JP2013534902A5 - - Google Patents

Download PDF

Info

Publication number
JP2013534902A5
JP2013534902A5 JP2013501421A JP2013501421A JP2013534902A5 JP 2013534902 A5 JP2013534902 A5 JP 2013534902A5 JP 2013501421 A JP2013501421 A JP 2013501421A JP 2013501421 A JP2013501421 A JP 2013501421A JP 2013534902 A5 JP2013534902 A5 JP 2013534902A5
Authority
JP
Japan
Prior art keywords
indol
dihydro
amine
acetyl
methyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2013501421A
Other languages
English (en)
Japanese (ja)
Other versions
JP5876031B2 (ja
JP2013534902A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2011/029511 external-priority patent/WO2011119663A1/en
Publication of JP2013534902A publication Critical patent/JP2013534902A/ja
Publication of JP2013534902A5 publication Critical patent/JP2013534902A5/ja
Application granted granted Critical
Publication of JP5876031B2 publication Critical patent/JP5876031B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2013501421A 2010-03-25 2011-03-23 化合物 Expired - Fee Related JP5876031B2 (ja)

Applications Claiming Priority (11)

Application Number Priority Date Filing Date Title
US31747610P 2010-03-25 2010-03-25
US61/317,476 2010-03-25
US35286310P 2010-06-09 2010-06-09
US61/352,863 2010-06-09
US38148010P 2010-09-10 2010-09-10
US61/381,480 2010-09-10
US38815110P 2010-09-30 2010-09-30
US61/388,151 2010-09-30
US41906810P 2010-12-02 2010-12-02
US61/419,068 2010-12-02
PCT/US2011/029511 WO2011119663A1 (en) 2010-03-25 2011-03-23 Chemical compounds

Publications (3)

Publication Number Publication Date
JP2013534902A JP2013534902A (ja) 2013-09-09
JP2013534902A5 true JP2013534902A5 (enExample) 2014-05-08
JP5876031B2 JP5876031B2 (ja) 2016-03-02

Family

ID=46160738

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013501421A Expired - Fee Related JP5876031B2 (ja) 2010-03-25 2011-03-23 化合物

Country Status (15)

Country Link
US (1) US20120077828A1 (enExample)
EP (1) EP2549868B1 (enExample)
JP (1) JP5876031B2 (enExample)
KR (1) KR101676077B1 (enExample)
CN (1) CN102917588B (enExample)
AR (1) AR080792A1 (enExample)
AU (1) AU2011232516B2 (enExample)
EA (1) EA022325B1 (enExample)
ES (1) ES2530955T3 (enExample)
IL (1) IL222120A (enExample)
MX (1) MX2012011045A (enExample)
SG (1) SG183954A1 (enExample)
TW (1) TW201202241A (enExample)
UY (1) UY33288A (enExample)
WO (1) WO2011119663A1 (enExample)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8598156B2 (en) 2010-03-25 2013-12-03 Glaxosmithkline Llc Chemical compounds
WO2012158123A1 (en) * 2011-05-13 2012-11-22 Agency For Science, Technology And Research Compounds and methods for treating insulin resistance syndrome
IN2014CN00408A (enExample) 2011-07-19 2015-04-03 Merck Sharp & Dohme
EP2548877A1 (en) 2011-07-19 2013-01-23 MSD Oss B.V. 4-(5-Membered fused pyridinyl)benzamides as BTK-inhibitors
WO2014055595A1 (en) 2012-10-05 2014-04-10 Merck Sharp & Dohme Corp. Indoline compounds as aldosterone synthase inhibitiors related applications
MX2015009270A (es) 2013-01-18 2015-10-30 Hoffmann La Roche Pirazoles sustituidos en posicion 3 y uso de los mismos como inhibidores de la cinasa cremallera de leucinas dual (dlk).
MX367772B (es) * 2013-04-04 2019-09-05 Janssen Pharmaceutica Nv Derivados de n-(2,3-dihidro-1h-pirrolo[2,3,b]piridin-5-il)-4-quina zolinamina y n-(2,3-dihidro-1h-indol-5-il)-4-quinazolinamina novedosos como inhibidores de perk.
TWI482757B (zh) * 2013-10-07 2015-05-01 Luminescence Technology Corp Vegf-2/3受體及蛋白質酪胺酸激酶抑制劑及其醫藥用途
WO2015056180A1 (en) * 2013-10-15 2015-04-23 Glaxosmithkline Intellectual Property (No.2) Limited Indoline derivatives as inhibitors of perk
KR20160093062A (ko) 2013-12-05 2016-08-05 아세르타 파마. 비.브이. Pi3k 억제제 및 btk 억제제의 치료적 조합
US10272083B2 (en) 2014-01-21 2019-04-30 Acerta Pharma B.V. Methods of treating chronic lymphocytic leukemia and small lymphocytic leukemia using a BTK inhibitor
WO2015136463A1 (en) * 2014-03-11 2015-09-17 Glaxosmithkline Intellectual Property (No.2) Limited Chemical compounds acting as perk inhibitors
US9937171B2 (en) 2014-04-11 2018-04-10 Acerta Pharma B.V. Methods of blocking the CXCR-4/SDF-1 signaling pathway with inhibitors of bruton's tyrosine kinase
US9949971B2 (en) 2014-06-17 2018-04-24 Acerta Pharma B.V. Therapeutic combinations of a BTK inhibitor, a PI3K inhibitor and/or a JAK-2 inhibitor
WO2016024230A1 (en) 2014-08-11 2016-02-18 Acerta Pharma B.V. Therapeutic combinations of a btk inhibitor, a pi3k inhibitor, a jak-2 inhibitor, and/or a bcl-2 inhibitor
LT3461821T (lt) 2014-10-24 2020-08-10 Bristol-Myers Squibb Company Indolo karboksamido junginiai, naudotini kaip kinazės inhibitoriai
AU2015345054B2 (en) 2014-11-14 2020-03-05 Nerviano Medical Sciences S.R.L. 6-amino-7-bicyclo-7-deaza-purine derivatives as protein kinase inhibitors
WO2016126026A2 (ko) * 2015-02-04 2016-08-11 서울대학교병원 당뇨병 치료 조성물 및 이의 용도
DK3317281T3 (da) 2015-07-02 2020-06-15 Acerta Pharma Bv Faste former og formuleringer af (s)-4-(8-amino-3-(1-(but-2-ynoyl)pyrrolidin-2-yl)imidazo[1,5-a]pyrazin-1-yl)-n-(pyridin-2-yl)benzamid
TW201722957A (zh) * 2015-09-15 2017-07-01 葛蘭素史克智慧財產(第二)有限公司 化學化合物
WO2017046739A1 (en) * 2015-09-15 2017-03-23 Glaxosmithkline Intellectual Property (No.2) Limited Imidazolidinone derivatives as inhibitors of perk
SG10201900628RA (en) * 2016-04-07 2019-02-27 Glaxosmithkline Ip Dev Ltd Heterocyclic amides useful as protein modulators
IL289793B2 (en) * 2016-04-15 2023-03-01 Cancer Research Tech Ltd Heterocyclic compounds as ret kinase inhibitors
US11026945B2 (en) * 2016-04-29 2021-06-08 The Trustees Of The University Of Pennsylvania Protein kinase RNA-like endoplasmic reticulum kinase (PERK) inhibitors for prevention and/or treatment of lung injury and/or inflammation
WO2017216792A1 (en) 2016-06-13 2017-12-21 Ramot At Tel-Aviv University Ltd. Perk inhibitors and uses thereof in treating diseases associated with aggregation-prone proteins
MX388660B (es) 2016-06-21 2025-03-20 Nerviano Medical Sciences Srl DERIVADOS DE N-(SUSTITUIDA-FENIL)-SULFONAMIDA COMO INHIBIDORES DE QUINASA N-(sustituida-fenil)-sulfonamida.
CA3031047A1 (en) * 2016-07-20 2018-01-25 Glaxosmithkline Intellectual Property Development Limited Isoquinoline derivatives as perk inhibitors
US11759437B2 (en) * 2016-09-22 2023-09-19 The University Of Hong Kong Preventive and therapeutic approach for aberrant cell differentiation and ISR-associated diseases
EP3656382A1 (en) 2017-01-30 2020-05-27 Université de Liège Perk and ire-1a inhibitors against neurodevelopmental disorders
CN106974910B (zh) * 2017-03-02 2019-11-12 深圳大学 含索拉非尼和gsk2656157的药物组合物及用途
CN106963769B (zh) * 2017-03-03 2019-10-25 深圳大学 含pi3k抑制剂和perk抑制剂的药物组合物及其应用
ES2997337T3 (en) * 2017-03-06 2025-02-17 Tsubota Lab Inc Composition for use in the prevention or suppression of myopia
HUE045261T2 (hu) * 2017-03-20 2019-12-30 Forma Therapeutics Inc Pirrolopirrol kompozíciók piruvát kináz (PKR) aktivátorokként
WO2019021208A1 (en) * 2017-07-27 2019-01-31 Glaxosmithkline Intellectual Property Development Limited USEFUL INDAZOLE DERIVATIVES AS PERK INHIBITORS
WO2019090088A1 (en) 2017-11-02 2019-05-09 Calico Life Sciences Llc Modulators of the integrated stress pathway
CN108003163B (zh) * 2017-11-30 2020-11-24 武汉九州钰民医药科技有限公司 用作激酶抑制剂的吡唑并嘧啶类化合物及其应用
CN111100130B (zh) * 2018-10-29 2022-07-15 四川大学 4-氨基吡咯并嘧啶衍生物及其制备方法和用途
CN111213632B (zh) * 2019-11-19 2022-03-01 长春中医药大学 动物药环氧树脂标本制作方法
CN116075513A (zh) 2020-06-08 2023-05-05 哈利亚治疗公司 Nek7激酶的抑制剂
WO2022140246A1 (en) 2020-12-21 2022-06-30 Hangzhou Jijing Pharmaceutical Technology Limited Methods and compounds for targeted autophagy
US20240382488A1 (en) 2021-03-29 2024-11-21 Halia Therapeutics, Inc. Nek7 inhibitors
EP4320127A1 (en) 2021-04-05 2024-02-14 Halia Therapeutics, Inc. Nek7 inhibitors
WO2023034236A1 (en) * 2021-08-31 2023-03-09 Wisconsin Alumni Research Foundation Deuterated inhibitors of rip kinases
GB202407386D0 (en) 2024-05-24 2024-07-10 Apollo Ap45 Ltd 1H-pyrazolo(4,3-D)pyrimidine derivatives

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1753428A4 (en) * 2004-05-14 2010-09-15 Abbott Lab INHIBITORS OF KINASES AS THERAPEUTIC AGENTS
BRPI0511967B8 (pt) * 2004-06-11 2021-05-25 Japan Tobacco Inc derivados de 5-amino-2,4,7-trioxo-3,4,7,8-tetrahidro-2h-pirido[2,3-d] pirimidina, seu uso e composição farmacêutica que os compreende
EP1951728A4 (en) * 2005-11-04 2011-04-20 Glaxosmithkline Llc THIENOPYRIDINES AS INHIBITORS OF B-RAF KINASE
WO2008008981A1 (en) * 2006-07-13 2008-01-17 Zymogenetics, Inc. Interleukin 21 and tyrosine kinase inhibitor combination therapy
WO2009151621A1 (en) 2008-06-13 2009-12-17 Arena Pharmaceuticals, Inc. Substituted (1, 2, 4-0xadiaz0l-3-yl) indolin-1-yl carboxylic acid derivatives useful as s1p1 agonists
ES2536730T3 (es) * 2008-09-19 2015-05-28 Nerviano Medical Sciences S.R.L. Derivados de 3,4-dihidro-2H-pirrolo[1,2-a]pirazin-1-ona

Similar Documents

Publication Publication Date Title
JP2013534902A5 (enExample)
ES2540996T3 (es) Compuestos de N-(1H-indazol-4-il)imidazo[1,2-a]piridin-3-carboxamida sustituidos como inhibidores de tirosina cinasa del receptor de tipo III
JP2022185110A (ja) C-kit阻害剤としてのベンズイミダゾール化合物
JP7654071B2 (ja) 複素環スピロ化合物及び使用方法
RU2019115115A (ru) Производные пиперидина в качестве ингибиторов убиквитин-специфической протеазы 7
CN112204027A (zh) Erk 抑制剂及其应用
JP2019535664A5 (enExample)
JP2020531498A5 (enExample)
RU2018123779A (ru) Новые соединения
WO2018218133A1 (en) Pyrazolo[3,4-b]pyrazine derivatives as shp2 phosphatase inhibitors
JP2009529047A5 (enExample)
HRP20120105T1 (hr) Aminoheterociklički spojevi
RU2012131124A (ru) Птеридиноны как ингибиторы polo-подобных киназ
JP2018500376A5 (enExample)
JP2015514783A (ja) ベンゾチアゾール−6−イル酢酸誘導体およびhiv感染を処置するためのそれらの使用
HRP20170349T1 (hr) Novi derivati pirola, postupak njihove priprave i farmaceutski pripravci koji ih sadrže
ME02514B (me) Derivati 8 -karbamoil- 2-(2,3-disupstituirani pirid-6- il)-1,2,3,4-tetrahidroizokinolina kao sredstva za izazivanje apoptoze za liječenje karcinoma i imunih i autoimunih bolesti
JP2010512338A5 (enExample)
AU2013225533A1 (en) Amido spirocyclic amide and sulfonamide derivatives
JP2013515729A5 (enExample)
JPWO2011078221A1 (ja) イミダゾピリダジン化合物
JP2012525367A5 (enExample)
JP2019535689A5 (enExample)
JP2013531684A5 (enExample)
RU2018113430A (ru) Производные l-фенилпирролидин-2-она в качестве ингибиторов perk