WO1987000613A1
(en)
*
|
1985-07-19 |
1987-01-29 |
Armtech Limited |
A disc magazine firearm
|
US7863444B2
(en)
*
|
1997-03-19 |
2011-01-04 |
Abbott Laboratories |
4-aminopyrrolopyrimidines as kinase inhibitors
|
US7223724B1
(en)
*
|
1999-02-08 |
2007-05-29 |
Human Genome Sciences, Inc. |
Use of vascular endothelial growth factor to treat photoreceptor cells
|
US6921763B2
(en)
*
|
1999-09-17 |
2005-07-26 |
Abbott Laboratories |
Pyrazolopyrimidines as therapeutic agents
|
WO2002011769A1
(en)
*
|
2000-08-04 |
2002-02-14 |
Human Genome Sciences, Inc. |
Vascular endothelial growth factor 2
|
MXPA03008560A
(es)
|
2001-03-22 |
2004-06-30 |
Abbot Gmbh & Co Kg |
Pirazolopirimidinas como agentes terapeuticos.
|
EP1385864B1
(de)
*
|
2001-04-13 |
2010-06-09 |
Human Genome Sciences, Inc. |
Anti-VEGF-2 Antikörper
|
US20050232921A1
(en)
*
|
2001-04-13 |
2005-10-20 |
Rosen Craig A |
Vascular endothelial growth factor 2
|
AU2002252631A1
(en)
*
|
2001-04-13 |
2002-10-28 |
Human Genome Sciences, Inc. |
Vascular endothelial growth factor 2
|
HUP0304054A2
(hu)
|
2001-04-30 |
2004-04-28 |
Glaxo Group Limited |
A kortikotropin-realising faktor (CRF) antagonistáiként alkalmazható kondenzált pirimidinek, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények
|
DE60228103D1
(de)
*
|
2001-10-02 |
2008-09-18 |
Smithkline Beecham Corp |
Chemische verbindungen
|
US20030187026A1
(en)
|
2001-12-13 |
2003-10-02 |
Qun Li |
Kinase inhibitors
|
US20030199525A1
(en)
*
|
2002-03-21 |
2003-10-23 |
Hirst Gavin C. |
Kinase inhibitors
|
US20030225273A1
(en)
*
|
2002-03-21 |
2003-12-04 |
Michaelides Michael R. |
Thiopyrimidine and isothiazolopyrimidine kinase inhibitors
|
US6695881B2
(en)
|
2002-04-29 |
2004-02-24 |
Alcon, Inc. |
Accommodative intraocular lens
|
US20040033986A1
(en)
*
|
2002-05-17 |
2004-02-19 |
Protopopova Marina Nikolaevna |
Anti tubercular drug: compositions and methods
|
US7456222B2
(en)
*
|
2002-05-17 |
2008-11-25 |
Sequella, Inc. |
Anti tubercular drug: compositions and methods
|
CN101404986B
(zh)
*
|
2002-05-17 |
2011-09-28 |
赛奎拉公司 |
用于诊断和治疗感染性疾病的组合物和制药方法
|
JP2006501200A
(ja)
*
|
2002-07-23 |
2006-01-12 |
スミスクライン ビーチャム コーポレーション |
キナーゼインヒビターとしてのピラゾロピリミジン
|
WO2004009602A1
(en)
*
|
2002-07-23 |
2004-01-29 |
Smithkline Beecham Corporation |
Pyrazolopyrimidines as kinase inhibitors
|
EP1534389A2
(de)
*
|
2002-07-23 |
2005-06-01 |
SmithKline Beecham Corporation |
Pyrazolopyrimidine als kinaseinhibitoren
|
DE60304718T2
(de)
*
|
2002-08-06 |
2007-04-26 |
Astrazeneca Ab |
Kondensierte pyridine und pyrimidine mit tie2 (tek) aktivität
|
GB0226370D0
(en)
*
|
2002-11-12 |
2002-12-18 |
Novartis Ag |
Organic compounds
|
GB0230089D0
(en)
*
|
2002-12-24 |
2003-01-29 |
Astrazeneca Ab |
Therapeutic agents
|
DK1599468T3
(da)
|
2003-01-14 |
2008-02-04 |
Arena Pharm Inc |
1,2,3-trisubstituerede aryl- og heteroarylderivater som modulatorer af metabolisme og forebyggelse og behandling af forstyrrelser forbundet dermed såsom diabetes og hyperglykæmi
|
WO2004100868A2
(en)
*
|
2003-04-23 |
2004-11-25 |
Abbott Laboratories |
Method of treating transplant rejection
|
US7429596B2
(en)
|
2003-06-20 |
2008-09-30 |
The Regents Of The University Of California |
1H-pyrrolo [2,3-D] pyrimidine derivatives and methods of use thereof
|
EP1644375A2
(de)
*
|
2003-07-14 |
2006-04-12 |
Arena Pharmaceuticals, Inc. |
Kondensierte aryl- und heteroarylderivate als stoffwechselmodulatoren und die prophylaxe und behandlung von damit in zusammenhang stehenden erkrankungen
|
WO2005034857A2
(en)
*
|
2003-09-05 |
2005-04-21 |
Sequella, Inc. |
Methods and compositions comprising diamines as new anti-tubercular therapeutics
|
CA2542886A1
(en)
|
2003-11-05 |
2005-05-19 |
Neelima M. Bhat |
Enhanced b cell cytotoxicity of cdim binding antibody
|
GB0401334D0
(en)
*
|
2004-01-21 |
2004-02-25 |
Novartis Ag |
Organic compounds
|
CA2553724A1
(en)
*
|
2004-02-03 |
2005-08-18 |
Abbott Laboratories |
Aminobenzoxazoles as therapeutic agents
|
JP2007523938A
(ja)
*
|
2004-02-27 |
2007-08-23 |
エフ.ホフマン−ラ ロシュ アーゲー |
ピラゾールの縮合誘導体
|
EP1744788A4
(de)
*
|
2004-03-19 |
2010-08-18 |
Penn State Res Found |
Kombinatorische verfahren und zusammensetzungen zur behandlung von melanomen
|
US20080287405A1
(en)
*
|
2004-05-14 |
2008-11-20 |
Thannickal Victor J |
Compositions and Methods Relating to Protein Kinase Inhibitors
|
WO2005117932A1
(en)
*
|
2004-06-04 |
2005-12-15 |
The Board Of Governors For Higher Education, State Of Rhode Island And Providence Plantations |
Bisubstrate inhibitors of protein tyrosine kinases as therapeutic agents
|
CA2571710A1
(en)
|
2004-06-24 |
2006-11-02 |
Nicholas Valiante |
Small molecule immunopotentiators and assays for their detection
|
US8377435B2
(en)
|
2004-11-05 |
2013-02-19 |
The Board Of Trustees Of The Leland Stanford Junior University |
Antibody induced cell membrane wounding
|
WO2006068760A2
(en)
*
|
2004-11-19 |
2006-06-29 |
The Regents Of The University Of California |
Anti-inflammatory pyrazolopyrimidines
|
DOP2006000009A
(es)
*
|
2005-01-13 |
2006-08-15 |
Arena Pharm Inc |
Procedimiento para preparar eteres de pirazolo [3,4-d] pirimidina
|
US8143285B2
(en)
|
2005-09-06 |
2012-03-27 |
Shionogi & Co., Ltd. |
Indolecarboxylic acid derivative having PGD2 receptor antagonistic activity
|
US20070072933A1
(en)
*
|
2005-09-26 |
2007-03-29 |
Peyman Gholam A |
Delivery of an ocular agent
|
JP5335432B2
(ja)
|
2005-11-17 |
2013-11-06 |
オーエスアイ・フアーマシユーテイカルズ・エル・エル・シー |
縮合2環系mTOR阻害剤
|
CN101448506A
(zh)
*
|
2005-12-02 |
2009-06-03 |
拜尔健康护理有限责任公司 |
通过抑制有丝分裂酶激酶治疗癌症的吡咯并三嗪衍生物
|
PE20070855A1
(es)
*
|
2005-12-02 |
2007-10-14 |
Bayer Pharmaceuticals Corp |
Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
|
KR20130141706A
(ko)
*
|
2005-12-02 |
2013-12-26 |
바이엘 헬스케어 엘엘씨 |
과다-증식성 장애 및 맥관형성과 관련된 질환의 치료에 유용한 치환된 4-아미노-피롤로트리아진 유도체
|
WO2007079164A2
(en)
*
|
2005-12-29 |
2007-07-12 |
Abbott Laboratories |
Protein kinase inhibitors
|
CA2636696A1
(en)
|
2006-01-13 |
2007-08-02 |
Pharmacyclics, Inc. |
Inhibitors of tyrosine kinases and uses thereof
|
ATE525072T1
(de)
*
|
2006-02-09 |
2011-10-15 |
Athersys Inc |
Pyrazole zur behandlung von adipositas und anderen zns-erkrankungen
|
CA2645137A1
(en)
*
|
2006-03-07 |
2007-09-13 |
James F. Blake |
Heterobicyclic pyrazole compounds and methods of use
|
PT2004654E
(pt)
*
|
2006-04-04 |
2013-08-27 |
Univ California |
Derivados de pirazolopirimidina para utilização como antagonistas da quinase
|
NL2000613C2
(nl)
*
|
2006-05-11 |
2007-11-20 |
Pfizer Prod Inc |
Triazoolpyrazinederivaten.
|
GB0610242D0
(en)
*
|
2006-05-23 |
2006-07-05 |
Novartis Ag |
Organic compounds
|
PL2529621T3
(pl)
|
2006-09-22 |
2017-06-30 |
Pharmacyclics Llc |
Inhibitory kinazy tyrozynowej brutona
|
ES2403546T3
(es)
|
2006-11-03 |
2013-05-20 |
Pharmacyclics, Inc. |
Sonda de actividad de la tirosina-cinasa de Bruton y procedimiento de utilización
|
JP2010514692A
(ja)
|
2006-12-20 |
2010-05-06 |
バイエル ヘルスケア リミティド ライアビリティ カンパニー |
癌の治療に有用なヒドロキシメチルフェニルピラゾリル尿素化合物
|
RU2446796C2
(ru)
*
|
2006-12-26 |
2012-04-10 |
Фармасайкликс, Инк. |
Способ использования ингибиторов гистондеацетилазы и мониторинга биомаркеров в комбинированной терапии
|
US20080200458A1
(en)
*
|
2007-01-18 |
2008-08-21 |
Joseph Barbosa |
Methods and compositions for the treatment of body composition disorders
|
US20080194557A1
(en)
*
|
2007-01-18 |
2008-08-14 |
Joseph Barbosa |
Methods and compositions for the treatment of pain, inflammation and cancer
|
US8809273B2
(en)
|
2007-03-28 |
2014-08-19 |
Pharmacyclics, Inc. |
Inhibitors of Bruton's tyrosine kinase
|
JP5347202B2
(ja)
|
2007-03-28 |
2013-11-20 |
ファーマサイクリックス,インク. |
ブルトンチロシンキナーゼインヒビター
|
MX2010000617A
(es)
|
2007-07-17 |
2010-05-17 |
Plexxikon Inc |
Compuestos y metodos para modulacion de cinasa, e indicaciones de estos.
|
KR20090018593A
(ko)
*
|
2007-08-17 |
2009-02-20 |
주식회사 엘지생명과학 |
세포괴사 저해제로서의 인돌 및 인다졸 화합물
|
GB2467670B
(en)
|
2007-10-04 |
2012-08-01 |
Intellikine Inc |
Chemical entities and therapeutic uses thereof
|
ES2647163T3
(es)
|
2008-01-04 |
2017-12-19 |
Intellikine, Inc. |
Derivados de isoquinolinona sustituidos con una purina útiles como inhibidores de la PI3K
|
US8193182B2
(en)
|
2008-01-04 |
2012-06-05 |
Intellikine, Inc. |
Substituted isoquinolin-1(2H)-ones, and methods of use thereof
|
US20110020326A1
(en)
*
|
2008-03-04 |
2011-01-27 |
Children's Medical Center Corporation |
Method of treating polycystic kidney disease
|
EP2252293B1
(de)
|
2008-03-14 |
2018-06-27 |
Intellikine, LLC |
Kinasehemmer und verwendungsverfahren
|
US8993580B2
(en)
|
2008-03-14 |
2015-03-31 |
Intellikine Llc |
Benzothiazole kinase inhibitors and methods of use
|
WO2009136965A1
(en)
*
|
2008-05-06 |
2009-11-12 |
Sequella, Inc. |
Compositions and methods comprising capuramycin analogues
|
US20090301928A1
(en)
*
|
2008-06-05 |
2009-12-10 |
United Comb & Novelty Corporation |
Packaging For Lipped Containers
|
KR20110039326A
(ko)
|
2008-07-08 |
2011-04-15 |
인텔리카인, 인크. |
키나제 억제제 및 사용 방법
|
WO2010006072A2
(en)
|
2008-07-08 |
2010-01-14 |
The Regents Of The University Of California |
Mtor modulators and uses thereof
|
US8946239B2
(en)
|
2008-07-10 |
2015-02-03 |
Duquesne University Of The Holy Spirit |
Substituted pyrrolo, -furano, and cyclopentylpyrimidines having antimitotic and/or antitumor activity and methods of use thereof
|
CN102159214A
(zh)
|
2008-07-16 |
2011-08-17 |
药品循环公司 |
用于实体肿瘤的治疗的布鲁顿酪氨酸激酶的抑制剂
|
CA2738429C
(en)
|
2008-09-26 |
2016-10-25 |
Intellikine, Inc. |
Heterocyclic kinase inhibitors
|
JP5819195B2
(ja)
*
|
2008-10-16 |
2015-11-18 |
ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア |
融合環ヘテロアリールキナーゼ阻害剤
|
US8476431B2
(en)
|
2008-11-03 |
2013-07-02 |
Itellikine LLC |
Benzoxazole kinase inhibitors and methods of use
|
WO2010051561A1
(en)
*
|
2008-11-03 |
2010-05-06 |
Chemocentryx, Inc. |
Compounds for the treatment of osteoporosis and cancers
|
WO2010119306A1
(en)
*
|
2009-04-15 |
2010-10-21 |
Fondazione Irccs Istituto Nazionale Dei Tumori |
Use of multi-kinase inhibitors in the treatment of vascular hyperpermeability
|
EP2427195B1
(de)
|
2009-05-07 |
2019-05-01 |
Intellikine, LLC |
Heterocyclische verbindungen und ihre verwendung
|
GEP201706639B
(en)
|
2009-08-17 |
2017-03-27 |
Intellikine Llc |
Heterocyclic compounds and uses thereof
|
EP2470539A1
(de)
*
|
2009-08-28 |
2012-07-04 |
Array Biopharma, Inc. |
Raf-hemmende verbindungen und anwendungsverfahren dafür
|
US7718662B1
(en)
*
|
2009-10-12 |
2010-05-18 |
Pharmacyclics, Inc. |
Pyrazolo-pyrimidine inhibitors of bruton's tyrosine kinase
|
US8980899B2
(en)
|
2009-10-16 |
2015-03-17 |
The Regents Of The University Of California |
Methods of inhibiting Ire1
|
WO2011090738A2
(en)
|
2009-12-29 |
2011-07-28 |
Dana-Farber Cancer Institute, Inc. |
Type ii raf kinase inhibitors
|
WO2011094008A1
(en)
|
2010-01-27 |
2011-08-04 |
Arena Pharmaceuticals, Inc. |
Processes for the preparation of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid and salts thereof
|
JP5764145B2
(ja)
*
|
2010-02-08 |
2015-08-12 |
メルク・シャープ・エンド・ドーム・ベー・フェー |
8−メチル−1−フェニル−イミダゾル[1,5−a]ピラジン化合物
|
AU2011255218B2
(en)
|
2010-05-21 |
2015-03-12 |
Infinity Pharmaceuticals, Inc. |
Chemical compounds, compositions and methods for kinase modulation
|
CA2800521A1
(en)
|
2010-05-24 |
2011-12-01 |
Toa Eiyo Ltd. |
Fused imidazole derivative
|
AU2011261185A1
(en)
|
2010-06-03 |
2013-01-10 |
Pharmacyclics, Inc. |
The use of inhibitors of Bruton's tyrosine kinase (Btk)
|
EP3323818A1
(de)
|
2010-09-22 |
2018-05-23 |
Arena Pharmaceuticals, Inc. |
Modulatoren des gpr119-rezeptors und behandlung von damit assoziierten erkrankungen
|
EP2637669A4
(de)
|
2010-11-10 |
2014-04-02 |
Infinity Pharmaceuticals Inc |
Heterocyclische verbindungen und ihre verwendung
|
CA2824197C
(en)
|
2011-01-10 |
2020-02-25 |
Michael Martin |
Processes for preparing isoquinolinones and solid forms of isoquinolinones
|
US8889684B2
(en)
*
|
2011-02-02 |
2014-11-18 |
Boehringer Ingelheim International Gmbh |
Azaindolylphenyl sulfonamides as serine/threonine kinase inhibitors
|
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
|
WO2012158795A1
(en)
|
2011-05-17 |
2012-11-22 |
Principia Biopharma Inc. |
Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors
|
JP5974084B2
(ja)
|
2011-05-17 |
2016-08-23 |
プリンシピア バイオファーマ インコーポレイテッド |
チロシンキナーゼ阻害剤
|
EP2726634B1
(de)
|
2011-07-01 |
2017-02-22 |
Dana-Farber Cancer Institute, Inc. |
Ermittlung einer somatischen mutation im gen myd88 in einem lymphoplasmazytischen lymphom
|
EP2731612A4
(de)
|
2011-07-13 |
2015-04-08 |
Pharmacyclics Inc |
Hemmer der bruton-tyrosinkinase
|
JP6027611B2
(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
|
AU2012284088B2
(en)
|
2011-07-19 |
2015-10-08 |
Infinity Pharmaceuticals Inc. |
Heterocyclic compounds and uses thereof
|
EP2548877A1
(de)
*
|
2011-07-19 |
2013-01-23 |
MSD Oss B.V. |
4-(5-Gliedrige kondensierte Pyridinyl)benzamide als BTK-Inhibitoren
|
CA2846431A1
(en)
|
2011-08-29 |
2013-03-07 |
Infinity Pharmaceuticals Inc. |
Heterocyclic compounds and uses thereof
|
JP6342805B2
(ja)
*
|
2011-09-02 |
2018-06-13 |
ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア |
置換ピラゾロ[3,4−d]ピリミジンおよびその用途
|
CN103917231B
(zh)
|
2011-09-13 |
2016-09-28 |
药品循环有限责任公司 |
组蛋白脱乙酰酶抑制剂与苯达莫司汀的联合制剂及其用途
|
US9382239B2
(en)
|
2011-11-17 |
2016-07-05 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of c-Jun-N-terminal kinase (JNK)
|
US8377946B1
(en)
|
2011-12-30 |
2013-02-19 |
Pharmacyclics, Inc. |
Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors
|
JP6335796B2
(ja)
|
2012-02-08 |
2018-06-06 |
アイジーエム バイオサイエンシズ インク.Igm Biosciences Inc. |
Cdim結合タンパク質及びその使用
|
US8940742B2
(en)
|
2012-04-10 |
2015-01-27 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
KR101972990B1
(ko)
*
|
2012-05-31 |
2019-04-26 |
파마사이언스 인크. |
단백질 키나제 저해제
|
CA3218491A1
(en)
|
2012-06-04 |
2013-12-12 |
Pharmacyclics Llc |
Crystalline forms of a bruton's tyrosine kinase inhibitor
|
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
|
GB201211309D0
(en)
*
|
2012-06-26 |
2012-08-08 |
Fujifilm Mfg Europe Bv |
Process for preparing membranes
|
KR20180088926A
(ko)
|
2012-07-24 |
2018-08-07 |
파마싸이클릭스 엘엘씨 |
브루톤 티로신 키나제(btk)의 억제제에 대한 내성과 관련된 돌연변이
|
JP6327713B2
(ja)
|
2012-07-27 |
2018-05-23 |
国立研究開発法人理化学研究所 |
急性骨髄性白血病の治療又は再発抑制剤
|
CA2882367C
(en)
|
2012-09-10 |
2021-11-09 |
Principia Biopharma Inc. |
Pyrazolopyrimidine compounds as kinase inhibitors
|
MX2015003874A
(es)
|
2012-09-26 |
2015-12-16 |
Univ California |
Modulacion de ire1.
|
EP2909194A1
(de)
|
2012-10-18 |
2015-08-26 |
Dana-Farber Cancer Institute, Inc. |
Hemmer der cyclinabhängigen kinase 7 (cdk7)
|
USRE48175E1
(en)
|
2012-10-19 |
2020-08-25 |
Dana-Farber Cancer Institute, Inc. |
Hydrophobically tagged small molecules as inducers of protein degradation
|
WO2014063054A1
(en)
|
2012-10-19 |
2014-04-24 |
Dana-Farber Cancer Institute, Inc. |
Bone marrow on x chromosome kinase (bmx) inhibitors and uses thereof
|
JP2015537033A
(ja)
|
2012-11-15 |
2015-12-24 |
ファーマサイクリックス,インク. |
キナーゼ阻害剤としてのピロロピリミジン化合物
|
JP6403219B2
(ja)
|
2012-12-07 |
2018-10-10 |
ベナトルクス ファーマシューティカルズ,インク. |
ベータ−ラクタマーゼ阻害剤
|
WO2014110442A1
(en)
|
2013-01-10 |
2014-07-17 |
VenatoRx Pharmaceuticals, Inc. |
Beta-lactamase inhibitors
|
WO2014122474A1
(en)
|
2013-02-07 |
2014-08-14 |
Takeda Pharmaceutical Company Limited |
Piperidin-1 -yl and azepin-1 -yl carboxylates as muscarinic m4 receptor agonists
|
EA201591685A1
(ru)
*
|
2013-03-15 |
2016-01-29 |
Янссен Фармацевтика Нв |
Способы и промежуточные соединения для получения лекарственного препарата
|
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
|
CA2907726A1
(en)
|
2013-03-22 |
2014-09-25 |
Millennium Pharmaceuticals, Inc. |
Combination of catalytic mtorc1/2 inhibitors and selective inhibitors of aurora a kinase
|
US8957080B2
(en)
|
2013-04-09 |
2015-02-17 |
Principia Biopharma Inc. |
Tyrosine kinase inhibitors
|
AU2014256633B2
(en)
|
2013-04-25 |
2017-02-02 |
Beigene Switzerland Gmbh |
Fused heterocyclic compounds as protein kinase inhibitors
|
TWI649081B
(zh)
|
2013-08-02 |
2019-02-01 |
製藥公司 |
治療固態腫瘤之方法
|
WO2015023703A1
(en)
|
2013-08-12 |
2015-02-19 |
Pharmacyclics, Inc. |
Methods for the treatment of her2 amplified cancer
|
CA3080200A1
(en)
|
2013-09-13 |
2015-03-19 |
Beigene Switzerland Gmbh |
Anti-pd1 antibodies and their use as therapeutics and diagnostics
|
BR112016006978A2
(pt)
|
2013-09-30 |
2017-08-01 |
Pharmacyclics Llc |
inibidores de tirosina quinase de bruton
|
US9359365B2
(en)
|
2013-10-04 |
2016-06-07 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
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)
|
WO2015058126A1
(en)
|
2013-10-18 |
2015-04-23 |
Syros Pharmaceuticals, Inc. |
Heteroaromatic compounds useful for the treatment of prolferative diseases
|
KR102452866B1
(ko)
|
2013-10-25 |
2022-10-07 |
파마싸이클릭스 엘엘씨 |
이식편 대 숙주 질환의 치료 및 예방 방법
|
US9856223B2
(en)
|
2013-12-13 |
2018-01-02 |
Dana-Farber Cancer Institute, Inc. |
Methods to treat lymphoplasmacytic lymphoma
|
MX2016009403A
(es)
|
2014-02-03 |
2016-09-16 |
Cadila Healthcare Ltd |
Compuestos heterociclicos.
|
EP3105238A4
(de)
*
|
2014-02-13 |
2017-11-08 |
Ligand Pharmaceuticals, Inc. |
Organische verbindungen und deren verwendungen
|
BR112016018948B1
(pt)
|
2014-02-21 |
2023-01-17 |
Principia Biopharma Inc |
Uso de composto ou sal farmaceuticamente aceitável, ácido sulfônico ou sal de ácido carboxílico de composto, forma amorfa de sal farmaceuticamente aceitável de composto, composição farmacêutica e respectivo uso
|
CA2943075C
(en)
|
2014-03-19 |
2023-02-28 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds for use in the treatment of pi3k-gamma mediated disorders
|
CA2942528A1
(en)
|
2014-03-20 |
2015-09-24 |
Pharmacyclics Inc. |
Phospholipase c gamma 2 and resistance associated mutations
|
WO2015160975A2
(en)
|
2014-04-16 |
2015-10-22 |
Infinity Pharmaceuticals, Inc. |
Combination therapies
|
US9862688B2
(en)
|
2014-04-23 |
2018-01-09 |
Dana-Farber Cancer Institute, Inc. |
Hydrophobically tagged janus kinase inhibitors and uses thereof
|
US10017477B2
(en)
|
2014-04-23 |
2018-07-10 |
Dana-Farber Cancer Institute, Inc. |
Janus kinase inhibitors and uses thereof
|
GB201410430D0
(en)
|
2014-06-11 |
2014-07-23 |
Redx Pharma Ltd |
Compounds
|
TWI687438B
(zh)
|
2014-07-03 |
2020-03-11 |
英屬開曼群島商百濟神州生物科技有限公司 |
抗pd-l1抗體及其作為治療及診斷之用途
|
EP3174539A4
(de)
|
2014-08-01 |
2017-12-13 |
Pharmacyclics, LLC |
Hemmer der bruton-tyrosinkinase
|
CN106573002A
(zh)
|
2014-08-07 |
2017-04-19 |
药品循环有限责任公司 |
布鲁顿氏酪氨酸激酶抑制剂的新型制剂
|
US9708348B2
(en)
|
2014-10-03 |
2017-07-18 |
Infinity Pharmaceuticals, Inc. |
Trisubstituted bicyclic heterocyclic compounds with kinase activities and uses thereof
|
ITRM20140620A1
(it)
|
2014-10-30 |
2016-04-30 |
Lead Discovery Siena S R L |
Compounds and uses thereof
|
CA2964276A1
(en)
|
2014-11-05 |
2016-05-12 |
Flexus Biosciences, Inc. |
Immunoregulatory agents
|
UY36390A
(es)
*
|
2014-11-05 |
2016-06-01 |
Flexus Biosciences Inc |
Compuestos moduladores de la enzima indolamina 2,3-dioxigenasa (ido), sus métodos de síntesis y composiciones farmacéuticas que los contienen
|
CN104478884A
(zh)
*
|
2014-12-05 |
2015-04-01 |
广东东阳光药业有限公司 |
一种中间体的制备方法
|
PL3233103T3
(pl)
|
2014-12-18 |
2021-04-19 |
Principia Biopharma Inc. |
Leczenie pęcherzycy
|
US10167451B2
(en)
|
2014-12-22 |
2019-01-01 |
The Chinese University Of Hong Kong |
Combinational use of mechanical manipulation and programin derivatives to increase Oct4, Sox2, or Nanog expression in fibroblasts
|
JP6736253B2
(ja)
*
|
2014-12-22 |
2020-08-05 |
ザ チャイニーズ ユニバーシティ オブ ホンコン |
体細胞から多能性幹細胞を作製するための機械的操作とプログラミンの併用
|
CA2972239A1
(en)
|
2014-12-23 |
2016-06-30 |
Dana-Farber Cancer Institute, Inc. |
Inhibitors of cyclin-dependent kinase 7 (cdk7)
|
EP3242666B1
(de)
|
2015-01-06 |
2024-10-16 |
Arena Pharmaceuticals, Inc. |
Wirkstoff zur behandlung von mit s1p1-rezeptor zusammenhängenden erkrankungen
|
CN105777755A
(zh)
*
|
2015-01-07 |
2016-07-20 |
常州百敖威生物科技有限公司 |
一种伊鲁替尼中间体3-碘-1h-吡唑并[3,4-d]嘧啶-4-胺的制备方法
|
IL315294A
(en)
|
2015-03-03 |
2024-10-01 |
Pharmacyclics Llc |
Pharmaceutical formulations of proton tyrosine kinase inhibitor
|
EP3273966B1
(de)
|
2015-03-27 |
2023-05-03 |
Dana-Farber Cancer Institute, Inc. |
Hemmer von cyclinabhängigen kinasen
|
AU2016276963C1
(en)
|
2015-06-12 |
2021-08-05 |
Dana-Farber Cancer Institute, Inc. |
Combination therapy of transcription inhibitors and kinase inhibitors
|
PT3310760T
(pt)
|
2015-06-22 |
2022-11-10 |
Arena Pharm Inc |
Sal cristalino de l-arginina de ácido (r)-2-(7-(4-ciclopentil-3-(trifluorometil)benziloxi)-1,2,3,4-tetrahidrociclo-penta[b]indol-3-il)acético para utilização em distúrbios associados a recetores de s1p1
|
EP3313839A1
(de)
|
2015-06-24 |
2018-05-02 |
Principia Biopharma Inc. |
Tyrosin-kinase-inhibitoren
|
EP4019515A1
(de)
|
2015-09-09 |
2022-06-29 |
Dana-Farber Cancer Institute, Inc. |
Hemmer von cyclinabhängigen kinasen
|
NZ740616A
(en)
|
2015-09-14 |
2023-05-26 |
Infinity Pharmaceuticals Inc |
Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same
|
US10611766B2
(en)
|
2015-09-16 |
2020-04-07 |
Loxo Oncology Inc. |
Pyrazolopyrimidine derivatives as BTK inhibitors for the treatment of cancer
|
MX2021003478A
(es)
|
2015-12-16 |
2022-07-25 |
Loxo Oncology Inc |
Compuestos utiles como inhibidores de cinasa.
|
WO2017161116A1
(en)
|
2016-03-17 |
2017-09-21 |
Infinity Pharmaceuticals, Inc. |
Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as pi3k kinase inhibitors
|
US10919914B2
(en)
|
2016-06-08 |
2021-02-16 |
Infinity Pharmaceuticals, Inc. |
Heterocyclic compounds and uses thereof
|
MX2018016227A
(es)
|
2016-06-24 |
2019-07-08 |
Infinity Pharmaceuticals Inc |
Terapias de combinacion.
|
KR102515813B1
(ko)
|
2016-06-29 |
2023-03-30 |
프린시피아 바이오파마, 인코퍼레이티드 |
2-[3-[4-아미노-3-(2-플루오로-4-페녹시-페닐)피라졸로[3,4-d]피리미딘-1-일]피페리딘-1-카르보닐]-4-메틸-4-[4-(옥세탄-3-일)피페라진-1-일]펜트-2-엔니트릴의 변형 방출 제제
|
WO2018007885A1
(en)
|
2016-07-05 |
2018-01-11 |
Beigene, Ltd. |
COMBINATION OF A PD-l ANTAGONIST AND A RAF INHIBITOR FOR TREATING CANCER
|
CA3033827A1
(en)
|
2016-08-16 |
2018-02-22 |
Beigene, Ltd. |
Crystalline form of (s)-7-(1-acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl )-4,5,6,7-tetra-hydropyrazolo[1,5-a]pyrimidine-3-carboxamide,preparation, and uses thereof
|
TWI739887B
(zh)
|
2016-08-19 |
2021-09-21 |
英屬開曼群島商百濟神州有限公司 |
使用包含btk抑制劑的組合產品治療癌症
|
EP3573989A4
(de)
|
2017-01-25 |
2020-11-18 |
Beigene, Ltd. |
Kristalline formen von (s)-7-(1-(but-2-ynoyl)-piperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-carboxamid, herstellung und verwendungen davon
|
CA3053418A1
(en)
|
2017-02-16 |
2018-08-23 |
Arena Pharmaceuticals, Inc. |
Compounds and methods for treatment of primary biliary cholangitis
|
EP3645569A4
(de)
|
2017-06-26 |
2021-03-24 |
BeiGene, Ltd. |
Immuntherapie für leberzellkarzinom
|
US11377449B2
(en)
|
2017-08-12 |
2022-07-05 |
Beigene, Ltd. |
BTK inhibitors with improved dual selectivity
|
WO2019108795A1
(en)
|
2017-11-29 |
2019-06-06 |
Beigene Switzerland Gmbh |
Treatment of indolent or aggressive b-cell lymphomas using a combination comprising btk inhibitors
|
US11970482B2
(en)
|
2018-01-09 |
2024-04-30 |
Ligand Pharmaceuticals Inc. |
Acetal compounds and therapeutic uses thereof
|
CN108299311A
(zh)
*
|
2018-02-28 |
2018-07-20 |
杭州福斯特药业有限公司 |
一种5-溴-2-氯-n-环戊基嘧啶-4-胺的制备方法
|
CN111171035B
(zh)
*
|
2018-11-13 |
2021-03-30 |
山东大学 |
4-苯氧基苯基吡唑并嘧啶酰胺衍生物的制备方法和应用
|
CN111454268B
(zh)
*
|
2019-01-18 |
2023-09-08 |
明慧医药(上海)有限公司 |
作为布鲁顿酪氨酸激酶抑制剂的环状分子
|
AU2020301399A1
(en)
*
|
2019-06-24 |
2021-12-02 |
Dana-Farber Cancer Institute, Inc. |
HCK degraders and uses thereof
|
CN110511225B
(zh)
*
|
2019-08-19 |
2023-07-18 |
杭州中美华东制药有限公司 |
一种伊布替尼中间体的合成方法
|
WO2021038540A1
(en)
|
2019-08-31 |
2021-03-04 |
Sun Pharma Advanced Research Company Limited |
Cycloalkylidene carboxylic acids and derivatives as btk inhibitors
|
US11370803B2
(en)
|
2019-09-18 |
2022-06-28 |
Takeda Pharmaceutical Company Limited |
Heteroaryl plasma kallikrein inhibitors
|
CN114728962A
(zh)
|
2019-09-18 |
2022-07-08 |
武田药品工业有限公司 |
血浆激肽释放酶抑制剂及其用途
|
JP2022551502A
(ja)
*
|
2019-10-08 |
2022-12-09 |
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 |
治療、特にmyd88変異疾患における使用のためのhck阻害剤としてのピラゾロピリミジン誘導体
|
CN112961158B
(zh)
*
|
2020-03-05 |
2022-07-01 |
四川大学华西医院 |
氨基嘧啶并吡唑/吡咯类衍生物及其制备方法和用途
|
AU2020436612A1
(en)
|
2020-03-16 |
2022-09-01 |
Flash Therapeutics, Llc |
Compounds for treating or inhibiting recurrence of acute myeloid leukemia
|
TWI797711B
(zh)
|
2020-08-13 |
2023-04-01 |
大陸商上海和譽生物醫藥科技有限公司 |
一種fgfr及其突變抑制劑,其製備方法和應用
|
US11912668B2
(en)
|
2020-11-18 |
2024-02-27 |
Deciphera Pharmaceuticals, Llc |
GCN2 and perk kinase inhibitors and methods of use thereof
|
EP4308229A1
(de)
*
|
2021-03-17 |
2024-01-24 |
Takeda Pharmaceutical Company Limited |
Plasmakallikreinhemmer
|
US11786531B1
(en)
|
2022-06-08 |
2023-10-17 |
Beigene Switzerland Gmbh |
Methods of treating B-cell proliferative disorder
|
CN115650986B
(zh)
*
|
2022-10-22 |
2024-07-30 |
浙江工业大学 |
肉桂酰氨基吡唑并[3,4-d]嘧啶类化合物及其制备和应用
|