WO2007070514A1
(en)
|
2005-12-13 |
2007-06-21 |
Incyte Corporation |
Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors
|
US7989459B2
(en)
|
2006-02-17 |
2011-08-02 |
Pharmacopeia, Llc |
Purinones and 1H-imidazopyridinones as PKC-theta inhibitors
|
WO2008043019A1
(en)
|
2006-10-04 |
2008-04-10 |
Pharmacopeia, Inc |
8-substituted 2-(benzimidazolyl) purine derivatives for immunosuppression
|
US7902187B2
(en)
|
2006-10-04 |
2011-03-08 |
Wyeth Llc |
6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression
|
US7919490B2
(en)
|
2006-10-04 |
2011-04-05 |
Wyeth Llc |
6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression
|
RS58449B1
(sr)
|
2007-06-13 |
2019-04-30 |
Incyte Holdings Corp |
Upotreba soli inhibitora janus kinaze (r)-3-(4-(7h-pirolo[2,3-d]pirimidin-4-il)-1h- pirazol-1-il)-3-ciklopentilpropionitrila
|
US20110118238A1
(en)
*
|
2007-08-23 |
2011-05-19 |
Astrazeneca Ab |
2-anilinopurin-8-ones as inhibitors of ttk/mps1 for the treatment of proliferative disorders
|
US8841312B2
(en)
|
2007-12-19 |
2014-09-23 |
Amgen Inc. |
Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors
|
AU2009211338B2
(en)
|
2008-02-06 |
2011-12-15 |
Novartis Ag |
Pyrrolo[2, 3-D] pyrimidines and use thereof as tyrosine kinase inhibitors
|
TW200942544A
(en)
*
|
2008-03-03 |
2009-10-16 |
Takeda Pharmaceutical |
Combination drug
|
US8389533B2
(en)
|
2008-04-07 |
2013-03-05 |
Amgen Inc. |
Gem-disubstituted and spirocyclic amino pyridines/pyrimidines as cell cycle inhibitors
|
TW201002713A
(en)
|
2008-04-09 |
2010-01-16 |
Organon Nv |
Pyrrolo[2,3-d]pyrimidin-2-yl-amine derivatives as PKC-theta inhibitors
|
JP2011518841A
(ja)
*
|
2008-04-24 |
2011-06-30 |
ニューリンク ジェネティクス, インコーポレイテッド |
Ido阻害剤
|
WO2009152027A1
(en)
*
|
2008-06-12 |
2009-12-17 |
Merck & Co., Inc. |
5,7-dihydro-6h-pyrrolo[2,3-d]pyrimidin-6-one derivatives for mark inhibition
|
PE20110419A1
(es)
|
2008-08-22 |
2011-07-13 |
Novartis Ag |
Compuestos de pirrolo-pirimidina como inhibidores de cdk
|
WO2010045451A1
(en)
*
|
2008-10-16 |
2010-04-22 |
Glaxosmithkline Llc |
Pyrrolopyrimidine compounds
|
GB0903759D0
(en)
*
|
2009-03-04 |
2009-04-15 |
Medical Res Council |
Compound
|
EP3025724B1
(en)
|
2009-05-13 |
2018-07-11 |
The University of North Carolina At Chapel Hill |
Cyclin dependent kinase inhibitors and methods of use
|
AU2010249380B2
(en)
|
2009-05-22 |
2015-08-20 |
Incyte Holdings Corporation |
N-(hetero)aryl-pyrrolidine derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines and pyrrol-3-yl-pyrrolo[2,3-d]pyrimidines as Janus kinase inhibitors
|
EP3643312A1
(en)
|
2009-05-22 |
2020-04-29 |
Incyte Holdings Corporation |
3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]octane- or heptane-nitrile as jak inhibitors
|
AR078012A1
(es)
|
2009-09-01 |
2011-10-05 |
Incyte Corp |
Derivados heterociclicos de las pirazol-4-il- pirrolo (2,3-d) pirimidinas como inhibidores de la quinasa janus
|
TWI478714B
(zh)
|
2009-10-29 |
2015-04-01 |
Vectura Ltd |
作為Janus激酶3(JAK3)抑制劑之含氮雜芳基衍生物類
|
WO2011082400A2
(en)
*
|
2010-01-04 |
2011-07-07 |
President And Fellows Of Harvard College |
Modulators of immunoinhibitory receptor pd-1, and methods of use thereof
|
EP4289838A3
(en)
|
2010-02-11 |
2024-03-13 |
Celgene Corporation |
Arylmethoxy isoindoline derivatives and compositions comprising and methods of using the same
|
UY33227A
(es)
*
|
2010-02-19 |
2011-09-30 |
Novartis Ag |
Compuestos de pirrolopirimidina como inhibidores de la cdk4/6
|
UY33226A
(es)
|
2010-02-19 |
2011-09-30 |
Novartis Ag |
Compuestos de pirrolopirimidina deuterada como inhibidores de la cdk4/6
|
CN102985417B
(zh)
|
2010-03-10 |
2015-01-28 |
因塞特公司 |
作为jak1抑制剂的哌啶-4-基氮杂环丁烷衍生物
|
ES2689177T3
(es)
*
|
2010-04-13 |
2018-11-08 |
Novartis Ag |
Combinación que comprende un inhibidor de cinasa 4 dependiente de ciclina o cinasa dependiente de ciclina (CDK4/6) y un inhibidor de mTOR para tratar cáncer
|
GB201007286D0
(en)
|
2010-04-30 |
2010-06-16 |
Astex Therapeutics Ltd |
New compounds
|
WO2011146313A1
(en)
|
2010-05-19 |
2011-11-24 |
The University Of North Carolina At Chapel Hill |
Pyrazolopyrimidine compounds for the treatment of cancer
|
EA035981B1
(ru)
|
2010-05-21 |
2020-09-09 |
Инсайт Холдингс Корпорейшн |
Композиция ингибитора jak для местного применения
|
RS55135B1
(sr)
*
|
2010-10-25 |
2016-12-30 |
G1 Therapeutics Inc |
Cdk inhibitori
|
US20120115878A1
(en)
*
|
2010-11-10 |
2012-05-10 |
John Vincent Calienni |
Salt(s) of 7-cyclopentyl-2-(5-piperazin-1-yl-pyridin-2-ylamino)-7h-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide and processes of making thereof
|
WO2012068381A2
(en)
|
2010-11-17 |
2012-05-24 |
The University Of North Carolina At Chapel Hill |
Protection of renal tissues from schema through inhibition of the proliferative kisses cdk4 and cdk6
|
TW201249845A
(en)
|
2010-11-19 |
2012-12-16 |
Incyte Corp |
Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as JAK inhibitors
|
EP2640725B1
(en)
|
2010-11-19 |
2015-01-07 |
Incyte Corporation |
Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors
|
CN103476776B
(zh)
*
|
2011-01-07 |
2016-09-28 |
北京赛林泰医药技术有限公司 |
作为FAK/Pyk2抑制剂的2,4-二氨基-6,7-二氢-5H-吡咯并[2,3]嘧啶衍生物
|
CN102093364B
(zh)
*
|
2011-01-07 |
2015-01-28 |
北京赛林泰医药技术有限公司 |
作为FAK/Pyk2抑制剂的2,4-二氨基-6,7-二氢-5H-吡咯并[2,3]嘧啶衍生物
|
WO2012110773A1
(en)
|
2011-02-17 |
2012-08-23 |
Cancer Therapeutics Crc Pty Limited |
Fak inhibitors
|
JP5937112B2
(ja)
|
2011-02-17 |
2016-06-22 |
カンサー・セラピューティクス・シーアールシー・プロプライエタリー・リミテッドCancer Therapeutics Crc Pty Limited |
選択的fak阻害剤
|
GB201104267D0
(en)
|
2011-03-14 |
2011-04-27 |
Cancer Rec Tech Ltd |
Pyrrolopyridineamino derivatives
|
BR112013024267A2
(pt)
|
2011-03-22 |
2018-06-26 |
Advinus Therapeutics Ltd |
compostos tricíclicos fundidos substituídos, composições e aplicações medicinais dos mesmos.
|
PT2937349T
(pt)
|
2011-03-23 |
2017-03-24 |
Amgen Inc |
Inibidores duais tricíclicos fusionados de cdk 4/6 e flt3
|
CA2836417A1
(en)
*
|
2011-05-17 |
2012-11-22 |
Principia Biopharma Inc. |
Azaindole derivatives as tyrosine kinase inhibitors
|
WO2012177606A1
(en)
|
2011-06-20 |
2012-12-27 |
Incyte Corporation |
Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors
|
EP2726074B1
(en)
|
2011-07-01 |
2018-04-04 |
Novartis AG |
Combination therapy comprising a cdk4/6 inhibitor and a pi3k inhibitor for use in the treatment of cancer
|
CA2840620A1
(en)
|
2011-07-01 |
2013-01-10 |
Novartis Ag |
Combination therapy
|
CA2841111A1
(en)
|
2011-07-08 |
2013-01-17 |
Novartis Ag |
Novel pyrrolo pyrimidine derivatives
|
WO2013017479A1
(en)
*
|
2011-07-29 |
2013-02-07 |
Cellzome Limited |
Pyrazolo[4,3-c]pyridine derivatives as jak inhibitors
|
WO2013017480A1
(en)
*
|
2011-07-29 |
2013-02-07 |
Cellzome Limited |
Pyrazolo[4,3-c]pyridine derivatives as jak inhibitors
|
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
|
UA111854C2
(uk)
|
2011-09-07 |
2016-06-24 |
Інсайт Холдінгс Корпорейшн |
Способи і проміжні сполуки для отримання інгібіторів jak
|
JP2014532060A
(ja)
|
2011-10-03 |
2014-12-04 |
ザ・ユニヴァーシティ・オヴ・ノース・キャロライナ・アト・チャペル・ヒル |
癌を治療するためのピロロピリミジン化合物
|
WO2013059634A1
(en)
|
2011-10-20 |
2013-04-25 |
The Regents Of The University Of California |
Use of cdk9 inhibitors to reduce cartilage degradation
|
TW201406761A
(zh)
|
2012-05-18 |
2014-02-16 |
Incyte Corp |
做爲jak抑制劑之哌啶基環丁基取代之吡咯并吡啶及吡咯并嘧啶衍生物
|
CA2873878A1
(en)
|
2012-05-22 |
2013-11-28 |
The University Of North Carolina At Chapel Hill |
Pyrimidine compounds for the treatment of cancer
|
EA201492104A1
(ru)
*
|
2012-06-14 |
2015-06-30 |
Эли Лилли Энд Компани |
Ингибитор jak1/2
|
EP2880448B1
(en)
|
2012-08-03 |
2022-06-29 |
Foundation Medicine, Inc. |
Human papilloma virus as predictor of cancer prognosis
|
GB201216018D0
(en)
|
2012-09-07 |
2012-10-24 |
Cancer Rec Tech Ltd |
Pharmacologically active compounds
|
GB201216017D0
(en)
|
2012-09-07 |
2012-10-24 |
Cancer Rec Tech Ltd |
Inhibitor compounds
|
WO2014045305A1
(en)
|
2012-09-21 |
2014-03-27 |
Advinus Therapeutics Limited |
Substituted fused tricyclic compounds, compositions and medicinal applications thereof
|
EP2912036A1
(en)
|
2012-10-04 |
2015-09-02 |
Pfizer Limited |
Pyrrolo[3,2-c]pyridine tropomyosin-related kinase inhibitors
|
WO2014062774A1
(en)
|
2012-10-17 |
2014-04-24 |
The University Of North Carolina At Chapel Hill |
Pyrazolopyrimidine compounds for the treatment of cancer
|
CN113384545A
(zh)
|
2012-11-15 |
2021-09-14 |
因赛特公司 |
鲁索利替尼的缓释剂型
|
US9771330B2
(en)
|
2012-11-27 |
2017-09-26 |
The University Of North Carolina At Chapel Hill |
Pyrimidine compounds for the treatment of cancer
|
EP3251673A1
(en)
|
2012-12-13 |
2017-12-06 |
IP Gesellschaft für Management mbH |
Combination therapy comprising a cdk4/6 inhibitor and a pi3k inhibitor for use in the treatment of cancer
|
EP2934515B1
(en)
*
|
2012-12-20 |
2018-04-04 |
Novartis AG |
A pharmaceutical combination comprising binimetinib
|
WO2014130693A1
(en)
*
|
2013-02-25 |
2014-08-28 |
Pharmacyclics, Inc. |
Inhibitors of bruton's tyrosine kinase
|
EP2959013A2
(en)
|
2013-02-25 |
2015-12-30 |
Novartis AG |
Novel androgen receptor mutation
|
CA2903901A1
(en)
*
|
2013-03-05 |
2014-09-12 |
Merck Patent Gmbh |
9-(aryl or heteroaryl)-2-(pyrazolyl, pyrrolidinyl or cyclopentyl)aminopurine derivatives as anticancer agents
|
SI3489239T1
(sl)
|
2013-03-06 |
2022-04-29 |
Incyte Holdings Corporation |
Postopki in intermediati za pripravo zaviralca JAK
|
JP6449234B2
(ja)
|
2013-03-21 |
2019-01-09 |
ノバルティス アーゲー |
併用療法
|
AU2014253932B2
(en)
|
2013-04-16 |
2020-04-30 |
Memorial Sloan-Kettering Cancer Center |
Companion diagnostic for CDK4 inhibitors
|
KR101793807B1
(ko)
|
2013-04-25 |
2017-11-03 |
베이진 엘티디 |
단백질 키나제 억제제로서의 융합된 헤테로시클릭 화합물
|
US8895611B1
(en)
|
2013-07-17 |
2014-11-25 |
King Fahd University Of Petroleum And Minerals |
Cytotoxic compounds for treating cancer
|
EA201690357A1
(ru)
|
2013-08-07 |
2016-07-29 |
Инсайт Корпорейшн |
Лекарственные формы с замедленным высвобождением для ингибитора jak1
|
CN103408546A
(zh)
*
|
2013-08-22 |
2013-11-27 |
中国药科大学 |
2-苯氨基嘌呤类plk1抑制剂及其用途
|
EP4130044A1
(en)
|
2013-09-13 |
2023-02-08 |
BeiGene Switzerland GmbH |
Anti-pd1 antibodies and their use as therapeutics and diagnostics
|
GB201403536D0
(en)
|
2014-02-28 |
2014-04-16 |
Cancer Rec Tech Ltd |
Inhibitor compounds
|
WO2015144808A1
(en)
|
2014-03-26 |
2015-10-01 |
Astex Therapeutics Ltd |
Combinations of an fgfr inhibitor and an igf1r inhibitor
|
KR102479693B1
(ko)
|
2014-03-26 |
2022-12-22 |
아스텍스 테라퓨틱스 리미티드 |
조합물
|
JO3512B1
(ar)
|
2014-03-26 |
2020-07-05 |
Astex Therapeutics Ltd |
مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز
|
WO2015157115A1
(en)
|
2014-04-11 |
2015-10-15 |
The University Of North Carolina At Chapel Hill |
Mertk-specific pyrimidine compounds
|
WO2015160986A2
(en)
|
2014-04-16 |
2015-10-22 |
Infinity Pharmaceuticals, Inc. |
Combination therapies
|
ES2873959T3
(es)
|
2014-05-28 |
2021-11-04 |
Piramal Entpr Ltd |
Combinación farmacéutica que comprende un inhibidor de CDK y un inhibidor de tiorredoxina reductasa para el tratamiento del cáncer
|
WO2015180642A1
(en)
*
|
2014-05-28 |
2015-12-03 |
Shanghai Fochon Pharmaceutical Co Ltd |
Certain protein kinase inhibitors
|
US9498467B2
(en)
|
2014-05-30 |
2016-11-22 |
Incyte Corporation |
Treatment of chronic neutrophilic leukemia (CNL) and atypical chronic myeloid leukemia (aCML) by inhibitors of JAK1
|
KR102130600B1
(ko)
|
2014-07-03 |
2020-07-08 |
베이진 엘티디 |
Pd-l1 항체와 이를 이용한 치료 및 진단
|
MY187555A
(en)
|
2014-07-24 |
2021-09-29 |
Beta Pharma Inc |
2-h-indazole derivatives as cyclin-dependent kinase (cdk) inhibitors and therapeutic uses thereof
|
SG10202009598VA
(en)
|
2014-10-06 |
2020-10-29 |
Signal Pharm Llc |
Substituted aminopurine compounds, compositions thereof, and methods of treatment therewith
|
JP6930913B2
(ja)
|
2014-10-14 |
2021-09-01 |
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The Regents Of The University Of California |
炎症を阻害するためのcdk9及びbrd4阻害剤の使用法
|
CN105111215B
(zh)
*
|
2014-12-12 |
2019-06-18 |
苏州晶云药物科技股份有限公司 |
一种周期蛋白依赖性激酶抑制剂的晶型及其制备方法
|
CN104610265A
(zh)
*
|
2014-12-31 |
2015-05-13 |
芜湖杨燕制药有限公司 |
一种化合物及其制备方法
|
CN104606197A
(zh)
*
|
2014-12-31 |
2015-05-13 |
芜湖杨燕制药有限公司 |
一种化合物的抗肿瘤用途
|
JOP20200201A1
(ar)
|
2015-02-10 |
2017-06-16 |
Astex Therapeutics Ltd |
تركيبات صيدلانية تشتمل على n-(3.5- ثنائي ميثوكسي فينيل)-n'-(1-ميثيل إيثيل)-n-[3-(ميثيل-1h-بيرازول-4-يل) كينوكسالين-6-يل]إيثان-1.2-ثنائي الأمين
|
EP3778604A1
(en)
*
|
2015-02-13 |
2021-02-17 |
Dana Farber Cancer Institute, Inc. |
Lrrk2 inhibitors and methods of making and using the same
|
CN106146515B
(zh)
*
|
2015-04-17 |
2020-09-04 |
常州隆赛医药科技有限公司 |
新型激酶抑制剂的制备及应用
|
MX2018003564A
(es)
|
2015-09-23 |
2018-06-18 |
Janssen Pharmaceutica Nv |
1,4-benzodiazepinas biheteroarilo sustituidas y usos de las mismas para el tratamiento del cancer.
|
LT3353177T
(lt)
|
2015-09-23 |
2020-08-25 |
Janssen Pharmaceutica Nv |
Tricikliniai heterociklai, skirti vėžio gydymui
|
WO2017114351A1
(en)
*
|
2015-12-27 |
2017-07-06 |
Chongqing Fochon Pharmaceutical Co., Ltd. |
Certain protein kinase inhibitors
|
WO2017114512A1
(zh)
|
2015-12-31 |
2017-07-06 |
上海医药集团股份有限公司 |
含氮稠杂环化合物、制备方法、中间体、组合物和应用
|
WO2017156263A1
(en)
|
2016-03-09 |
2017-09-14 |
Memorial Sloan-Kettering Cancer Center |
Enigma and cdh18 as companion diagnostics for cdk4 inhibitors
|
US10709708B2
(en)
|
2016-03-17 |
2020-07-14 |
The University Of North Carolina At Chapel Hill |
Method of treating cancer with a combination of MER tyrosine kinase inhibitor and an epidermal growth factor receptor (EGFR) inhibitor
|
US10576085B2
(en)
|
2016-04-01 |
2020-03-03 |
Signal Pharmaceuticals, Llc |
Substituted aminopurine compounds, compositions thereof, and methods of treatment therewith
|
AU2017240050B2
(en)
|
2016-04-01 |
2021-12-16 |
Signal Pharmaceuticals, Llc |
Solid forms of (1s,4s)-4-(2-(((3S4R)-3-fluorotetrahydro-2H-pyran-4-yl) amino)-8-((2,4,6-trichlorophenyl) amino)-9H-purin-9-yl)-1-methylcyclohexane-1-carboxamide and methods of their use
|
AU2017293423B2
(en)
|
2016-07-05 |
2023-05-25 |
Beigene, Ltd. |
Combination of a PD-1 antagonist and a RAF inhibitor for treating cancer
|
WO2018033853A2
(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
|
WO2018033135A1
(en)
|
2016-08-19 |
2018-02-22 |
Beigene, Ltd. |
Use of a combination comprising a btk inhibitor for treating cancers
|
CA3034875A1
(en)
|
2016-08-23 |
2018-03-01 |
Eisai R&D Management Co., Ltd. |
Combination therapies for the treatment of hepatocellular carcinoma
|
IL292938A
(en)
|
2016-09-19 |
2022-07-01 |
Mei Pharma Inc |
Combined treatment
|
AU2017345367A1
(en)
*
|
2016-10-20 |
2019-04-04 |
Pfizer Inc. |
Anti-proliferative agents for treating PAH
|
WO2018081211A1
(en)
*
|
2016-10-26 |
2018-05-03 |
Li George Y |
Deuterated 7-cyclopentyl-n, n-dimethyl-2-((5-(piperazin-1-yl)pyridin-2-yl)amino)-7h-pyrrolo[2,3-d]pyrimdine-6-carboxamide
|
JP2020502062A
(ja)
*
|
2016-11-17 |
2020-01-23 |
ザ ユニバーシティ オブ ノース カロライナ アット チャペル ヒル |
アルキルピロロピリミジン類似体、及びその製造方法と使用方法
|
MX2019007189A
(es)
|
2016-12-20 |
2019-10-09 |
Astrazeneca Ab |
Compuestos de amino-triazolopiridina y su uso en el trataniento del cancer.
|
WO2018117177A1
(ja)
*
|
2016-12-21 |
2018-06-28 |
小野薬品工業株式会社 |
Brk阻害化合物
|
CA3048376A1
(en)
|
2016-12-27 |
2018-07-05 |
Riken |
Bmp-signal-inhibiting compound
|
WO2018137681A1
(en)
|
2017-01-25 |
2018-08-02 |
Beigene, Ltd. |
Crystalline forms of (s) -7- (1- (but-2-ynoyl) piperidin-4-yl) -2- (4-phenoxyphenyl) -4, 5, 6, 7-tetrahy dropyrazolo [1, 5-a] pyrimidine-3-carboxamide, preparation, and uses thereof
|
JP7142846B2
(ja)
*
|
2017-01-30 |
2022-09-28 |
国立大学法人京都大学 |
新規化合物及び制御性t細胞の製造方法
|
WO2018170447A1
(en)
|
2017-03-16 |
2018-09-20 |
Eisai R&D Management Co., Ltd. |
Combination therapies for the treatment of breast cancer
|
EA201992744A1
(ru)
|
2017-06-16 |
2020-05-27 |
Бета Фарма, Инк. |
Фармацевтические композиции n-(2-(2-(диметиламино)этокси)-4-метокси-5-((4-(1-метил-1h-индол-3-ил)пиримидин-2-ил)амино)фенил)акриламида и его солей
|
GB201709840D0
(en)
|
2017-06-20 |
2017-08-02 |
Inst Of Cancer Research: Royal Cancer Hospital |
Methods and medical uses
|
CA3066518A1
(en)
|
2017-06-26 |
2019-01-03 |
Beigene, Ltd. |
Immunotherapy for hepatocellular carcinoma
|
WO2019034009A1
(en)
|
2017-08-12 |
2019-02-21 |
Beigene, Ltd. |
BTK INHIBITOR WITH ENHANCED DOUBLE SELECTIVITY
|
US11174254B2
(en)
*
|
2017-09-28 |
2021-11-16 |
Yangtze River Pharmaceutical Group Co., Ltd. |
Aniline-substituted 1,2-dihydropyrrol[3,4-C]pyridin/pyrimidin-3-one derivative and use thereof
|
JP2020536100A
(ja)
|
2017-10-04 |
2020-12-10 |
セルジーン コーポレイション |
シス−4−[2−{[(3s,4r)−3−フルオロキサン−4−イル]アミノ}−8−(2,4,6−トリクロロアニリノ)−9h−プリン−9−イル]−1−メチルシクロヘキサン−1−カルボキサミドの製造プロセス
|
EA202090884A1
(ru)
|
2017-10-04 |
2020-06-26 |
Селджин Корпорейшн |
Композиции и способы применения цис-4-[2-{[(3s,4r)-3-фтороксан-4-ил]амино}-8-(2,4,6-трихлоранилино)-9н-пурин-9-ил]-1-метилциклогексан-1-карбоксамида
|
US11786529B2
(en)
|
2017-11-29 |
2023-10-17 |
Beigene Switzerland Gmbh |
Treatment of indolent or aggressive B-cell lymphomas using a combination comprising BTK inhibitors
|
US10596161B2
(en)
|
2017-12-08 |
2020-03-24 |
Incyte Corporation |
Low dose combination therapy for treatment of myeloproliferative neoplasms
|
BR112020015405A2
(pt)
*
|
2018-01-29 |
2020-12-08 |
Beta Pharma, Inc. |
Compostos de 2h-indazóis como inibidores cdk4 e cdk6, composições farmacêuticas que os compreendem, seus usos terapêuticos e métodos de preparação
|
SI3746429T1
(sl)
|
2018-01-30 |
2023-01-31 |
Incyte Corporation |
Postopki za pripravo (1-(3-fluoro-2-(trifluorometil)izonikotinil) piperidin-4-ona)
|
WO2019191684A1
(en)
|
2018-03-30 |
2019-10-03 |
Incyte Corporation |
Treatment of hidradenitis suppurativa using jak inhibitors
|
WO2019195959A1
(en)
|
2018-04-08 |
2019-10-17 |
Cothera Biosciences, Inc. |
Combination therapy for cancers with braf mutation
|
CA3043066A1
(en)
|
2018-05-14 |
2019-11-14 |
Apotex Inc. |
Processes for the preparation of ribociclib and intermediates thereof
|
WO2019222524A1
(en)
*
|
2018-05-16 |
2019-11-21 |
The University Of North Carolina At Chapel Hill |
Alkyl pyrrolopyrimidines as pan-tam inhibitors and their application in cancer treatment
|
CN110577524B
(zh)
*
|
2018-06-07 |
2022-01-28 |
北京大学深圳研究生院 |
一种激酶选择性抑制剂
|
CN109438447B
(zh)
*
|
2018-09-11 |
2020-10-16 |
北京工业大学 |
5,7-二氢-6H-吡咯并[2,3-d]嘧啶-6-酮类衍生物制备方法和应用
|
US11066404B2
(en)
|
2018-10-11 |
2021-07-20 |
Incyte Corporation |
Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
|
WO2020140052A1
(en)
*
|
2018-12-28 |
2020-07-02 |
Spv Therapeutics Inc. |
Cyclin-dependent kinase inhibitors
|
US20230065740A1
(en)
*
|
2018-12-28 |
2023-03-02 |
Spv Therapeutics Inc. |
Cyclin-dependent kinase inhibitors
|
US11384083B2
(en)
|
2019-02-15 |
2022-07-12 |
Incyte Corporation |
Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors
|
WO2020180959A1
(en)
|
2019-03-05 |
2020-09-10 |
Incyte Corporation |
Pyrazolyl pyrimidinylamine compounds as cdk2 inhibitors
|
US11919904B2
(en)
|
2019-03-29 |
2024-03-05 |
Incyte Corporation |
Sulfonylamide compounds as CDK2 inhibitors
|
WO2020223469A1
(en)
|
2019-05-01 |
2020-11-05 |
Incyte Corporation |
N-(1-(methylsulfonyl)piperidin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine derivatives and related compounds as cyclin-dependent kinase 2 (cdk2) inhibitors for treating cancer
|
WO2020223558A1
(en)
|
2019-05-01 |
2020-11-05 |
Incyte Corporation |
Tricyclic amine compounds as cdk2 inhibitors
|
KR20220052859A
(ko)
|
2019-05-08 |
2022-04-28 |
비말란 바이오사이언스즈, 인크. |
Jak 억제제
|
KR20230031981A
(ko)
|
2019-05-14 |
2023-03-07 |
프로벤션 바이오, 인코포레이티드 |
제1형 당뇨병을 예방하기 위한 방법 및 조성물
|
TW202110849A
(zh)
*
|
2019-05-27 |
2021-03-16 |
大陸商迪哲(江蘇)醫藥股份有限公司 |
Dna依賴性蛋白激酶抑制劑
|
CN110305140B
(zh)
*
|
2019-07-30 |
2020-08-04 |
上海勋和医药科技有限公司 |
二氢吡咯并嘧啶类选择性jak2抑制剂
|
CN115038436A
(zh)
*
|
2019-08-08 |
2022-09-09 |
维玛兰生物科学公司 |
Jak抑制剂
|
EP4013750A1
(en)
|
2019-08-14 |
2022-06-22 |
Incyte Corporation |
Imidazolyl pyrimidinylamine compounds as cdk2 inhibitors
|
GB201911868D0
(en)
*
|
2019-08-19 |
2019-10-02 |
Galapagos Nv |
Novel compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders
|
EP4034107A4
(en)
*
|
2019-09-25 |
2023-08-30 |
Vimalan Biosciences, Inc. |
JAK INHIBITORS
|
EP4041731A1
(en)
|
2019-10-11 |
2022-08-17 |
Incyte Corporation |
Bicyclic amines as cdk2 inhibitors
|
CN114555600B
(zh)
*
|
2019-10-17 |
2024-03-01 |
辰欣药业股份有限公司 |
作为cdk2/4/6三重抑制剂的氨基嘧啶类化合物
|
US20230357248A1
(en)
*
|
2019-11-13 |
2023-11-09 |
Medshine Discovery Inc. |
Pyrrolopyrimidine compound as btk inhibitor and use thereof
|
CN114901666A
(zh)
*
|
2019-12-16 |
2022-08-12 |
卢内拉生物技术有限公司 |
选择性cdk4/6抑制剂型癌症治疗药物
|
US11833155B2
(en)
|
2020-06-03 |
2023-12-05 |
Incyte Corporation |
Combination therapy for treatment of myeloproliferative neoplasms
|
WO2021257857A1
(en)
|
2020-06-19 |
2021-12-23 |
Incyte Corporation |
Naphthyridinone compounds as jak2 v617f inhibitors
|
WO2021257863A1
(en)
|
2020-06-19 |
2021-12-23 |
Incyte Corporation |
Pyrrolotriazine compounds as jak2 v617f inhibitors
|
KR102409595B1
(ko)
*
|
2020-06-29 |
2022-06-17 |
한국과학기술연구원 |
단백질 카이네이즈 csf-1r 억제제로서의 신규 퓨리논 유도체
|
CR20230057A
(es)
|
2020-07-02 |
2023-08-15 |
Incyte Corp |
Compuestos tríciclicos de urea como inhibidores de jak2 v617f
|
WO2022006456A1
(en)
|
2020-07-02 |
2022-01-06 |
Incyte Corporation |
Tricyclic pyridone compounds as jak2 v617f inhibitors
|
WO2022046989A1
(en)
|
2020-08-27 |
2022-03-03 |
Incyte Corporation |
Tricyclic urea compounds as jak2 v617f inhibitors
|
CZ309356B6
(cs)
*
|
2020-09-15 |
2022-09-28 |
Ústav experimentální botaniky AV ČR, v. v. i |
Substituované purinové sloučeniny jako inhibitory proteinkináz, jejich použití jako léčiva a farmaceutické přípravky obsahující tyto deriváty
|
CN112375081B
(zh)
*
|
2020-11-23 |
2022-04-12 |
中国医学科学院医药生物技术研究所 |
具有抑制CDK4、6或9活性的吡咯[2,3-d]嘧啶衍生物及其制备方法和应用
|
US11919908B2
(en)
|
2020-12-21 |
2024-03-05 |
Incyte Corporation |
Substituted pyrrolo[2,3-d]pyrimidine compounds as JAK2 V617F inhibitors
|
TW202241901A
(zh)
*
|
2020-12-21 |
2022-11-01 |
大陸商江蘇恆瑞醫藥股份有限公司 |
嘌呤酮衍生物、其製備方法及其在醫藥上的應用
|
WO2022207788A2
(en)
|
2021-04-01 |
2022-10-06 |
Krka, D.D., Novo Mesto |
Process for the preparation of ribociclib and pharmaceutically acceptable salts thereof
|
WO2022226290A1
(en)
*
|
2021-04-22 |
2022-10-27 |
H. Lee Moffitt Cancer Center And Research Institute, Inc. |
2-phenylamino pyrrolopyrimidines as ack1 inhibitors
|
WO2023283425A1
(en)
|
2021-07-09 |
2023-01-12 |
Plexium, Inc. |
Aryl compounds and pharmaceutical compositions that modulate ikzf2
|
US11786531B1
(en)
|
2022-06-08 |
2023-10-17 |
Beigene Switzerland Gmbh |
Methods of treating B-cell proliferative disorder
|
WO2023241620A1
(en)
*
|
2022-06-14 |
2023-12-21 |
Suzhou Keen Therapeutics Co., Ltd. |
Biologically active compounds and methods thereof
|
WO2024049926A1
(en)
|
2022-08-31 |
2024-03-07 |
Arvinas Operations, Inc. |
Dosage regimens of estrogen receptor degraders
|
CN117720532A
(zh)
*
|
2022-09-16 |
2024-03-19 |
华东师范大学 |
作为rsk抑制剂的吡咯并嘧啶衍生物及其应用
|