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
|
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
|
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
|
US3936454A
(en)
|
1973-08-14 |
1976-02-03 |
Warner-Lambert Company |
5-Amino-4-chloro-6-(substituted amino)-pyrimidines
|
US3862189A
(en)
|
1973-08-14 |
1975-01-21 |
Warner Lambert Co |
Aralkyl-substituted purines and pyrimidines as antianginal bronchodilator agents
|
DK3375A
(fr)
|
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
|
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
|
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
|
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
|
JPS6067709U
(ja)
|
1983-10-14 |
1985-05-14 |
三洋電機株式会社 |
ヘア−ドライヤ−
|
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
|
JPS6263591U
(fr)
|
1985-06-29 |
1987-04-20 |
|
|
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
|
JPS635783Y2
(fr)
|
1985-10-17 |
1988-02-17 |
|
|
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
(fr)
|
1986-07-30 |
1993-11-23 |
Eastman Kodak Company |
Element et processus photographiques
|
JPS6427257U
(fr)
|
1987-08-11 |
1989-02-16 |
|
|
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
|
WO1989008113A1
(fr)
|
1988-03-02 |
1989-09-08 |
Yoshitomi Pharmaceutical Industries, Ltd. |
COMPOSES DE 3,4-DIHYDROTHIENO[2,3-d]PYRIMIDINE ET LEURS APPLICATIONS PHARMACOLOGIQUES
|
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
|
JPH054831Y2
(fr)
|
1988-11-22 |
1993-02-08 |
|
|
DK0482208T3
(da)
|
1990-04-25 |
2000-09-18 |
Nissan Chemical Ind Ltd |
Pyridazinonderivat
|
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
(fr)
|
1990-06-28 |
1998-05-13 |
Fuji Photo Film Co., Ltd. |
Matériaux photographiques à l'halogénure d'argent
|
EP0481614A1
(fr)
|
1990-10-01 |
1992-04-22 |
Merck & Co. Inc. |
Pyridopyrimidinones substituées et hétérocyles apparantés comme antagonistes de la angiotensine II
|
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
|
AU1625192A
(en)
|
1991-05-31 |
1992-12-03 |
Zeneca Limited |
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
|
AU3933493A
(en)
|
1992-04-24 |
1993-11-29 |
E.I. Du Pont De Nemours And Company |
Arthropodicidal and fungicidal aminopyrimidines
|
TW229140B
(fr)
|
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
|
EP0934307B1
(fr)
|
1996-06-19 |
2011-04-27 |
Aventis Pharma Limited |
Composes azabicycliques substitues et leur utilisation en tant qu'inhibiteurs de la production de tnf et de la photodiesterase cyclique d'amp
|
NZ329798A
(en)
|
1996-07-03 |
1999-04-29 |
Japan Energy Corp |
Purine derivatives their tautomers and salts thereof and interferon secretion inducers, antiviral agents and anticancer drugs containing the same
|
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
|
IL137540A0
(en)
|
1998-02-25 |
2001-07-24 |
Genetics Inst |
Inhibitors of phospholipase a2
|
US6828344B1
(en)
|
1998-02-25 |
2004-12-07 |
Genetics Institute, Llc |
Inhibitors of phospholipase enzymes
|
AU2782699A
(en)
|
1998-02-25 |
1999-09-15 |
Genetics Institute, Llc |
Inhibitors of phospholipase enzymes
|
US6479487B1
(en)
|
1998-02-26 |
2002-11-12 |
Aventis Pharmaceuticals Inc. |
6, 9-disubstituted 2-[trans-(4-aminocyclohexyl)amino] purines
|
CZ20003960A3
(cs)
|
1998-05-04 |
2002-04-17 |
Zentaris Ag |
Deriváty indolu a jejich pouľití pro léčení maligních a jiných chorob vyvolaných patologickou proliferací buněk
|
EP1086950B1
(fr)
|
1998-05-26 |
2010-09-29 |
Chugai Seiyaku Kabushiki Kaisha |
Derives d'indole heterocycliques et derives de mono ou de di-azaindole
|
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
|
JP4516690B2
(ja)
|
1998-08-11 |
2010-08-04 |
ノバルティス アーゲー |
血管形成阻害活性を有するイソキノリン誘導体
|
CA2341506A1
(fr)
|
1998-08-25 |
2000-03-02 |
The Uab Research Foundation |
Inhibiteurs de la nad synthetase bacterienne
|
US6133031A
(en)
|
1999-08-19 |
2000-10-17 |
Isis Pharmaceuticals Inc. |
Antisense inhibition of focal adhesion kinase expression
|
IL144675A0
(en)
|
1999-02-01 |
2002-05-23 |
Cv Therapeutics Inc |
PURINE INHIBITORS OF CYCLIN DEPENDENT KINASE 2 AND IkB-α
|
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
(fr)
|
2000-03-29 |
2001-10-04 |
Eli Lilly And Company Limited |
Dérivés du naphthalène comme médicaments du SNC
|
US6667300B2
(en)
|
2000-04-25 |
2003-12-23 |
Icos Corporation |
Inhibitors of human phosphatidylinositol 3-kinase delta
|
AU1560802A
(en)
|
2000-06-28 |
2002-01-08 |
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
|
PL360294A1
(en)
|
2000-07-05 |
2004-09-06 |
Yamanouchi Pharmaceutical Co.Ltd. |
Propane-1,3-dione derivatives
|
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
|
KR20030078958A
(ko)
|
2001-03-01 |
2003-10-08 |
시오노기세이야쿠가부시키가이샤 |
Hiv 인테그라제 저해 활성을 갖는 질소 함유의헤테로아릴 화합물
|
UA76977C2
(en)
|
2001-03-02 |
2006-10-16 |
Icos Corp |
Aryl- and heteroaryl substituted chk1 inhibitors and their use as radiosensitizers and chemosensitizers
|
JP2004525150A
(ja)
|
2001-03-30 |
2004-08-19 |
スミスクライン ビーチャム コーポレーション |
治療用化合物としてのピラゾロピリジン類の使用
|
JP4237497B2
(ja)
|
2001-03-30 |
2009-03-11 |
スミスクライン ビーチャム コーポレーション |
ピラゾロピリジン類、その調製方法及びその治療用化合物としての使用
|
WO2002088124A2
(fr)
|
2001-04-27 |
2002-11-07 |
Smithkline Beecham Corporation |
Composes therapeutiques
|
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
|
MXPA04002243A
(es)
|
2001-09-19 |
2004-06-29 |
Aventis Pharma Sa |
Compuestos quimicos.
|
EP1432711A1
(fr)
|
2001-09-26 |
2004-06-30 |
Bayer Corporation |
Derives de 1,6-naphthyridine et leur utilisation dans le traitement du diabete et de troubles associes
|
ES2309206T3
(es)
|
2001-10-02 |
2008-12-16 |
Smithkline Beecham Corporation |
Compuestos quimicos.
|
CN1582150B
(zh)
|
2001-10-30 |
2011-09-07 |
诺瓦提斯公司 |
作为flt3受体酪氨酸激酶活性抑制剂的星形孢菌素衍生物
|
US7262164B2
(en)
|
2001-11-09 |
2007-08-28 |
Enzon, Inc. |
Polymeric thiol-linked prodrugs employing benzyl elimination systems
|
EP1314733A1
(fr)
|
2001-11-22 |
2003-05-28 |
Aventis Pharma Deutschland GmbH |
Indole-2-carboxamides comme inhibiteurs du facteur Xa
|
ES2291543T3
(es)
|
2001-12-06 |
2008-03-01 |
MERCK & CO., INC. |
Inhibicion de kinesina mitotica.
|
DE60231439D1
(de)
|
2001-12-06 |
2009-04-16 |
Merck & Co Inc |
Mitotische kinesinhemmer
|
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
|
CA2476162A1
(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
|
ATE370145T1
(de)
|
2002-04-03 |
2007-09-15 |
Bristol Myers Squibb Co |
Tricyclische verbindungen auf thiophengrundlage und pharmazeutische zusammensetzungen, die diese enthalten
|
NZ536123A
(en)
|
2002-05-06 |
2006-09-29 |
Genelabs Tech Inc |
Nucleoside derivatives for treating hepatitis C virus infection
|
TW200406374A
(en)
|
2002-05-29 |
2004-05-01 |
Novartis Ag |
Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases
|
GB0215676D0
(en)
|
2002-07-05 |
2002-08-14 |
Novartis Ag |
Organic compounds
|
AU2003257822A1
(en)
|
2002-08-13 |
2004-04-30 |
Shionogi And Co., Ltd. |
Heterocyclic compound having hiv integrase inhibitory activity
|
JP4190232B2
(ja)
|
2002-08-26 |
2008-12-03 |
富士通株式会社 |
機械研磨を行う方法
|
CA2497765A1
(fr)
|
2002-09-27 |
2004-04-08 |
Sumitomo Pharmaceuticals Co., Ltd. |
Nouveau compose d'adenine et son application
|
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
|
CA2507100C
(fr)
|
2002-11-21 |
2012-10-09 |
Chiron Corporation |
Pyrimidines 2,4,6-trisubstitutees utilisees comme inhibiteurs de phosphotidylinositol (pi) 3-kinase et leur utilisation dans le traitement du cancer
|
WO2004048326A1
(fr)
|
2002-11-25 |
2004-06-10 |
Mochida Pharmaceutical Co., Ltd. |
Agent therapeutique pour maladies respiratoires contenant un derive de 4-hydroxypiperidine en tant qu'ingredient actif
|
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
|
US20060247245A1
(en)
|
2003-05-05 |
2006-11-02 |
Yuelian Xu |
Substituted imidazolopyrazine and triazolopyrazine derivatives: gabaa receptor ligands
|
EP1636225B1
(fr)
|
2003-06-20 |
2010-02-24 |
Novartis Vaccines and Diagnostics, Inc. |
Composes de pyridino 1,2-a pyrimidin-4-one servant d'agents anticancereux
|
WO2005000309A2
(fr)
|
2003-06-27 |
2005-01-06 |
Ionix Pharmaceuticals Limited |
Composes chimiques
|
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
|
US20050124637A1
(en)
|
2003-08-15 |
2005-06-09 |
Irm Llc |
Compounds and compositions as inhibitors of receptor tyrosine kinase activity
|
US7138401B2
(en)
|
2003-09-18 |
2006-11-21 |
Conforma Therapeutics Corporation |
2-aminopurine analogs having HSP90-inhibiting activity
|
AU2004289186B2
(en)
|
2003-09-23 |
2010-12-16 |
Merck Sharp & Dohme Corp. |
Isoquinolinone potassium channel inhibitors
|
PE20050952A1
(es)
|
2003-09-24 |
2005-12-19 |
Novartis Ag |
Derivados de isoquinolina como inhibidores de b-raf
|
CA2553724A1
(fr)
|
2004-02-03 |
2005-08-18 |
Abbott Laboratories |
Utilisation d'aminobenzoxazoles comme agents therapeutiques
|
WO2005077948A1
(fr)
|
2004-02-16 |
2005-08-25 |
Daiichi Pharmaceutical Co., Ltd. |
Composes heterocycliques fongicides
|
WO2005091857A2
(fr)
|
2004-03-12 |
2005-10-06 |
Bayer Pharmaceuticals Corporation |
Derives de 1,6-naphtyridine et 1,8-naphtyridine et leur utilisation pour le traitement du diabete et de troubles associes
|
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
|
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
|
US7217702B2
(en)
|
2004-04-02 |
2007-05-15 |
Adenosine Therapeutics, Llc |
Selective antagonists of A2A adenosine receptors
|
US7932260B2
(en)
|
2004-05-13 |
2011-04-26 |
Icos Corporation |
Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta
|
EP1753428A4
(fr)
|
2004-05-14 |
2010-09-15 |
Abbott Lab |
Inhibiteurs de kinases en tant qu'agents therapeutiques
|
JP2008506759A
(ja)
|
2004-07-22 |
2008-03-06 |
アストラゼネカ アクチボラグ |
癌の処置および予防に有用な縮合ピリミドン類
|
AU2005273705B8
(en)
|
2004-08-18 |
2010-01-28 |
Astrazeneca Ab |
Enantiomers of selected fused pyrimidones and uses in the treatment and prevention of cancer
|
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
(fr)
|
2004-10-19 |
2006-05-11 |
Novartis Vaccines And Diagnostics Inc. |
Derives d'indole et de benzimidazole
|
EP1807417A2
(fr)
|
2004-11-04 |
2007-07-18 |
Neurogen Corporation |
Dérivés hétéroaryles de pyrazolylméthyle
|
WO2006068760A2
(fr)
|
2004-11-19 |
2006-06-29 |
The Regents Of The University Of California |
Pyrazolopyrimidines anti-inflammatoires
|
RU2007123675A
(ru)
|
2004-11-24 |
2008-12-27 |
Новартис АГ (CH) |
Комбинации ингибиторов jak
|
EP1885356A2
(fr)
|
2005-02-17 |
2008-02-13 |
Icos Corporation |
Inhibiteurs de la phosphoinositide 3-kinase pour inhiber l'accumulation des leucocytes
|
JP2008546843A
(ja)
|
2005-06-27 |
2008-12-25 |
アムゲン インコーポレイティッド |
抗炎症性アリールニトリル化合物
|
FR2889192A1
(fr)
|
2005-07-27 |
2007-02-02 |
Cytomics Systems Sa |
Composes antifongiques, compositions contenant ces composes et leurs utilisations
|
JP2009504769A
(ja)
|
2005-08-16 |
2009-02-05 |
ジェンザイム・コーポレーション |
ケモカイン受容体結合化合物
|
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
|
US20090118263A1
(en)
|
2005-09-22 |
2009-05-07 |
Dainippon Sumitomo Pharma Co., Ltd. |
Novel Adenine Compound
|
GB0520657D0
(en)
|
2005-10-11 |
2005-11-16 |
Ludwig Inst Cancer Res |
Pharmaceutical compounds
|
RU2589878C2
(ru)
|
2005-11-01 |
2016-07-10 |
Таргеджен, Инк. |
Би-арил-мета-пиримидиновые ингибиторы киназ
|
EP1783114A1
(fr)
|
2005-11-03 |
2007-05-09 |
Novartis AG |
Dérivés de N-(hétéro)aryle indole comme pesticides
|
EP2314590A1
(fr)
|
2005-11-10 |
2011-04-27 |
ChemoCentryx, Inc. |
Quinolones substituées et procédés d'utilisation
|
LT2474545T
(lt)
|
2005-12-13 |
2017-02-27 |
Incyte Holdings Corporation |
Heteroarilu pakeisti pirolo[2,3-b]piridinai ir pirolo[2,3-b]pirimidinai kaip janus kinazės inhibitoriai
|
US7989461B2
(en)
|
2005-12-23 |
2011-08-02 |
Amgen Inc. |
Substituted quinazolinamine compounds for the treatment of cancer
|
JP2009524689A
(ja)
|
2006-01-25 |
2009-07-02 |
スミスクライン ビーチャム コーポレーション |
化合物
|
PE20071025A1
(es)
|
2006-01-31 |
2007-10-17 |
Mitsubishi Tanabe Pharma Corp |
Compuesto amina trisustituido
|
PE20070978A1
(es)
|
2006-02-14 |
2007-11-15 |
Novartis Ag |
COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE FOSFATIDILINOSITOL 3-QUINASAS (PI3Ks)
|
JPWO2007102392A1
(ja)
|
2006-03-03 |
2009-07-23 |
塩野義製薬株式会社 |
Mmp−13選択的阻害剤
|
US20100273776A1
(en)
|
2006-03-29 |
2010-10-28 |
FOLDRx PHARMACEUTICALS, INC |
Inhibition of alpha-synuclein toxicity
|
MX2008012928A
(es)
|
2006-04-04 |
2009-03-06 |
Univ California |
Antagonistas de pi3-cinasa.
|
ES2436028T3
(es)
|
2006-06-23 |
2013-12-26 |
Radius Health, Inc. |
Tratamiento de síntomas vasomotores con moduladores selectivos de receptores de estrógeno
|
WO2008005303A2
(fr)
|
2006-06-30 |
2008-01-10 |
Janssen Pharmaceutica N.V. |
Modulateurs de trpv1 à base de thiazolopyrimidine
|
US20080009508A1
(en)
|
2006-07-10 |
2008-01-10 |
Lucie Szucova |
6,9-Disubstituted Purine Derivatives And Their Use For Treating Skin
|
AU2007272009A1
(en)
|
2006-07-12 |
2008-01-17 |
Syngenta Limited |
Triazolopyridine derivatives as herbicides
|
RU2448109C2
(ru)
|
2006-08-08 |
2012-04-20 |
Чугаи Сейяку Кабусики Кайся |
Производное пиримидина в качестве ингибитора pi3k и его применение
|
WO2008025821A1
(fr)
|
2006-08-30 |
2008-03-06 |
Cellzome Limited |
Dérivés de triazole en tant qu'inhibiteurs de kinase
|
WO2008032033A1
(fr)
|
2006-09-14 |
2008-03-20 |
Astrazeneca Ab |
Dérivés de 4-benzimidazolyl-2-morpholino-6-pipérazinylpyrimidine utilisés en tant que pi3k et inhibiteurs de mtor destinés au traitement de troubles prolifératifs
|
EP1972631A1
(fr)
|
2007-03-23 |
2008-09-24 |
Novartis AG |
Imidazopyridazines comme inhibiteurs de kinase lipide PI3K
|
WO2008055013A2
(fr)
|
2006-10-31 |
2008-05-08 |
Janssen Pharmaceutica N.V. |
5-oxo-5,8-dihydro-pyrido-pyrimidines comme inhibiteurs de la kinase c-fms
|
US20100216820A1
(en)
|
2006-11-13 |
2010-08-26 |
White Stephen L |
Thienopyrimidiones for treatment of inflammatory disorders and cancers
|
LT3034075T
(lt)
|
2006-11-22 |
2018-11-26 |
Incyte Holdings Corporation |
Imidazotriazinai ir imidazopirimidinai kaip kinazės inhibitoriai
|
CN101631786A
(zh)
|
2006-12-20 |
2010-01-20 |
先灵公司 |
新颖的jnk抑制剂
|
CA2674154A1
(fr)
|
2006-12-29 |
2008-07-10 |
F. Hoffmann-La Roche Ag |
Derives azaspiro
|
TW200838539A
(en)
|
2007-02-05 |
2008-10-01 |
Xenon Pharmaceuticals Inc |
Pyridopyrimidinone compounds useful in treating sodium channel-mediated diseases or conditions
|
CN101687789A
(zh)
|
2007-02-12 |
2010-03-31 |
因特蒙公司 |
C型肝炎病毒复制的新颖抑制剂
|
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
|
MX2009009913A
(es)
|
2007-03-23 |
2009-10-16 |
Amgen Inc |
Derivados de quinolina o benzopirazina y sus usos para el tratamiento de enfermedades inflamatorias, enfermedades autoinmunitarias o varias clases de canceres.
|
KR101504773B1
(ko)
|
2007-03-23 |
2015-03-20 |
암젠 인크 |
헤테로시클릭 화합물 및 그의 용도
|
US8039505B2
(en)
|
2007-04-11 |
2011-10-18 |
University Of Utah Research Foundation |
Compounds for modulating T-cells
|
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
|
JP2010531304A
(ja)
|
2007-06-18 |
2010-09-24 |
ユニバーシティ オブ ルイビル リサーチ ファウンデーション、インコーポレイテッド |
抗悪性腫瘍活性を有するpfkfb3阻害物質ファミリー
|
US7968544B2
(en)
|
2007-06-29 |
2011-06-28 |
Gilead Sciences, Inc. |
Modulators of toll-like receptor 7
|
EP2190466A4
(fr)
|
2007-08-10 |
2011-12-21 |
Burnham Inst Medical Research |
Activateurs de la phosphatase alcaline non spécifique des tissus (tnap) et leurs utilisations
|
WO2009026701A1
(fr)
|
2007-08-29 |
2009-03-05 |
Methylgene Inc. |
Inhibiteurs de sirtuine
|
JP2009076865A
(ja)
|
2007-08-29 |
2009-04-09 |
Fujifilm Corp |
有機電界発光素子
|
WO2009034386A1
(fr)
|
2007-09-13 |
2009-03-19 |
Astrazeneca Ab |
Dérivés de l'adénine et de la 8-aza-adénine et leurs utilisations
|
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
|
CN101917999A
(zh)
|
2007-11-07 |
2010-12-15 |
弗尔德里克斯制药股份有限公司 |
蛋白质运输的调节
|
WO2009063235A1
(fr)
|
2007-11-13 |
2009-05-22 |
Astrazeneca Ab |
Dérivés de 1,9-dihydro-6h-purin-6-one et leurs utilisations -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。
|
US7820665B2
(en)
|
2007-12-19 |
2010-10-26 |
Amgen Inc. |
Imidazopyridazine inhibitors of PI3 kinase for cancer treatment
|
AU2008345681A1
(en)
|
2007-12-21 |
2009-07-09 |
Wyeth Llc |
Imidazo [1,2-a] pyridine compounds
|
JP2011507910A
(ja)
|
2007-12-21 |
2011-03-10 |
ユニバーシティー オブ ロチェスター |
真核生物の寿命を変更するための方法
|
WO2009081105A2
(fr)
|
2007-12-21 |
2009-07-02 |
Ucb Pharma S.A. |
Dérivés de quinoxaline et de quinoléine en tant qu'inhibiteurs de kinase
|
WO2009082845A1
(fr)
|
2007-12-28 |
2009-07-09 |
Topharman Shanghai Co., Ltd. |
N-{1-[3-(2-éthoxy-5-(4-éthylpipérazinyl)benzènesulfonyl)-4,5-dihydro-5-oxo-1,2,4-triazin-6-yl]éthyl}butyramide, son procédé de préparation et son utilisation
|
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
|
US8193182B2
(en)
|
2008-01-04 |
2012-06-05 |
Intellikine, Inc. |
Substituted isoquinolin-1(2H)-ones, and methods of use thereof
|
NZ586642A
(en)
|
2008-01-11 |
2012-04-27 |
Natco Pharma Ltd |
Novel pyrazolo [3, 4 -d] pyrimidine derivatives as anti -cancer agents
|
US9089572B2
(en)
|
2008-01-17 |
2015-07-28 |
California Institute Of Technology |
Inhibitors of p97
|
US8987280B2
(en)
|
2008-01-30 |
2015-03-24 |
Genentech, Inc. |
Pyrazolopyrimidine PI3K inhibitor compounds and methods of use
|
WO2009128520A1
(fr)
|
2008-04-18 |
2009-10-22 |
塩野義製薬株式会社 |
Composé hétérocyclique présentant une activité inhibitrice sur p13k
|
US8119647B2
(en)
|
2008-04-23 |
2012-02-21 |
Glenmark Pharmaceuticals S.A. |
Fused pyrimidineone compounds as TRPV3 modulators
|
WO2009140215A2
(fr)
|
2008-05-11 |
2009-11-19 |
Geraghty, Erin |
Procédé pour traiter des infections bactériennes résistant au médicament et d'autres infections par du clioquinol, de la phanquinone et des composés apparentés
|
WO2009151972A1
(fr)
|
2008-05-28 |
2009-12-17 |
, The United States Of America, As Represented By The Secretary Of The Army, On Behalf Of U.S. Army Medical Research And Materiel Command |
Inhibiteurs à petites molécules de neurotoxines botuliniques
|
WO2010008739A2
(fr)
|
2008-06-20 |
2010-01-21 |
Metabolex, Inc. |
Agonistes des récepteurs gpr119 aryles et utilisations associées
|
US8026271B2
(en)
|
2008-07-11 |
2011-09-27 |
National Health Research Institutes |
Formulations of indol-3-yl-2-oxoacetamide compounds
|
WO2010018458A2
(fr)
|
2008-08-12 |
2010-02-18 |
Crystalgenomics, Inc. |
Dérivés de phénol et leurs procédés d'utilisation
|
WO2010036380A1
(fr)
|
2008-09-26 |
2010-04-01 |
Intellikine, Inc. |
Inhibiteurs hétérocycliques de kinases
|
ES2674719T3
(es)
|
2008-11-13 |
2018-07-03 |
Gilead Calistoga Llc |
Terapias para neoplasias hematológicas
|
WO2010075068A1
(fr)
|
2008-12-16 |
2010-07-01 |
Schering Corporation |
Dérivés de pyridopyrimidine et leurs procédés d'utilisation
|
CN105399731A
(zh)
|
2008-12-24 |
2016-03-16 |
比亚尔-珀特拉和Ca股份公司 |
药物化合物
|
EP2387575B1
(fr)
|
2009-01-15 |
2013-09-04 |
Anvyl, LLC |
Modulateurs allostériques des récepteurs nicotiniques de l'acétylcholine de type alpha7, leurs dérivés et leurs utilisations
|
ES2598358T3
(es)
|
2009-02-13 |
2017-01-27 |
Ucb Pharma, S.A. |
Derivados de quinolina como inhibidores de PI3K quinasa
|
WO2010114900A1
(fr)
|
2009-03-31 |
2010-10-07 |
Arqule, Inc. |
Composés indolo-pipéridine substitués
|
WO2010118367A2
(fr)
|
2009-04-10 |
2010-10-14 |
Progenics Pharmaceuticals, Inc. |
Pyrimidines antivirales
|
CN102458410A
(zh)
|
2009-04-20 |
2012-05-16 |
吉联亚·卡利斯托加有限责任公司 |
治疗实体瘤的方法
|
WO2010127208A1
(fr)
|
2009-04-30 |
2010-11-04 |
Forest Laboratories Holdings Limited |
Inhibiteurs de l'acétyl-coa carboxylase
|
EP2427195B1
(fr)
|
2009-05-07 |
2019-05-01 |
Intellikine, LLC |
Composés hétérocycliques et leurs utilisations
|
BRPI1012159B1
(pt)
|
2009-05-22 |
2022-01-25 |
Incyte Holdings Corporation |
Compostos derivados de n-(hetero)aril-pirrolidina de pirazol-4-il-pirrolo[2,3-d] pirimidinas e pirrol-3-il-pirrolo[2,3-d] pirimidinas como inibidores de janus cinase, composições farmacêuticas compreendendo os referidos compostos e usos dos mesmos
|
TW201111362A
(en)
|
2009-06-25 |
2011-04-01 |
Amgen Inc |
Heterocyclic compounds and their uses
|
MX2011013901A
(es)
|
2009-06-25 |
2012-05-08 |
Amgen Inc |
Derivados de 4h-pirido [1,2-a] pirimidin-4-ona 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
|
ME01838B
(me)
|
2009-06-29 |
2014-12-20 |
Lncyte Holdings Corp |
Pirimidinoni kao inhibitori pi3k
|
FR2947269B1
(fr)
|
2009-06-29 |
2013-01-18 |
Sanofi Aventis |
Nouveaux composes anticancereux
|
NZ597379A
(en)
|
2009-06-29 |
2014-04-30 |
Agios Pharmaceuticals Inc |
Therapeutic compounds and compositions
|
CN102647987A
(zh)
|
2009-07-21 |
2012-08-22 |
吉里德卡利斯托加公司 |
使用pi3k抑制剂治疗肝脏障碍
|
AR077974A1
(es)
|
2009-08-28 |
2011-10-05 |
Takeda Pharmaceutical |
Compuestos de hexahidrooxazinopterina para uso como inhibidores de mtor
|
TW201113285A
(en)
|
2009-09-01 |
2011-04-16 |
Incyte Corp |
Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors
|
CA2775009A1
(fr)
|
2009-10-20 |
2011-04-28 |
Cellzome Limited |
Analogues d'heterocyclyl pyrazolopyrimidine en tant qu'inhibiteurs de jak
|
SI2491035T1
(sl)
|
2009-10-22 |
2017-10-30 |
Gilead Sciences, Inc. |
Derivati purina ali deazapurina uporabni za zdravljenje (med drugimi) virusnih okužb
|
DK2496567T3
(en)
|
2009-11-05 |
2017-10-30 |
Rhizen Pharmaceuticals S A |
PRESENT UNKNOWN BENZOPYRANKINA MODULATORS
|
ES2444543T3
(es)
|
2009-11-10 |
2014-02-25 |
Pfizer Inc |
Inhibidores de la N1-pirazoloespirocetona acetil-CoA carboxilasa
|
WO2011058111A1
(fr)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Dérivés d'aminopurine en tant qu'inhibiteurs de kinase
|
WO2011058113A1
(fr)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Dérivés de pyridine et de pyrazine bicycliques condensés comme inhibiteurs de kinases
|
EP2511283A4
(fr)
|
2009-12-10 |
2013-07-03 |
Inst Materia Medica Cams |
Dérivés d'adénosine à substitution n6, dérivés d'adénine à substitution n6 et leurs utilisations
|
US8759359B2
(en)
|
2009-12-18 |
2014-06-24 |
Incyte Corporation |
Substituted heteroaryl fused derivatives as PI3K inhibitors
|
CA2784566A1
(fr)
|
2009-12-18 |
2011-06-23 |
Amgen Inc. |
Composes heterocycliques et leurs utilisations
|
AR079529A1
(es)
|
2009-12-18 |
2012-02-01 |
Incyte Corp |
Derivados arilo y heteroarilo sustituidos y fundidos como inhibidores de la pi3k
|
JP2011136925A
(ja)
|
2009-12-28 |
2011-07-14 |
Dainippon Sumitomo Pharma Co Ltd |
含窒素二環性化合物
|
IN2012DN06323A
(fr)
|
2010-01-07 |
2015-10-02 |
Dow Agrosciences Llc |
|
UY33199A
(es)
|
2010-01-26 |
2011-08-31 |
Boehringer Ingelheim Int |
5-alquinil-pirimidinas.
|
KR20220015492A
(ko)
|
2010-03-10 |
2022-02-08 |
인사이트 홀딩스 코포레이션 |
Jak1 저해제로서의 피페리딘4일 아제티딘 유도체
|
MA34075B1
(fr)
|
2010-03-22 |
2013-03-05 |
Glenmark Pharmaceuticals Sa |
Composition pharmaceutique comprenant un dérivé pyrimidineone
|
UY33304A
(es)
|
2010-04-02 |
2011-10-31 |
Amgen Inc |
Compuestos heterocíclicos y sus usos
|
EP2558463A1
(fr)
|
2010-04-14 |
2013-02-20 |
Incyte Corporation |
Dérivés condensés en tant qu'inhibiteurs de i3
|
CN103002738A
(zh)
|
2010-05-21 |
2013-03-27 |
英特利凯恩有限责任公司 |
用于激酶调节的化学化合物、组合物和方法
|
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
|
JP2013530238A
(ja)
|
2010-07-01 |
2013-07-25 |
アムジエン・インコーポレーテツド |
Pi3k活性の阻害剤としての複素環化合物及びその使用
|
MX2012014996A
(es)
|
2010-07-01 |
2013-03-21 |
Amgen Inc |
Compuestos heterociclicos y su uso como inhibidores de la actividad pi3k.
|
WO2012003271A1
(fr)
|
2010-07-02 |
2012-01-05 |
Amgen Inc. |
Composés hétérocycliques et leur utilisation comme inhibiteurs de l'activité pi3k
|
EP2619209A1
(fr)
|
2010-09-24 |
2013-07-31 |
Gilead Calistoga LLC |
Atropisomères de composés inhibiteur de pi3k
|
MX2013005005A
(es)
|
2010-11-04 |
2013-10-25 |
Amgen Inc |
Derivados de ciano-4,6-diaminopirimidina o 6-aminopurina como inhibidores de pi3k-delta.
|
AU2011326427B2
(en)
|
2010-11-10 |
2016-01-07 |
Infinity Pharmaceuticals Inc. |
Heterocyclic compounds and uses thereof
|
AU2011329806A1
(en)
|
2010-11-17 |
2013-05-30 |
Amgen Inc. |
Quinoline derivatives as PIK3 inhibitors
|
CA2818542A1
(fr)
|
2010-11-19 |
2012-05-24 |
Incyte Corporation |
Derives pyrrolopyridine et pyrrolopyrimidine a substitution cyclobutyle utilises comme inhibiteurs des jak
|
ES2536415T3
(es)
|
2010-11-19 |
2015-05-25 |
Incyte Corporation |
Pirrolopiridinas y pirrolopirimidinas sustituidas heterocíclicas como inhibidores de JAK
|
JP2014503528A
(ja)
|
2010-12-14 |
2014-02-13 |
エレクトロプホレトイクス リミテッド |
カゼインキナーゼ1δ(CK1δ)阻害剤及びタウオパチーなどの神経変性疾患の治療におけるその使用
|
EP2655374B1
(fr)
|
2010-12-20 |
2019-10-23 |
Incyte Holdings Corporation |
N-(1-(phényl substitué)éthyl)-9h-purin-6-amines en tant qu'inhibiteurs de pi3k
|
MX2013007261A
(es)
|
2010-12-23 |
2013-11-04 |
Amgen Inc |
Compuestos heterociclicos y sus usos.
|
BR112013017670B1
(pt)
|
2011-01-10 |
2022-07-19 |
Infinity Pharmaceuticals, Inc |
Processos de preparação de isoquinolinonas e formas sólidas de isoquinolinonas
|
USRE47009E1
(en)
|
2011-02-01 |
2018-08-28 |
The Children's Hospital Of Philadelphia |
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
|
WO2012135009A1
(fr)
|
2011-03-25 |
2012-10-04 |
Incyte Corporation |
Dérivés de pyrimidine-4,6-diamine en tant qu'inhibiteurs de pi3k
|
EP2721028B1
(fr)
|
2011-06-20 |
2015-11-04 |
Incyte Corporation |
Dérivés d'azétidinyl-phényl-, de pyridyl- ou de pyrazinyl-carboxamide en tant qu'inhibiteurs des jak
|
WO2013012915A1
(fr)
|
2011-07-19 |
2013-01-24 |
Infinity Pharmaceuticals Inc. |
Composés hétérocycliques et leurs utilisations
|
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
|
KR102371532B1
(ko)
|
2011-09-02 |
2022-03-07 |
인사이트 홀딩스 코포레이션 |
Pi3k 억제제로서 헤테로시클릴아민
|
WO2013052699A2
(fr)
|
2011-10-04 |
2013-04-11 |
Gilead Calistoga Llc |
Nouveaux inhibiteurs de quinoxaline de la voie pi3k
|
AR090548A1
(es)
|
2012-04-02 |
2014-11-19 |
Incyte Corp |
Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
|
WO2013173720A1
(fr)
|
2012-05-18 |
2013-11-21 |
Incyte Corporation |
Dérivés de pyrrolopyridine et de pyrrolopyrimidine substitués par un pipéridinylcyclobutyle à titre d'inhibiteurs jak
|
NZ707495A
(en)
|
2012-11-01 |
2019-01-25 |
Incyte Holdings Corp |
Tricyclic fused thiophene derivatives as jak inhibitors
|
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
|
EP2970291B1
(fr)
*
|
2013-03-15 |
2022-05-11 |
Janssen Pharmaceutica, N.V. |
Procédés et intermédiaires pour la préparation d'un médicament
|
HUE033587T2
(hu)
|
2013-05-17 |
2017-12-28 |
Incyte Corp |
Bipirazol-származékok mint JAK inhibitorok
|
CA3158254C
(fr)
|
2014-04-08 |
2024-05-21 |
Incyte Corporation |
Traitement des malignites de cellules b par une combinaison d'inhibiteurs de jak et de pi3k
|
CA2941429A1
(fr)
|
2014-05-27 |
2015-12-03 |
Almirall, S.A. |
Usage medical
|
US10077277B2
(en)
|
2014-06-11 |
2018-09-18 |
Incyte Corporation |
Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors
|
TWI770525B
(zh)
|
2014-12-30 |
2022-07-11 |
美商瓦洛健康公司 |
作為泛素特異性蛋白酶7抑制劑之吡咯并及吡唑并嘧啶
|
NZ734993A
(en)
|
2015-02-27 |
2024-03-22 |
Incyte Holdings 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
|
US9732097B2
(en)
|
2015-05-11 |
2017-08-15 |
Incyte Corporation |
Process for the synthesis of a phosphoinositide 3-kinase inhibitor
|
WO2016183062A1
(fr)
|
2015-05-11 |
2016-11-17 |
Incyte Corporation |
Sels de (s)-7-(1-(9h-purin-6-ylamino)éthyl)-6-(3-fluorophényl)-3-méthyl-5h-thiazolo[3,2-a]pyrimidin-5-one
|
MA52761A
(fr)
|
2018-06-01 |
2021-04-14 |
Incyte Corp |
Schéma posologique destiné au traitement de troubles liés à la pi3k
|