JP2016512488A5 - - Google Patents

Download PDF

Info

Publication number
JP2016512488A5
JP2016512488A5 JP2015557554A JP2015557554A JP2016512488A5 JP 2016512488 A5 JP2016512488 A5 JP 2016512488A5 JP 2015557554 A JP2015557554 A JP 2015557554A JP 2015557554 A JP2015557554 A JP 2015557554A JP 2016512488 A5 JP2016512488 A5 JP 2016512488A5
Authority
JP
Japan
Prior art keywords
methyl
oxo
tetrahydrobenzo
carboxamide
oxazepin
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
JP2015557554A
Other languages
English (en)
Japanese (ja)
Other versions
JP6321045B2 (ja
JP2016512488A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2014/059004 external-priority patent/WO2014125444A1/en
Publication of JP2016512488A publication Critical patent/JP2016512488A/ja
Publication of JP2016512488A5 publication Critical patent/JP2016512488A5/ja
Application granted granted Critical
Publication of JP6321045B2 publication Critical patent/JP6321045B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2015557554A 2013-02-15 2014-02-14 キナーゼ阻害剤としての複素環式アミド Active JP6321045B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201361765664P 2013-02-15 2013-02-15
US61/765,664 2013-02-15
US201361790044P 2013-03-15 2013-03-15
US61/790,044 2013-03-15
PCT/IB2014/059004 WO2014125444A1 (en) 2013-02-15 2014-02-14 Heterocyclic amides as kinase inhibitors

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2018044611A Division JP6352571B1 (ja) 2013-02-15 2018-03-12 キナーゼ阻害剤としての複素環式アミド

Publications (3)

Publication Number Publication Date
JP2016512488A JP2016512488A (ja) 2016-04-28
JP2016512488A5 true JP2016512488A5 (cg-RX-API-DMAC7.html) 2017-03-23
JP6321045B2 JP6321045B2 (ja) 2018-05-09

Family

ID=50151350

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2015557554A Active JP6321045B2 (ja) 2013-02-15 2014-02-14 キナーゼ阻害剤としての複素環式アミド
JP2018044611A Active JP6352571B1 (ja) 2013-02-15 2018-03-12 キナーゼ阻害剤としての複素環式アミド
JP2018107215A Pending JP2018150372A (ja) 2013-02-15 2018-06-04 キナーゼ阻害剤としての複素環式アミド

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2018044611A Active JP6352571B1 (ja) 2013-02-15 2018-03-12 キナーゼ阻害剤としての複素環式アミド
JP2018107215A Pending JP2018150372A (ja) 2013-02-15 2018-06-04 キナーゼ阻害剤としての複素環式アミド

Country Status (37)

Country Link
US (6) US9556152B2 (cg-RX-API-DMAC7.html)
EP (4) EP3375780B1 (cg-RX-API-DMAC7.html)
JP (3) JP6321045B2 (cg-RX-API-DMAC7.html)
KR (2) KR102228764B1 (cg-RX-API-DMAC7.html)
CN (3) CN108774214B (cg-RX-API-DMAC7.html)
AU (1) AU2014217453B2 (cg-RX-API-DMAC7.html)
BR (4) BR122017002951A2 (cg-RX-API-DMAC7.html)
CA (1) CA2900695C (cg-RX-API-DMAC7.html)
CL (1) CL2015002279A1 (cg-RX-API-DMAC7.html)
CR (3) CR20190512A (cg-RX-API-DMAC7.html)
CY (2) CY1120320T1 (cg-RX-API-DMAC7.html)
DK (2) DK3342771T3 (cg-RX-API-DMAC7.html)
DO (3) DOP2015000196A (cg-RX-API-DMAC7.html)
EA (2) EA028991B1 (cg-RX-API-DMAC7.html)
ES (3) ES2672530T3 (cg-RX-API-DMAC7.html)
HR (2) HRP20180900T1 (cg-RX-API-DMAC7.html)
HU (2) HUE037763T2 (cg-RX-API-DMAC7.html)
IL (3) IL240280B (cg-RX-API-DMAC7.html)
LT (2) LT3342771T (cg-RX-API-DMAC7.html)
MA (1) MA44820B1 (cg-RX-API-DMAC7.html)
MX (3) MX373867B (cg-RX-API-DMAC7.html)
MY (2) MY195183A (cg-RX-API-DMAC7.html)
NZ (1) NZ628447A (cg-RX-API-DMAC7.html)
PE (1) PE20151752A1 (cg-RX-API-DMAC7.html)
PH (4) PH12015501675A1 (cg-RX-API-DMAC7.html)
PL (2) PL2956452T3 (cg-RX-API-DMAC7.html)
PT (2) PT2956452T (cg-RX-API-DMAC7.html)
RS (2) RS61439B1 (cg-RX-API-DMAC7.html)
SG (1) SG11201505796TA (cg-RX-API-DMAC7.html)
SI (2) SI2956452T1 (cg-RX-API-DMAC7.html)
SM (2) SMT201800289T1 (cg-RX-API-DMAC7.html)
TR (1) TR201808112T4 (cg-RX-API-DMAC7.html)
TW (4) TWI648273B (cg-RX-API-DMAC7.html)
UA (1) UA118259C2 (cg-RX-API-DMAC7.html)
UY (1) UY35330A (cg-RX-API-DMAC7.html)
WO (1) WO2014125444A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA201505267B (cg-RX-API-DMAC7.html)

Families Citing this family (111)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI648273B (zh) 2013-02-15 2019-01-21 英商葛蘭素史克智慧財產發展有限公司 作為激酶抑制劑之雜環醯胺類(三)
US20170266199A1 (en) 2014-08-21 2017-09-21 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as rip1 kinase inhibitors as medicaments
EP3218371B1 (en) * 2014-11-14 2018-09-26 Boehringer Ingelheim International GmbH Aryl and heteroaryl-fused tetrahydro-1,4-oxazepine amides as somatostatin receptor subtype 4 (sstr4) agonists
AU2015360291A1 (en) 2014-12-11 2017-07-13 President And Fellows Of Harvard College Inhibitors of cellular necrosis and related methods
EP3256467A1 (en) * 2015-02-13 2017-12-20 GlaxoSmithKline Intellectual Property Management Limited Crystalline forms of (s)-5-benzyl-n-(5-methyl-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-4h-1,2,4-triazole-3-carboxamide
JP6727224B2 (ja) 2015-03-02 2020-07-22 アペイロン・バイオロジックス・アクチェンゲゼルシャフトAPEIRON Biologics AG 新生物疾患および/または感染性疾患の治療にとって有用な二環式テトラヒドロチアゼピン誘導体
UY36680A (es) * 2015-05-19 2016-12-30 Glaxosmithkline Ip Dev Ltd Amidas heterocíclicas como inhibidores de quinasa
KR20180030545A (ko) * 2015-06-22 2018-03-23 다이닛본 스미토모 세이야꾸 가부시끼가이샤 바이사이클릭 헤테로사이클릭 아미드 유도체
CA2988601C (en) * 2015-07-02 2021-12-07 F. Hoffmann-La Roche Ag Bicyclic lactams and methods of use thereof
MX381798B (es) 2015-07-22 2025-03-13 Enanta Pharm Inc Derivados de benzodiazepina como inhibidores de rsv
EP3366684B1 (en) * 2015-10-23 2020-09-02 Takeda Pharmaceutical Company Limited Heterocyclic compound
WO2017096301A1 (en) * 2015-12-04 2017-06-08 Denali Therapeutics Inc. Isoxazolidine derived inhibitors of receptor interacting protein kinase 1 (ripk 1)
US10961258B2 (en) 2015-12-21 2021-03-30 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as kinase inhibitors
EP3402799B1 (en) 2016-01-15 2022-05-04 Enanta Pharmaceuticals, Inc. Heterocyclic compounds as rsv inhibitors
EA201891620A1 (ru) * 2016-02-05 2019-02-28 Денали Терапьютикс Инк. Ингибиторы взаимодействующей с рецептором протеинкиназы 1
US10898469B2 (en) 2016-02-26 2021-01-26 Sumitomo Dainippon Pharma Co., Ltd. Imidazolylamide derivative
WO2018007973A2 (en) 2016-07-06 2018-01-11 Glaxosmithkline Intellectual Property Development Limited Process and intermediates for preparing benzoxazepines
EP3526219B1 (en) 2016-10-17 2021-12-15 F. Hoffmann-La Roche AG Bicyclic pyridone lactams and methods of use thereof
TW201822637A (zh) 2016-11-07 2018-07-01 德商拜耳廠股份有限公司 用於控制動物害蟲的經取代磺醯胺類
TW201831464A (zh) 2016-11-18 2018-09-01 英商葛蘭素史克智慧財產發展有限公司 作為激酶抑制劑之雜環醯胺
TW201831478A (zh) 2016-12-02 2018-09-01 瑞士商赫孚孟拉羅股份公司 雙環醯胺化合物及其使用方法
EP3552017B1 (en) 2016-12-09 2022-02-23 Denali Therapeutics Inc. Compounds useful as ripk1 inhibitors
US11072607B2 (en) 2016-12-16 2021-07-27 Genentech, Inc. Inhibitors of RIP1 kinase and methods of use thereof
JPWO2018117196A1 (ja) 2016-12-20 2019-10-31 大日本住友製薬株式会社 がん幹細胞を標的とする医薬
US10398706B2 (en) 2017-01-06 2019-09-03 Enanta Pharmaceuticals, Inc. Heteroaryldiazepine derivatives as RSV inhibitors
CN110809472B (zh) 2017-02-16 2023-05-23 英安塔制药有限公司 用于制备苯二氮䓬衍生物的方法
CA3052767A1 (en) 2017-02-27 2018-08-30 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as kinase inhibitors
JOP20190233A1 (ar) * 2017-04-14 2019-10-02 Biogen Ma Inc نظائر بنزوازيبين بوصفها عوامل مثبطة لتيروزين كيناز بروتون
CN110769853B (zh) * 2017-04-17 2022-06-03 北京生命科学研究所 治疗雄性衰老
KR102638151B1 (ko) 2017-05-17 2024-02-16 데날리 테라퓨틱스 인크. 키나아제 억제제 및 이의 용도
US10752598B2 (en) 2017-06-07 2020-08-25 Enanta Pharmaceuticals, Inc. Aryldiazepine derivatives as RSV inhibitors
WO2019006291A1 (en) 2017-06-30 2019-01-03 Enanta Pharmaceuticals, Inc. HETEROCYCLIC COMPOUNDS AS RSV INHIBITORS
WO2019006295A1 (en) 2017-06-30 2019-01-03 Enanta Pharmaceuticals, Inc. HETEROCYCLIC COMPOUNDS AS RSV INHIBITORS
EP4397309A3 (en) 2017-07-14 2024-09-04 F. Hoffmann-La Roche AG Bicyclic ketone compounds and methods of use thereof
UY37861A (es) 2017-08-28 2019-03-29 Enanta Pharm Inc Agentes antivirales contra la hepatitis b
US10881666B2 (en) 2017-09-29 2021-01-05 Enanta Pharmaceuticals, Inc. Combination pharmaceutical agents as RSV inhibitors
BR112020007067A2 (pt) 2017-10-11 2020-10-06 F. Hoffmann-La Roche Ag compostos bicíclicos para uso como inibidores rip1 quinase
EP3704097B1 (en) 2017-10-31 2023-10-25 F. Hoffmann-La Roche AG Bicyclic sulfones and sulfoxides and methods of use thereof
JP7228588B2 (ja) 2017-11-13 2023-02-24 エナンタ ファーマシューティカルズ インコーポレイテッド ベンゾジアゼピン-2-オンおよびベンゾアゼピン-2-オン誘導体の分割方法
US10647711B2 (en) 2017-11-13 2020-05-12 Enanta Pharmaceuticals, Inc. Azepin-2-one derivatives as RSV inhibitors
WO2019123219A1 (en) 2017-12-20 2019-06-27 Glaxosmithkline Intellectual Property Development Limited Crystalline salt form of (s)-5-benzyl-n-(5-methyl-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-4h-1,2,4-triazole-3-carboxamide
JP2021509113A (ja) 2017-12-29 2021-03-18 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 キナーゼ阻害剤としての複素環式アミド
WO2019199908A1 (en) 2018-04-11 2019-10-17 Enanta Pharmaceuticals, Inc. Heterocyclic compounds as rsv inhibitors
WO2019204537A1 (en) 2018-04-20 2019-10-24 Genentech, Inc. N-[4-oxo-2,3-dihydro-1,5-benzoxazepin-3-yl]-5,6-dihydro-4h-pyrrolo[1,2-b]pyrazol e-2-carboxamide derivatives and related compounds as rip1 kinase inhibitors for treating e.g. irritable bowel syndrome (ibs)
CN110407770B (zh) * 2018-04-27 2022-12-30 复旦大学 3-取代-1,5-苯并氮杂䓬类化合物及其药物用途
DK3788045T3 (da) * 2018-05-03 2023-06-26 Rigel Pharmaceuticals Inc RIP1-hæmmende forbindelser og fremgangsmåder til fremstilling og anvendelse deraf
BR112020022420A2 (pt) * 2018-05-03 2021-03-02 Rigel Pharmaceuticals, Inc. composto, composição farmacêutica, método, método para tratar uma doença em um indivíduo e método para produzir o composto
WO2019224774A1 (en) 2018-05-23 2019-11-28 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as rip1 kinase inhibitors
WO2019224773A1 (en) 2018-05-23 2019-11-28 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as rip1 kinase inhibitors
WO2020001420A1 (zh) * 2018-06-26 2020-01-02 中国科学院上海有机化学研究所 一类细胞坏死抑制剂及其制备方法和用途
CN110642874B (zh) * 2018-06-26 2023-03-28 中国科学院上海有机化学研究所 一类细胞坏死抑制剂及其制备方法和用途
PT3594199T (pt) * 2018-07-09 2020-09-04 Amgen Inc 2-fluoro-3-nitrotolueno cristalino e processo para a sua preparação
WO2020044206A1 (en) 2018-08-29 2020-03-05 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as kinase inhibitors for use in the treatment cancer
CN109134448B (zh) * 2018-10-16 2020-11-27 中南大学湘雅医院 杂环化合物及其盐、制备方法、用途和药物
WO2020088194A1 (zh) 2018-11-02 2020-05-07 中国科学院上海药物研究所 抑制rip1激酶的杂环酰胺及其用途
CN111138448B (zh) * 2018-11-02 2022-08-02 中国科学院上海药物研究所 抑制rip1激酶的杂环酰胺及其用途
KR102819704B1 (ko) 2018-11-21 2025-06-11 이난타 파마슈티칼스, 인코포레이티드 항바이러스제로서의 작용화된 헤테로사이클
JP7585205B2 (ja) 2019-01-11 2024-11-18 エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト 二環式ピロロトリアゾールケトン化合物及びその使用方法
JP7268921B2 (ja) * 2019-01-25 2023-05-08 北京賽特明強医薬科技有限公司 アミド基架橋複素環式化合物、その組成物および応用
BR112021018335A2 (pt) 2019-03-18 2021-11-23 Enanta Pharm Inc Derivados de benzodiazepina como inibidores de rsv
WO2020210246A1 (en) 2019-04-09 2020-10-15 Enanta Pharmaceuticals, Inc, Heterocyclic compounds as rsv inhibitors
WO2020234716A1 (en) 2019-05-17 2020-11-26 Glaxosmithkline Intellectual Property Development Limited Matrix composition comprising (s)-5-benzyl-n-(5-methyl-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-4h-1,2,4-triazole-3-carboxamide
EP3978492B1 (en) * 2019-05-31 2025-12-31 Medshine Discovery Inc. BICYCLIC COMPOUND AS A RIP-1 KINASE INHIBITOR AND ITS APPLICATION
US12365695B2 (en) * 2019-08-09 2025-07-22 Bisichem Co., Ltd. Fused ring heteroaryl compounds as RIPK1 inhibitors
MY198690A (en) 2019-09-06 2023-09-16 Rigel Pharmaceuticals Inc Rip1 inhibitory compounds and methods for making and using the same
WO2021043966A1 (en) * 2019-09-06 2021-03-11 Inflazome Limited Nlrp3 inhibitors
JP7376218B2 (ja) * 2019-09-06 2023-11-08 ライジェル ファーマシューティカルズ, インコーポレイテッド Rip1阻害化合物ならびにそれを作製および使用するための方法
WO2021046515A1 (en) 2019-09-06 2021-03-11 Board Of Regents, The University Of Texas System Inhibitors of receptor interacting protein kinase i for the treatment of disease
IL291665B2 (en) 2019-09-27 2025-07-01 Univ Texas Inhibitors of receptor interacting protein kinase i for the treatment of disease
US11505558B1 (en) 2019-10-04 2022-11-22 Enanta Pharmaceuticals, Inc. Antiviral heterocyclic compounds
TWI864048B (zh) 2019-10-04 2024-12-01 美商安塔製藥公司 抗病毒雜環化合物、其醫藥組成物及其用途
KR102824962B1 (ko) * 2019-11-07 2025-06-26 리겔 파마슈티칼스, 인크. 헤테로시클릭 rip1 억제 화합물
AU2020391425A1 (en) 2019-11-26 2022-06-16 Board Of Regents, The University Of Texas System Inhibitors of Receptor Interacting Protein Kinase 1 for the treatment of disease
UY39032A (es) 2020-01-24 2021-07-30 Enanta Pharm Inc Compuestos heterocíclicos como agentes antivirales
WO2021173917A1 (en) * 2020-02-28 2021-09-02 Board Of Regents, The University Of Texas System Inhibitors of receptor interacting protein kinase i for the treatment of disease
AR121717A1 (es) * 2020-04-02 2022-06-29 Rigel Pharmaceuticals Inc Inhibidores de rip1k
TW202214617A (zh) 2020-06-02 2022-04-16 法商賽諾菲公司 作為ripk1抑制劑之異㗁唑啶及其用途
TWI840311B (zh) * 2020-07-01 2024-04-21 美商雷傑製藥公司 Rip1k抑制劑
WO2022010882A1 (en) 2020-07-07 2022-01-13 Enanta Pharmaceuticals, Inc, Dihydroquinoxaline and dihydropyridopyrazine derivatives as rsv inhibitors
IL300471A (en) * 2020-08-18 2023-04-01 Hutchison Medipharma Ltd Pyrimidinone compounds and their uses
WO2022086840A1 (en) 2020-10-19 2022-04-28 Enanta Pharmaceuticals, Inc. Heterocyclic compounds as anti-viral agents
CN114716427B (zh) * 2021-01-07 2024-04-26 成都贝诺科成生物科技有限公司 一种作为rip抑制剂的化合物及其制备方法和用途
WO2022171111A1 (en) * 2021-02-10 2022-08-18 Zai Lab (Us) Llc Heteroaryl-fused bicyclic compound as rip1-kinase inhibitors and uses thereof
WO2022171110A1 (en) * 2021-02-10 2022-08-18 Zai Lab (Us) Llc Fused tricyclic compounds as rip1-kinase inhibitors and uses thereof
TW202300490A (zh) * 2021-03-11 2023-01-01 美商雷傑製藥公司 雜環rip1激酶抑制劑
CN113045560B (zh) * 2021-03-30 2022-09-06 港科鹏禾生物(苏州)有限公司 一种酰胺类衍生物及其制备方法和应用
CA3214802A1 (en) 2021-04-02 2022-10-06 Genentech, Inc. Processes for making bicyclic ketone compounds
US20240228506A1 (en) * 2021-04-27 2024-07-11 Merck Sharp & Dohme Llc Ripk1 inhibitors and methods of use
CN115246796A (zh) * 2021-04-27 2022-10-28 中国科学院上海有机化学研究所 一种抑制细胞程序性死亡的化合物及其制备方法
US11767310B2 (en) 2021-08-10 2023-09-26 Abbvie Inc. Nicotinamide RIPK1 inhibitors
CN119528915A (zh) * 2021-09-14 2025-02-28 中国科学院上海有机化学研究所 抑制细胞程序性死亡的化合物及其制备方法
AU2022346718A1 (en) * 2021-09-17 2024-03-28 Bisichem Co., Ltd. Fused heterocyclic rings as ripk1 inhibitors
EP4421077A4 (en) * 2021-10-22 2025-09-24 Voronoi Inc ARYL OR HETEROARYL DERIVATIVE, AND PHARMACEUTICAL COMPOSITION COMPRISING IT AS AN ACTIVE INGREDIENT FOR THE PREVENTION OR TREATMENT OF KINASE-ASSOCIATED DISEASES
CN113876778B (zh) * 2021-11-05 2023-04-14 中日友好医院(中日友好临床医学研究所) Kw2449在制备改善类风湿性关节炎药物中的应用
CA3237975A1 (en) 2021-11-11 2023-05-19 Elisabeth Defossa Isoxazolidines as ripk1 inhibitors and use thereof
WO2023119210A1 (ko) * 2021-12-24 2023-06-29 제일약품주식회사 Ripk1 저해제로서의 신규한 화합물 및 이를 포함하는 약학적 조성물
KR20240132504A (ko) 2022-01-12 2024-09-03 데날리 테라퓨틱스 인크. (s)-5-벤질-n-(5-메틸-4-옥소-2,3,4,5-테트라하이드로피리도 [3,2-b][1,4]옥사제핀-3-일)-4h-1,2,4-트리아졸-3-카복사미드의 결정질 형태
EP4495119A4 (en) 2022-03-16 2025-06-25 Jiangsu Hengrui Pharmaceuticals Co., Ltd. FUSED HETEROCYCLIC COMPOUND, PREPARATION METHOD AND MEDICAL USE THEREOF
AR129003A1 (es) 2022-04-07 2024-07-03 Enanta Pharm Inc Compuestos heterocíclicos antivirales
WO2023211997A1 (en) 2022-04-27 2023-11-02 Enanta Pharmaceuticals, Inc. Antiviral compounds
WO2023240379A1 (zh) * 2022-06-13 2023-12-21 南京医工医药技术有限公司 咪唑啉酮衍生物及其用途
CN114736197B (zh) * 2022-06-13 2022-09-13 南京医工医药技术有限公司 咪唑啉酮衍生物及其用途
CN117447460A (zh) * 2022-07-13 2024-01-26 南京天印健华医药科技有限公司 作为ripk1抑制剂的杂环化合物
WO2024040155A1 (en) 2022-08-19 2024-02-22 Genzyme Corporation Isoxazolidines as ripk1 inhibitors and use thereof
TW202423921A (zh) * 2022-08-22 2024-06-16 美商安塔製藥公司 稠合的雜雙環抗病毒劑
CN117645579A (zh) * 2022-09-02 2024-03-05 科辉智药生物科技(深圳)有限公司 作为ripk1抑制剂的氮杂䓬类稠环化合物及其应用
TW202444357A (zh) * 2023-01-23 2024-11-16 美商健臻公司 4-(3,3-二氟-2,2-二甲基-丙醯基)-3,5-二氫-2h-吡啶并[3,4-f][1,4]氧氮呯-9-甲腈之藥品調配物
CN121127467A (zh) 2023-05-10 2025-12-12 建新公司 作为ripk1抑制剂的异噁唑烷及其用途
WO2024233547A1 (en) 2023-05-10 2024-11-14 Genzyme Corporation Isoxazolidines as ripk1 inhibitors and use thereof
WO2024233554A1 (en) 2023-05-10 2024-11-14 Genzyme Corporation Isoxazolidines as ripk1 inhibitors and use thereof
US20250000872A1 (en) * 2023-06-26 2025-01-02 Eli Lilly And Company Formulations and dosing regimens for rip1 kinase inhibitors for treating autoimmune and inflammatory diseases

Family Cites Families (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5239065B2 (cg-RX-API-DMAC7.html) 1971-11-17 1977-10-03
EP0166357A3 (en) * 1984-06-26 1988-10-26 Merck & Co. Inc. Benzofused lactams and pharmaceutical compositions containing them
US4692522A (en) 1985-04-01 1987-09-08 Merck & Co., Inc. Benzofused lactams useful as cholecystokinin antagonists
US5206234A (en) 1990-10-22 1993-04-27 Merck & Co., Inc. Benzolactam analogs as antagonists of cck
JP3358069B2 (ja) * 1991-12-24 2002-12-16 武田薬品工業株式会社 三環性複素環類、その製造法及び剤
ATE235472T1 (de) 1995-06-07 2003-04-15 Merck & Co Inc N-(2-oxo-2,3,4,5-tetrahydro-1h-1,5-benzodiazepi - 3-yl)-3-amide
WO1998041510A1 (en) * 1997-03-14 1998-09-24 Shionogi & Co., Ltd. Novel benzolactam derivatives and medicinal compositions comprising the same
US6228854B1 (en) 1997-08-11 2001-05-08 Cor Therapeutics, Inc. Selective factor Xa inhibitors
FR2781483A1 (fr) * 1998-07-21 2000-01-28 Hoechst Marion Roussel Inc Derives de thioazepinone, procede de preparation et intermediaires de ce procede, application a titre de medicament et compositions pharmaceutiques les renfermant
JP2003503476A (ja) 1999-07-06 2003-01-28 バーテックス ファーマシューティカルズ インコーポレイテッド 環化アミド誘導体
US6514965B1 (en) 1999-11-18 2003-02-04 Antex Pharma Inc. Substituted 1-benzazepines and derivatives thereof
IL151576A0 (en) 2000-04-03 2003-04-10 Bristol Myers Squibb Pharma Co Cyclic lactams as inhibitors of a-beta protein production
MXPA02009729A (es) 2000-04-03 2003-03-27 Bristol Myers Squibb Pharma Co Lactamas ciclicas como inhibidores de la produccion de la proteina a-beta.
WO2001092235A1 (en) 2000-06-01 2001-12-06 Bristol-Myers Squibb Pharma Company LACTAMS SUBSTITUTED BY CYCLIC SUCCINATES AS INHIBITORS OF Aβ PROTEIN PRODUCTION
DE10054279A1 (de) 2000-11-02 2002-05-16 Apotech Res & Dev Ltd Verwendung von Liganden von Todesrezeptoren oder RIP zur Auslösung des Caspase-unabhängigen Zelltods und Verbindungen zur Inhibition des Caspase-unabhängigen Zelltods
CA2447687A1 (en) 2001-05-16 2002-12-19 Antexpharma, Inc. Substituted 1-benzazepines and derivatives thereof
US7057046B2 (en) * 2002-05-20 2006-06-06 Bristol-Myers Squibb Company Lactam glycogen phosphorylase inhibitors and method of use
AU2003229678A1 (en) 2003-04-15 2004-11-04 Dirk Koczan Method for diagnosing rheumatoid arthritis or osteoarthritis
TW200509910A (en) * 2003-05-02 2005-03-16 Elan Pharm Inc Substituted pyrazole derivatives and related compounds as bradykinin B1 receptor antagonists
WO2005028664A2 (en) 2003-09-17 2005-03-31 University Of Massachusetts Modulation of programmed necrosis
EP1640012A1 (de) 2004-09-24 2006-03-29 Salama, Zoser B. nat.rer.Dr. Pharmazeutisches Mittel enthaltend Blutbestandteile 10 kDa und deren Verwendung zur Prophylaxe und Behandlung von Defekten des Immunsystems
US20060067942A1 (en) 2004-09-24 2006-03-30 Salama Zoser B Pharmaceutical agent comprising amino acids, peptides, proteins and/or fractions and fragments thereof and the use of same in the prophylaxis and treatment of immune system deficiency in humans and animals
AU2006331754B9 (en) * 2005-12-20 2013-07-11 President And Fellows Of Harvard College Compounds, screens, and methods of treatment
FR2894968B1 (fr) 2005-12-20 2008-02-22 Trophos Sa Nouveaux derives de l'oxime de cholest-4-en-3-one, compositions pharmaceutiques les renfermant, et procede de preparation
FR2899108B1 (fr) 2006-03-31 2012-02-03 Trophos Utilisation de derives du cholest-4-en-3-one pour l'obtention d'un medicament cytoprotecteur
US8007790B2 (en) 2006-04-03 2011-08-30 Stowers Institute For Medical Research Methods for treating polycystic kidney disease (PKD) or other cyst forming diseases
FR2907783A1 (fr) 2006-10-30 2008-05-02 Trophos Sa Nouveaux composes chimiques, leurs procedes de synthese et leur utilisation a titre de medicament, particulierement a titre de medicament cytoprotecteur, neuroprotecteur ou cardioprotecteur
WO2008086043A2 (en) 2007-01-10 2008-07-17 Wyeth Methods and compositions for assessment and treatment of asthma
AU2008219723A1 (en) 2007-02-28 2008-09-04 Merck Sharp & Dohme Corp. Substituted benzodiazepinones, benzoxazepinones and benzothiazepinones as sodium channel blockers
JP5239065B2 (ja) 2007-04-20 2013-07-17 株式会社大一商会 遊技機
EP3034494A1 (en) 2007-08-15 2016-06-22 President and Fellows of Harvard College Heterocyclic inhibitors of necroptosis
FR2934596B1 (fr) 2008-07-30 2015-04-10 Trophos Nouveaux derives de l'oxime de cholest-4-en-3-one, compositions pharmaceutiques les renfermant, et procede de preparation
US8257921B1 (en) 2008-12-22 2012-09-04 Schering Corporation NRIP1 regulation of apolipoprotein A1
WO2010075290A1 (en) 2008-12-22 2010-07-01 President And Fellows Of Harvard College Unsaturated heterocyclic inhibitors of necroptosis
EP2381775A4 (en) 2008-12-23 2012-08-15 Harvard College INHIBITORS OF NECROPTOSIS OF SMALL MOLECULAR SIZE
FR2940650B1 (fr) 2008-12-29 2017-01-27 Trophos Nouveaux derives d'oxime du 3,5-seco-4-nor-cholestane, compositions pharmaceutiques les renfermant,et procede de preparation
US7622106B1 (en) 2009-03-06 2009-11-24 Board Of Regents, The University Of Texas System Necrosis assay
KR101155506B1 (ko) 2009-07-08 2012-06-15 고려대학교 산학협력단 활성산소조절 유전자를 이용한 tnf-알파 유도 질병의 치료제 및 예방제의 스크리닝 방법
EP2519260A2 (en) 2009-12-31 2012-11-07 Deutsches Krebsforschungszentrum Novel modulators of trail signalling
WO2011112588A2 (en) 2010-03-08 2011-09-15 Case Western Reserve University Compositions and methods for treating inflammatory disorders
AU2011242465B2 (en) 2010-04-23 2017-01-19 Massachusetts Eye And Ear Infirmary Methods and compositions for preserving photoreceptor and retinal pigment epithelial cells
MX342951B (es) 2010-07-16 2016-10-18 Agios Pharmaceuticals Inc * Composiciones terapeuticamente activas y su metodo de uso.
US20120022116A1 (en) 2010-07-20 2012-01-26 Huayun Deng Compositions and methods for the treatment of pathological condition(s) related to gpr35 and/or gpr35-herg complex
US20140024598A1 (en) 2010-11-01 2014-01-23 Demetrios Vavvas Methods and compositions for preserving retinal ganglion cells
WO2012125544A2 (en) 2011-03-11 2012-09-20 President And Fellows Of Harvard College Necroptosis inhibitors and methods of use therefor
WO2013013826A1 (en) 2011-07-27 2013-01-31 Friedrich-Alexander-Universität Erlangen-Nürnberg Necroptosis inhibitors for the treatment of inflammatory diseases of the gastrointestinal tract
WO2013043662A1 (en) 2011-09-22 2013-03-28 Marv Enterprises Llc Method for the treatment of multiple sclerosis
CN102343102A (zh) 2011-10-19 2012-02-08 柳忠辉 激活素受体相互作用蛋白2基因在制备药物中的应用
CA2888805C (en) 2011-10-21 2020-07-14 Massachusetts Eye And Ear Infirmary Methods and compositions for promoting axon regeneration and nerve function
KR101410332B1 (ko) 2012-02-29 2014-06-24 코아스템(주) 중간엽 기질세포 배양용 항산화 조성물 및 이의 용도
ES2446494B1 (es) 2012-03-28 2015-03-16 Consejo Superior De Investigaciones Científicas (Csic) Aplicación terapéutica de necrostatina-1 en esteatohepatitis
WO2014022102A1 (en) 2012-08-01 2014-02-06 Amgen Inc. Methods of using anti-apoptotic compounds to modulate one or more properties of a cell culture
WO2014024183A1 (en) 2012-08-06 2014-02-13 Brainstorm Cell Therapeutics Ltd. Methods of generating mesenchymal stem cells which secrete neurotrophic factors
MX376594B (es) 2012-12-26 2025-03-07 Innosign B V Evaluacion de la actividad de la via de señalizacion celular utilizando combinacion(es) lineal(es) de expresiones de genes objetivo.
JPWO2014126127A1 (ja) 2013-02-13 2017-02-02 国立大学法人北海道大学 ネクロプトーシス関連疾患の治療用医薬組成物及びその有効成分のスクリーニング方法
TWI648273B (zh) * 2013-02-15 2019-01-21 英商葛蘭素史克智慧財產發展有限公司 作為激酶抑制劑之雜環醯胺類(三)
EP2961849A2 (en) 2013-02-27 2016-01-06 The Broad Institute, Inc. T cell balance gene expression, compositions of matters and methods of use thereof
JP2016514693A (ja) 2013-03-15 2016-05-23 プレジデント アンド フェローズ オブ ハーバード カレッジ ハイブリッド型ネクロトーシス阻害剤
US20170266199A1 (en) 2014-08-21 2017-09-21 Glaxosmithkline Intellectual Property Development Limited Heterocyclic amides as rip1 kinase inhibitors as medicaments
EA201891620A1 (ru) 2016-02-05 2019-02-28 Денали Терапьютикс Инк. Ингибиторы взаимодействующей с рецептором протеинкиназы 1

Similar Documents

Publication Publication Date Title
JP2016512488A5 (cg-RX-API-DMAC7.html)
CA2849169C (en) Pyrazole carboxamides as janus kinase inhibitors
JP2012525349A5 (cg-RX-API-DMAC7.html)
JP2010513444A5 (cg-RX-API-DMAC7.html)
JP6017313B2 (ja) 化合物および方法
CA2670605A1 (en) Substituted arylpyrazoles
JP2017524028A (ja) 薬剤としてのrip1キナーゼ阻害剤である複素環式アミド
JP2017538750A5 (cg-RX-API-DMAC7.html)
RU2017125520A (ru) Соединения, ингибирующие parg
JP2010533158A5 (cg-RX-API-DMAC7.html)
RU2011116226A (ru) Пиразолопиридиновые производные как ингибиторы надфн-оксидазы
WO2002062804A1 (en) Oxazolyl-pyrazole derivatives as kinase inhibitors
JP2008525502A (ja) 抗炎症薬
AU2002246076A1 (en) Oxazolyl-pyrazole derivatives as kinase inhibitors
JP2017512794A5 (cg-RX-API-DMAC7.html)
RU2019132212A (ru) Селективные ингибиторы hdac6
SG175640A1 (en) Kinase inhibitors useful for the treatment of myleoproliferative diseases and other proliferative diseases
CA2521201A1 (en) Substituted pyrazoles for use in the prophylaxis or treatment of a disease which can be influenced by the binding of the substitued pyrazoles to 5ht receptors
JP2010504280A5 (cg-RX-API-DMAC7.html)
CA2554686A1 (en) Compounds
RU2016102137A (ru) Первичные карбоксамиды в качестве ингибиторов bik
JP2014525444A5 (cg-RX-API-DMAC7.html)
RU2012143794A (ru) Производные n-(имидазопиримидин-7-ил)-гетероаламидов и их применение в качестве ингибиторов pde10a
KR20070007103A (ko) 벤즈아미드 유도체 및 이의 글루코키나아제 활성화제로서의용도
RU2017124425A (ru) Производные 2,4-диоксо-хиназолин-6-сульфонамида в качестве ингибиторов parg