US3169967A
(en)
|
1957-11-14 |
1965-02-16 |
Ciba Geigy Corp |
Methyl o-lower alkanoyl-reserpates
|
US3037980A
(en)
|
1955-08-18 |
1962-06-05 |
Burroughs Wellcome Co |
Pyrrolopyrimidine vasodilators and method of making them
|
DE1770420U
(de)
|
1958-02-27 |
1958-07-17 |
Tara Union G M B H |
Blumentopf aus kunststoff.
|
US3506643A
(en)
|
1966-12-09 |
1970-04-14 |
Max Thiel |
N**6-aralkyl-adenosine derivatives
|
DE2139107A1
(de)
|
1971-08-04 |
1973-02-15 |
Merck Patent Gmbh |
Heterocyclisch substituierte adenosinverbindungen
|
US3814251A
(en)
|
1972-08-09 |
1974-06-04 |
Sperry Rand Corp |
Power transmission
|
US3962443A
(en)
|
1972-08-14 |
1976-06-08 |
Dainippon Pharmaceutical Co., Ltd. |
Antibacterial pharmaceutical compositions and processes for preparation thereof
|
DE2248232A1
(de)
|
1972-10-02 |
1974-04-11 |
Basf Ag |
4-thiopyrimido eckige klammer auf 4,5-d eckige klammer zu pyrimidine
|
AR204003A1
(es)
|
1973-04-03 |
1975-11-12 |
Dainippon Pharmaceutical Co |
Procedimiento para preparar compuestos derivados del acido 2-(1-piperazinil)-5-oxopirido-(2,3-d)pirimidino-6-carboxilico y sus sales farmaceuticamente aceptables
|
US3862189A
(en)
|
1973-08-14 |
1975-01-21 |
Warner Lambert Co |
Aralkyl-substituted purines and pyrimidines as antianginal bronchodilator agents
|
US3936454A
(en)
|
1973-08-14 |
1976-02-03 |
Warner-Lambert Company |
5-Amino-4-chloro-6-(substituted amino)-pyrimidines
|
DK3375A
(es)
|
1974-01-25 |
1975-09-15 |
Ciba Geigy Ag |
|
JPS587626B2
(ja)
|
1974-02-13 |
1983-02-10 |
大日本製薬株式会社 |
ナフチリジン オヨビ キノリンユウドウタイノセイホウ
|
JPS50111080U
(es)
|
1974-02-21 |
1975-09-10 |
|
|
JPS5625234Y2
(es)
|
1976-01-17 |
1981-06-15 |
|
|
JPS5359663A
(en)
|
1976-11-09 |
1978-05-29 |
Sumitomo Chem Co Ltd |
2-halogeno methyl indole derivatives and process for praparation of the same
|
JPS52106897A
(en)
|
1977-01-10 |
1977-09-07 |
Dainippon Pharmaceut Co Ltd |
Synthesis of piperazine derivatives
|
JPS5392767A
(en)
|
1977-01-27 |
1978-08-15 |
Sumitomo Chem Co Ltd |
Preparation of 2-phthalimidomethylindole derivatives
|
JPS5625234A
(en)
|
1979-08-02 |
1981-03-11 |
Hitachi Denshi Ltd |
Dropout display system
|
JPS56123981U
(es)
|
1980-02-20 |
1981-09-21 |
|
|
JPS56123981A
(en)
|
1981-02-23 |
1981-09-29 |
Dainippon Pharmaceut Co Ltd |
Preparation of 1,4-disubstituted piperazine
|
JPS5883698A
(ja)
|
1981-11-13 |
1983-05-19 |
Takeda Chem Ind Ltd |
キノン化合物およびその製造法
|
JPS5883698U
(ja)
|
1981-11-27 |
1983-06-06 |
石川島播磨重工業株式会社 |
熱交換器
|
JPS58162949A
(ja)
|
1982-03-20 |
1983-09-27 |
Konishiroku Photo Ind Co Ltd |
ハロゲン化銀カラ−写真感光材料
|
JPS60140373U
(ja)
|
1984-02-28 |
1985-09-17 |
東洋ハ−ネス株式会社 |
ワイヤハ−ネスのア−ス構造
|
JPS6190153A
(ja)
|
1984-10-09 |
1986-05-08 |
Fuji Photo Film Co Ltd |
ハロゲン化銀写真感光材料の処理方法
|
JPS62103640A
(ja)
|
1985-07-18 |
1987-05-14 |
Fuji Photo Film Co Ltd |
ハロゲン化銀カラ−写真感光材料
|
JPS62103640U
(es)
|
1985-12-18 |
1987-07-02 |
|
|
JPH07119970B2
(ja)
|
1986-04-18 |
1995-12-20 |
富士写真フイルム株式会社 |
画像形成方法
|
JPS6310746A
(ja)
|
1986-07-01 |
1988-01-18 |
Tanabe Seiyaku Co Ltd |
ナフタレン誘導体
|
CA1324609C
(en)
|
1986-07-30 |
1993-11-23 |
Eastman Kodak Company |
Photographic element and process
|
US4861701A
(en)
|
1987-10-05 |
1989-08-29 |
Eastman Kodak Company |
Photographic element and process comprising a compound which comprises two timing groups in sequence
|
AT388372B
(de)
|
1987-10-08 |
1989-06-12 |
Tanabe Seiyaku Co |
Neue naphthalinderivate und sie enthaltende pharmazeutika
|
JPH01250316A
(ja)
|
1987-12-28 |
1989-10-05 |
Tanabe Seiyaku Co Ltd |
抗脂血剤
|
EP0364598A4
(en)
|
1988-03-02 |
1992-01-15 |
Yoshitomi Pharmaceutical Industries, Ltd. |
3,4-dihydrothieno 2,3-d¨pyrimidine compounds and pharmaceutical application thereof
|
US5208250A
(en)
|
1988-05-25 |
1993-05-04 |
Warner-Lambert Company |
Known and selected novel arylmethylenyl derivatives of thiazolidinones, imidazolidinones and oxazolidinones useful as antiallergy agents and anti-inflammatory agents
|
AU634655B2
(en)
|
1990-04-25 |
1993-02-25 |
Nissan Chemical Industries Ltd. |
Pyridazinone derivative
|
SU1712359A1
(ru)
|
1990-05-07 |
1992-02-15 |
Уфимский Нефтяной Институт |
Гидрохлорид 8 @ -гидроксихинолинового эфира 8-гидроксихинолин-7-карбоновой кислоты, в качестве бактерицида дл подавлени сульфатвосстанавливающих бактерий и культур РSеUDомоNаS и АRтнRовастеR
|
EP0464612B1
(en)
|
1990-06-28 |
1998-05-13 |
Fuji Photo Film Co., Ltd. |
Silver halide photographic materials
|
EP0481614A1
(en)
|
1990-10-01 |
1992-04-22 |
Merck & Co. Inc. |
Substituted pyridopyrimidinones and related heterocycles as angiotensin II antagonists
|
JPH04190232A
(ja)
|
1990-11-26 |
1992-07-08 |
Fuji Photo Film Co Ltd |
ハロゲン化銀カラー写真感光材料
|
US5480883A
(en)
|
1991-05-10 |
1996-01-02 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
|
IL101860A0
(en)
|
1991-05-31 |
1992-12-30 |
Ici Plc |
Heterocyclic derivatives
|
JP3108483B2
(ja)
|
1991-09-30 |
2000-11-13 |
日清製粉株式会社 |
インドール誘導体およびこれを有効成分とする抗潰瘍薬
|
HUT64064A
(en)
|
1992-02-13 |
1993-11-29 |
Chinoin Gyogyszer Es Vegyeszet |
Process for producing puyrido/1,2-a/pyrimidine derivatives and pharmaceutical compositions comprising same as active ingredient
|
US5521184A
(en)
|
1992-04-03 |
1996-05-28 |
Ciba-Geigy Corporation |
Pyrimidine derivatives and processes for the preparation thereof
|
WO1993022291A1
(en)
|
1992-04-24 |
1993-11-11 |
E.I. Du Pont De Nemours And Company |
Arthropodicidal and fungicidal aminopyrimidines
|
TW229140B
(es)
|
1992-06-05 |
1994-09-01 |
Shell Internat Res Schappej B V |
|
FR2714907B1
(fr)
|
1994-01-07 |
1996-03-29 |
Union Pharma Scient Appl |
Nouveaux dérivés de l'Adénosine, leurs procédés de préparation, compositions pharmaceutiques les contenant.
|
US6342501B1
(en)
|
1994-02-25 |
2002-01-29 |
The Regents Of The University Of Michigan |
Pyrrolo[2,3-d] pyrimidines as antiviral agents
|
JPH0987282A
(ja)
|
1995-09-21 |
1997-03-31 |
Kyowa Hakko Kogyo Co Ltd |
チアゾール誘導体
|
JPH09176162A
(ja)
|
1995-12-22 |
1997-07-08 |
Toubishi Yakuhin Kogyo Kk |
チアゾリジンジオン誘導体及びその製造法並びにそれを含む医薬組成物
|
JPH09176116A
(ja)
|
1995-12-27 |
1997-07-08 |
Toray Ind Inc |
複素環誘導体およびその医薬用途
|
JPH1025294A
(ja)
|
1996-03-26 |
1998-01-27 |
Akira Matsuda |
縮合ヘテロ環誘導体、その製造法及びそれを含有する悪性腫瘍治療剤
|
WO1997048697A1
(en)
|
1996-06-19 |
1997-12-24 |
Rhone-Poulenc Rorer Limited |
Substituted azabicylic compounds and their use as inhibitors of the production of tnf and cyclic amp phosphodiesterase
|
AU698419B2
(en)
|
1996-07-03 |
1998-10-29 |
Dainippon Sumitomo Pharma Co., Ltd. |
A novel purine derivative
|
US5866702A
(en)
|
1996-08-02 |
1999-02-02 |
Cv Therapeutics, Incorporation |
Purine inhibitors of cyclin dependent kinase 2
|
US6630496B1
(en)
|
1996-08-26 |
2003-10-07 |
Genetics Institute Llc |
Inhibitors of phospholipase enzymes
|
JPH10231297A
(ja)
|
1997-02-20 |
1998-09-02 |
Japan Energy Corp |
新規なアデニン−1−n−オキシド誘導体およびその医薬用途
|
KR100540046B1
(ko)
|
1997-11-12 |
2006-01-10 |
미쓰비시 가가꾸 가부시키가이샤 |
퓨린유도체 및 이를 유효성분으로 함유하는 의약
|
TW572758B
(en)
|
1997-12-22 |
2004-01-21 |
Sumitomo Pharma |
Type 2 helper T cell-selective immune response inhibitors comprising purine derivatives
|
US6828344B1
(en)
|
1998-02-25 |
2004-12-07 |
Genetics Institute, Llc |
Inhibitors of phospholipase enzymes
|
SK12742000A3
(sk)
|
1998-02-25 |
2001-05-10 |
Genetics Institute, Inc. |
Inhibítory fosfolipázových enzýmov, farmaceutický prostriedok s ich obsahom a ich použitie
|
IL137540A0
(en)
|
1998-02-25 |
2001-07-24 |
Genetics Inst |
Inhibitors of phospholipase a2
|
US6479487B1
(en)
|
1998-02-26 |
2002-11-12 |
Aventis Pharmaceuticals Inc. |
6, 9-disubstituted 2-[trans-(4-aminocyclohexyl)amino] purines
|
EP1109785B1
(de)
|
1998-05-04 |
2003-01-02 |
Zentaris AG |
Indolderivate und deren verwendung zur behandlung von malignen und anderen, auf pathologischen zellproliferationen beruhenden erkrankungen
|
ATE482945T1
(de)
|
1998-05-26 |
2010-10-15 |
Chugai Pharmaceutical Co Ltd |
Heterozyklische indolderivate und mono- oder diazaindol-derivate
|
JP3997651B2
(ja)
|
1998-06-24 |
2007-10-24 |
コニカミノルタホールディングス株式会社 |
新規色素及び画像記録材料及び感熱転写材料及びインクジェット記録液
|
AU5620299A
(en)
|
1998-08-11 |
2000-03-06 |
Novartis Ag |
Isoquinoline derivatives with angiogenesis inhibiting activity
|
JP2002523412A
(ja)
|
1998-08-25 |
2002-07-30 |
ザ ユーエイビー リサーチ ファウンデイション |
細菌nadシンテターゼ阻害剤
|
US6133031A
(en)
|
1999-08-19 |
2000-10-17 |
Isis Pharmaceuticals Inc. |
Antisense inhibition of focal adhesion kinase expression
|
CN1353713A
(zh)
|
1999-02-01 |
2002-06-12 |
Cv治疗公司 |
依赖细胞周期蛋白的激酶2和IκB-α的嘌呤抑制剂
|
GB9905075D0
(en)
|
1999-03-06 |
1999-04-28 |
Zeneca Ltd |
Chemical compounds
|
JP2000281654A
(ja)
|
1999-03-26 |
2000-10-10 |
Tanabe Seiyaku Co Ltd |
イソキノリン誘導体
|
DE19932571A1
(de)
|
1999-07-13 |
2001-01-18 |
Clariant Gmbh |
Verfahren zur Herstellung von Biarylen unter Palladophosphacyclobutan-Katalyse
|
JP2001151771A
(ja)
|
1999-09-10 |
2001-06-05 |
Kyowa Hakko Kogyo Co Ltd |
含窒素芳香族複素環誘導体
|
GB0004890D0
(en)
|
2000-03-01 |
2000-04-19 |
Astrazeneca Uk Ltd |
Chemical compounds
|
US6436965B1
(en)
|
2000-03-02 |
2002-08-20 |
Merck Frosst Canada & Co. |
PDE IV inhibiting amides, compositions and methods of treatment
|
EP1138328A1
(en)
|
2000-03-29 |
2001-10-04 |
Eli Lilly And Company Limited |
Naphthalene derivatives as CNS drugs
|
US6667300B2
(en)
|
2000-04-25 |
2003-12-23 |
Icos Corporation |
Inhibitors of human phosphatidylinositol 3-kinase delta
|
EP1294358B1
(en)
|
2000-06-28 |
2004-08-18 |
Smithkline Beecham Plc |
Wet milling process
|
CN1331340A
(zh)
|
2000-06-30 |
2002-01-16 |
上海博德基因开发有限公司 |
一种新的多肽——人拓扑异构酶12.1和编码这种多肽的多核苷酸
|
DK1300398T3
(da)
|
2000-07-05 |
2006-07-17 |
Astellas Pharma Inc |
Propan-1,3-dionderivat
|
FR2814073B1
(fr)
|
2000-09-21 |
2005-06-24 |
Yang Ji Chemical Company Ltd |
Composition pharmaceutique antifongique et/ou antiparasitaire et nouveaux derives de l'indole a titre de principes actifs d'une telle composition
|
DOP2002000334A
(es)
|
2001-02-14 |
2002-08-30 |
Warner Lambert Co |
Pirimidinas biciclicas como inhibidores de metaloproteinasas de matriz
|
SE0100568D0
(sv)
|
2001-02-20 |
2001-02-20 |
Astrazeneca Ab |
Compounds
|
JP3616628B2
(ja)
|
2001-03-01 |
2005-02-02 |
塩野義製薬株式会社 |
Hivインテグラーゼ阻害活性を有する含窒素芳香族複素環化合物
|
UA76977C2
(en)
|
2001-03-02 |
2006-10-16 |
Icos Corp |
Aryl- and heteroaryl substituted chk1 inhibitors and their use as radiosensitizers and chemosensitizers
|
WO2002078701A1
(en)
|
2001-03-30 |
2002-10-10 |
Smithkline Beecham Corporation |
Use of pyrazolopyridines as therapeutic compounds
|
US7034030B2
(en)
|
2001-03-30 |
2006-04-25 |
Smithkline Beecham Corporation |
Pyralopyridines, process for their preparation and use as therapeutic compounds
|
ES2242028T3
(es)
|
2001-04-27 |
2005-11-01 |
Smithkline Beecham Corporation |
Derivados de pirazolo(1,5-a)piridina.
|
CZ294535B6
(cs)
|
2001-08-02 |
2005-01-12 |
Ústav Experimentální Botaniky Avčr |
Heterocyklické sloučeniny na bázi N6-substituovaného adeninu, způsoby jejich přípravy, jejich použití pro přípravu léčiv, kosmetických přípravků a růstových regulátorů, farmaceutické přípravky, kosmetické přípravky a růstové regulátory tyto sloučeniny obsahující
|
GB0121033D0
(en)
|
2001-08-30 |
2001-10-24 |
Novartis Ag |
Organic compounds
|
US8124625B2
(en)
|
2001-09-14 |
2012-02-28 |
Shionogi & Co., Ltd. |
Method of enhancing the expression of apolipoprotein AI using olefin derivatives
|
PL369530A1
(en)
|
2001-09-19 |
2005-05-02 |
Aventis Pharma S.A. |
Chemical compounds
|
PL369567A1
(en)
|
2001-09-26 |
2005-05-02 |
Bayer Pharmaceuticals Corporation |
1,6-naphthyridine derivatives as antidiabetics
|
US7217710B2
(en)
|
2001-10-02 |
2007-05-15 |
Smithkline Beecham Corporation |
Substituted pyrazolopyrimidines
|
IL161156A0
(en)
|
2001-10-30 |
2004-08-31 |
Novartis Ag |
Staurosporine derivatives as inhibitors of flt3 receptor tyrosine kinase activity
|
WO2003041642A2
(en)
|
2001-11-09 |
2003-05-22 |
Enzon, Inc. |
Polymeric thiol-linked prodrugs employing benzyl elimination systems
|
EP1314733A1
(en)
|
2001-11-22 |
2003-05-28 |
Aventis Pharma Deutschland GmbH |
Indole-2-carboxamides as factor Xa inhibitors
|
ATE424388T1
(de)
|
2001-12-06 |
2009-03-15 |
Merck & Co Inc |
Mitotische kinesinhemmer
|
CA2467722A1
(en)
|
2001-12-06 |
2003-06-19 |
Merck & Co., Inc. |
Thienopyrimidinone derivatives as mitotic kinesin inhibitors
|
TW200301135A
(en)
|
2001-12-27 |
2003-07-01 |
Otsuka Maryland Res Inst Inc |
Pharmaceutical compositions comprising a multifunctional phosphodiesterase inhibitor and an adenosine uptake inhibitor
|
WO2003068750A1
(fr)
|
2002-02-13 |
2003-08-21 |
Takeda Chemical Industries, Ltd. |
Inhibiteur de jnk
|
AU2003225668A1
(en)
|
2002-03-01 |
2003-09-16 |
Pintex Pharmaceutical, Inc. |
Pin1-modulating compounds and methods of use thereof
|
WO2003084959A1
(en)
|
2002-04-03 |
2003-10-16 |
Bristol-Myers Squibb Company |
Thiopene-based tricyclic compounds and pharmaceutical compositions comprising same
|
CN1653077A
(zh)
|
2002-05-06 |
2005-08-10 |
健亚生物科技公司 |
治疗c型肝炎病毒感染的核苷衍生物
|
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
|
WO2004024693A1
(ja)
|
2002-08-13 |
2004-03-25 |
Shionogi & Co., Ltd. |
Hivインテグラーゼ阻害活性を有するヘテロ環化合物
|
JP4190232B2
(ja)
|
2002-08-26 |
2008-12-03 |
富士通株式会社 |
機械研磨を行う方法
|
WO2004029054A1
(ja)
|
2002-09-27 |
2004-04-08 |
Sumitomo Pharmaceuticals Company, Limited |
新規アデニン化合物及びその用途
|
TWI335913B
(en)
|
2002-11-15 |
2011-01-11 |
Vertex Pharma |
Diaminotriazoles useful as inhibitors of protein kinases
|
CA2507100C
(en)
|
2002-11-21 |
2012-10-09 |
Chiron Corporation |
2,4,6-trisubstituted pyrimidines as phosphotidylinositol (pi) 3-kinase inhibitors and their use in the treatment of cancer
|
US7494987B2
(en)
|
2002-11-25 |
2009-02-24 |
Mochida Pharmaceutical Co., Ltd. |
Agent for treating respiratory diseases containing 4-hydroxypiperidine derivative as active ingredient
|
UA80767C2
(en)
|
2002-12-20 |
2007-10-25 |
Pfizer Prod Inc |
Pyrimidine derivatives for the treatment of abnormal cell growth
|
JP4500689B2
(ja)
|
2002-12-26 |
2010-07-14 |
エーザイ・アール・アンド・ディー・マネジメント株式会社 |
選択的エストロゲン受容体モジュレーター
|
CZ294538B6
(cs)
|
2002-12-30 |
2005-01-12 |
Ústav Experimentální Botaniky Akademie Vědčeské Re |
Substituční deriváty N6-benzyladenosinu, způsob jejich přípravy, jejich použití pro přípravu léčiv, kosmetických přípravků a růstových regulátorů, farmaceutické přípravky, kosmetické přípravky a růstové regulátory tyto sloučeniny obsahující
|
RU2233842C1
(ru)
|
2003-01-13 |
2004-08-10 |
Петров Владимир Иванович |
Производные пурина, обладающие противовирусной активностью
|
PE20050068A1
(es)
|
2003-02-06 |
2005-03-11 |
Novartis Ag |
2-cianopirrolopirimidinas como inhibidores de la catepsina s
|
GB0304640D0
(en)
|
2003-02-28 |
2003-04-02 |
Novartis Ag |
Organic compounds
|
GB0305929D0
(en)
|
2003-03-14 |
2003-04-23 |
Novartis Ag |
Organic compounds
|
SE0300908D0
(sv)
|
2003-03-31 |
2003-03-31 |
Astrazeneca Ab |
Azaindole derivatives, preparations thereof, uses thereof and compositions containing them
|
US7129264B2
(en)
|
2003-04-16 |
2006-10-31 |
Bristol-Myers Squibb Company |
Biarylmethyl indolines and indoles as antithromboembolic agents
|
WO2004107863A1
(en)
|
2003-05-05 |
2004-12-16 |
Neurogen Corporation |
Sustituted imidazolopyrazine and triazolopyrazine derivatives: gabaa receptor ligands
|
WO2004113335A2
(en)
|
2003-06-20 |
2004-12-29 |
Chiron Corporation |
Pyridino[1,2-a]pyrimidin-4-one compounds as anticancer agents
|
WO2005000309A2
(en)
|
2003-06-27 |
2005-01-06 |
Ionix Pharmaceuticals Limited |
Chemical compounds
|
JP4570015B2
(ja)
|
2003-07-14 |
2010-10-27 |
クミアイ化学工業株式会社 |
2−イソオキサゾリン誘導体及びそれを有効成分として含有する除草剤
|
WO2005016528A2
(en)
|
2003-08-15 |
2005-02-24 |
Irm Llc |
6-substituted anilino purines as rtk inhibitors
|
JP2007505933A
(ja)
|
2003-09-18 |
2007-03-15 |
コンフォーマ・セラピューティクス・コーポレイション |
Hsp90インヒビターとしての新規なヘテロ環化合物
|
CN1856474A
(zh)
|
2003-09-23 |
2006-11-01 |
默克公司 |
异喹啉钾通道抑制剂
|
PE20050952A1
(es)
|
2003-09-24 |
2005-12-19 |
Novartis Ag |
Derivados de isoquinolina como inhibidores de b-raf
|
CA2553724A1
(en)
|
2004-02-03 |
2005-08-18 |
Abbott Laboratories |
Aminobenzoxazoles as therapeutic agents
|
WO2005077948A1
(ja)
|
2004-02-16 |
2005-08-25 |
Daiichi Pharmaceutical Co., Ltd. |
抗真菌作用複素環化合物
|
CN1560035A
(zh)
|
2004-03-12 |
2005-01-05 |
沈阳药科大学 |
5-羟基吲哚-3-羧酸脂类衍生物
|
WO2005091857A2
(en)
|
2004-03-12 |
2005-10-06 |
Bayer Pharmaceuticals Corporation |
1,6-naphthyridine and 1,8-naphthyridine derivatives and their use to treat diabetes and related disorders
|
JPWO2005092892A1
(ja)
|
2004-03-26 |
2008-02-14 |
大日本住友製薬株式会社 |
8−オキソアデニン化合物
|
JP2007531729A
(ja)
|
2004-04-02 |
2007-11-08 |
アデノシン、セラピューティックス、リミテッド、ライアビリティ、カンパニー |
A2aアデノシンレセプターの選択的アンタゴニスト
|
ES2605792T3
(es)
|
2004-05-13 |
2017-03-16 |
Icos Corporation |
Quinazolinona usada como inhibidor de la fosfatidilinositol 3-quinasa delta humana
|
CA2566158A1
(en)
|
2004-05-14 |
2005-11-24 |
Abbott Laboratories |
Kinase inhibitors as therapeutic agents
|
RU2007106552A
(ru)
|
2004-07-22 |
2008-08-27 |
Астразенека Аб (Se) |
Конденсированные пиримидоны, пригодные для лечения и предотвращения злокачественного новообразования
|
MY141233A
(en)
|
2004-08-18 |
2010-03-31 |
Astrazeneca Ab |
Enantiomers of selected fused heterocyclics and uses thereof
|
DE102004044221A1
(de)
|
2004-09-14 |
2006-03-16 |
Boehringer Ingelheim Pharma Gmbh & Co. Kg |
Neue 3-Methyl-7-butinyl-xanthine, deren Herstellung und deren Verwendung als Arzneimittel
|
GB0420719D0
(en)
|
2004-09-17 |
2004-10-20 |
Addex Pharmaceuticals Sa |
Novel allosteric modulators
|
WO2006049835A2
(en)
|
2004-10-19 |
2006-05-11 |
Novartis Vaccines And Diagnostics Inc. |
Indole and benzimidazole derivatives
|
US20080004269A1
(en)
|
2004-11-04 |
2008-01-03 |
Yuelian Xu |
Pyrazolylmethy Heteroaryl Derivatives
|
JP2008520744A
(ja)
|
2004-11-19 |
2008-06-19 |
ザ・レジェンツ・オブ・ザ・ユニバーシティ・オブ・カリフォルニア |
抗炎症性ピラゾロピリミジン
|
MX2007006204A
(es)
|
2004-11-24 |
2007-06-20 |
Novartis Ag |
Combinaciones que comprenden inhibidores de jak y cuando menos uno de entre inhibidores de bcr-abl, flt-3, fak o raf cinasa.
|
CA2598409A1
(en)
|
2005-02-17 |
2006-08-24 |
Icos Corporation |
Phosphoinositide 3-kinase inhibitors for inhibiting leukocyte accumulation
|
WO2007002701A2
(en)
|
2005-06-27 |
2007-01-04 |
Amgen Inc. |
Anti-inflammatory aryl nitrile compounds
|
FR2889192A1
(fr)
|
2005-07-27 |
2007-02-02 |
Cytomics Systems Sa |
Composes antifongiques, compositions contenant ces composes et leurs utilisations
|
CA2619881A1
(en)
|
2005-08-16 |
2007-02-22 |
Genzyme Corporation |
Chemokine receptor binding compounds
|
US7642270B2
(en)
|
2005-09-14 |
2010-01-05 |
Janssen Pharmaceutica N.V. |
5-oxo-5,8-dihydro-pyrido-pyrimidine as inhibitors of c-fms kinase
|
WO2007034817A1
(ja)
|
2005-09-22 |
2007-03-29 |
Dainippon Sumitomo Pharma Co., Ltd. |
新規アデニン化合物
|
GB0520657D0
(en)
*
|
2005-10-11 |
2005-11-16 |
Ludwig Inst Cancer Res |
Pharmaceutical compounds
|
PT1951684T
(pt)
|
2005-11-01 |
2016-10-13 |
Targegen Inc |
Inibidores de cinases de tipo biaril-meta-pirimidina
|
EP1783114A1
(en)
|
2005-11-03 |
2007-05-09 |
Novartis AG |
N-(hetero)aryl indole derivatives as pesticides
|
WO2007059108A2
(en)
|
2005-11-10 |
2007-05-24 |
Chemocentryx, Inc. |
Substituted quinolones and methods of use
|
TWI553008B
(zh)
|
2005-12-13 |
2016-10-11 |
英塞特控股公司 |
作為傑納斯激酶(JANUS KINASE)抑制劑之經雜芳基取代之吡咯并[2,3-b]吡啶及吡咯并[2,3-b]嘧啶
|
US7989461B2
(en)
|
2005-12-23 |
2011-08-02 |
Amgen Inc. |
Substituted quinazolinamine compounds for the treatment of cancer
|
WO2007087548A2
(en)
|
2006-01-25 |
2007-08-02 |
Smithkline Beecham Corporation |
Chemical compounds
|
UY30118A1
(es)
|
2006-01-31 |
2007-06-29 |
Tanabe Seiyaku Co |
Compueto amina trisustituido
|
PE20070978A1
(es)
|
2006-02-14 |
2007-11-15 |
Novartis Ag |
COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE FOSFATIDILINOSITOL 3-QUINASAS (PI3Ks)
|
US20090069304A1
(en)
|
2006-03-03 |
2009-03-12 |
Shionogi & Co., Ltd. |
Mmp-13 selective inhibitor
|
JP2009531443A
(ja)
|
2006-03-29 |
2009-09-03 |
フォールドアールエックス ファーマシューティカルズ インコーポレーティッド |
α−シヌクレイン毒性の抑制
|
KR20090017498A
(ko)
*
|
2006-04-04 |
2009-02-18 |
더 리젠트스 오브 더 유니이버시티 오브 캘리포니아 |
Pi3 키나제 길항물질
|
DE102006029074A1
(de)
*
|
2006-06-22 |
2007-12-27 |
Friedrich-Schiller-Universität Jena |
4-Amino-3-arylamino-6-arylpyrazolo[3,4-d]pyrimidin-Derivate, Verfahren zu ihrer Herstellung und deren Verwendung als antivirale Wirkstoffe
|
US8933130B2
(en)
|
2006-06-23 |
2015-01-13 |
Radius Health, Inc. |
Treatment of vasomotor symptoms with selective estrogen receptor modulators
|
EP2044086A2
(en)
|
2006-06-30 |
2009-04-08 |
Janssen Pharmaceutica N.V. |
Thiazolopyrimidine modulators of trpv1
|
US20080009508A1
(en)
|
2006-07-10 |
2008-01-10 |
Lucie Szucova |
6,9-Disubstituted Purine Derivatives And Their Use For Treating Skin
|
WO2008006540A1
(en)
|
2006-07-12 |
2008-01-17 |
Syngenta Participations Ag |
Triazolopyridine derivatives as herbicides
|
HUE035116T2
(hu)
|
2006-08-08 |
2018-05-02 |
Chugai Pharmaceutical Co Ltd |
PI3K inhibitor pirimidinszármazékok és alkalmazásuk
|
BRPI0716239A2
(pt)
|
2006-08-30 |
2013-08-13 |
Cellzome Ltd |
derivados de triazol como inibidores de cinase
|
WO2008032033A1
(en)
|
2006-09-14 |
2008-03-20 |
Astrazeneca Ab |
4-benzimidazolyl-2-morpholino-6-piperazinylpyrimidine derivatives as pi3k and mtor inhibitors for the treatment of proliferative disorders
|
EP1972631A1
(en)
|
2007-03-23 |
2008-09-24 |
Novartis AG |
Imidazopyridazines as PI3K lipid kinase inhibitors
|
WO2008055013A2
(en)
|
2006-10-31 |
2008-05-08 |
Janssen Pharmaceutica N.V. |
5-oxo-5,8 - dihydro - pyrido - pyrimidines as inhibitors of c-fms kinase
|
EP2441768A1
(en)
|
2006-11-13 |
2012-04-18 |
Eli Lilly & Co. |
Thienopyrimidinones for treatment of inflammatory disorders and cancers
|
DK2497470T3
(en)
|
2006-11-22 |
2015-12-07 |
Incyte Holdings Corp |
Imidazotriaziner and imidazopyrimidines as kinase inhibitors
|
EP2134713A2
(en)
|
2006-12-20 |
2009-12-23 |
Schering Corporation |
Novel jnk inhibitors
|
WO2008080844A1
(en)
|
2006-12-29 |
2008-07-10 |
F. Hoffmann-La Roche Ag |
Azaspiro derivatives
|
EP2079737A1
(en)
|
2007-02-05 |
2009-07-22 |
Xenon Pharmaceuticals Inc. |
Pyridopyrimidinone compounds useful in treating sodium channel-mediated diseases or conditions
|
CA2676906A1
(en)
|
2007-02-12 |
2008-08-21 |
Intermune, Inc. |
Novel inhibitors hepatitis c virus replication
|
PE20081887A1
(es)
|
2007-03-20 |
2009-01-16 |
Dainippon Sumitomo Pharma Co |
Nuevo compuesto de adenina
|
US20080233127A1
(en)
|
2007-03-21 |
2008-09-25 |
Wyeth |
Imidazolopyrimidine analogs and their use as pi3 kinase and mtor inhibitors
|
AU2008231384B2
(en)
|
2007-03-23 |
2011-09-15 |
Amgen Inc. |
Heterocyclic compounds and their use
|
MX2009009968A
(es)
|
2007-03-23 |
2009-10-08 |
Amgen Inc |
Compuestos heterociclicos y sus usos.
|
US8039505B2
(en)
|
2007-04-11 |
2011-10-18 |
University Of Utah Research Foundation |
Compounds for modulating T-cells
|
US8633186B2
(en)
|
2007-06-08 |
2014-01-21 |
Senomyx Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
US9603848B2
(en)
|
2007-06-08 |
2017-03-28 |
Senomyx, Inc. |
Modulation of chemosensory receptors and ligands associated therewith
|
EP2167058B1
(en)
|
2007-06-18 |
2015-08-12 |
University Of Louisville Research Foundation, Inc. |
Family of pfkfb3 inhibitors with anti-neoplastic activities
|
CA2691444C
(en)
|
2007-06-29 |
2016-06-14 |
Gilead Sciences, Inc. |
Purine derivatives and their use as modulators of toll-like receptor 7
|
EP2190466A4
(en)
|
2007-08-10 |
2011-12-21 |
Burnham Inst Medical Research |
Tissue-specific alkaline phosphatase (TNAP) activators and their use
|
TW200916447A
(en)
|
2007-08-29 |
2009-04-16 |
Methylgene Inc |
Sirtuin inhibitors
|
JP2009076865A
(ja)
|
2007-08-29 |
2009-04-09 |
Fujifilm Corp |
有機電界発光素子
|
WO2009034386A1
(en)
|
2007-09-13 |
2009-03-19 |
Astrazeneca Ab |
Derivatives of adenine and 8-aza-adenine and uses thereof-796
|
JP2009080233A
(ja)
|
2007-09-26 |
2009-04-16 |
Kyocera Mita Corp |
電子写真感光体
|
CZ300774B6
(cs)
|
2007-10-05 |
2009-08-05 |
Univerzita Palackého |
Substituované 6-(alkylbenzylamino)purinové deriváty pro použití jako antagonisté cytokininových receptoru a prípravky obsahující tyto slouceniny
|
WO2009062118A2
(en)
|
2007-11-07 |
2009-05-14 |
Foldrx Pharmaceuticals, Inc. |
Modulation of protein trafficking
|
WO2009063235A1
(en)
|
2007-11-13 |
2009-05-22 |
Astrazeneca Ab |
Derivatives of 1,9-dihydro-6h-purin-6-one and uses thereof-018
|
JP2009120686A
(ja)
|
2007-11-14 |
2009-06-04 |
Toyo Ink Mfg Co Ltd |
光重合開始剤、重合性組成物、および重合物の製造方法。
|
PE20091268A1
(es)
|
2007-12-19 |
2009-09-19 |
Amgen Inc |
Derivados heterociclicos como inhibidores de pi3 quinasa
|
AU2008345681A1
(en)
|
2007-12-21 |
2009-07-09 |
Wyeth Llc |
Imidazo [1,2-a] pyridine compounds
|
EP2219646A4
(en)
|
2007-12-21 |
2010-12-22 |
Univ Rochester |
METHOD FOR MODIFYING THE LIFETIME OF EUKARYOTIC ORGANISMS
|
EP2231641B1
(en)
|
2007-12-21 |
2016-06-01 |
UCB Biopharma SPRL |
Quinoxaline and quinoline derivatives as kinase inhibitors
|
US7960397B2
(en)
|
2007-12-28 |
2011-06-14 |
Institute Of Experimental Botany, Academy Of Sciences Of The Czech Republic |
6,9-disubstituted purine derivatives and their use as cosmetics and cosmetic compositions
|
WO2009082845A1
(en)
|
2007-12-28 |
2009-07-09 |
Topharman Shanghai Co., Ltd. |
N-{1-[3-(2-ethoxy-5-(4-ethylpiperazinyl)benzenesulfonyl)-4,5-dihydro-5-oxo-1,2,4-triazin-6-yl]ethyl}butyramide, the preparation method and use thereof
|
US8193182B2
(en)
*
|
2008-01-04 |
2012-06-05 |
Intellikine, Inc. |
Substituted isoquinolin-1(2H)-ones, and methods of use thereof
|
MX2010007523A
(es)
|
2008-01-11 |
2010-08-18 |
Natco Pharma Ltd |
Nuevos derivados de pirazolo[3,4-d]pirimidina como farmacos anticancer.
|
US9089572B2
(en)
|
2008-01-17 |
2015-07-28 |
California Institute Of Technology |
Inhibitors of p97
|
WO2009097446A1
(en)
|
2008-01-30 |
2009-08-06 |
Genentech, Inc. |
Pyrazolopyrimidine pi3k inhibitor compounds and methods of use
|
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
|
US8119647B2
(en)
|
2008-04-23 |
2012-02-21 |
Glenmark Pharmaceuticals S.A. |
Fused pyrimidineone compounds as TRPV3 modulators
|
WO2009140215A2
(en)
|
2008-05-11 |
2009-11-19 |
Geraghty, Erin |
Method for treating drug-resistant bacterial and other infections with clioquinol, phanquinone, and related compounds
|
US10301265B2
(en)
|
2008-05-28 |
2019-05-28 |
Virginia I. Roxas-Duncan |
Small molecule inhibitors of botulinum neurotoxins
|
MX2010013876A
(es)
|
2008-06-20 |
2011-03-04 |
Metabolex Inc |
Agonistas de arilo grpr119 y sus usos .
|
US8026271B2
(en)
|
2008-07-11 |
2011-09-27 |
National Health Research Institutes |
Formulations of indol-3-yl-2-oxoacetamide compounds
|
WO2010018458A2
(en)
|
2008-08-12 |
2010-02-18 |
Crystalgenomics, Inc. |
Phenol derivatives and methods of use thereof
|
EP2346508B1
(en)
*
|
2008-09-26 |
2016-08-24 |
Intellikine, LLC |
Heterocyclic kinase inhibitors
|
CA2975473C
(en)
|
2008-11-13 |
2021-01-19 |
Gilead Calistoga Llc |
Therapies for hematologic malignancies
|
WO2010075068A1
(en)
|
2008-12-16 |
2010-07-01 |
Schering Corporation |
Pyridopyrimidine derivatives and methods of use thereof
|
BR122013027950A2
(pt)
|
2008-12-24 |
2019-12-10 |
BIAL PORTELA & Cª S A |
compostos farmacêuticos
|
WO2010083444A1
(en)
|
2009-01-15 |
2010-07-22 |
Anvyl, Llc |
Alpha7 nicotinic acetylcholine receptor allosteric modulators, their derivatives and uses thereof
|
ES2598358T3
(es)
|
2009-02-13 |
2017-01-27 |
Ucb Pharma, S.A. |
Derivados de quinolina como inhibidores de PI3K quinasa
|
US8497276B2
(en)
|
2009-03-31 |
2013-07-30 |
Arqule, Inc. |
Substituted indolo-piperidine compounds
|
WO2010118367A2
(en)
|
2009-04-10 |
2010-10-14 |
Progenics Pharmaceuticals, Inc. |
Antiviral pyrimidines
|
WO2010123931A1
(en)
|
2009-04-20 |
2010-10-28 |
Calistoga Pharmaceuticals Inc. |
Methods of treatment for solid tumors
|
WO2010127208A1
(en)
|
2009-04-30 |
2010-11-04 |
Forest Laboratories Holdings Limited |
Inhibitors of acetyl-coa carboxylase
|
EP2427195B1
(en)
|
2009-05-07 |
2019-05-01 |
Intellikine, LLC |
Heterocyclic compounds and uses thereof
|
CN102458581B
(zh)
|
2009-05-22 |
2016-03-30 |
因塞特控股公司 |
作为JANUS激酶抑制剂的吡唑-4-基-吡咯并[2,3-d]嘧啶和吡咯-3-基-吡咯并[2,3-d]嘧啶的N-(杂)芳基-吡咯烷衍生物
|
AU2010265974B2
(en)
*
|
2009-06-25 |
2014-09-11 |
Amgen Inc. |
Polycyclic derivatives of pyridine and their use in the treatment of (inter alia) rheumatoid arthritis and similar diseases
|
WO2010151735A2
(en)
|
2009-06-25 |
2010-12-29 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
EP3708169A1
(en)
|
2009-06-29 |
2020-09-16 |
Agios Pharmaceuticals, Inc. |
2,3-dihydrobenzo[b][1,4]dioxine-6-sulfonamide derivatives having an anticancer activity
|
MX2011013816A
(es)
|
2009-06-29 |
2012-04-11 |
Incyte Corp |
Pirimidinonas como inhibidores de pi3k.
|
AR077252A1
(es)
|
2009-06-29 |
2011-08-10 |
Xenon Pharmaceuticals Inc |
Enantiomeros de compuestos de espirooxindol y sus usos como agentes terapeuticos
|
FR2947269B1
(fr)
|
2009-06-29 |
2013-01-18 |
Sanofi Aventis |
Nouveaux composes anticancereux
|
EA201270184A1
(ru)
|
2009-07-21 |
2012-08-30 |
ГИЛИЭД КАЛИСТОГА ЭлЭлСи |
Лечение расстройств печени ингибиторами pi3k
|
SI2470546T1
(sl)
|
2009-08-28 |
2013-12-31 |
Takeda Pharmaceutical Company Limited |
Spojine heksahidrooksazinopteridina za uporabo kot MTOR inhibitorji
|
AR078012A1
(es)
|
2009-09-01 |
2011-10-05 |
Incyte Corp |
Derivados heterociclicos de las pirazol-4-il- pirrolo (2,3-d) pirimidinas como inhibidores de la quinasa janus
|
EP2491039A1
(en)
|
2009-10-20 |
2012-08-29 |
Cellzome Limited |
Heterocyclyl pyrazolopyrimidine analogues as jak inhibitors
|
AU2010310813B2
(en)
|
2009-10-22 |
2015-06-18 |
Gilead Sciences, Inc. |
Derivatives of purine or deazapurine useful for the treatment of (inter alia) viral infections
|
EP2496567B1
(en)
*
|
2009-11-05 |
2017-07-12 |
Rhizen Pharmaceuticals S.A. |
Novel benzopyran kinase modulators
|
CU24077B1
(es)
|
2009-11-10 |
2015-03-30 |
Pfizer |
DERIVADOS DE N1-PIRAZOLOESPIROCETONA ÚTILES COMO INHIBIDORES DE ACETIL-CoA CARBOXILASA
|
WO2011058111A1
(en)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Aminopurine derivatives as kinase inhibitors
|
ES2534096T3
(es)
|
2009-11-12 |
2015-04-17 |
Ucb Pharma, S.A. |
Derivados de piridina y pirazina bicíclicos condensados como inhibidores de quinasa
|
CA2783859A1
(en)
|
2009-12-10 |
2011-06-16 |
Institute Of Materia Medica, Chinese Academy Of Medical Sciences |
N6-substituted adenosine derivatives and n6-substituted adenine derivatives and uses thereof
|
WO2011075630A1
(en)
|
2009-12-18 |
2011-06-23 |
Incyte Corporation |
Substituted fused aryl and heteroaryl derivatives as pi3k inhibitors
|
MX2012006953A
(es)
|
2009-12-18 |
2012-10-09 |
Amgen Inc |
Compuestos heterociclicos y sus usos.
|
WO2011075643A1
(en)
|
2009-12-18 |
2011-06-23 |
Incyte Corporation |
Substituted heteroaryl fused derivatives as pi3k inhibitors
|
UA107818C2
(en)
*
|
2009-12-23 |
2015-02-25 |
Medicis Pharmaceutical Corp Usa |
Alkyl amino pyrimidine derivatives as antagonists district h4-histamine receptors
|
JP2011136925A
(ja)
|
2009-12-28 |
2011-07-14 |
Dainippon Sumitomo Pharma Co Ltd |
含窒素二環性化合物
|
ES2529247T3
(es)
|
2010-01-07 |
2015-02-18 |
Dow Agrosciences Llc |
Tiazolo[5,4-d]pirimidinas y su uso como productos agroquímicos
|
US8633183B2
(en)
|
2010-01-26 |
2014-01-21 |
Boehringer Ingelheim International Gmbh |
5-alkynyl-pyrimidines
|
RS60680B1
(sr)
|
2010-03-10 |
2020-09-30 |
Incyte Holdings Corp |
Piperidin-4-il azetidin derivati kao inhibitori jak1
|
WO2011117711A1
(en)
|
2010-03-22 |
2011-09-29 |
Glenmark Pharmaceuticals S.A. |
Pharmaceutical composition comprising a pyrimidineone derivative
|
UY33304A
(es)
|
2010-04-02 |
2011-10-31 |
Amgen Inc |
Compuestos heterocíclicos y sus usos
|
US9193721B2
(en)
|
2010-04-14 |
2015-11-24 |
Incyte Holdings Corporation |
Fused derivatives as PI3Kδ inhibitors
|
CA2799579A1
(en)
|
2010-05-21 |
2011-11-24 |
Intellikine, Inc. |
Chemical compounds, compositions and methods for kinase modulation
|
AU2011265258A1
(en)
|
2010-06-11 |
2013-01-10 |
Calistoga Pharmaceuticals, Inc. |
Methods of treating hematological disorders with quinazolinone compounds in selected patients
|
US9062055B2
(en)
|
2010-06-21 |
2015-06-23 |
Incyte Corporation |
Fused pyrrole derivatives as PI3K inhibitors
|
US20130085131A1
(en)
|
2010-07-01 |
2013-04-04 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
AU2011271460B2
(en)
|
2010-07-01 |
2014-02-06 |
Amgen Inc. |
Heterocyclic compounds and their use as inhibitors of P13K activity
|
CA2803624A1
(en)
|
2010-07-02 |
2012-01-05 |
Jason A. Duquette |
Heterocyclic compounds and their use as inhibitors of pi3k activity
|
US20130324561A1
(en)
|
2010-09-24 |
2013-12-05 |
Gilead Calistroga Llc. |
Atropisomers of p13k-inhibiting compounds
|
MX2013005005A
(es)
|
2010-11-04 |
2013-10-25 |
Amgen Inc |
Derivados de ciano-4,6-diaminopirimidina o 6-aminopurina como inhibidores de pi3k-delta.
|
CN103298474B
(zh)
|
2010-11-10 |
2016-06-29 |
无限药品股份有限公司 |
杂环化合物及其用途
|
US8765768B2
(en)
|
2010-11-17 |
2014-07-01 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
AR083933A1
(es)
|
2010-11-19 |
2013-04-10 |
Incyte Corp |
Derivados de pirrolopiridina y pirrolopirimidina sustituidos con ciclobutilo como inhibidores de jak
|
EP2640725B1
(en)
|
2010-11-19 |
2015-01-07 |
Incyte Corporation |
Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors
|
ES2650744T3
(es)
|
2010-12-14 |
2018-01-22 |
Electrophoretics Limited |
Inhibidores de la caseína quinasa 1 delta (CK1delta)
|
CA2822070C
(en)
|
2010-12-20 |
2019-09-17 |
Incyte Corporation |
N-(1-(substituted-phenyl)ethyl)-9h-purin-6-amines as pi3k inhibitors
|
AU2011349669A1
(en)
|
2010-12-23 |
2013-07-11 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
BR112013017670B1
(pt)
|
2011-01-10 |
2022-07-19 |
Infinity Pharmaceuticals, Inc |
Processos de preparação de isoquinolinonas e formas sólidas de isoquinolinonas
|
EP2670733B1
(en)
|
2011-02-01 |
2019-04-10 |
The Board of Trustees of the University of Illionis |
N-hydroxybenzamide derivatives as hdac inhibitors and therapeutic methods using the same
|
US9108984B2
(en)
|
2011-03-14 |
2015-08-18 |
Incyte Corporation |
Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors
|
US9126948B2
(en)
|
2011-03-25 |
2015-09-08 |
Incyte Holdings Corporation |
Pyrimidine-4,6-diamine derivatives as PI3K inhibitors
|
CA2839767A1
(en)
|
2011-06-20 |
2012-12-27 |
Incyte Corporation |
Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors
|
WO2013012915A1
(en)
|
2011-07-19 |
2013-01-24 |
Infinity Pharmaceuticals Inc. |
Heterocyclic compounds and uses thereof
|
TW201313721A
(zh)
|
2011-08-18 |
2013-04-01 |
Incyte Corp |
作為jak抑制劑之環己基氮雜環丁烷衍生物
|
ES2722524T3
(es)
|
2011-09-02 |
2019-08-13 |
Incyte Holdings Corp |
Heterociclaminas como inhibidores de pi3k
|
CN104024257A
(zh)
|
2011-10-04 |
2014-09-03 |
吉利德卡利斯托加有限责任公司 |
Pi3k的新的喹喔啉抑制剂
|
AR090548A1
(es)
|
2012-04-02 |
2014-11-19 |
Incyte Corp |
Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
|
TW201406761A
(zh)
|
2012-05-18 |
2014-02-16 |
Incyte Corp |
做爲jak抑制劑之哌啶基環丁基取代之吡咯并吡啶及吡咯并嘧啶衍生物
|
TWI646099B
(zh)
|
2012-11-01 |
2019-01-01 |
英塞特控股公司 |
作爲jak抑制劑之三環稠合噻吩衍生物
|
TWI657090B
(zh)
|
2013-03-01 |
2019-04-21 |
英塞特控股公司 |
吡唑并嘧啶衍生物治療PI3Kδ 相關病症之用途
|
SG10201809696UA
(en)
|
2013-03-15 |
2018-11-29 |
Janssen Pharmaceutica Nv |
Processes and intermediates for preparing a medicament
|
EA039660B1
(ru)
|
2013-05-17 |
2022-02-24 |
Инсайт Корпорейшн |
Твердая форма производного бипиразола
|
US10077277B2
(en)
|
2014-06-11 |
2018-09-18 |
Incyte Corporation |
Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors
|
TWI698436B
(zh)
|
2014-12-30 |
2020-07-11 |
美商佛瑪治療公司 |
作為泛素特異性蛋白酶7抑制劑之吡咯并及吡唑并嘧啶
|
SG11201706917WA
(en)
|
2015-02-27 |
2017-09-28 |
Incyte Corp |
Salts of pi3k inhibitor and processes for their preparation
|
US9988401B2
(en)
|
2015-05-11 |
2018-06-05 |
Incyte Corporation |
Crystalline forms of a PI3K inhibitor
|
WO2016183062A1
(en)
|
2015-05-11 |
2016-11-17 |
Incyte Corporation |
Salts of (s)-7-(1-(9h-purin-6-ylamino)ethyl)-6-(3-fluorophenyl)-3-methyl-5h-thiazolo[3,2-a]pyrimidin-5-one
|
WO2016183060A1
(en)
|
2015-05-11 |
2016-11-17 |
Incyte Corporation |
Process for the synthesis of a phosphoinositide 3-kinase inhibitor
|
CN112469418A
(zh)
|
2018-06-01 |
2021-03-09 |
因赛特公司 |
治疗pi3k相关病症的给药方案
|