劑及其用途
|
AU2012382373A1
(en)
|
2012-06-12 |
2014-12-11 |
Abbvie Inc. |
Pyridinone and pyridazinone derivatives
|
KR20150045423A
(ko)
|
2012-06-25 |
2015-04-28 |
온코에틱스 에스에이 |
티에노트리아졸로디아제핀 화합물을 사용하여 림프종을 치료하는 방법
|
US9610332B2
(en)
|
2012-07-18 |
2017-04-04 |
Massachusetts Institute Of Technology |
Compositions and methods for modulating BRD4 bioactivity
|
AU2013304146A1
(en)
|
2012-08-16 |
2015-02-26 |
Bayer Pharma Aktiengesellschaft |
2,3-benzodiazepines
|
BR112015002824A2
(pt)
|
2012-08-16 |
2017-08-08 |
Glaxosmithkline Llc |
composto, uso de um composto, composição farmacêutica, e, produto farmacêutico de combinação.
|
JP2015531365A
(ja)
|
2012-09-28 |
2015-11-02 |
オンコエシックス エスエー |
チエノトリアゾロジアゼピン化合物を含む医薬製剤
|
WO2014048945A1
(de)
|
2012-09-28 |
2014-04-03 |
Bayer Pharma Aktiengesellschaft |
Bet-proteininhibitorische 5-aryl-triazolo-azepine
|
US9422290B2
(en)
|
2012-11-13 |
2016-08-23 |
Boehringer Ingelheim International Gmbh |
Triazolopyridazine
|
ES2625945T3
(es)
|
2012-11-14 |
2017-07-21 |
Glaxosmithkline Llc |
Tieno[3,2-c]piridin-4(5H)-onas como inhibidores de bet
|
WO2014080291A2
(en)
|
2012-11-21 |
2014-05-30 |
Rvx Therapeutics Inc. |
Biaryl derivatives as bromodomain inhibitors
|
WO2014080290A2
(en)
|
2012-11-21 |
2014-05-30 |
Rvx Therapeutics Inc. |
Cyclic amines as bromodomain inhibitors
|
CA2895426A1
(en)
|
2012-12-20 |
2014-06-26 |
Bayer Pharma Aktiengesellschaft |
Bet-protein-inhibiting dihydroquinoxalinones
|
WO2014095774A1
(de)
|
2012-12-20 |
2014-06-26 |
Bayer Pharma Aktiengesellschaft |
Bet-proteininhibitorische dihydropyridopyrazinone
|
CA2895905A1
(en)
|
2012-12-21 |
2014-06-26 |
Zenith Epigenetics Corp. |
Novel heterocyclic compounds as bromodomain inhibitors
|
WO2014128655A1
(en)
|
2013-02-25 |
2014-08-28 |
Aurigene Discovery Technologies Limited |
Substituted imidazo[4,5-c]quinoline derivatives as bromodomain inhibitors
|
US9492460B2
(en)
|
2013-02-27 |
2016-11-15 |
Bristol-Myers Squibb Company |
Carbazole compounds useful as bromodomain inhibitors
|
JP6404838B2
(ja)
|
2013-02-27 |
2018-10-17 |
ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company |
ブロモドメイン阻害剤として有用なカルバゾール化合物
|
JP2016516701A
(ja)
|
2013-03-11 |
2016-06-09 |
アッヴィ・インコーポレイテッド |
縮合四環系ブロモドメイン阻害剤
|
EP2970312B1
(en)
|
2013-03-11 |
2017-11-15 |
The Regents of The University of Michigan |
Bet bromodomain inhibitors and therapeutic methods using the same
|
MX2015012005A
(es)
|
2013-03-11 |
2016-04-04 |
Abbvie Inc |
Inhibidores de bromodominio.
|
CA2903910C
(en)
|
2013-03-12 |
2023-08-15 |
Steven D. FIDANZE |
Triazadibenzo[cd,f]azulene derivatives and pharmaceutical compositions thereof useful as bromodomain inhibitors
|
WO2014165127A1
(en)
|
2013-03-12 |
2014-10-09 |
Abbvie Inc. |
Pyrrole amide inhibitors
|
EP2970276A1
(en)
|
2013-03-12 |
2016-01-20 |
AbbVie Inc. |
Dihydro-pyrrolopyridinone bromodomain inhibitors
|
WO2014159392A1
(en)
|
2013-03-14 |
2014-10-02 |
Dana-Farber Cancer Institute, Inc. |
Bromodomain binding reagents and uses thereof
|
BR112015022417A2
(pt)
|
2013-03-14 |
2017-07-18 |
Convergene Llc |
métodos e composições para inibição de proteínas contendo bromodomínio
|
CA2903357A1
(en)
|
2013-03-14 |
2014-09-18 |
Glaxosmithkline Intellectual Property (No.2) Limited |
Furanopyridines as bromodomain lnhibitors
|
PT2970127T
(pt)
|
2013-03-14 |
2019-01-16 |
Glaxosmithkline Ip No 2 Ltd |
Derivados de 1-acil-4-amino-1,2,3,4-tetra-hidroquinolina 2,3-dissubstituída e sua utilização como inibidores de bromodomínio
|
AU2014236606A1
(en)
|
2013-03-15 |
2015-09-24 |
Epigenetix, Inc. |
Oxazolo(5,4-c)quinolin-2-one compounds as bromodomain inhibitors
|
KR102355670B1
(ko)
|
2013-03-15 |
2022-02-08 |
인사이트 홀딩스 코포레이션 |
Bet 단백질 저해제로서의 삼환식 복소환
|
KR102244719B1
(ko)
|
2013-03-15 |
2021-04-26 |
플렉시콘 인코퍼레이티드 |
헤테로시클릭 화합물 및 그의 용도
|
JP6453845B2
(ja)
|
2013-03-27 |
2019-01-16 |
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 |
Brd4阻害薬としてのジヒドロキナゾリノン類似体
|
EP2978757B1
(en)
|
2013-03-27 |
2017-02-08 |
Boehringer Ingelheim International GmbH |
Indolinone analogues as brd4 inhibitors
|
TWI530499B
(zh)
|
2013-03-28 |
2016-04-21 |
吉李德科學股份有限公司 |
作為溴結構域(bromodomain)抑制劑之苯並咪唑酮衍生物類
|
US10435364B2
(en)
|
2013-04-17 |
2019-10-08 |
Albert Ludwigs Universität Freiburg |
Compounds for use as bromodomain inhibitors
|
CA2901083A1
(en)
|
2013-04-26 |
2014-10-30 |
Beigene, Ltd. |
Substituted 5-(3,5-dimethylisoxazol-4-yl)indoline-2-ones
|
TWI527811B
(zh)
|
2013-05-09 |
2016-04-01 |
吉李德科學股份有限公司 |
作爲溴結構域抑制劑的苯並咪唑衍生物
|
EA029312B1
(ru)
|
2013-05-27 |
2018-03-30 |
Новартис Аг |
Производные имидазопирролидинона и их применение при лечении заболеваний
|
US8975417B2
(en)
|
2013-05-27 |
2015-03-10 |
Novartis Ag |
Pyrazolopyrrolidine derivatives and their use in the treatment of disease
|
AU2014272700B2
(en)
|
2013-05-28 |
2016-12-01 |
Novartis Ag |
Pyrazolo-pyrrolidin-4-one derivatives and their use in the treatment of disease
|
ES2656471T3
(es)
|
2013-05-28 |
2018-02-27 |
Novartis Ag |
Derivados de pirazolo-pirrolidin-4-ona como inhibidores de BET y su uso en el tratamiento de enfermedades
|
CA2915419A1
(en)
|
2013-06-17 |
2014-12-24 |
Bayer Pharma Aktiengesellschaft |
Substituted phenyl-2,3-benzodiazepines
|
SG10201710705UA
(en)
|
2013-06-21 |
2018-02-27 |
Zenith Epigenetics Ltd |
Novel bicyclic bromodomain inhibitors
|
US9662311B2
(en)
|
2013-06-21 |
2017-05-30 |
Zenith Epigenetics Ltd. |
Substituted bicyclic compounds as bromodomain inhibitors
|
MX2015017963A
(es)
|
2013-06-28 |
2016-11-10 |
Abbvie Inc |
Inhibidores de bromodominio.
|
AR096758A1
(es)
|
2013-06-28 |
2016-02-03 |
Abbvie Inc |
Inhibidores cristalinos de bromodominios
|
CA2917319A1
(en)
|
2013-07-08 |
2015-01-15 |
Incyte Holdings Corporation |
Tricyclic heterocycles as bet protein inhibitors
|
BR112016001457A2
(pt)
|
2013-07-25 |
2017-08-29 |
Dana Farber Cancer Inst Inc |
Inibidores de fatores de transcrição e usos dos mesmos
|
KR101672096B1
(ko)
|
2013-09-30 |
2016-11-02 |
주식회사 엘지화학 |
헤테로환 화합물 및 이를 포함하는 유기 발광 소자
|
WO2015081189A1
(en)
|
2013-11-26 |
2015-06-04 |
Incyte Corporation |
Bicyclic heterocycles as bet protein inhibitors
|
US20150148372A1
(en)
|
2013-11-26 |
2015-05-28 |
Incyte Corporation |
Bicyclic heterocycles as bet protein inhibitors
|
US9399640B2
(en)
|
2013-11-26 |
2016-07-26 |
Incyte Corporation |
Substituted pyrrolo[2,3-c]pyridines and pyrazolo[3,4-c]pyridines as BET protein inhibitors
|
US9428514B2
(en)
|
2013-12-09 |
2016-08-30 |
Abbvie Inc. |
Bromodomain inhibitors
|
WO2015095492A1
(en)
|
2013-12-19 |
2015-06-25 |
Incyte Corporation |
Tricyclic heterocycles as bet protein inhibitors
|
UA119870C2
(uk)
|
2014-04-23 |
2019-08-27 |
Інсайт Корпорейшн |
1H-ПІРОЛО[2,3-c]ПІРИДИН-7(6H)-ОНИ ТА ПІРАЗОЛО[3,4-c]ПІРИДИН-7(6H)-ОНИ ЯК ІНГІБІТОРИ БІЛКІВ BET
|
US9956228B2
(en)
|
2014-05-02 |
2018-05-01 |
Oncoethix Gmbh |
Method of treating acute myeloid leukemia and/or acute lymphoblastic leukemia using thienotriazolodiazepine compounds
|
AU2015252940A1
(en)
|
2014-05-02 |
2016-11-17 |
Kay NOEL |
Method of treating resistant non-Hodgkin lymphoma, medulloblastoma, and/or ALK+non-small cell lung cancer using thienotriazolodiazepine compounds
|
BR112016026046A8
(pt)
|
2014-05-08 |
2021-07-20 |
Oncoethix Gmbh |
uso de compostos de tienotriazolodiazepina
|
WO2015169953A1
(en)
|
2014-05-08 |
2015-11-12 |
Oncoethix Gmbh |
Method of treating glioma using thienotriazolodiazepine compounds
|
EP3148543B1
(en)
|
2014-05-30 |
2020-04-08 |
Icahn School of Medicine at Mount Sinai |
Small molecule transcription modulators of bromodomains
|
ES2855225T3
(es)
|
2014-09-15 |
2021-09-23 |
Incyte Corp |
Heterociclos tricíclicos para su uso como inhibidores de proteínas BET
|
WO2016186453A1
(en)
|
2015-05-20 |
2016-11-24 |
Kainos Medicine, Inc. |
Quinoline derivatives as bromodomain inhibitors
|
CN107922423B
(zh)
|
2015-05-29 |
2020-10-27 |
盐野义制药株式会社 |
具有hiv复制抑制作用的含氮三环性衍生物
|
AR106520A1
(es)
|
2015-10-29 |
2018-01-24 |
Incyte Corp |
Forma sólida amorfa de un inhibidor de proteína bet
|