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
JP2013534902A (ja
JP5876031B2 (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 (OSRAM) 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 (OSRAM)
EP (1) EP2549868B1 (OSRAM)
JP (1) JP5876031B2 (OSRAM)
KR (1) KR101676077B1 (OSRAM)
CN (1) CN102917588B (OSRAM)
AR (1) AR080792A1 (OSRAM)
AU (1) AU2011232516B2 (OSRAM)
EA (1) EA022325B1 (OSRAM)
ES (1) ES2530955T3 (OSRAM)
IL (1) IL222120A (OSRAM)
MX (1) MX2012011045A (OSRAM)
SG (1) SG183954A1 (OSRAM)
TW (1) TW201202241A (OSRAM)
UY (1) UY33288A (OSRAM)
WO (1) WO2011119663A1 (OSRAM)

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
US20140227289A1 (en) * 2011-05-13 2014-08-14 Stephen Michael Cohen Compounds and methods for treating insulin resistance syndrome
EP3495368B1 (en) 2011-07-19 2023-05-31 Merck Sharp & Dohme B.V. (s)-4-(8-amino-3-(1-(but-2-ynoyl)pyrrolidin-2-yl)imidazo[1,5-a]pyrazin-1-yl)-2-methoxy-n-(pyridin-2-yl)benzamide as btk-inhibitor
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
CN104918934B (zh) 2013-01-18 2017-12-22 霍夫曼-拉罗奇有限公司 3‑取代的吡唑及其作为dlk抑制剂的用途
EA027811B1 (ru) * 2013-04-04 2017-09-29 Янссен Фармацевтика Нв ПРОИЗВОДНЫЕ N-(2,3-ДИГИДРО-1H-ПИРРОЛО[2,3-b]ПИРИДИН-5-ИЛ)-4-ХИНАЗОЛИНАМИНА И N-(2,3-ДИГИДРО-1H-ИНДОЛ-5-ИЛ)-4-ХИНАЗОЛИНАМИНА В КАЧЕСТВЕ ИНГИБИТОРОВ 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
EP3076974A1 (en) 2013-12-05 2016-10-12 Acerta Pharma B.V. Therapeutic combination of a pi3k inhibitor and a btk inhibitor
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
JP2017507967A (ja) * 2014-03-11 2017-03-23 グラクソスミスクライン、インテレクチュアル、プロパティー、(ナンバー2)、リミテッドGlaxosmithkline Intellectual Property (No.2) Limited Perk阻害剤として作用する化合物
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
TW201613644A (en) 2014-06-17 2016-04-16 Acerta Pharma Bv Therapeutic combinations of a BTK inhibitor, a PI3K inhibitor, and/or a JAK-2 inhibitor
TW201618772A (zh) 2014-08-11 2016-06-01 艾森塔製藥公司 Btk抑制劑、pi3k抑制劑、jak-2抑制劑及/或bcl-2抑制劑之治療組合物
HUE050706T2 (hu) * 2014-10-24 2020-12-28 Bristol Myers Squibb Co Indol karboxamid vegyületek, amelyek hasznosak kináz inhibitorokként
CA2967125C (en) 2014-11-14 2022-10-25 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
SI3317281T1 (sl) 2015-07-02 2020-08-31 Acerta Pharma B.V. Trdne oblike in formulacije (s)-4-(8-amino-3-(1-(but-2-inoil)pirolidin -2-il)imidazo(1,5-a)pirazin-1-il)-n-(piridin-2-il)benzamida
WO2017046739A1 (en) * 2015-09-15 2017-03-23 Glaxosmithkline Intellectual Property (No.2) Limited Imidazolidinone derivatives as inhibitors of perk
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
CN113549110B (zh) * 2016-04-07 2024-08-16 葛兰素史密斯克莱知识产权发展有限公司 用作蛋白质调节剂的杂环酰胺
SG11201808878UA (en) * 2016-04-15 2018-11-29 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
EP3472133B1 (en) 2016-06-13 2023-10-11 Ramot at Tel-Aviv University Ltd. Perk inhibitors and uses thereof in treating diseases associated with aggregation-prone proteins
CN109311894B (zh) 2016-06-21 2022-03-22 内尔维阿诺医学科学有限公司 作为激酶抑制剂的n-(取代的-苯基)-磺酰胺衍生物
JP2019521166A (ja) * 2016-07-20 2019-07-25 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited Perk阻害剤としてのイソキノリン誘導体
WO2018055578A1 (en) * 2016-09-22 2018-03-29 The University Of Hong Kong Preventive and therapeutic approach for aberrant cell differentiation and isr-associated diseases
EP3573608A1 (en) 2017-01-30 2019-12-04 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
FI3593817T3 (fi) * 2017-03-06 2025-02-05 Tsubota Lab Inc Koostumus käytettäväksi likinäköisyyden ehkäisyssä tai vähentämisessä
DK3448859T3 (da) * 2017-03-20 2019-09-23 Forma Therapeutics Inc Pyrrolopyrrolsammensætninger som pyruvatkinase- (pkr) aktivatorer
WO2019021208A1 (en) * 2017-07-27 2019-01-31 Glaxosmithkline Intellectual Property Development Limited USEFUL INDAZOLE DERIVATIVES AS PERK INHIBITORS
JP2021501785A (ja) 2017-11-02 2021-01-21 カリコ ライフ サイエンシーズ エルエルシー 統合的ストレス経路の調節剤
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
AU2021289345A1 (en) 2020-06-08 2023-01-19 Halia Therapeutics, Inc. Inhibitors of NEK7 kinase
US20240100172A1 (en) 2020-12-21 2024-03-28 Hangzhou Jijing Pharmaceutical Technology Limited Methods and compounds for targeted autophagy
US20240382488A1 (en) 2021-03-29 2024-11-21 Halia Therapeutics, Inc. Nek7 inhibitors
WO2022216680A1 (en) 2021-04-05 2022-10-13 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
US20060074102A1 (en) * 2004-05-14 2006-04-06 Kevin Cusack Kinase inhibitors as therapeutic agents
PT1761528E (pt) * 2004-06-11 2008-04-15 Japan Tobacco Inc Derivados de 5-amino-2,4,7-trioxo-3,4,7,8-tetra-hidro-2hpirido[ 2,3-d]pirimidina e compostos relacionados para o tratamento do cancro
US20080255184A1 (en) * 2005-11-04 2008-10-16 Smithkline Beecham Corporation Thienopyridine B-Raf Kinase Inhibitors
AU2007272330A1 (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 (OSRAM)
JP7158383B2 (ja) C-kit阻害剤としてのベンズイミダゾール化合物
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
JP7654071B2 (ja) 複素環スピロ化合物及び使用方法
HRP20200624T1 (hr) Derivati 2-(2,4,5-supstituiranog-anilino)pirimidina kao modulatori egfr korisni za liječenje raka
RU2019115115A (ru) Производные пиперидина в качестве ингибиторов убиквитин-специфической протеазы 7
JP2019535664A5 (OSRAM)
JP2020531498A5 (OSRAM)
RU2018123779A (ru) Новые соединения
WO2018218133A1 (en) Pyrazolo[3,4-b]pyrazine derivatives as shp2 phosphatase inhibitors
CN112204027A (zh) Erk 抑制剂及其应用
JP2009529047A5 (OSRAM)
HRP20120105T1 (hr) Aminoheterociklički spojevi
RU2012131124A (ru) Птеридиноны как ингибиторы polo-подобных киназ
JP2018500376A5 (OSRAM)
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 (OSRAM)
AU2013225533A1 (en) Amido spirocyclic amide and sulfonamide derivatives
JP2013515729A5 (OSRAM)
JP2012525367A5 (OSRAM)
JP2019535689A5 (OSRAM)
JP2013531684A5 (OSRAM)
RU2011125314A (ru) Новое производное пиразол-3-карбоксамида, обладающее антагонистической активностью в отношении рецептора 5-нт2в