|
EP1386922B1
(en)
*
|
1996-12-03 |
2012-04-11 |
Sloan-Kettering Institute For Cancer Research |
Synthesis of epothilones, intermediates thereof, analogues and uses thereof
|
|
US20020058286A1
(en)
*
|
1999-02-24 |
2002-05-16 |
Danishefsky Samuel J. |
Synthesis of epothilones, intermediates thereto and analogues thereof
|
|
BR0309398A
(pt)
|
2002-04-19 |
2005-02-01 |
Cellular Genomics Inc |
Composto ou um seu sal, hidrato, solvato, forma cristalina, diastereÈmero, prodroga farmaceuticamente aceitável, ou misturas deles, composição farmacêutica, e, métodos para tratar uma condição envolvida com a cinase em um mamìfero, para tratar câncer, e para identificar uma cinase
|
|
US6921769B2
(en)
|
2002-08-23 |
2005-07-26 |
Sloan-Kettering Institute For Cancer Research |
Synthesis of epothilones, intermediates thereto and analogues thereof
|
|
US7649006B2
(en)
|
2002-08-23 |
2010-01-19 |
Sloan-Kettering Institute For Cancer Research |
Synthesis of epothilones, intermediates thereto and analogues thereof
|
|
ATE350383T1
(de)
*
|
2002-08-23 |
2007-01-15 |
Sloan Kettering Inst Cancer |
Synthese von epothilonen, zwischenprodukte dafür, analoga und deren verwendungen
|
|
AU2003270489A1
(en)
|
2002-09-09 |
2004-03-29 |
Cellular Genomics, Inc. |
6-ARYL-IMIDAZO(1,2-a)PYRAZIN-8-YLAMINES, METHOD OF MAKING, AND METHOD OF USE THEREOF
|
|
JP4799864B2
(ja)
*
|
2002-09-23 |
2011-10-26 |
シェーリング コーポレイション |
サイクリン依存性キナーゼインヒビターとしてのイミダゾピラジン
|
|
KR20060010709A
(ko)
*
|
2002-09-23 |
2006-02-02 |
쉐링 코포레이션 |
사이클린 의존성 키나제 억제제로서의 신규한 이미다조피라진
|
|
US7576085B2
(en)
*
|
2002-09-23 |
2009-08-18 |
Schering Corporation |
Imidazopyrazines as cyclin dependent kinase inhibitors
|
|
US7189723B2
(en)
|
2003-02-10 |
2007-03-13 |
Cgi Pharmaceuticals, Inc. |
Certain 8-heteroaryl-6-phenyl-imidazo[1,2-a]pyrazines as modulators of kinase activity
|
|
US7157460B2
(en)
*
|
2003-02-20 |
2007-01-02 |
Sugen Inc. |
Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
|
|
US7186832B2
(en)
*
|
2003-02-20 |
2007-03-06 |
Sugen Inc. |
Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
|
|
US7405295B2
(en)
|
2003-06-04 |
2008-07-29 |
Cgi Pharmaceuticals, Inc. |
Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds
|
|
US20060183746A1
(en)
*
|
2003-06-04 |
2006-08-17 |
Currie Kevin S |
Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds
|
|
US7393848B2
(en)
*
|
2003-06-30 |
2008-07-01 |
Cgi Pharmaceuticals, Inc. |
Certain heterocyclic substituted imidazo[1,2-A]pyrazin-8-ylamines and methods of inhibition of Bruton's tyrosine kinase by such compounds
|
|
WO2005019220A2
(en)
*
|
2003-08-11 |
2005-03-03 |
Cellular Genomics Inc. |
Substituted imidazo[1,2-a]pyrazines as modulators of kinase activity
|
|
US7572914B2
(en)
|
2003-12-19 |
2009-08-11 |
Takeda Pharmaceutical Company Limited |
Kinase inhibitors
|
|
WO2006023931A2
(en)
|
2004-08-18 |
2006-03-02 |
Takeda San Diego, Inc. |
Kinase inhibitors
|
|
CA2576159A1
(en)
*
|
2004-08-27 |
2006-03-02 |
Cyclacel Limited |
Purine and pyrimidine cdk inhibitors and their use for the treatment of autoimmune diseases
|
|
EP1812439B2
(en)
*
|
2004-10-15 |
2017-12-06 |
Takeda Pharmaceutical Company Limited |
Kinase inhibitors
|
|
EP2397478A1
(en)
*
|
2005-01-14 |
2011-12-21 |
CGI Pharmaceuticals, Inc. |
1,3-diaryl substituted ureas as modulators of kinase activity.
|
|
US7777040B2
(en)
|
2005-05-03 |
2010-08-17 |
Cgi Pharmaceuticals, Inc. |
Certain substituted ureas, as modulators of kinase activity
|
|
EP1928237A4
(en)
*
|
2005-09-02 |
2011-03-09 |
Abbott Lab |
NEW HETEROCYCLES BASED ON IMIDAZO
|
|
CA2621983A1
(en)
*
|
2005-09-09 |
2007-03-22 |
Schering Corporation |
Azafused cyclin dependent kinase inhibitors
|
|
US8119655B2
(en)
*
|
2005-10-07 |
2012-02-21 |
Takeda Pharmaceutical Company Limited |
Kinase inhibitors
|
|
EP1945216A1
(en)
*
|
2005-11-10 |
2008-07-23 |
Schering Corporation |
Methods for inhibiting protein kinases
|
|
EP1945644A2
(en)
*
|
2005-11-10 |
2008-07-23 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
|
HRP20100378T1
(hr)
*
|
2006-05-31 |
2010-08-31 |
Galapagos N.V. |
Spojevi triazolopirazina učinkoviti za tretman degenerativnih i upalnih bolesti
|
|
JP2009539840A
(ja)
*
|
2006-06-06 |
2009-11-19 |
シェーリング コーポレイション |
プロテインキナーゼ阻害剤としてのイミダゾピラジン
|
|
US20090175852A1
(en)
|
2006-06-06 |
2009-07-09 |
Schering Corporation |
Imidazopyrazines as protein kinase inhibitors
|
|
EP2223925A1
(en)
*
|
2006-10-09 |
2010-09-01 |
Takeda Pharmaceutical Company Limited |
Kinase inhibitors
|
|
JP2010505962A
(ja)
|
2006-10-09 |
2010-02-25 |
武田薬品工業株式会社 |
キナーゼ阻害剤
|
|
PE20080931A1
(es)
*
|
2006-11-08 |
2008-07-19 |
Schering Corp |
Imidazopirazinas como inhibidores de proteina quinasa
|
|
EP2086644A2
(en)
*
|
2006-11-17 |
2009-08-12 |
Schering Corporation |
Combination of an inhibitor of dna polymerase-alpha and an inhibitor of a checkpoint kinase for proliferative disorders
|
|
ATE495743T1
(de)
*
|
2006-12-01 |
2011-02-15 |
Galapagos Nv |
Triazolopyridinverbindungen zur behandlung von degenerations- und entzündungskrankheiten
|
|
CN101652069A
(zh)
*
|
2007-03-27 |
2010-02-17 |
艾博特公司 |
新的基于咪唑并的杂环化合物
|
|
WO2008138843A1
(en)
*
|
2007-05-10 |
2008-11-20 |
Galapagos N.V. |
Imidazopyridines and triazolopyrimidines useful for the treatment of joint degenerative & inflammatory diseases
|
|
US8148369B2
(en)
*
|
2007-05-10 |
2012-04-03 |
Janssen Pharmaceutica Nv |
Fused pyrazine compounds useful for the treatment of degenerative and inflammatory diseases
|
|
PE20090365A1
(es)
*
|
2007-06-14 |
2009-04-04 |
Schering Corp |
Imidazopirazinas como inhibidores de proteina quinasa
|
|
DE102007032349A1
(de)
*
|
2007-07-11 |
2009-01-15 |
Bayer Healthcare Ag |
Imidazo-, Pyrazolopyrazine und Imidazotriazine und ihre Verwendung
|
|
KR20100042287A
(ko)
*
|
2007-07-31 |
2010-04-23 |
쉐링 코포레이션 |
항암요법으로서의 항-유사분열제 및 아우로라 키나제 억제제 조합물
|
|
GB0716292D0
(en)
|
2007-08-21 |
2007-09-26 |
Biofocus Dpi Ltd |
Imidazopyrazine compounds
|
|
PE20091074A1
(es)
*
|
2007-12-13 |
2009-07-26 |
Bayer Healthcare Ag |
Triazolotriazinas y triazolopirazinas y su uso
|
|
JP5496915B2
(ja)
|
2008-02-13 |
2014-05-21 |
シージーアイ ファーマシューティカルズ,インコーポレーテッド |
6−アリール−イミダゾ[1,2−a]ピラジン誘導体、その製造方法、及びその使用方法
|
|
DE102008023801A1
(de)
|
2008-05-15 |
2009-11-19 |
Bayer Schering Pharma Aktiengesellschaft |
Substituierte Imidazo- und Triazolopyrimidine, Imidazo- und Pyrazolopyrazine und Imidazotriazine
|
|
EA020461B1
(ru)
|
2008-12-08 |
2014-11-28 |
Джилид Коннектикут, Инк. |
ИМИДАЗОПИРАЗИНОВЫЕ ИНГИБИТОРЫ Syk
|
|
PE20120121A1
(es)
*
|
2008-12-08 |
2012-02-20 |
Gilead Connecticut Inc |
Derivados de imidazopirazina como inhibidores de syk
|
|
US8450321B2
(en)
|
2008-12-08 |
2013-05-28 |
Gilead Connecticut, Inc. |
6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor
|
|
NZ596185A
(en)
*
|
2009-04-16 |
2013-01-25 |
Ct Nac Investigaciones Oncologicas Cnio |
Imidazopyrazines for use as kinase inhibitors
|
|
WO2011028638A1
(en)
|
2009-09-04 |
2011-03-10 |
Schering Corporation |
Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors
|
|
PH12012500778A1
(en)
|
2009-10-30 |
2012-11-26 |
Janssen Pharmaceutica Nv |
IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS
|
|
WO2011092120A1
(en)
*
|
2010-01-29 |
2011-08-04 |
Nerviano Medical Sciences S.R.L. |
6,7- dihydroimidazo [1,5-a] pyrazin-8 (5h) - one derivatives as protein kinase modulators
|
|
AR080754A1
(es)
|
2010-03-09 |
2012-05-09 |
Janssen Pharmaceutica Nv |
Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10
|
|
JP5938352B2
(ja)
|
2010-03-11 |
2016-06-22 |
ギリアード コネチカット, インコーポレイテッド |
イミダゾピリジンsyk阻害剤
|
|
ES2551407T3
(es)
|
2010-03-18 |
2015-11-18 |
Bayer Intellectual Property Gmbh |
Imidazopirazinas
|
|
CN103038235B
(zh)
|
2010-06-01 |
2015-07-29 |
拜耳知识产权有限责任公司 |
取代的咪唑并吡嗪
|
|
AR081587A1
(es)
|
2010-06-09 |
2012-10-03 |
Janssen Pharmaceutica Nv |
DERIVADOS DE 5,6-DIHIDRO-2H-[1,4]OXAZIN-3-IL-AMINA UTILES COMO INHIBIDORES DE LA b-SECRETASA (BACE)
|
|
US20140187548A1
(en)
|
2010-12-17 |
2014-07-03 |
Bayer Intellectual Property Gmbh |
6 substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
|
|
US9284317B2
(en)
*
|
2010-12-17 |
2016-03-15 |
Bayer Intellectual Property Gmbh |
Substituted imidazo[1,2-a]pyrazines as MPS-1 inhibitors
|
|
WO2012080228A1
(en)
|
2010-12-17 |
2012-06-21 |
Bayer Pharma Aktiengesellschaft |
6-thio-substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
|
|
US20140135319A1
(en)
|
2010-12-17 |
2014-05-15 |
Bayer Intellectual Property Gmbh |
6-substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
|
|
ES2648143T3
(es)
*
|
2010-12-22 |
2017-12-28 |
Janssen Pharmaceutica Nv |
Derivados de 5,6-dihidro-imidazo[1,2-a]pirazin-8-ilamina útiles como inhibidores de la beta-secretasa (BACE)
|
|
US9346811B2
(en)
|
2011-03-01 |
2016-05-24 |
Janssen Pharmaceutica Nv |
6,7-dihydro-pyrazolo[1,5-a]pyrazin-4-ylamine derivatives useful as inhibitors of beta-secretase (BACE)
|
|
JP5853035B2
(ja)
|
2011-03-09 |
2016-02-09 |
ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプJanssen Pharmaceutica Naamloze Vennootschap |
β−セクレターゼ(BACE)の阻害剤として有用な3,4−ジヒドロ−ピロロ[1,2−a]ピラジン−1−イルアミン誘導体
|
|
JP6115962B2
(ja)
|
2011-06-27 |
2017-04-19 |
ヤンセン ファーマシューティカ エヌ.ベー. |
1−アリール−4−メチル−[1,2,4]トリアゾロ[4,3−a]キノキサリン誘導体
|
|
WO2014001314A1
(en)
|
2012-06-26 |
2014-01-03 |
Janssen Pharmaceutica Nv |
Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl- [1,2,4] triazolo [4,3-a] quinoxaline compounds and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders
|
|
AU2013289284B2
(en)
|
2012-07-09 |
2017-03-30 |
Janssen Pharmaceutica Nv |
Inhibitors of phosphodiesterase 10 enzyme
|
|
EP3008067B1
(en)
|
2013-06-12 |
2017-03-29 |
Janssen Pharmaceutica N.V. |
4-amino-6-phenyl-5,6-dihydroimidazo[1,5-a]pyrazin-3(2h)-one derivatives as inhibitors of beta-secretase (bace)
|
|
BR112015030597A2
(pt)
|
2013-06-12 |
2017-07-25 |
Janssen Pharmaceutica Nv |
derivados 4-amino-6-fenil-6,7-di-hidro[1,2,3]triazolo[1,5-a]pirazina como inibidores de beta-secretase (bace)
|
|
KR102243134B1
(ko)
|
2013-06-12 |
2021-04-22 |
얀센 파마슈티카 엔.브이. |
베타-세크레타제(bace) 저해제로서의 4-아미노-6-페닐-5,6-디하이드로이미다조[1,5-a]피라진 유도체
|
|
PL3027171T3
(pl)
|
2013-07-30 |
2020-08-24 |
Gilead Connecticut, Inc. |
Formulacja inhibitorów syk
|
|
EA029281B1
(ru)
|
2013-07-30 |
2018-03-30 |
Джилид Коннектикут, Инк. |
Полиморф ингибиторов syk
|
|
AU2014360537B2
(en)
|
2013-12-04 |
2017-09-07 |
Gilead Sciences, Inc. |
Methods for treating cancers
|
|
TWI662037B
(zh)
|
2013-12-23 |
2019-06-11 |
美商基利科學股份有限公司 |
脾酪胺酸激酶抑制劑
|
|
US9290505B2
(en)
|
2013-12-23 |
2016-03-22 |
Gilead Sciences, Inc. |
Substituted imidazo[1,2-a]pyrazines as Syk inhibitors
|
|
RU2671494C2
(ru)
*
|
2014-05-28 |
2018-11-01 |
Шанхай Фокон Фармасьютикал Ко., Лтд |
Некоторые ингибиторы протеинкиназы
|
|
CN106687139A
(zh)
|
2014-07-14 |
2017-05-17 |
吉利德科学公司 |
用于治疗癌症的组合
|
|
JP2017538753A
(ja)
|
2014-12-18 |
2017-12-28 |
ヤンセン ファーマシューティカ エヌ.ベー. |
2,3,4,5−テトラヒドロピリジン−6−アミンおよび3,4−ジヒドロ−2H−ピロール−5−アミンの化合物のβセクレターゼ阻害剤
|
|
CN108700594B
(zh)
|
2015-11-18 |
2021-06-29 |
建新公司 |
多囊性肾病的生物标志物及其用途
|
|
KR20220070056A
(ko)
|
2017-08-25 |
2022-05-27 |
길리애드 사이언시즈, 인코포레이티드 |
Syk 억제제의 다형체
|
|
AU2020225455A1
(en)
|
2019-02-22 |
2021-09-09 |
Kronos Bio, Inc. |
Solid forms of condensed pyrazines as Syk inhibitors
|
|
TW202214634A
(zh)
*
|
2020-06-09 |
2022-04-16 |
大陸商賽諾哈勃藥業(成都)有限公司 |
雜環化合物及其衍生物
|