CZ303692B6
(cs)
|
1999-02-10 |
2013-03-13 |
Astrazeneca Ab |
Chinazolinové deriváty jako inhibitory angiogeneze
|
PE20010306A1
(es)
*
|
1999-07-02 |
2001-03-29 |
Agouron Pharma |
Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa
|
SK287882B6
(sk)
|
1999-12-24 |
2012-02-03 |
Aventis Pharma Limited |
Azaindoles derivatives, pharmaceutical composition containing thereof and their use
|
CA2399274A1
(en)
|
2000-02-07 |
2001-08-09 |
Mark E. Salvati |
3-aminopyrazole inhibitors of cyclin dependent kinases
|
US20040087798A1
(en)
*
|
2000-03-14 |
2004-05-06 |
Akira Yamada |
Novel amide compounds
|
ES2236217T3
(es)
|
2000-04-25 |
2005-07-16 |
Bristol-Myers Squibb Company |
Uso de 5.tio.,sulfinil- y sulfonilpirazolo 3,4-b)-piridinas como inhibidores de la quinasa dependiente de la ciclina.
|
BR0113057A
(pt)
|
2000-08-09 |
2003-07-08 |
Astrazeneca Ab |
Composto, processo para a preparação de um composto, composição farmacêutica, uso de um composto, e, método para produzir um efeito antiangiogênico e/ou efeito de redução da permeabilidade vascular em um animal de sangue quente em necessidade de tal tratamento
|
US7371765B2
(en)
|
2000-08-09 |
2008-05-13 |
Astrazeneca Ab |
Quinoline derivatives having VEGF inhibiting activity
|
WO2002018383A2
(en)
|
2000-09-01 |
2002-03-07 |
Chiron Corporation |
Aza heterocyclic derivatives and their therapeutic use
|
AP1666A
(en)
|
2000-09-11 |
2006-09-29 |
Chiron Corp |
Quinolinone derivatives as tyrosine kinase inhibitors.
|
AU9598601A
(en)
|
2000-10-20 |
2002-04-29 |
Eisai Co Ltd |
Nitrogenous aromatic ring compounds
|
TWI243164B
(en)
|
2001-02-13 |
2005-11-11 |
Aventis Pharma Gmbh |
Acylated indanyl amines and their use as pharmaceuticals
|
GB0115109D0
(en)
|
2001-06-21 |
2001-08-15 |
Aventis Pharma Ltd |
Chemical compounds
|
US7642278B2
(en)
|
2001-07-03 |
2010-01-05 |
Novartis Vaccines And Diagnostics, Inc. |
Indazole benzimidazole compounds
|
US7064215B2
(en)
|
2001-07-03 |
2006-06-20 |
Chiron Corporation |
Indazole benzimidazole compounds
|
WO2003024969A1
(en)
|
2001-09-14 |
2003-03-27 |
Merck & Co., Inc. |
Tyrosine kinase inhibitors
|
FR2831536A1
(fr)
*
|
2001-10-26 |
2003-05-02 |
Aventis Pharma Sa |
Nouveaux derives de benzimidazoles, leur procede de preparation, leur application a titre de medicament, compositions pharmaceutiques et nouvelle utilisation notamment comme inhibiteurs de kdr
|
US6897208B2
(en)
*
|
2001-10-26 |
2005-05-24 |
Aventis Pharmaceuticals Inc. |
Benzimidazoles
|
JP5039268B2
(ja)
*
|
2001-10-26 |
2012-10-03 |
アベンティス・ファーマスーティカルズ・インコーポレイテツド |
ベンゾイミダゾールおよび類縁体および蛋白キナーゼ阻害剤としてのその使用
|
FR2831537B1
(fr)
*
|
2001-10-26 |
2008-02-29 |
Aventis Pharma Sa |
Nouveaux derives de benzimidazoles, leur procede de preparation, leur application a titre de medicament, compositions pharmaceutiques et nouvelle utilisation
|
PL371486A1
(en)
|
2002-02-01 |
2005-06-13 |
Astrazeneca Ab |
Quinazoline compounds
|
US7166293B2
(en)
|
2002-03-29 |
2007-01-23 |
Carlsbad Technology, Inc. |
Angiogenesis inhibitors
|
US20050119278A1
(en)
*
|
2002-05-16 |
2005-06-02 |
Che-Ming Teng |
Anti-angiogenesis methods
|
CA2495216A1
(en)
|
2002-08-12 |
2004-02-19 |
Sugen, Inc. |
3-pyrrolyl-pyridopyrazoles and 3-pyrrolyl-indazoles as novel kinase inhibitors
|
AU2003288899B2
(en)
|
2002-08-23 |
2009-09-03 |
Novartis Vaccines And Diagnostics, Inc. |
Benzimidazole quinolinones and uses thereof
|
AU2003289287A1
(en)
*
|
2002-12-03 |
2004-06-23 |
Kyowa Hakko Kogyo Co., Ltd. |
Jnk inhibitor
|
DK1585743T3
(da)
*
|
2002-12-19 |
2007-09-17 |
Pfizer |
2-(H-indazol-6-ylamino)-benzamid forbindelser som protein kinase inhibitorer, nyttige til behandling opthalmiske sygdomme
|
US7192976B2
(en)
|
2002-12-21 |
2007-03-20 |
Angion Biomedica Corporation |
Small molecule modulators of hepatocyte growth factor (scatter factor) activity
|
US7135575B2
(en)
|
2003-03-03 |
2006-11-14 |
Array Biopharma, Inc. |
P38 inhibitors and methods of use thereof
|
PL214032B1
(pl)
|
2003-03-03 |
2013-06-28 |
Array Biopharma |
Zwiazki bedace inhibitorami kinazy p38, kompozycja farmaceutyczna je zawierajaca oraz ich zastosowanie do wytwarzania leku do leczenia stanu, w którym posredniczy kinaza p38
|
JP2006522087A
(ja)
*
|
2003-04-03 |
2006-09-28 |
ファイザー・インク |
Ag013736を含んでなる剤形
|
WO2004092217A1
(en)
*
|
2003-04-17 |
2004-10-28 |
Pfizer Inc. |
Crystal structure of vegfrkd: ligand complexes and methods of use thereof
|
FR2854159B1
(fr)
*
|
2003-04-25 |
2008-01-11 |
Aventis Pharma Sa |
Nouveaux derives de l'indole, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de kdr
|
TWI372050B
(en)
|
2003-07-03 |
2012-09-11 |
Astex Therapeutics Ltd |
(morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles
|
WO2005012256A1
(en)
|
2003-07-22 |
2005-02-10 |
Astex Therapeutics Limited |
3, 4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases (cdk) and glycogen synthase kinase-3 (gsk-3) modulators
|
JP4836788B2
(ja)
*
|
2003-07-23 |
2011-12-14 |
エグゼリクシス, インコーポレイテッド |
未分化リンパ腫キナーゼ変調因子及びその使用法
|
ES2384568T3
(es)
|
2003-07-30 |
2012-07-09 |
Kyowa Hakko Kirin Co., Ltd. |
Derivados de indazol
|
EP1650194A4
(en)
*
|
2003-07-30 |
2008-10-01 |
Kyowa Hakko Kogyo Kk |
INHIBITOR OF PROTEIN KINASE
|
JP2007504236A
(ja)
*
|
2003-09-04 |
2007-03-01 |
メルク エンド カムパニー インコーポレーテッド |
高眼圧症を治療するための眼用組成物
|
US20050164300A1
(en)
*
|
2003-09-15 |
2005-07-28 |
Plexxikon, Inc. |
Molecular scaffolds for kinase ligand development
|
US20050182061A1
(en)
*
|
2003-10-02 |
2005-08-18 |
Jeremy Green |
Phthalimide compounds useful as protein kinase inhibitors
|
EP1692085A4
(en)
|
2003-11-07 |
2010-10-13 |
Novartis Vaccines & Diagnostic |
INHIBITION OF FGFR3 AND TREATMENT OF MULTIPLE MYELOMA
|
JP4303726B2
(ja)
|
2003-11-11 |
2009-07-29 |
エーザイ・アール・アンド・ディー・マネジメント株式会社 |
ウレア誘導体およびその製造方法
|
WO2005051942A1
(en)
*
|
2003-11-19 |
2005-06-09 |
Signal Pharmaceuticals, Llc |
Indazole compounds and methods of use thereof as protein kinase inhibitors
|
GB0330002D0
(en)
|
2003-12-24 |
2004-01-28 |
Astrazeneca Ab |
Quinazoline derivatives
|
RU2006134022A
(ru)
*
|
2004-02-27 |
2008-04-10 |
Ф.Хоффманн-Ля Рош Аг (Ch) |
Производные индазола и содержащие их фармацевтические композиции
|
EP1720855A4
(en)
*
|
2004-03-02 |
2008-12-17 |
Smithkline Beecham Corp |
HEMMER OF ACT ACTIVITY
|
WO2005094823A1
(ja)
*
|
2004-03-30 |
2005-10-13 |
Kyowa Hakko Kogyo Co., Ltd. |
Flt-3阻害剤
|
WO2005108370A1
(ja)
*
|
2004-04-16 |
2005-11-17 |
Ajinomoto Co., Inc. |
ベンゼン化合物
|
EP1742627A4
(en)
|
2004-05-06 |
2009-08-26 |
Plexxikon Inc |
PDE4B HEMMER AND ITS USE
|
AU2005264996A1
(en)
*
|
2004-06-17 |
2006-01-26 |
Wyeth |
Gonadotropin releasing hormone receptor antagonists
|
RU2007101509A
(ru)
*
|
2004-06-17 |
2008-07-27 |
Уайт (Us) |
Способ получения антагонистов рецепторов гормона, высвобождающего гонадотропин
|
WO2006021886A1
(en)
*
|
2004-08-26 |
2006-03-02 |
Pfizer Inc. |
Aminoheteroaryl compounds as protein tyrosine kinase inhibitors
|
AU2005279795A1
(en)
*
|
2004-09-03 |
2006-03-09 |
Plexxikon, Inc. |
Bicyclic heteroaryl PDE4B inhibitors
|
JP4834553B2
(ja)
|
2004-09-17 |
2011-12-14 |
エーザイ・アール・アンド・ディー・マネジメント株式会社 |
医薬組成物
|
EP1647549A1
(en)
*
|
2004-10-14 |
2006-04-19 |
Laboratoire Theramex |
Indazoles, benzisoxazoles and benzisothiazoles as estrogenic agents
|
RU2007120635A
(ru)
*
|
2004-11-02 |
2008-12-10 |
Пфайзер Инк. (US) |
Способы получения индазольных соединений
|
CA2586176A1
(en)
*
|
2004-11-02 |
2006-05-11 |
Srinivasan Babu |
Methods for preparing indazole compounds
|
EP1819696A1
(en)
*
|
2004-11-02 |
2007-08-22 |
Pfizer, Inc. |
Polymorphic forms of 6-2-(methylcarbamoyl)phenysulfanyl|-3-e-2-(pyridin-2-yl)ethenyl indazole
|
EP1831225A2
(en)
|
2004-11-19 |
2007-09-12 |
The Regents of the University of California |
Anti-inflammatory pyrazolopyrimidines
|
FR2878442B1
(fr)
*
|
2004-11-29 |
2008-10-24 |
Aventis Pharma Sa |
THIENO(2,3-c)PYRAZOLES SUBSTITUES, PROCEDE DE PREPARATION, COMPOSITIONS LES CONTENANT ET UTILISATION
|
US20060142247A1
(en)
*
|
2004-12-17 |
2006-06-29 |
Guy Georges |
Tricyclic heterocycles
|
RU2416610C2
(ru)
|
2004-12-30 |
2011-04-20 |
Астекс Терапьютикс Лимитед |
Фармацевтические соединения
|
US7622583B2
(en)
|
2005-01-14 |
2009-11-24 |
Chemocentryx, Inc. |
Heteroaryl sulfonamides and CCR2
|
US8404718B2
(en)
|
2005-01-21 |
2013-03-26 |
Astex Therapeutics Limited |
Combinations of pyrazole kinase inhibitors
|
AR054425A1
(es)
|
2005-01-21 |
2007-06-27 |
Astex Therapeutics Ltd |
Sales de adicion de piperidin 4-il- amida de acido 4-(2,6-dicloro-benzoilamino) 1h-pirazol-3-carboxilico.
|
WO2006077424A1
(en)
|
2005-01-21 |
2006-07-27 |
Astex Therapeutics Limited |
Pharmaceutical compounds
|
ES2552338T3
(es)
|
2005-01-21 |
2015-11-27 |
Astex Therapeutics Limited |
Compuestos farmacéuticos
|
ATE451363T1
(de)
*
|
2005-01-26 |
2009-12-15 |
Schering Corp |
3-(indazol-5-yl)-(1,2,4)triazinderivate und verwandte verbindungen als proteinkinaseinhibitoren zur behandlung von krebs
|
JPWO2006080450A1
(ja)
|
2005-01-27 |
2008-06-19 |
協和醗酵工業株式会社 |
Igf−1r阻害剤
|
US7534796B2
(en)
|
2005-02-18 |
2009-05-19 |
Wyeth |
Imidazo[4,5-b]pyridine antagonists of gonadotropin releasing hormone receptor
|
US7538113B2
(en)
|
2005-02-18 |
2009-05-26 |
Wyeth |
4-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor
|
US7582634B2
(en)
|
2005-02-18 |
2009-09-01 |
Wyeth |
7-substituted imidazo[4,5-c]pyridine antagonists of gonadotropin releasing hormone receptor
|
JP5545925B2
(ja)
|
2005-05-17 |
2014-07-09 |
ノバルティス アーゲー |
ヘテロ環化合物の合成方法
|
US7531542B2
(en)
|
2005-05-18 |
2009-05-12 |
Wyeth |
Benzooxazole and benzothiazole antagonists of gonadotropin releasing hormone receptor
|
WO2006123223A1
(en)
*
|
2005-05-19 |
2006-11-23 |
Pfizer Inc. |
Pharmaceutical compostions comprising an amorphous form of a vegf-r inhibitor
|
WO2006127587A1
(en)
*
|
2005-05-20 |
2006-11-30 |
Vertex Pharmaceuticals Incorporated |
Pyrrolopyridines useful as inhibitors of protein kinase
|
US7582636B2
(en)
|
2005-05-26 |
2009-09-01 |
Wyeth |
Piperazinylimidazopyridine and piperazinyltriazolopyridine antagonists of Gonadotropin Releasing Hormone receptor
|
US7541367B2
(en)
|
2005-05-31 |
2009-06-02 |
Janssen Pharmaceutica, N.V. |
3-benzoimidazolyl-pyrazolopyridines useful in treating kinase disorders
|
US7888381B2
(en)
|
2005-06-14 |
2011-02-15 |
Bristol-Myers Squibb Company |
Modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity, and use thereof
|
US9006240B2
(en)
|
2005-08-02 |
2015-04-14 |
Eisai R&D Management Co., Ltd. |
Method for assay on the effect of vascularization inhibitor
|
AU2006320591B2
(en)
|
2005-11-29 |
2010-06-03 |
Novartis Ag |
Formulations of quinolinones
|
TW200732305A
(en)
*
|
2005-12-23 |
2007-09-01 |
Yung Shin Pharmaceutical Ind |
Cancer chemotherapy
|
SI1981851T1
(sl)
|
2006-01-31 |
2012-05-31 |
Array Biopharma Inc |
Kinazni inhibitorji in postopki za njihovo uporabo
|
JP2009530337A
(ja)
*
|
2006-03-23 |
2009-08-27 |
エフ.ホフマン−ラ ロシュ アーゲー |
置換インダゾール誘導体、その製造方法、及びその薬剤としての利用法
|
CA2909277A1
(en)
|
2006-04-04 |
2007-10-11 |
Kevan M. Shokat |
Kinase antagonists
|
CN101443009A
(zh)
|
2006-05-18 |
2009-05-27 |
卫材R&D管理有限公司 |
针对甲状腺癌的抗肿瘤剂
|
WO2008001885A1
(fr)
|
2006-06-30 |
2008-01-03 |
Kyowa Hakko Kirin Co., Ltd. |
INHIBITEUR DE KINASE Abl
|
JPWO2008001886A1
(ja)
|
2006-06-30 |
2009-11-26 |
協和発酵キリン株式会社 |
オーロラ(Aurora)阻害剤
|
US8519135B2
(en)
|
2006-07-14 |
2013-08-27 |
Chemocentryx, Inc. |
Heteroaryl sulfonamides and CCR2/CCR9
|
JPWO2008020606A1
(ja)
*
|
2006-08-16 |
2010-01-07 |
協和発酵キリン株式会社 |
血管新生阻害剤
|
US8865737B2
(en)
|
2006-08-28 |
2014-10-21 |
Eisai R&D Management Co., Ltd. |
Antitumor agent for undifferentiated gastric cancer
|
CL2007002617A1
(es)
|
2006-09-11 |
2008-05-16 |
Sanofi Aventis |
Compuestos derivados de pirrolo[2,3-b]pirazin-6-ilo; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar inflamacion de las articulaciones, artritis reumatoide, tumores, linfoma de las celulas del manto.
|
CA2676796C
(en)
|
2007-01-29 |
2016-02-23 |
Eisai R & D Management Co., Ltd. |
Composition for treatment of undifferentiated gastric cancer
|
WO2008111441A1
(ja)
|
2007-03-05 |
2008-09-18 |
Kyowa Hakko Kirin Co., Ltd. |
医薬組成物
|
CN101730703B
(zh)
*
|
2007-03-16 |
2012-12-26 |
中国人民解放军军事医学科学院放射与辐射医学研究所 |
具有抗增殖活性的苯甲酰胺类衍生物及其药用制剂
|
PT2134702T
(pt)
*
|
2007-04-05 |
2017-07-31 |
Pfizer Prod Inc |
Formas cristalinas de 6-[2-(metilcarbamoil)fenilsulfanil]-3-e-[2-(piridin-2-il)etenil]indazol adequadas para o tratamento de crescimento celular anormal em mamíferos
|
DE602008003055D1
(de)
|
2007-05-31 |
2010-12-02 |
Nerviano Medical Sciences Srl |
Zyklokondensierte Azaindole, die als Kinase-Hemmer wirken
|
AU2008275000B2
(en)
|
2007-07-12 |
2013-02-07 |
Chemocentryx, Inc. |
Fused heteroaryl pyridyl and phenyl benzenesulfonamides as CCR2 modulators for the treatment of inflammation
|
GB2467670B
(en)
|
2007-10-04 |
2012-08-01 |
Intellikine Inc |
Chemical entities and therapeutic uses thereof
|
US8779197B2
(en)
*
|
2007-10-11 |
2014-07-15 |
Vertex Pharmaceuticals Incorporated |
Aryl amides useful as inhibitors of voltage-gated sodium channels
|
NZ585063A
(en)
|
2007-11-02 |
2012-05-25 |
Vertex Pharma |
[1h- pyrazolo [3, 4-b] pyridine-4-yl] -phenyle or -pyridin-2-yle derivatives as protein kinase c-theta
|
WO2009060945A1
(ja)
|
2007-11-09 |
2009-05-14 |
Eisai R & D Management Co., Ltd. |
血管新生阻害物質と抗腫瘍性白金錯体との併用
|
SG10201605472WA
(en)
|
2008-01-04 |
2016-09-29 |
Intellikine Llc |
Certain Chemical Entities, Compositions And Methods
|
US8193182B2
(en)
|
2008-01-04 |
2012-06-05 |
Intellikine, Inc. |
Substituted isoquinolin-1(2H)-ones, and methods of use thereof
|
WO2009114870A2
(en)
|
2008-03-14 |
2009-09-17 |
Intellikine, Inc. |
Kinase inhibitors and methods of use
|
WO2009114874A2
(en)
|
2008-03-14 |
2009-09-17 |
Intellikine, Inc. |
Benzothiazole kinase inhibitors and methods of use
|
KR101269393B1
(ko)
|
2008-04-28 |
2013-05-29 |
아사히 가세이 파마 가부시키가이샤 |
페닐프로피온산 유도체 및 이의 용도
|
WO2010006072A2
(en)
|
2008-07-08 |
2010-01-14 |
The Regents Of The University Of California |
Mtor modulators and uses thereof
|
MX2011000216A
(es)
|
2008-07-08 |
2011-03-29 |
Intellikine Inc |
Inhibidores de cinasa y metodos para su uso.
|
CA2767331A1
(en)
|
2008-07-10 |
2010-01-14 |
Angion Biomedica Corp. |
Methods and compositions of small molecule modulators of hepatocyte growth factor (scatter factor) activity
|
CA2738429C
(en)
|
2008-09-26 |
2016-10-25 |
Intellikine, Inc. |
Heterocyclic kinase inhibitors
|
CA2740885C
(en)
|
2008-10-16 |
2018-04-03 |
The Regents Of The University Of California |
Fused ring heteroaryl kinase inhibitors
|
US8476282B2
(en)
|
2008-11-03 |
2013-07-02 |
Intellikine Llc |
Benzoxazole kinase inhibitors and methods of use
|
EP2414328B1
(en)
|
2009-04-02 |
2021-05-26 |
Merck Serono S.A. |
Dihydroorotate dehydrogenase inhibitors
|
WO2010129816A2
(en)
|
2009-05-07 |
2010-11-11 |
Intellikine, Inc. |
Heterocyclic compounds and uses thereof
|
EP2987487B1
(en)
|
2009-08-10 |
2020-10-07 |
Samumed, LLC |
Indazole inhibitors of the wnt signal pathway and therapeutic uses thereof
|
US8980899B2
(en)
|
2009-10-16 |
2015-03-17 |
The Regents Of The University Of California |
Methods of inhibiting Ire1
|
WO2011073521A1
(en)
|
2009-12-15 |
2011-06-23 |
Petri Salven |
Methods for enriching adult-derived endothelial progenitor cells and uses thereof
|
SMT201700581T1
(it)
|
2009-12-21 |
2018-01-11 |
Samumed Llc |
1h-pirazolo[3,4-b]piridine e loro usi terapeutici
|
WO2011090738A2
(en)
|
2009-12-29 |
2011-07-28 |
Dana-Farber Cancer Institute, Inc. |
Type ii raf kinase inhibitors
|
UY33236A
(es)
|
2010-02-25 |
2011-09-30 |
Novartis Ag |
Inhibidores dimericos de las iap
|
JP2013522292A
(ja)
*
|
2010-03-16 |
2013-06-13 |
デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド |
インダゾール化合物およびそれらの使用
|
AU2011255218B2
(en)
|
2010-05-21 |
2015-03-12 |
Infinity Pharmaceuticals, Inc. |
Chemical compounds, compositions and methods for kinase modulation
|
CA2802644C
(en)
|
2010-06-25 |
2017-02-21 |
Eisai R & D Management Co., Ltd. |
Antitumor agent using compounds having kinase inhibitory effect in combination
|
CN103261225A
(zh)
|
2010-07-23 |
2013-08-21 |
波士顿大学董事会 |
作为用于抑制病理性血管生成和肿瘤细胞侵袭力的治疗剂以及用于分子成像和靶向递送的抗DEspR抑制剂
|
CA2817577A1
(en)
|
2010-11-10 |
2012-05-18 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
UY33794A
(es)
|
2010-12-13 |
2012-07-31 |
Novartis Ag |
Inhibidores diméricos de las iap
|
CN103261186A
(zh)
|
2010-12-13 |
2013-08-21 |
诺瓦提斯公司 |
二聚化iap抑制剂
|
WO2012088266A2
(en)
|
2010-12-22 |
2012-06-28 |
Incyte Corporation |
Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3
|
TWI659956B
(zh)
|
2011-01-10 |
2019-05-21 |
美商英菲尼提製藥股份有限公司 |
製備異喹啉酮之方法及異喹啉酮之固體形式
|
TWI592411B
(zh)
|
2011-02-23 |
2017-07-21 |
英特爾立秦有限責任公司 |
激酶抑制劑之組合及其用途
|
JP2014509660A
(ja)
|
2011-04-01 |
2014-04-21 |
ユニバーシティ・オブ・ユタ・リサーチ・ファウンデイション |
PDK1キナーゼの阻害剤としての置換3−(1H−ベンゾ{d}イミダゾール−2−イル)−1H−インダゾール類似体
|
BR112013021941B1
(pt)
|
2011-04-18 |
2022-11-16 |
Eisai R & D Management Co., Ltd |
Agente terapêutico para tumor
|
ES2841809T3
(es)
|
2011-06-03 |
2021-07-09 |
Eisai R&D Man Co Ltd |
Biomarcadores para pronosticar y evaluar el grado de respuesta de sujetos con cáncer de tiroides y de riñón a compuestos de lenvatinib
|
HK1198475A1
(en)
|
2011-07-19 |
2015-05-08 |
无限药品股份有限公司 |
Heterocyclic compounds and uses thereof
|
JP6027610B2
(ja)
|
2011-07-19 |
2016-11-16 |
インフィニティー ファーマシューティカルズ, インコーポレイテッド |
複素環式化合物及びその使用
|
US8575336B2
(en)
*
|
2011-07-27 |
2013-11-05 |
Pfizer Limited |
Indazoles
|
AR091790A1
(es)
|
2011-08-29 |
2015-03-04 |
Infinity Pharmaceuticals Inc |
Derivados de isoquinolin-1-ona y sus usos
|
MX370814B
(es)
|
2011-09-02 |
2020-01-08 |
Univ California |
Pirazolo[3,4-d]pirimidinas sustituidas y usos de las mismas.
|
MX390742B
(es)
|
2011-09-14 |
2025-03-21 |
Samumed Llc |
Indazol-3-carboxamidas y su uso como inhibidores de la trayectoria de señalizacion de wnt/b-catenina.
|
CN102432595B
(zh)
*
|
2011-09-14 |
2013-09-25 |
湖南有色凯铂生物药业有限公司 |
N-吲哚-1-酰胺类化合物及作为抗癌药物的应用
|
EA025183B1
(ru)
|
2011-09-27 |
2016-11-30 |
Новартис Аг |
3-пиримидин-4-ил-оксазолидин-2-оны в качестве ингибиторов мутантной idh
|
CA2856291C
(en)
|
2011-11-17 |
2020-08-11 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of c-jun-n-terminal kinase (jnk)
|
KR20140098242A
(ko)
|
2011-12-05 |
2014-08-07 |
노파르티스 아게 |
안드로겐 수용체 길항제로서의 시클릭 우레아 유도체
|
FR2985257B1
(fr)
*
|
2011-12-28 |
2014-02-14 |
Sanofi Sa |
Composes dimeres agonistes des recepteurs des fgfs (fgfrs), leur procede de preparation et leur application en therapeutique
|
AU2013208720A1
(en)
|
2012-01-09 |
2014-07-24 |
Arrowhead Research Corporation |
RNAi agents to treat Beta-Catenin related diseases
|
JO3357B1
(ar)
|
2012-01-26 |
2019-03-13 |
Novartis Ag |
مركبات إيميدازوبيروليدينون
|
PH12017500997A1
(en)
|
2012-04-04 |
2018-02-19 |
Samumed Llc |
Indazole inhibitors of the wnt signal pathway and therapeutic uses thereof
|
US8940742B2
(en)
|
2012-04-10 |
2015-01-27 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
PT2770994T
(pt)
|
2012-05-04 |
2019-11-04 |
Samumed Llc |
1h-pirazolo[3,4-b]piridinas e utilizações terapêuticas destas
|
PT3495367T
(pt)
|
2012-06-13 |
2020-11-12 |
Incyte Holdings Corp |
Compostos tricíclicos substituídos como inibidores de fgfr
|
JP6231262B2
(ja)
*
|
2012-06-20 |
2017-11-15 |
大日本印刷株式会社 |
ピタバスタチンカルシウムの前駆体の製造法
|
US8828998B2
(en)
|
2012-06-25 |
2014-09-09 |
Infinity Pharmaceuticals, Inc. |
Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors
|
US9388185B2
(en)
|
2012-08-10 |
2016-07-12 |
Incyte Holdings Corporation |
Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
|
SG11201502331RA
(en)
|
2012-09-26 |
2015-04-29 |
Univ California |
Modulation of ire1
|
EP2909194A1
(en)
|
2012-10-18 |
2015-08-26 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of cyclin-dependent kinase 7 (cdk7)
|
WO2014063054A1
(en)
|
2012-10-19 |
2014-04-24 |
Dana-Farber Cancer Institute, Inc. |
Bone marrow on x chromosome kinase (bmx) inhibitors and uses thereof
|
USRE48175E1
(en)
|
2012-10-19 |
2020-08-25 |
Dana-Farber Cancer Institute, Inc. |
Hydrophobically tagged small molecules as inducers of protein degradation
|
CN103804349A
(zh)
*
|
2012-11-01 |
2014-05-21 |
杨子娇 |
一类治疗青光眼的化合物及其用途
|
NZ744567A
(en)
|
2012-11-01 |
2020-03-27 |
Infinity Pharmaceuticals Inc |
Treatment of cancers using pi3 kinase isoform modulators
|
US9266892B2
(en)
|
2012-12-19 |
2016-02-23 |
Incyte Holdings Corporation |
Fused pyrazoles as FGFR inhibitors
|
EP2937337A4
(en)
|
2012-12-21 |
2016-06-22 |
Eisai R&D Man Co Ltd |
AMORPHIC FORM OF CHINOLINE DERIVATIVES AND METHOD FOR THE PRODUCTION THEREOF
|
EP2943198B1
(en)
|
2013-01-08 |
2019-07-17 |
Samumed, LLC |
3-(benzoimidazol-2-yl)-indazole inhibitors of the wnt signaling pathway and therapeutic uses thereof
|
CN104370889A
(zh)
*
|
2013-01-24 |
2015-02-25 |
韩冰 |
一类降低眼压的化合物及其制备方法和用途
|
PT2952510T
(pt)
*
|
2013-02-02 |
2019-04-16 |
Centaurus Biopharma Co Ltd |
Inibidor de proteína-cinase de 2-aminopiridina substituída
|
PE20151428A1
(es)
|
2013-02-19 |
2015-09-24 |
Novartis Ag |
Derivados de benzotiofeno y composiciones de los mismos como degradantes selectivos de los receptores de estrogeno
|
EA028033B1
(ru)
|
2013-03-14 |
2017-09-29 |
Новартис Аг |
3-пиримидин-4-ил-оксазолидин-2-оны в качестве ингибиторов мутантного idh
|
EA028122B1
(ru)
|
2013-03-14 |
2017-10-31 |
Новартис Аг |
3-пиримидин-4-илоксазолидин-2-оны в качестве ингибиторов мутантного idh
|
US9481667B2
(en)
|
2013-03-15 |
2016-11-01 |
Infinity Pharmaceuticals, Inc. |
Salts and solid forms of isoquinolinones and composition comprising and methods of using the same
|
WO2014147586A1
(en)
|
2013-03-22 |
2014-09-25 |
Novartis Ag |
1-(2-(ethylamino)pyrimidin-4-yl)pyrrolidin-2-ones as inhibitors of mutant idh
|
PE20152033A1
(es)
|
2013-04-19 |
2016-01-21 |
Incyte Holdings Corp |
Heterociclos bicicliclos como inhibidores de fgfr
|
MX368099B
(es)
|
2013-05-14 |
2019-09-19 |
Eisai R&D Man Co Ltd |
Biomarcadores para predecir y evaluar el grado de respuesta de sujetos con cancer de endometrio a compuestos de tipo lenvatinib.
|
US20150018376A1
(en)
*
|
2013-05-17 |
2015-01-15 |
Novartis Ag |
Pyrimidin-4-yl)oxy)-1h-indole-1-carboxamide derivatives and use thereof
|
CN103387565B
(zh)
*
|
2013-07-29 |
2014-10-29 |
苏州明锐医药科技有限公司 |
阿西替尼的制备方法
|
TWI657085B
(zh)
|
2013-10-04 |
2019-04-21 |
英菲尼提製藥股份有限公司 |
雜環化合物及其用途
|
US9751888B2
(en)
|
2013-10-04 |
2017-09-05 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
WO2015058140A1
(en)
|
2013-10-18 |
2015-04-23 |
Dana-Farber Cancer Institute, Inc. |
Polycyclic inhibitors of cyclin-dependent kinase 7 (cdk7)
|
EP3057955B1
(en)
|
2013-10-18 |
2018-04-11 |
Syros Pharmaceuticals, Inc. |
Heteroaromatic compounds useful for the treatment of prolferative diseases
|
CN103570696B
(zh)
*
|
2013-11-06 |
2016-02-24 |
湖南欧亚生物有限公司 |
一种阿西替尼中间体的制备方法以及在制备阿西替尼中的应用
|
WO2015067224A1
(en)
|
2013-11-08 |
2015-05-14 |
Zentiva, K.S. |
Salts of 6-[2-(methylcarbamoyl)phenylsulfanyl]-3-e-[2-(pyridin-2-yl)ethanyl] indazole
|
WO2015092634A1
(en)
|
2013-12-16 |
2015-06-25 |
Novartis Ag |
1,2,3,4-tetrahydroisoquinoline compounds and compositions as selective estrogen receptor antagonists and degraders
|
CN105899491B
(zh)
|
2014-01-17 |
2019-04-02 |
诺华股份有限公司 |
用于抑制shp2活性的1-哒嗪-/三嗪-3-基-哌(-嗪)/啶/吡咯烷衍生物及其组合物
|
EP3094629B1
(en)
|
2014-01-17 |
2018-08-22 |
Novartis AG |
1-(triazin-3-yl/pyridazin-3-yl)-piper(-azine)idine derivatives and compositions thereof for inhibiting the activity of shp2
|
JO3517B1
(ar)
|
2014-01-17 |
2020-07-05 |
Novartis Ag |
ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2
|
NZ724368A
(en)
|
2014-03-19 |
2023-07-28 |
Infinity Pharmaceuticals Inc |
Heterocyclic compounds for use in the treatment of pi3k-gamma mediated disorders
|
CN106458920B
(zh)
*
|
2014-03-31 |
2019-02-15 |
千寿制药株式会社 |
炔基吲唑衍生物及其用途
|
WO2015160975A2
(en)
|
2014-04-16 |
2015-10-22 |
Infinity Pharmaceuticals, Inc. |
Combination therapies
|
WO2015164614A1
(en)
|
2014-04-23 |
2015-10-29 |
Dana-Farber Cancer Institute, Inc. |
Janus kinase inhibitors and uses thereof
|
WO2015164604A1
(en)
|
2014-04-23 |
2015-10-29 |
Dana-Farber Cancer Institute, Inc. |
Hydrophobically tagged janus kinase inhibitors and uses thereof
|
WO2015181624A2
(en)
|
2014-05-28 |
2015-12-03 |
Idenix Pharmaceuticals, Inc |
Nucleoside derivatives for the treatment of cancer
|
CN104072484B
(zh)
*
|
2014-07-07 |
2016-07-06 |
渤海大学 |
氮-(4-(芳巯基)-1氢-吲唑-3-基)-1-(芳杂环取代)甲基亚胺类化合物及其药学上可接受的盐及其制备方法和应用
|
AR101196A1
(es)
|
2014-07-16 |
2016-11-30 |
Gruenenthal Gmbh |
Compuestos de pirimidina sustituidos
|
AR101198A1
(es)
|
2014-07-16 |
2016-11-30 |
Gruenenthal Gmbh |
Pirimidinas 2,5-sustituidas como inhibidores de pde4b
|
SI3524595T1
(sl)
|
2014-08-28 |
2022-10-28 |
Eisai R&D Management Co., Ltd. |
Derivat kinolina visoke čistosti in postopek njegove proizvodnje
|
WO2016040190A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridine and therapeutic uses thereof
|
WO2016040181A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof
|
WO2016040193A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridine and therapeutic uses thereof
|
WO2016040182A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
2-(1h-indazol-3-yl)-1h-imidazo[4,5-c]pyridine and therapeutic uses thereof
|
WO2016040184A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof
|
WO2016040185A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
2-(1h-indazol-3-yl)-3h-imidazo[4,5-b]pyridine and therapeutic uses thereof
|
WO2016040188A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
3-(3h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof
|
WO2016040180A1
(en)
|
2014-09-08 |
2016-03-17 |
Samumed, Llc |
3-(1h-benzo[d]imidazol-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof
|
BR112017005510A2
(pt)
|
2014-09-17 |
2018-08-14 |
Celgene Quanticel Res Inc |
inibidores da histona-desmetilase.
|
WO2016054491A1
(en)
|
2014-10-03 |
2016-04-07 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
US10851105B2
(en)
|
2014-10-22 |
2020-12-01 |
Incyte Corporation |
Bicyclic heterocycles as FGFR4 inhibitors
|
US10508108B2
(en)
|
2014-12-05 |
2019-12-17 |
Merck Sharp & Dohme Corp. |
Tricyclic compounds as inhibitors of mutant IDH enzymes
|
WO2016089797A1
(en)
|
2014-12-05 |
2016-06-09 |
Merck Sharp & Dohme Corp. |
Novel tricyclic compounds as inhibitors of mutant idh enzymes
|
EP3226690B1
(en)
|
2014-12-05 |
2020-05-20 |
Merck Sharp & Dohme Corp. |
Novel tricyclic compounds as inhibitors of mutant idh enzymes
|
MA41140A
(fr)
|
2014-12-12 |
2017-10-17 |
Cancer Research Tech Ltd |
Dérivés de 2,4-dioxo-quinazoline-6-sulfonamide en tant qu'inhibiteurs de la parg
|
MA41179A
(fr)
*
|
2014-12-19 |
2017-10-24 |
Cancer Research Tech Ltd |
Composés inhibiteurs de parg
|
AU2015371251B2
(en)
|
2014-12-23 |
2020-06-11 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of cyclin-dependent kinase 7 (CDK7)
|
EP3246046A4
(en)
|
2015-01-13 |
2018-12-05 |
Kyoto University |
Agent for preventing and/or treating amyotrophic lateral sclerosis
|
US9580423B2
(en)
|
2015-02-20 |
2017-02-28 |
Incyte Corporation |
Bicyclic heterocycles as FGFR4 inhibitors
|
PE20171514A1
(es)
|
2015-02-20 |
2017-10-20 |
Incyte Corp |
Heterociclos biciclicos como inhibidores de fgfr
|
MA41551A
(fr)
|
2015-02-20 |
2017-12-26 |
Incyte Corp |
Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
|
US20180028662A1
(en)
|
2015-02-25 |
2018-02-01 |
Eisai R&D Management Co., Ltd. |
Method for Suppressing Bitterness of Quinoline Derivative
|
CA2978226A1
(en)
|
2015-03-04 |
2016-09-09 |
Merck Sharpe & Dohme Corp. |
Combination of a pd-1 antagonist and a vegfr/fgfr/ret tyrosine kinase inhibitor for treating cancer
|
AU2016243529B2
(en)
|
2015-03-27 |
2021-03-25 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of cyclin-dependent kinases
|
US9580406B2
(en)
|
2015-04-28 |
2017-02-28 |
Signa S.A. De C.V. |
Processes for the preparation of axitinib
|
US10815264B2
(en)
|
2015-05-27 |
2020-10-27 |
Southern Research Institute |
Nucleotides for the treatment of cancer
|
EP3302379B1
(en)
|
2015-06-06 |
2023-11-22 |
Cloudbreak Therapeutics, LLC |
Compositions and methods for treating pterygium
|
EP3307728A4
(en)
|
2015-06-12 |
2019-07-17 |
Dana Farber Cancer Institute, Inc. |
COMBINATION THERAPY OF TRANSCRIPTION INHIBITORS AND CHINESE INHIBITORS
|
MX373231B
(es)
|
2015-06-16 |
2020-05-08 |
Eisai R&D Man Co Ltd |
Agente anticancerigeno.
|
ES2741746T3
(es)
|
2015-06-19 |
2020-02-12 |
Novartis Ag |
Compuestos y composiciones para inhibir la actividad de SHP2
|
US10287266B2
(en)
|
2015-06-19 |
2019-05-14 |
Novartis Ag |
Compounds and compositions for inhibiting the activity of SHP2
|
ES2824576T3
(es)
|
2015-06-19 |
2021-05-12 |
Novartis Ag |
Compuestos y composiciones para inhibir la actividad de SHP2
|
GB201511382D0
(en)
|
2015-06-29 |
2015-08-12 |
Imp Innovations Ltd |
Novel compounds and their use in therapy
|
GB201511790D0
(en)
|
2015-07-06 |
2015-08-19 |
Iomet Pharma Ltd |
Pharmaceutical compound
|
WO2017024004A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(1h-pyrrolo[2,3-b]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
US10463651B2
(en)
|
2015-08-03 |
2019-11-05 |
Samumed, Llc |
3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1H-indazoles and therapeutic uses thereof
|
WO2017024021A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc |
3-(1h-pyrrolo[2,3-b]pyridin-2-yl)-1h-indazoles and therapeutic uses thereof
|
WO2017024025A1
(en)
|
2015-08-03 |
2017-02-09 |
Sunil Kumar Kc |
3-(1h-pyrrolo[2,3-c]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
US10206908B2
(en)
|
2015-08-03 |
2019-02-19 |
Samumed, Llc |
3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof
|
US10383861B2
(en)
|
2015-08-03 |
2019-08-20 |
Sammumed, LLC |
3-(1H-pyrrolo[2,3-C]pyridin-2-yl)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof
|
US10195185B2
(en)
|
2015-08-03 |
2019-02-05 |
Samumed, Llc |
3-(1H-imidazo[4,5-C]pyridin-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
US10166218B2
(en)
|
2015-08-03 |
2019-01-01 |
Samumed, Llc |
3-(1H-indol-2-yl)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof
|
US10392383B2
(en)
|
2015-08-03 |
2019-08-27 |
Samumed, Llc |
3-(1H-benzo[d]imidazol-2-yl)-1H-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
WO2017024003A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc |
3-(1h-pyrrolo[3,2-c]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
US10226453B2
(en)
|
2015-08-03 |
2019-03-12 |
Samumed, Llc |
3-(1H-indol-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof
|
WO2017023988A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(3h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
US10604512B2
(en)
|
2015-08-03 |
2020-03-31 |
Samumed, Llc |
3-(1H-indol-2-yl)-1H-indazoles and therapeutic uses thereof
|
WO2017023987A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(1h-pyrrolo[3,2-c]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridines and therapeutic uses thereof
|
US10285983B2
(en)
|
2015-08-03 |
2019-05-14 |
Samumed, Llc |
3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[3,4-B] pyridines and therapeutic uses thereof
|
WO2017024015A1
(en)
|
2015-08-03 |
2017-02-09 |
Samumed, Llc. |
3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof
|
US10285982B2
(en)
|
2015-08-03 |
2019-05-14 |
Samumed, Llc |
3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof
|
US11453697B1
(en)
|
2015-08-13 |
2022-09-27 |
Merck Sharp & Dohme Llc |
Cyclic di-nucleotide compounds as sting agonists
|
CA2995365C
(en)
|
2015-08-13 |
2021-10-12 |
Merck Sharp & Dohme Corp. |
Cyclic di-nucleotide compounds as sting agonists
|
KR102587702B1
(ko)
|
2015-08-20 |
2023-10-12 |
에자이 알앤드디 매니지먼트 가부시키가이샤 |
종양 치료제
|
CA2996978A1
(en)
|
2015-09-09 |
2017-03-16 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of cyclin-dependent kinases
|
US10160761B2
(en)
|
2015-09-14 |
2018-12-25 |
Infinity Pharmaceuticals, Inc. |
Solid forms of isoquinolinones, and process of making, composition comprising, and methods of using the same
|
KR102317700B1
(ko)
*
|
2015-10-07 |
2021-10-26 |
아이비바 바이오파마, 인크. |
피부 섬유성 장애를 치료하는 조성물 및 방법
|
BR112018007720A2
(pt)
*
|
2015-10-22 |
2018-10-23 |
Selvita S A |
novos derivados de piridona e seu uso como inibidores da quinase
|
EP3371187A4
(en)
|
2015-11-06 |
2019-09-04 |
Samumed, LLC |
2- (1H-INDAZOLE-3-YL) -3H-IMIDAZO [4,5-C] PYRIDINE AND ITS USE AS AN INHIBITOR OF INHIBITOR
|
WO2017106062A1
(en)
|
2015-12-15 |
2017-06-22 |
Merck Sharp & Dohme Corp. |
Novel compounds as indoleamine 2,3-dioxygenase inhibitors
|
WO2017161116A1
(en)
|
2016-03-17 |
2017-09-21 |
Infinity Pharmaceuticals, Inc. |
Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as pi3k kinase inhibitors
|
AR108325A1
(es)
|
2016-04-27 |
2018-08-08 |
Samumed Llc |
Isoquinolin-3-il carboxamidas y preparación y uso de las mismas
|
US10577362B2
(en)
|
2016-05-04 |
2020-03-03 |
Genoscience Pharma |
Substituted 2, 4-diamino-quinoline derivatives for use in the treatment of proliferative diseases
|
HUE060797T2
(hu)
|
2016-06-01 |
2023-04-28 |
Biosplice Therapeutics Inc |
Eljárás N-(5-(3-(7-(3-fluorfenil)-3H-imidazo[4,5-c]piridin-2-il)-1H-indazol-5-il)- piridin-3-il)-3-metilbutánamid elõállítására
|
US10919914B2
(en)
|
2016-06-08 |
2021-02-16 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
KR102457146B1
(ko)
|
2016-06-14 |
2022-10-19 |
노파르티스 아게 |
Shp2의 활성을 억제하기 위한 화합물 및 조성물
|
UA125216C2
(uk)
|
2016-06-24 |
2022-02-02 |
Інфініті Фармасьютікалз, Інк. |
Комбінована терапія
|
MX386187B
(es)
|
2016-10-04 |
2025-03-18 |
Merck Sharp & Dohme Llc |
Compuestos de benzo[b]tiofeno como agonistas de sting.
|
MX391624B
(es)
|
2016-10-21 |
2025-03-04 |
Samumed Llc |
Métodos de uso de indazol-3-carboxamidas y su uso como inhibidores de la ruta de señalización de wnt/b-catenina.
|
EP3534878A1
(en)
|
2016-11-07 |
2019-09-11 |
Samumed, LLC |
Single-dose, ready-to-use injectable formulations
|
WO2018091542A1
(en)
|
2016-11-21 |
2018-05-24 |
Idenix Pharmaceuticals Llc |
Cyclic phosphate substituted nucleoside derivatives for the treatment of liver diseases
|
JP7013464B2
(ja)
|
2016-11-23 |
2022-02-15 |
ケモセントリックス, インコーポレイテッド |
巣状分節性糸球体硬化症を治療する方法
|
WO2018138685A2
(en)
|
2017-01-27 |
2018-08-02 |
Janssen Biotech, Inc. |
Cyclic dinucleotides as sting agonists
|
CN110234404A
(zh)
|
2017-01-27 |
2019-09-13 |
詹森生物科技公司 |
作为sting激动剂的环状二核苷酸
|
JP6581320B2
(ja)
|
2017-02-08 |
2019-09-25 |
エーザイ・アール・アンド・ディー・マネジメント株式会社 |
腫瘍治療用医薬組成物
|
US20190388407A1
(en)
|
2017-02-12 |
2019-12-26 |
Aiviva Biopharma, Inc. |
Multikinase inhibitors of vegf and tfg beta and uses thereof
|
EP3584241B1
(en)
|
2017-02-14 |
2023-04-26 |
FUJIFILM Corporation |
Method for producing indazole compound, and indazole compound
|
WO2018208667A1
(en)
|
2017-05-12 |
2018-11-15 |
Merck Sharp & Dohme Corp. |
Cyclic di-nucleotide compounds as sting agonists
|
MX2019013014A
(es)
|
2017-05-16 |
2020-08-06 |
Eisai R&D Man Co Ltd |
Tratamiento de carcinoma hepatocelular.
|
CN108947961B
(zh)
*
|
2017-05-18 |
2021-06-04 |
四川大学 |
吲唑类衍生物及其制备方法和用途
|
AR111960A1
(es)
|
2017-05-26 |
2019-09-04 |
Incyte Corp |
Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
|
EP3661499A4
(en)
|
2017-08-04 |
2021-04-21 |
Merck Sharp & Dohme Corp. |
COMBINATIONS OF PD-1 ANTAGONISTS AND STING BENZO AGONISTS [B
|
WO2019027858A1
(en)
|
2017-08-04 |
2019-02-07 |
Merck Sharp & Dohme Corp. |
BENZO [B] STING THIOPHEN AGONISTS FOR THE TREATMENT OF CANCER
|
EP4360651A3
(en)
|
2017-08-24 |
2024-07-17 |
Novo Nordisk A/S |
Glp-1 compositions and uses thereof
|
CN111201223B
(zh)
|
2017-09-11 |
2024-07-09 |
克鲁松制药公司 |
SHP2的八氢环戊二烯并[c]吡咯别构抑制剂
|
WO2019067332A1
(en)
|
2017-09-27 |
2019-04-04 |
Merck Sharp & Dohme Corp. |
COMPOSITIONS AND METHODS FOR TREATING CANCER THROUGH A COMBINATION OF PROGRAMMED DEATH ANTIBODY ANTIBODIES (PD-1) AND A CXCR2 ANTAGONIST
|
JP2020536919A
(ja)
|
2017-10-11 |
2020-12-17 |
ケモセントリックス, インコーポレイテッド |
Ccr2アンタゴニストによる巣状分節性糸球体硬化症の治療
|
WO2019089412A1
(en)
|
2017-11-01 |
2019-05-09 |
Merck Sharp & Dohme Corp. |
Novel substituted tetrahydroquinolin compounds as indoleamine 2,3-dioxygenase (ido) inhibitors
|
EP3709986B1
(en)
|
2017-11-14 |
2023-11-01 |
Merck Sharp & Dohme LLC |
Novel substituted biaryl compounds as indoleamine 2,3-dioxygenase (ido) inhibitors
|
JP7269928B2
(ja)
|
2017-11-14 |
2023-05-09 |
メルク・シャープ・アンド・ドーム・エルエルシー |
インドールアミン 2,3-ジオキシゲナーゼ(ido)阻害剤としての新規の置換ビアリール化合物
|
KR20200099178A
(ko)
|
2017-12-15 |
2020-08-21 |
얀센 바이오테크 인코포레이티드 |
Sting 작용제로서의 환상 다이뉴클레오티드
|
EP3727401A4
(en)
|
2017-12-20 |
2022-04-06 |
Merck Sharp & Dohme Corp. |
CYCLIC DI-NUCLEOTIDE COMPOUNDS AS STING AGONISTS
|
US12215116B2
(en)
|
2018-03-13 |
2025-02-04 |
Merck Sharp & Dohme Llc |
Arginase inhibitors and methods of use
|
US11702430B2
(en)
|
2018-04-03 |
2023-07-18 |
Merck Sharp & Dohme Llc |
Aza-benzothiophene compounds as STING agonists
|
CN111971277B
(zh)
|
2018-04-03 |
2023-06-06 |
默沙东有限责任公司 |
作为sting激动剂的苯并噻吩及相关化合物
|
CR20200591A
(es)
|
2018-05-04 |
2021-03-31 |
Incyte Corp |
Sales de un inhibidor de fgfr
|
CN119241541A
(zh)
|
2018-05-04 |
2025-01-03 |
因赛特公司 |
Fgfr抑制剂的固体形式和其制备方法
|
CN110452176A
(zh)
*
|
2018-05-07 |
2019-11-15 |
四川大学 |
吲唑类衍生物及其制备方法和用途
|
WO2019231870A1
(en)
|
2018-05-31 |
2019-12-05 |
Merck Sharp & Dohme Corp. |
Novel substituted [1.1.1] bicyclo compounds as indoleamine 2,3-dioxygenase inhibitors
|
EP3810615A4
(en)
|
2018-06-20 |
2022-03-30 |
Merck Sharp & Dohme Corp. |
Arginase inhibitors and methods of use
|
CA3099763A1
(en)
|
2018-06-25 |
2020-01-02 |
Dana-Farber Cancer Institute, Inc. |
Taire family kinase inhibitors and uses thereof
|
AU2019344897B2
(en)
|
2018-09-18 |
2024-01-18 |
Nikang Therapeutics, Inc. |
Tri-substituted heteroaryl derivatives AS SRC homology-2 phosphatase inhibitors
|
SG11202102981SA
(en)
|
2018-09-25 |
2021-04-29 |
Black Diamond Therapeutics Inc |
Quinazoline derivatives as tyrosine kinase inhibitor, compositions, methods of making them and their use
|
WO2020068873A1
(en)
|
2018-09-25 |
2020-04-02 |
Black Diamond Therapeutics, Inc. |
Tyrosine kinase inhibitor compositions, methods of making and methods of use
|
IL305106B1
(en)
|
2018-09-29 |
2025-04-01 |
Novartis Ag |
Process for producing a compound for inhibiting the activity of SHP2
|
WO2020092183A1
(en)
|
2018-11-01 |
2020-05-07 |
Merck Sharp & Dohme Corp. |
Novel substituted pyrazole compounds as indoleamine 2,3-dioxygenase inhibitors
|
US12065438B2
(en)
|
2018-11-06 |
2024-08-20 |
Merck Sharp & Dohme Llc |
Substituted tricyclic compounds as indoleamine 2,3-dioxygenase inhibitors
|
CN111205227A
(zh)
*
|
2018-11-22 |
2020-05-29 |
四川大学 |
3-乙烯基吲唑类衍生物及其制备方法和用途
|
US12264134B2
(en)
|
2018-11-28 |
2025-04-01 |
Merck Sharp & Dohme Llc |
Substituted piperazine amide compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors
|
WO2020131598A1
(en)
|
2018-12-18 |
2020-06-25 |
Merck Sharp & Dohme Corp. |
Arginase inhibitors and methods of use
|
US12281126B2
(en)
|
2018-12-28 |
2025-04-22 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of cyclin-dependent kinase 7 and uses thereof
|
JP7532385B2
(ja)
*
|
2019-01-31 |
2024-08-13 |
杏林製薬株式会社 |
15-pgdh阻害薬
|
US11628162B2
(en)
|
2019-03-08 |
2023-04-18 |
Incyte Corporation |
Methods of treating cancer with an FGFR inhibitor
|
EP3946324B1
(en)
|
2019-04-04 |
2025-07-30 |
Merck Sharp & Dohme LLC |
Inhibitors of histone deacetylase-3 useful for the treatment of cancer, inflammation, neurodegeneration diseases and diabetes
|
JP2022526827A
(ja)
|
2019-04-11 |
2022-05-26 |
アンジオン バイオメディカ コーポレーション |
(e)-3-[2-(2-チエニル)ビニル]-1h-ピラゾールの固体形態
|
WO2020212253A1
(en)
|
2019-04-18 |
2020-10-22 |
Synthon B.V. |
Process for preparing axitinib, process for purifying the intermediate 2-((3-iodo-1h-indazol-6-yl)thio)-n-methylbenzamide, process for purifying axitinib via the axitinib hcl salt, solid form of the axitinib hcl salt
|
WO2020225413A1
(en)
|
2019-05-09 |
2020-11-12 |
Synthon B.V. |
Pharmaceutical composition comprising axitinib
|
WO2020260547A1
(en)
|
2019-06-27 |
2020-12-30 |
Rigontec Gmbh |
Design method for optimized rig-i ligands
|
US11591329B2
(en)
|
2019-07-09 |
2023-02-28 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
AU2020324388A1
(en)
|
2019-08-02 |
2022-02-24 |
Mersana Therapeutics, Inc. |
Bis-[N-((5-carbamoyl)-1H-benzo[d]imidazol-2-yl)-pyrazol-5-carboxamide] derivatives and related compounds as STING (Stimulator of Interferon Genes) agonists for the treatment of cancer
|
EP4013749A1
(en)
|
2019-08-15 |
2022-06-22 |
Black Diamond Therapeutics, Inc. |
Alkynyl quinazoline compounds
|
CN112442011B
(zh)
*
|
2019-08-30 |
2023-11-14 |
润佳(苏州)医药科技有限公司 |
一种前药化合物及其在治疗癌症方面的应用
|
CN112442010B
(zh)
*
|
2019-08-30 |
2023-10-03 |
润佳(苏州)医药科技有限公司 |
一类前药化合物及其在治疗癌症方面的应用
|
CA3147801A1
(en)
*
|
2019-08-30 |
2021-03-04 |
Jiasheng LU |
Prodrugs of the tyrosine kinase inhibitor for treating cancer
|
US12122767B2
(en)
|
2019-10-01 |
2024-10-22 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
AU2020366006A1
(en)
|
2019-10-14 |
2022-04-21 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
US11566028B2
(en)
|
2019-10-16 |
2023-01-31 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
CN112694474B
(zh)
*
|
2019-10-23 |
2022-03-18 |
四川大学 |
吲唑类衍生物及其制备方法和用途
|
WO2021113479A1
(en)
|
2019-12-04 |
2021-06-10 |
Incyte Corporation |
Tricyclic heterocycles as fgfr inhibitors
|
KR20220131900A
(ko)
|
2019-12-04 |
2022-09-29 |
인사이트 코포레이션 |
Fgfr 억제제의 유도체
|
EP4069683A1
(en)
|
2019-12-06 |
2022-10-12 |
Mersana Therapeutics, Inc. |
Dimeric compounds as sting agonists
|
WO2021126725A1
(en)
|
2019-12-17 |
2021-06-24 |
Merck Sharp & Dohme Corp. |
Novel substituted 1,3,8-triazaspiro[4,5]decane-2,4-dione compounds as indoleamine 2,3-dioxygenase (ido) and/or tryptophan 2,3-dioxygenase (tdo) inhibitors
|
US20230140132A1
(en)
|
2020-01-07 |
2023-05-04 |
Merck Sharp & Dohme Llc |
Arginase inhibitors and methods of use
|
US12012409B2
(en)
|
2020-01-15 |
2024-06-18 |
Incyte Corporation |
Bicyclic heterocycles as FGFR inhibitors
|
CN111829859B
(zh)
*
|
2020-01-20 |
2024-01-05 |
北京林业大学 |
一种高效杨树种子透明染色及其三维成像的方法
|
CA3168543A1
(en)
|
2020-01-29 |
2021-08-05 |
Gilead Sciences, Inc. |
Glp-1r modulating compounds
|
TWI878456B
(zh)
|
2020-02-18 |
2025-04-01 |
丹麥商諾佛 儂迪克股份有限公司 |
Glp-1組成物及其用途
|
BR102020005423A2
(pt)
*
|
2020-03-18 |
2021-09-28 |
Faculdades Catolicas |
Compostos n-acil-hidrazônicos, uso no tratamento de agregopatias degenerativas amiloides e não-amiloides, e composição farmacêutica
|
WO2021195206A1
(en)
|
2020-03-24 |
2021-09-30 |
Black Diamond Therapeutics, Inc. |
Polymorphic forms and related uses
|
BR112022019919A2
(pt)
|
2020-04-02 |
2023-02-14 |
Mersana Therapeutics Inc |
Conjugado de anticorpo-fármaco compreendendo agonistas de sting
|
CR20220565A
(es)
|
2020-05-06 |
2023-01-13 |
Merck Sharp & Dohme Llc |
Inhibidores de il4i1 y métodos de uso
|
WO2021232367A1
(zh)
*
|
2020-05-21 |
2021-11-25 |
四川大学 |
3-乙烯基吲唑类衍生物及其制备方法和用途
|
CN113943271B
(zh)
*
|
2020-07-15 |
2023-11-14 |
鲁南制药集团股份有限公司 |
一种阿昔替尼晶型及其制备方法
|
CN112028831A
(zh)
*
|
2020-09-24 |
2020-12-04 |
山东大学 |
一种苯并吡唑类化合物、其制备方法及作为抗肿瘤药物的应用
|
EP4259619A1
(en)
*
|
2020-12-08 |
2023-10-18 |
Disarm Therapeutics, Inc. |
Benzopyrazole inhibitors of sarm1
|
IL303661A
(en)
|
2020-12-22 |
2023-08-01 |
Nikang Therapeutics Inc |
Compounds for degrading cyclin-dependent kinase 2 via ubiquitin proteosome pathway
|
CA3208313A1
(en)
|
2021-01-13 |
2022-07-21 |
Monte Rosa Therapeutics Ag |
Isoindolinone compounds
|
WO2022170052A1
(en)
|
2021-02-05 |
2022-08-11 |
Black Diamond Therapeutics, Inc. |
Quinazoline derivatives, pyridopyrimidine derivatives, pyrimidopyrimidine derivatives, and uses thereof
|
EP4323405A1
(en)
|
2021-04-12 |
2024-02-21 |
Incyte Corporation |
Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent
|
WO2022219407A1
(en)
|
2021-04-14 |
2022-10-20 |
Monte Rosa Therapeutics Ag |
Isoindolinone compounds
|
EP4323349A1
(en)
|
2021-04-14 |
2024-02-21 |
Monte Rosa Therapeutics AG |
Isoindolinone amide compounds useful to treat diseases associated with gspt1
|
WO2022227015A1
(en)
|
2021-04-30 |
2022-11-03 |
Merck Sharp & Dohme Corp. |
Il4i1 inhibitors and methods of use
|
US11939331B2
(en)
|
2021-06-09 |
2024-03-26 |
Incyte Corporation |
Tricyclic heterocycles as FGFR inhibitors
|
EP4370522A1
(en)
|
2021-07-14 |
2024-05-22 |
Nikang Therapeutics, Inc. |
Alkylidene derivatives as kras inhibitors
|
CN115701423B
(zh)
*
|
2021-08-02 |
2025-03-25 |
沈阳化工大学 |
三氟乙基硫醚(亚砜)取代苯类化合物的制备方法及其中间体
|
IL315722A
(en)
|
2022-03-23 |
2024-11-01 |
Ideaya Biosciences Inc |
Piperazine-substituted indazole compounds as PARG inhibitors
|
TW202346292A
(zh)
|
2022-03-28 |
2023-12-01 |
美商尼坎醫療公司 |
作為週期蛋白依賴性激酶2抑制劑的磺醯胺基衍生物
|
EP4282415A1
(en)
|
2022-05-26 |
2023-11-29 |
Genepharm S.A. |
A stable tablet composition of axitinib
|
WO2023240024A1
(en)
|
2022-06-08 |
2023-12-14 |
Nikang Therapeutics, Inc. |
Sulfamide derivatives as cyclin-dependent kinase 2 inhibitors
|
WO2024032584A1
(zh)
*
|
2022-08-08 |
2024-02-15 |
苏州必扬医药科技有限公司 |
一种蛋白酪氨酸激酶抑制剂及其医疗用途
|
AU2023375457A1
(en)
|
2022-11-11 |
2025-05-01 |
Nikang Therapeutics, Inc. |
Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 via ubiquitin proteasome pathway
|
US20240336608A1
(en)
|
2023-03-29 |
2024-10-10 |
Merck Sharp & Dohme Llc |
Il4i1 inhibitors and methods of use
|
WO2025072462A1
(en)
|
2023-09-27 |
2025-04-03 |
Nikang Therapeutics, Inc. |
Sulfonamide derivatives as cyclin-dependent kinase 2 inhibitors
|
WO2025082316A1
(zh)
*
|
2023-10-17 |
2025-04-24 |
苏州必扬医药科技有限公司 |
一种眼用制剂及其制备方法和应用
|
WO2025117616A1
(en)
|
2023-11-27 |
2025-06-05 |
Nikang Therapeutics, Inc. |
Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 and cyclin-dependent kinase 4 via ubiquitin proteasome pathway
|
WO2025117981A1
(en)
|
2023-12-02 |
2025-06-05 |
Nikang Therapeutics, Inc. |
Bifunctional compounds containing 2,5-substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 via ubiquitin proteasome pathway
|