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
|
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
(it)
|
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
(it)
|
1974-02-21 |
1975-09-10 |
|
|
JPS5625234Y2
(it)
|
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
(it)
|
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
|
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
(it)
|
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
(it)
|
1985-10-17 |
1988-02-17 |
|
|
JPS62103640U
(it)
|
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
|
JPS6427257U
(it)
|
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
|
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
|
JPH054831Y2
(it)
|
1988-11-22 |
1993-02-08 |
|
|
JPH07107055B1
(it)
|
1990-04-25 |
1995-11-15 |
|
|
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
|
DE69129389T2
(de)
|
1990-06-28 |
1998-10-08 |
Fuji Photo Film Co Ltd |
Photographische Silberhalogenidmaterialien
|
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
|
AU3933493A
(en)
|
1992-04-24 |
1993-11-29 |
E.I. Du Pont De Nemours And Company |
Arthropodicidal and fungicidal aminopyrimidines
|
TW229140B
(it)
|
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
|
JP4373497B2
(ja)
|
1996-06-19 |
2009-11-25 |
ローン−プーラン・ロレ・リミテツド |
置換されたアザビシクロ化合物、ならびにtnfおよびサイクリックampホスホジエステラーゼ産生の阻害剤としてのそれらの使用
|
CA2230808C
(en)
|
1996-07-03 |
2006-08-15 |
Japan Energy Corporation |
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
|
DE69824632T2
(de)
|
1997-11-12 |
2005-06-09 |
Mitsubishi Chemical Corp. |
Purinderivate und medikamente, welche dieselben als aktiven bestandteil enthalten
|
TW572758B
(en)
|
1997-12-22 |
2004-01-21 |
Sumitomo Pharma |
Type 2 helper T cell-selective immune response inhibitors comprising purine derivatives
|
PL342516A1
(en)
|
1998-02-25 |
2001-06-18 |
Genetics Inst |
Phospholipase a2 inhibitors
|
US6828344B1
(en)
|
1998-02-25 |
2004-12-07 |
Genetics Institute, Llc |
Inhibitors of phospholipase enzymes
|
CN1299347A
(zh)
|
1998-02-25 |
2001-06-13 |
遗传研究所有限公司 |
磷脂酶抑制剂
|
US6479487B1
(en)
|
1998-02-26 |
2002-11-12 |
Aventis Pharmaceuticals Inc. |
6, 9-disubstituted 2-[trans-(4-aminocyclohexyl)amino] purines
|
IL139056A0
(en)
|
1998-05-04 |
2001-11-25 |
Asta Medica Ag |
Indole derivatives and their use in the treatment of malignant and other diseases caused by pathological cell proliferation
|
AU3851199A
(en)
|
1998-05-26 |
1999-12-13 |
Chugai Seiyaku Kabushiki Kaisha |
Heterocyclic indole derivatives and mono- or diazaindole derivatives
|
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
|
BR9912938B1
(pt)
|
1998-08-11 |
2011-06-28 |
|
derivados de isoquinolina, composição que os compreende, processo para preparação e uso dos mesmos.
|
DE69913712T2
(de)
|
1998-08-25 |
2004-10-07 |
Uab Res Foundation Birmingham |
Inhibitoren der bakteriellen nad synthetase
|
US6133031A
(en)
|
1999-08-19 |
2000-10-17 |
Isis Pharmaceuticals Inc. |
Antisense inhibition of focal adhesion kinase expression
|
UA74142C2
(uk)
|
1999-02-01 |
2005-11-15 |
Сіві Серапьютікс, Інк. |
ПУРИНОВІ ІНГІБІТОРИ ЦИКЛІНОЗАЛЕЖНОЇ КІНАЗИ 2 ТА Ik-<font face="Symbol">a</font>
|
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
|
MXPA03000051A
(es)
|
2000-06-28 |
2003-08-19 |
Smithkline Beecham Plc |
Procedimiento de molido en humedo.
|
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
|
DE60118564T2
(de)
|
2000-07-05 |
2007-01-18 |
Astellas Pharma Inc. |
Propan-1,3-dion-derivate
|
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
|
EP1375486B1
(en)
|
2001-03-01 |
2008-10-15 |
Shionogi & Co., Ltd. |
Nitrogen-containing heteroaryl compounds having hiv integrase inhibitory activity
|
UA76977C2
(en)
|
2001-03-02 |
2006-10-16 |
Icos Corp |
Aryl- and heteroaryl substituted chk1 inhibitors and their use as radiosensitizers and chemosensitizers
|
WO2002078700A1
(en)
|
2001-03-30 |
2002-10-10 |
Smithkline Beecham Corporation |
Pyralopyridines, process for their preparation and use as therapteutic compounds
|
US20050107400A1
(en)
|
2001-03-30 |
2005-05-19 |
Boyd Leslie F. |
Use of pyrazolopyridines as therapeutic compounds
|
DE60204452T2
(de)
|
2001-04-27 |
2005-12-15 |
Smithkline Beecham Corp. |
Pyrazolo[1,5a]Pyridinderivate
|
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
|
IL160915A0
(en)
|
2001-09-19 |
2004-08-31 |
Aventis Pharma Sa |
Indolizines inhibiting kinase proteins
|
MXPA04002035A
(es)
|
2001-09-26 |
2004-06-07 |
Bayer Pharmaceuticals Corp |
Derivados de 1, 8-naftiridina y su uso para el tratamiento de la diabetes y trastornos relacionados.
|
EP1432714B1
(en)
|
2001-10-02 |
2008-08-06 |
Smithkline Beecham Corporation |
Chemical compounds
|
KR100926194B1
(ko)
|
2001-10-30 |
2009-11-09 |
노파르티스 아게 |
Flt3 수용체 티로신 키나아제 활성의 억제제로서의스타우로스포린 유도체
|
US7262164B2
(en)
|
2001-11-09 |
2007-08-28 |
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
|
US20050107404A1
(en)
|
2001-12-06 |
2005-05-19 |
Fraley Mark E. |
Mitotic kinesin inhibitors
|
ES2291543T3
(es)
|
2001-12-06 |
2008-03-01 |
MERCK & CO., INC. |
Inhibicion de kinesina mitotica.
|
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
|
US7402595B2
(en)
|
2002-02-13 |
2008-07-22 |
Takeda Pharmaceutical Company Limited |
JNK inhibitor
|
WO2003074497A1
(en)
|
2002-03-01 |
2003-09-12 |
Pintex Pharmaceutical, Inc. |
Pin1-modulating compounds and methods of use thereof
|
DE60315615T2
(de)
|
2002-04-03 |
2008-10-02 |
Bristol-Myers Squibb Co. |
Tricyclische verbindungen basierend auf thiophen und arzneimittel, die diese umfassen
|
EP1501850A2
(en)
|
2002-05-06 |
2005-02-02 |
Genelabs Technologies, 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
|
NZ539064A
(en)
|
2002-09-27 |
2007-09-28 |
Dainippon Sumitomo Pharma Co |
Novel adenine compound and use thereof
|
AR042052A1
(es)
|
2002-11-15 |
2005-06-08 |
Vertex Pharma |
Diaminotriazoles utiles como inhibidores de proteinquinasas
|
AU2003295776B2
(en)
|
2002-11-21 |
2011-05-12 |
Novartis Vaccines And Diagnostics, Inc. |
2,4,6-trisubstituted pyrimidines as phosphotidylinositol (PI) 3-kinase inhibitors and their use in the treatment of cancer
|
AU2003302416A1
(en)
|
2002-11-25 |
2004-06-18 |
Mochida Pharmaceutical Co., Ltd. |
Therapeutic agent for respiratory disease 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
|
AU2003292625B2
(en)
|
2002-12-26 |
2008-07-24 |
Eisai R & D Management Co., Ltd. |
Selective estrogen receptor modulators
|
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
|
AR043692A1
(es)
|
2003-02-06 |
2005-08-10 |
Novartis Ag |
2-cianopirrolopirimidinas y sus usos farmaceuticos
|
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
|
EP1619948A4
(en)
|
2003-05-05 |
2007-02-14 |
Neurogen Corp |
SUBSTITUTED 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
|
CA2535620A1
(en)
|
2003-08-15 |
2005-02-24 |
Irm Llc |
6-substituted anilino purines as rtk inhibitors
|
EP1670802A4
(en)
|
2003-09-18 |
2010-07-07 |
Conforma Therapeutics Corp |
NOVEL HETEROCYCLIC COMPOUNDS AS INHIBITORS OF HSP90 PROTEIN
|
US7709476B2
(en)
|
2003-09-23 |
2010-05-04 |
Merck Sharp & Dohme Corp. |
Isoquinolinone potassium channel inhibitors
|
AR045944A1
(es)
|
2003-09-24 |
2005-11-16 |
Novartis Ag |
Derivados de isoquinolina 1.4-disustituidas
|
CA2553724A1
(en)
|
2004-02-03 |
2005-08-18 |
Abbott Laboratories |
Aminobenzoxazoles as therapeutic agents
|
JPWO2005077948A1
(ja)
|
2004-02-16 |
2008-01-10 |
第一製薬株式会社 |
抗真菌作用複素環化合物
|
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
|
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
|
US20070225303A1
(en)
|
2004-03-26 |
2007-09-27 |
Haruhisa Ogita |
8-Oxoadenine Compound
|
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
|
EP2612862B1
(en)
|
2004-05-13 |
2016-09-14 |
Icos Corporation |
Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta
|
US20060074102A1
(en)
|
2004-05-14 |
2006-04-06 |
Kevin Cusack |
Kinase inhibitors as therapeutic agents
|
KR20070044458A
(ko)
|
2004-07-22 |
2007-04-27 |
아스트라제네카 아베 |
암의 예방 및 치료에 유용한 융합 피리미돈
|
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
(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
|
EP1831225A2
(en)
|
2004-11-19 |
2007-09-12 |
The Regents of the University of California |
Anti-inflammatory pyrazolopyrimidines
|
RU2007123675A
(ru)
|
2004-11-24 |
2008-12-27 |
Новартис АГ (CH) |
Комбинации ингибиторов jak
|
CA2598409A1
(en)
|
2005-02-17 |
2006-08-24 |
Icos Corporation |
Phosphoinositide 3-kinase inhibitors for inhibiting leukocyte accumulation
|
CA2612585A1
(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
|
BRPI0614801A2
(pt)
|
2005-08-16 |
2009-05-19 |
Genzyme Corp |
compostos de ligação a receptor de quimiocina
|
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
|
JPWO2007034817A1
(ja)
|
2005-09-22 |
2009-03-26 |
大日本住友製薬株式会社 |
新規アデニン化合物
|
GB0520657D0
(en)
*
|
2005-10-11 |
2005-11-16 |
Ludwig Inst Cancer Res |
Pharmaceutical compounds
|
BR122021011788B1
(pt)
|
2005-11-01 |
2022-01-25 |
Impact Biomedicines, Inc |
Inibidores de biaril meta pirimidina de cinases, composição farmacêutica e processo para preparar uma composição farmacêutica
|
EP1783114A1
(en)
|
2005-11-03 |
2007-05-09 |
Novartis AG |
N-(hetero)aryl indole derivatives as pesticides
|
DK1954274T3
(da)
|
2005-11-10 |
2011-01-31 |
Chemocentryx Inc |
Substituerede quinoloner og fremgangsmåder til anvendelse
|
ES2373688T3
(es)
|
2005-12-13 |
2012-02-07 |
Incyte Corporation |
Pirrolo[2,3-b]piridinas y pirrolo[2,3-b]pirimidinas sustituidas con heteroarilo como inhibidores de quinasas janus.
|
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)
|
WO2007102392A1
(ja)
|
2006-03-03 |
2007-09-13 |
Shionogi & Co., Ltd. |
Mmp-13選択的阻害剤
|
BRPI0709699A2
(pt)
|
2006-03-29 |
2011-07-26 |
Foldrx Pharmaceuticals Inc |
inibiÇço da toxidez da alfa-sinucleina
|
AU2007233302C1
(en)
*
|
2006-04-04 |
2013-06-06 |
The Regents Of The University Of California |
Kinase antagonists
|
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
|
EP2037905B1
(en)
|
2006-06-23 |
2013-05-01 |
Radius Health, Inc. |
Treatment of vasomotor symptoms with selective estrogen receptor modulators
|
WO2008005303A2
(en)
|
2006-06-30 |
2008-01-10 |
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
|
AU2007272009A1
(en)
|
2006-07-12 |
2008-01-17 |
Syngenta Limited |
Triazolopyridine derivatives as herbicides
|
HUE035116T2
(hu)
|
2006-08-08 |
2018-05-02 |
Chugai Pharmaceutical Co Ltd |
PI3K inhibitor pirimidinszármazékok és alkalmazásuk
|
WO2008025821A1
(en)
|
2006-08-30 |
2008-03-06 |
Cellzome Limited |
Triazole derivatives as kinase inhibitors
|
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
|
RS57741B1
(sr)
|
2006-11-22 |
2018-12-31 |
Incyte Holdings Corp |
Imidazotriazini i imidazopirimidini kao inhibitori kinaze
|
CA2672960A1
(en)
|
2006-12-20 |
2008-07-10 |
Schering Corporation |
Novel jnk inhibitors
|
WO2008080844A1
(en)
|
2006-12-29 |
2008-07-10 |
F. Hoffmann-La Roche Ag |
Azaspiro derivatives
|
JP2010518026A
(ja)
|
2007-02-05 |
2010-05-27 |
ゼノン・ファーマシューティカルズ・インコーポレイテッド |
ナトリウムチャネルが介在する疾患または状態の治療に有用なピリドピリミジノン化合物
|
MX2009008439A
(es)
|
2007-02-12 |
2009-08-13 |
Intermune Inc |
Nuevos inhibidores de la replicacion del virus de hepatitis c.
|
TW200902018A
(en)
|
2007-03-20 |
2009-01-16 |
Dainippon Sumitomo Pharma Co |
Novel adenine compound
|
US20080233127A1
(en)
|
2007-03-21 |
2008-09-25 |
Wyeth |
Imidazolopyrimidine analogs and their use as pi3 kinase and mtor inhibitors
|
EP2132207A2
(en)
|
2007-03-23 |
2009-12-16 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
CA2681136C
(en)
|
2007-03-23 |
2012-05-22 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
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
|
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
|
WO2009005687A1
(en)
|
2007-06-29 |
2009-01-08 |
Gilead Sciences, Inc. |
Purine derivatives and their use as modulators of toll-like receptor 7
|
WO2009042294A2
(en)
|
2007-08-10 |
2009-04-02 |
Burnham Institute For Medical Research |
Tissue-nonspecific alkaline phosphatase (tnap) activators and uses thereof
|
WO2009026701A1
(en)
|
2007-08-29 |
2009-03-05 |
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
|
US20100331297A1
(en)
|
2007-11-07 |
2010-12-30 |
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
|
WO2009081105A2
(en)
|
2007-12-21 |
2009-07-02 |
Ucb Pharma S.A. |
Quinoxaline and quinoline derivatives as kinase inhibitors
|
AU2008345225A1
(en)
|
2007-12-21 |
2009-07-09 |
University Of Rochester |
Method for altering the lifespan of eukaryotic organisms
|
AU2008345681A1
(en)
|
2007-12-21 |
2009-07-09 |
Wyeth Llc |
Imidazo [1,2-a] pyridine compounds
|
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
|
US8410098B2
(en)
|
2007-12-28 |
2013-04-02 |
Topharman Shanghai Co., Ltd. |
N-{1-[3-(2-ethoxy-5-(4-ethylpiperazinyl)sulfonylphenyl)-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
|
KR20100116607A
(ko)
|
2008-01-11 |
2010-11-01 |
낫코 파마 리미티드 |
항암제로서의 신규한 피라졸로[3,4-d]피리미딘 유도체
|
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
|
EP2444403A1
(en)
|
2008-04-18 |
2012-04-25 |
Shionogi Co., Ltd. |
Heterocyclic compound having inhibitory activity on PI3K
|
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
|
EP2300005A4
(en)
|
2008-05-28 |
2011-07-13 |
Us Of America As Represented By The Secretary Of The Army On Behalf Of U S Army Medical Res And Mate |
Small-molecule inhibitors of botulinum neurotoxins
|
KR20110026481A
(ko)
|
2008-06-20 |
2011-03-15 |
메타볼렉스, 인코포레이티드 |
아릴 gpr119 작동약 및 이의 용도
|
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
|
CA2738429C
(en)
*
|
2008-09-26 |
2016-10-25 |
Intellikine, Inc. |
Heterocyclic kinase inhibitors
|
NZ611764A
(en)
|
2008-11-13 |
2015-01-30 |
Gilead Calistoga Llc |
Therapies for hematologic malignancies
|
US20110245209A1
(en)
|
2008-12-16 |
2011-10-06 |
Schering Corporation |
Pyridopyrimidine derivatives and methods of use thereof
|
EP2382012A2
(en)
|
2008-12-24 |
2011-11-02 |
Bial-Portela & CA, S.A. |
Pharmaceutical compounds
|
US8563579B2
(en)
|
2009-01-15 |
2013-10-22 |
Anvyl Llc |
α-7 nicotinic acetylcholine receptor allosteric modulators, their derivatives and uses thereof
|
EP2396315B1
(en)
|
2009-02-13 |
2016-08-31 |
UCB Biopharma SPRL |
Quinoline derivatives as pi3k kinase inhibitors
|
TW201100428A
(en)
|
2009-03-31 |
2011-01-01 |
Arqule Inc |
Substituted indolo-piperidine compounds
|
WO2010118367A2
(en)
|
2009-04-10 |
2010-10-14 |
Progenics Pharmaceuticals, Inc. |
Antiviral pyrimidines
|
SG175259A1
(en)
|
2009-04-20 |
2011-11-28 |
Gilead Calistoga Llc |
Methods of treatment for solid tumors
|
WO2010127208A1
(en)
|
2009-04-30 |
2010-11-04 |
Forest Laboratories Holdings Limited |
Inhibitors of acetyl-coa carboxylase
|
JP5789252B2
(ja)
|
2009-05-07 |
2015-10-07 |
インテリカイン, エルエルシー |
複素環式化合物およびその使用
|
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
|
WO2010151735A2
(en)
|
2009-06-25 |
2010-12-29 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
EP2445900B1
(en)
*
|
2009-06-25 |
2016-03-02 |
Amgen, Inc |
Polycyclic derivatives of pyridine and their use in the treatment of (inter alia) rheumatoid arthritis and similar diseases
|
PL2448938T3
(pl)
|
2009-06-29 |
2014-11-28 |
Incyte Holdings Corp |
Pirymidynony jako inhibitory PI3K
|
KR101712035B1
(ko)
|
2009-06-29 |
2017-03-03 |
아지오스 파마슈티컬스 아이엔씨. |
치료용 화합물 및 조성물
|
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
|
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
|
ES2432315T3
(es)
|
2009-08-28 |
2013-12-02 |
Takeda Pharmaceutical Company Limited |
Compuestos de hexahidrooxazinopterina para su uso como inhibidores de mTOR
|
WO2011028685A1
(en)
|
2009-09-01 |
2011-03-10 |
Incyte Corporation |
Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors
|
WO2011048082A1
(en)
|
2009-10-20 |
2011-04-28 |
Cellzome Limited |
Heterocyclyl pyrazolopyrimidine analogues as jak inhibitors
|
AP3103A
(en)
|
2009-10-22 |
2015-01-31 |
Gilead Sciences Inc |
Derivatives of purine or deazapurine useful for the treatment of (inter alia)viral infections
|
CN102812013B
(zh)
|
2009-11-05 |
2016-05-25 |
理森制药股份公司 |
新型苯并吡喃激酶调节剂
|
JP5114610B1
(ja)
|
2009-11-10 |
2013-01-09 |
ファイザー・インク |
N1−ピラゾロスピロケトンアセチル−CoAカルボキシラーゼ阻害薬
|
WO2011058111A1
(en)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Aminopurine derivatives as kinase inhibitors
|
WO2011058113A1
(en)
|
2009-11-12 |
2011-05-19 |
Ucb Pharma S.A. |
Fused bicyclic pyridine and pyrazine derivatives as kinase inhibitors
|
EP2511283A4
(en)
|
2009-12-10 |
2013-07-03 |
Inst Materia Medica Cams |
N6-SUBSTITUTED ADENOSINE DERIVATIVES, N6-SUBSTITUTED ADENINE DERIVATIVES AND THEIR USE
|
AU2010330875B2
(en)
|
2009-12-18 |
2013-08-01 |
Amgen Inc. |
Heterocyclic compounds and their uses
|
US8759359B2
(en)
|
2009-12-18 |
2014-06-24 |
Incyte Corporation |
Substituted heteroaryl fused derivatives as PI3K inhibitors
|
TW201130842A
(en)
|
2009-12-18 |
2011-09-16 |
Incyte Corp |
Substituted fused aryl and heteroaryl derivatives as PI3K inhibitors
|
RU2573828C2
(ru)
*
|
2009-12-23 |
2016-01-27 |
Медисиз Фармасьютикал Корпорейшн |
Производные аминоалкилпиримидина в качестве антагонистов h4 рецептора гистамина
|
JP2011136925A
(ja)
|
2009-12-28 |
2011-07-14 |
Dainippon Sumitomo Pharma Co Ltd |
含窒素二環性化合物
|
IN2012DN06323A
(it)
|
2010-01-07 |
2015-10-02 |
Dow Agrosciences Llc |
|
US8633183B2
(en)
|
2010-01-26 |
2014-01-21 |
Boehringer Ingelheim International Gmbh |
5-alkynyl-pyrimidines
|
TWI592413B
(zh)
|
2010-03-10 |
2017-07-21 |
英塞特公司 |
作為jak1抑制劑之哌啶-4-基三亞甲亞胺衍生物
|
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
|
ME02445B
(me)
|
2010-05-21 |
2016-09-20 |
Incyte Holdings Corp |
Topikalna formulacija za inhibiciju jak-a
|
AU2011255218B2
(en)
|
2010-05-21 |
2015-03-12 |
Infinity Pharmaceuticals, Inc. |
Chemical compounds, compositions and methods for kinase modulation
|
CA2802484A1
(en)
|
2010-06-11 |
2011-12-15 |
Gilead Calistoga Llc |
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
|
EP2588468B1
(en)
|
2010-07-01 |
2014-03-26 |
Amgen Inc. |
Heterocyclic compounds and their use as inhibitors of pi3k activity
|
CA2803009A1
(en)
|
2010-07-01 |
2012-01-05 |
Amgen Inc. |
Heterocyclic compounds and their use as inhibitors of pi3k activity
|
CA2803624A1
(en)
|
2010-07-02 |
2012-01-05 |
Jason A. Duquette |
Heterocyclic compounds and their use as inhibitors of pi3k activity
|
WO2012040634A1
(en)
|
2010-09-24 |
2012-03-29 |
Gilead Calistoga Llc |
Atropisomers of pi3k-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
|
WO2012068343A1
(en)
|
2010-11-17 |
2012-05-24 |
Amgen Inc. |
Quinoline derivatives as pik3 inhibitors
|
CA2818542A1
(en)
|
2010-11-19 |
2012-05-24 |
Incyte Corporation |
Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors
|
CA2818545C
(en)
|
2010-11-19 |
2019-04-16 |
Incyte Corporation |
Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors
|
EP2651404B1
(en)
|
2010-12-14 |
2015-10-14 |
Electrophoretics Limited |
Casein kinase 1delta (ck1delta) inhibitors
|
JP5961187B2
(ja)
|
2010-12-20 |
2016-08-02 |
インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation |
Pi3k阻害剤としてのn−(1−(置換フェニル)エチル)−9h−プリン−6−アミン
|
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
|
WO2012125629A1
(en)
|
2011-03-14 |
2012-09-20 |
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
|
MY165963A
(en)
|
2011-06-20 |
2018-05-18 |
Incyte Holdings Corp |
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
|
ES2616477T3
(es)
|
2011-09-02 |
2017-06-13 |
Incyte Holdings Corporation |
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
|
US9193733B2
(en)
|
2012-05-18 |
2015-11-24 |
Incyte Holdings Corporation |
Piperidinylcyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as JAK inhibitors
|
MX2015005428A
(es)
|
2012-11-01 |
2015-07-21 |
Incyte Corp |
Derivados triciclicos fusionados de tiofeno como inhibidores de la cinasa janus (jak).
|
TWI736135B
(zh)
|
2013-03-01 |
2021-08-11 |
美商英塞特控股公司 |
吡唑并嘧啶衍生物治療PI3Kδ相關病症之用途
|
SI2970291T1
(sl)
|
2013-03-15 |
2022-07-29 |
Janssen Pharmaceutica, N.V. |
Postopki in vmesne spojine za pripravo zdravila
|
AR096330A1
(es)
|
2013-05-17 |
2015-12-23 |
Incyte Corp |
Derivados del bipirazol como inhibidores jak
|
PL3129021T3
(pl)
|
2014-04-08 |
2021-05-31 |
Incyte Corporation |
Leczenie nowotworów złośliwych z komórek b za pomocą skojarzenia inhibitora jak i pi3k
|
BR112016024538A2
(pt)
|
2014-05-27 |
2017-08-15 |
Almirall Sa |
sais de adição de (s)-2-(1-(6-amino-5-cianopirimidin-4-ilamino)etil)-4-oxo-3-fenil-3,4-di-hidro¬pirrolo[1,2-f][1,2,4]triazina-5-carbonitrila
|
WO2015191677A1
(en)
|
2014-06-11 |
2015-12-17 |
Incyte Corporation |
Bicyclic heteroarylaminoalkyl phenyl derivatives as pi3k inhibitors
|
AR103297A1
(es)
|
2014-12-30 |
2017-05-03 |
Forma Therapeutics Inc |
Pirrolo y pirazolopirimidinas como inhibidores de la proteasa 7 específica de ubiquitina
|
PH12017501538B1
(en)
|
2015-02-27 |
2024-02-14 |
Incyte Holdings Corp |
Salts of p13k inhibitor and processes for their preparation
|
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
|
WO2016183063A1
(en)
|
2015-05-11 |
2016-11-17 |
Incyte Corporation |
Crystalline forms of a pi3k inhibitor
|
WO2016183060A1
(en)
|
2015-05-11 |
2016-11-17 |
Incyte Corporation |
Process for the synthesis of a phosphoinositide 3-kinase inhibitor
|
CA3101323A1
(en)
|
2018-06-01 |
2019-12-05 |
Incyte Corporation |
Dosing regimen for the treatment of pi3k related disorders
|
US20230190755A1
(en)
|
2021-12-16 |
2023-06-22 |
Incyte Corporation |
Topical formulations of PI3K-delta inhibitors
|