MA44007A - Inhibiteurs du récepteur interagissant avec protéine kinase 1 - Google Patents
Inhibiteurs du récepteur interagissant avec protéine kinase 1Info
- Publication number
- MA44007A MA44007A MA044007A MA44007A MA44007A MA 44007 A MA44007 A MA 44007A MA 044007 A MA044007 A MA 044007A MA 44007 A MA44007 A MA 44007A MA 44007 A MA44007 A MA 44007A
- Authority
- MA
- Morocco
- Prior art keywords
- kinase
- protein
- receptor inhibitors
- interacting
- inhibitors interacting
- Prior art date
Links
- 108091000080 Phosphotransferase Proteins 0.000 title 1
- 102000020233 phosphotransferase Human genes 0.000 title 1
- 108090000623 proteins and genes Proteins 0.000 title 1
- 102000004169 proteins and genes Human genes 0.000 title 1
- 108091006082 receptor inhibitors Proteins 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
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- Physical Education & Sports Medicine (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Psychology (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Psychiatry (AREA)
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- Addiction (AREA)
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Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201662292202P | 2016-02-05 | 2016-02-05 | |
US201662341019P | 2016-05-24 | 2016-05-24 | |
US201662363775P | 2016-07-18 | 2016-07-18 | |
US201662385217P | 2016-09-08 | 2016-09-08 | |
US201662417219P | 2016-11-03 | 2016-11-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
MA44007A true MA44007A (fr) | 2018-12-19 |
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EP (1) | EP3414239A2 (fr) |
JP (2) | JP6974331B2 (fr) |
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AU (1) | AU2017213628B2 (fr) |
CA (1) | CA3012832A1 (fr) |
CL (1) | CL2018002081A1 (fr) |
CO (1) | CO2018008707A2 (fr) |
CR (1) | CR20180413A (fr) |
DO (1) | DOP2018000175A (fr) |
EA (1) | EA201891620A1 (fr) |
EC (1) | ECSP18066138A (fr) |
IL (2) | IL287136B2 (fr) |
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MX (3) | MX2018009448A (fr) |
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PH (1) | PH12018501583A1 (fr) |
SA (1) | SA518392146B1 (fr) |
SG (2) | SG10201913587WA (fr) |
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Families Citing this family (77)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI648274B (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 (二) |
AU2016287581B2 (en) | 2015-07-02 | 2019-06-06 | F. Hoffmann-La Roche Ag | Bicyclic lactams and methods of use thereof |
MX2018000916A (es) | 2015-07-22 | 2018-09-05 | Enanta Pharm Inc | Derivados de benzodiazepina como inhibidores de rsv. |
US10961258B2 (en) | 2015-12-21 | 2021-03-30 | Glaxosmithkline Intellectual Property Development Limited | Heterocyclic amides as kinase inhibitors |
US20170226129A1 (en) | 2016-01-15 | 2017-08-10 | Enanta Pharmaceuticals, Inc. | Heterocyclic compounds as rsv inhibitors |
SG10201913587WA (en) * | 2016-02-05 | 2020-02-27 | Denali Therapeutics Inc | Inhibitors of receptor-interacting protein kinase 1 |
TWI759301B (zh) | 2016-05-24 | 2022-04-01 | 美商安美基公司 | 聚乙二醇化卡非佐米化合物 |
SI3472153T1 (sl) * | 2016-06-16 | 2022-01-31 | Denali Therapeutics Inc. | Pirimidin-2-ilamino-1H-pirazoli kot zaviralci LRRK2 za uporabo pri zdravljenju nevrodegenerativnih motenj |
JP7349359B2 (ja) | 2016-10-17 | 2023-09-22 | エフ. ホフマン-ラ ロシュ アーゲー | 二環式ピリドンラクタム及びその使用方法。 |
JP6890179B2 (ja) | 2016-12-02 | 2021-06-18 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | 二環式アミド化合物及びその使用方法 |
US11072607B2 (en) * | 2016-12-16 | 2021-07-27 | Genentech, Inc. | Inhibitors of RIP1 kinase and methods of use thereof |
EP3582784B1 (fr) | 2017-02-16 | 2022-06-08 | Enanta Pharmaceuticals, Inc. | Procédés pour la préparation de dérivés de benzodiazépine |
BR112019017738A2 (pt) | 2017-02-27 | 2020-04-07 | Glaxosmithkline Ip Dev Ltd | combinação, composição farmacêutica, uso de uma combinação ou composição farmacêutica, método para tratar câncer em um humano, e, composto |
WO2018226801A1 (fr) | 2017-06-07 | 2018-12-13 | Enanta Pharmaceuticals, Inc. | Dérivés d'aryldiazépine utilisés en tant qu'inhibiteurs du vrs |
US11091501B2 (en) | 2017-06-30 | 2021-08-17 | Enanta Pharmaceuticals, Inc. | Heterocyclic compounds as RSV inhibitors |
US10851115B2 (en) | 2017-06-30 | 2020-12-01 | Enanta Pharmaceuticals, Inc. | Heterocyclic compounds as RSV inhibitors |
SG11202000333UA (en) | 2017-07-14 | 2020-02-27 | Hoffmann La Roche | Bicyclic ketone compounds and methods of use thereof |
CN107759574B (zh) * | 2017-08-29 | 2020-07-03 | 南京药石科技股份有限公司 | 一种5-氟-1h-吡唑-3-甲酸酯中间体及其合成方法 |
WO2019067864A1 (fr) | 2017-09-29 | 2019-04-04 | Enanta Pharmaceuticals, Inc. | Agents pharmaceutiques en combinaison en tant qu'inhibiteurs de rsv |
SG11202003283TA (en) | 2017-10-11 | 2020-05-28 | Hoffmann La Roche | Bicyclic compounds for use as rip1 kinase inhibitors |
MX2020003451A (es) * | 2017-10-31 | 2020-08-03 | Hoffmann La Roche | Sulfonas y sulfoxidos biciclicos y metodos de uso de los mismos. |
AU2018365174B2 (en) | 2017-11-13 | 2023-03-30 | Enanta Pharmaceuticals, Inc. | Processes for the resolution of benzodiazepin-2-one and benzoazepin-2-one derivatives |
WO2019094920A1 (fr) * | 2017-11-13 | 2019-05-16 | Enanta Pharmaceuticals, Inc. | Dérivés d'azépin-2-one en tant qu'inhibiteurs du vrs |
CN108129288B (zh) * | 2017-12-27 | 2021-01-22 | 上海毕得医药科技股份有限公司 | 一种反式-3-羟基环丁基甲酸的合成方法 |
WO2019199908A1 (fr) | 2018-04-11 | 2019-10-17 | Enanta Pharmaceuticals, Inc. | Composés hétérocycliques en tant qu'inhibiteurs de vrs |
WO2019204537A1 (fr) * | 2018-04-20 | 2019-10-24 | Genentech, Inc. | Dérivés de n-[4-oxo-2,3-dihydro-1,5-benzoxazépin-3-yl]-5,6-dihydro-4h-pyrrolo[1,2-b]pyrazol e-2-carboxamide et composés apparentés en tant qu'inhibiteurs de la kinase rip1 pour le traitement, par exemple, du syndrome du côlon irritable (ibs) |
MD3788044T2 (ro) | 2018-05-03 | 2023-12-31 | Rigel Pharmaceuticals Inc | Compuși inhibitori ai RIP1 și procedee de obţinere și utilizare a acestora |
PL3788045T3 (pl) * | 2018-05-03 | 2023-10-09 | Rigel Pharmaceuticals, Inc. | Związki hamujące rip1 oraz sposoby ich wytwarzania i wykorzystania |
WO2020001420A1 (fr) * | 2018-06-26 | 2020-01-02 | 中国科学院上海有机化学研究所 | Inhibiteur de nécrose cellulaire, son procédé de préparation et son utilisation |
WO2020044206A1 (fr) | 2018-08-29 | 2020-03-05 | Glaxosmithkline Intellectual Property Development Limited | Amides hétérocycliques utiles en tant qu'inhibiteurs de kinases destinés à être utilisés dans le traitement du cancer |
JP7467349B2 (ja) * | 2018-09-10 | 2024-04-15 | 科研製薬株式会社 | 新規ヘテロ芳香族アミド誘導体及びそれを含有する医薬 |
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 |
WO2020088194A1 (fr) * | 2018-11-02 | 2020-05-07 | 中国科学院上海药物研究所 | Amide hétérocyclique inhibant la kinase rip1 et ses applications |
AU2020210455B2 (en) * | 2019-01-25 | 2023-02-02 | Beijing Scitech-Mq Pharmaceuticals Limited | Acylamino bridged heterocyclic compound, and composition and application thereof |
US11254664B2 (en) | 2019-03-18 | 2022-02-22 | Enanta Pharmaceuticals, Inc. | Benzodiazepine derivatives as RSV inhibitors |
WO2020210246A1 (fr) | 2019-04-09 | 2020-10-15 | Enanta Pharmaceuticals, Inc, | Composés hétérocycliques utilisés comme inhibiteurs du vrs |
EP3978492A4 (fr) * | 2019-05-31 | 2023-06-28 | Medshine Discovery Inc. | Composé bicyclique en tant qu'inhibiteur de la kinase rip-1 et son application |
CN110172068A (zh) * | 2019-06-05 | 2019-08-27 | 河南龙湖生物技术有限公司 | 具有抗肿瘤活性的苯并噻唑类化合物及其制备方法和应用 |
US20210040115A1 (en) * | 2019-08-09 | 2021-02-11 | Bisichem Co., Ltd. | Fused ring heteroaryl compounds as ripk1 inhibitors |
US11718612B2 (en) | 2019-09-06 | 2023-08-08 | Board Of Regents, The University Of Texas System | Inhibitors of receptor interacting protein kinase I for the treatment of disease |
US11564930B2 (en) | 2019-09-06 | 2023-01-31 | Rigel Pharmaceuticals, Inc. | RIP1 inhibitory compounds and methods for making and using the same |
EP4025568A1 (fr) * | 2019-09-06 | 2022-07-13 | Rigel Pharmaceuticals, Inc. | Composés inhibiteurs de rip1 et leurs procédés de fabrication et d'utilisation |
US20220340568A1 (en) * | 2019-09-11 | 2022-10-27 | Ohio State Innovation Foundation | Kinase inhibitors for the treatment of neurodegenerative diseases |
US11753381B2 (en) | 2019-09-27 | 2023-09-12 | Board Of Regents, The University Of Texas System | Inhibitors of receptor interacting protein kinase I for the treatment of disease |
KR20220101083A (ko) | 2019-10-04 | 2022-07-19 | 이난타 파마슈티칼스, 인코포레이티드 | 항바이러스 헤테로사이클릭 화합물 |
US11505558B1 (en) | 2019-10-04 | 2022-11-22 | Enanta Pharmaceuticals, Inc. | Antiviral heterocyclic compounds |
CA3156594A1 (fr) | 2019-11-07 | 2021-05-14 | Yan Chen | Composes heterocycliques inhibiteurs de rip1 |
BR112022010082A2 (pt) | 2019-11-26 | 2022-08-30 | Univ Texas | Composto de fórmula estrutural i ou sal do mesmo, composição farmacêutica, uso do composto e uso da composição farmacêutica |
UY39032A (es) | 2020-01-24 | 2021-07-30 | Enanta Pharm Inc | Compuestos heterocíclicos como agentes antivirales |
AR121717A1 (es) * | 2020-04-02 | 2022-06-29 | Rigel Pharmaceuticals Inc | Inhibidores de rip1k |
JP2023522623A (ja) * | 2020-04-17 | 2023-05-31 | ジェンザイム・コーポレーション | 全身性過炎症反応を伴う状態の処置に使用するエクリタセルチブ |
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 |
AR122703A1 (es) * | 2020-07-01 | 2022-09-28 | Rigel Pharmaceuticals Inc | Inhibidores de rip1k |
US11534439B2 (en) | 2020-07-07 | 2022-12-27 | Enanta Pharmaceuticals, Inc. | Dihydroquinoxaline and dihydropyridopyrazine derivatives as RSV inhibitors |
WO2022086840A1 (fr) | 2020-10-19 | 2022-04-28 | Enanta Pharmaceuticals, Inc. | Composés hétérocycliques en tant qu'agents antiviraux |
US11976084B2 (en) | 2020-11-23 | 2024-05-07 | Enanta Pharmaceuticals, Inc. | Spiropyrrolidine derived antiviral 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 |
WO2022171110A1 (fr) * | 2021-02-10 | 2022-08-18 | Zai Lab (Us) Llc | Composés tricycliques fusionnés en tant qu'inhibiteurs de rip1-kinase et leurs utilisations |
WO2022171111A1 (fr) * | 2021-02-10 | 2022-08-18 | Zai Lab (Us) Llc | Composé bicyclique fusionné hétéroaryle utile en tant qu'inhibiteur de la rip1-kinase et ses utilisations |
JP2024507561A (ja) | 2021-02-26 | 2024-02-20 | 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 | 抗ウイルス複素環式化合物 |
TW202300490A (zh) * | 2021-03-11 | 2023-01-01 | 美商雷傑製藥公司 | 雜環rip1激酶抑制劑 |
JP2022165218A (ja) | 2021-04-19 | 2022-10-31 | 住友ゴム工業株式会社 | ゴム組成物及びタイヤ |
US11970502B2 (en) | 2021-05-04 | 2024-04-30 | Enanta Pharmaceuticals, Inc. | Macrocyclic antiviral agents |
CN114989156B (zh) * | 2021-05-19 | 2024-07-05 | 成都贝诺科成生物科技有限公司 | 一种受体相互作用蛋白抑制剂及其制备方法和用途 |
TW202321211A (zh) | 2021-08-10 | 2023-06-01 | 美商艾伯維有限公司 | 菸鹼醯胺ripk1抑制劑 |
WO2023043284A1 (fr) * | 2021-09-17 | 2023-03-23 | Bisichem Co., Ltd. | Hétérocycles fusionnés utiles comme inhibiteurs de ripk1 |
IL312739A (en) | 2021-11-11 | 2024-07-01 | Genzyme Corp | Isoxazolidines as RIPK1 inhibitors and their use |
WO2023086352A1 (fr) | 2021-11-12 | 2023-05-19 | Enanta Pharmaceuticals, Inc. | Nouveaux agents antiviraux dérivés de spiropyrrolidine |
WO2023086350A1 (fr) | 2021-11-12 | 2023-05-19 | Enanta Pharmaceuticals, Inc. | Agents antiviraux contenant des alcynes |
US11919910B2 (en) | 2021-11-12 | 2024-03-05 | Enanta Pharmaceuticals, Inc. | Spiropyrrolidine derived antiviral agents |
US11993600B2 (en) | 2021-12-08 | 2024-05-28 | Enanta Pharmaceuticals, Inc. | Saturated spirocyclics as antiviral agents |
WO2023119210A1 (fr) | 2021-12-24 | 2023-06-29 | 제일약품주식회사 | Nouveau composé utilisé en tant qu'inhibiteur de ripk1 et composition pharmaceutique le comprenant |
EP4209213A1 (fr) | 2022-01-05 | 2023-07-12 | Universität zu Köln | Combinaisons d'inhibiteur de trajet de signalisation destinées à être utilisées dans le traitement de cancers |
US12006291B2 (en) | 2022-01-11 | 2024-06-11 | Enanta Pharmaceuticals, Inc. | Processes for the preparation of 4,6,7-trifluoro-1H-indole-2-carboxylic acid |
US11999750B2 (en) | 2022-01-12 | 2024-06-04 | Denali Therapeutics Inc. | Crystalline forms of (S)-5-benzyl-N-(5-methyl-4-oxo-2,3,4,5-tetrahydropyrido [3,2-B][1,4]oxazepin-3-yl)-4H-1,2,4-triazole-3-carboxamide |
WO2024170776A1 (fr) | 2023-02-17 | 2024-08-22 | Universität Zu Köln | Inhibition de la triple kinase pour le traitement de troubles associés à la réponse interféron de type i |
CN117849327A (zh) * | 2024-03-06 | 2024-04-09 | 军科正源(北京)药物研究有限责任公司 | 用于检测苏金单抗抗药性抗体的方法 |
Family Cites Families (167)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6204261B1 (en) | 1995-12-20 | 2001-03-20 | Vertex Pharmaceuticals Incorporated | Inhibitors of interleukin-1β Converting enzyme inhibitors |
US4477464A (en) | 1983-02-10 | 1984-10-16 | Ciba-Geigy Corporation | Hetero-benzazepine derivatives and their pharmaceutical use |
EP0187037A3 (fr) | 1984-12-21 | 1988-03-23 | Takeda Chemical Industries, Ltd. | Dérivés de pipéridine, leur production et emploi |
EP0322779A3 (fr) | 1987-12-29 | 1991-05-08 | Yoshitomi Pharmaceutical Industries, Ltd. | Composés de benzolactame et leur utilisation pharmaceutique |
JPH0334977A (ja) | 1989-06-29 | 1991-02-14 | Yoshitomi Pharmaceut Ind Ltd | イミダゾリルベンゾラクタム化合物 |
AU641769B2 (en) | 1990-06-18 | 1993-09-30 | Merck & Co., Inc. | Inhibitors of HIV reverse transcriptase |
EP0481614A1 (fr) | 1990-10-01 | 1992-04-22 | Merck & Co. Inc. | Pyridopyrimidinones substituées et hétérocyles apparantés comme antagonistes de la angiotensine II |
US5206234A (en) | 1990-10-22 | 1993-04-27 | Merck & Co., Inc. | Benzolactam analogs as antagonists of cck |
US5206235A (en) | 1991-03-20 | 1993-04-27 | Merck & Co., Inc. | Benzo-fused lactams that promote the release of growth hormone |
US5457196A (en) | 1991-09-27 | 1995-10-10 | Merrell Dow Pharmaceuticals Inc. | 2-substituted indane-2-carboxyalkyl derivatives useful as inhibitors of enkephalinase and ACE |
ATE155143T1 (de) | 1991-09-27 | 1997-07-15 | Merrell Pharma Inc | 2-substituierte indan-2-mercaptoacetylamid- verbindungen mit enkephalinase und ace- hemmwirkung |
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 |
US5484917A (en) | 1993-06-16 | 1996-01-16 | Pfizer Inc. | Substituted tetrahydrobenzazepinones |
AU4282993A (en) | 1992-07-01 | 1994-01-31 | Pfizer Inc. | Benzothiazepine and benzoxazepine derivatives as cholecystokinin receptor antagonists |
WO1994004531A1 (fr) | 1992-08-24 | 1994-03-03 | Merrell Dow Pharmaceuticals Inc. | Nouveaux derives tricycliques de l'indane-2-mercaptoacetylamide a substitution en position 2 utilises comme inhibiteurs de l'enkephalinase |
US5420271A (en) | 1992-08-24 | 1995-05-30 | Merrell Dow Pharmaceuticals, Inc. | 2-substituted indane-2-mercaptoacetylamide tricyclic derivatives useful as inhibitors of enkephalinase |
US5283241A (en) | 1992-08-28 | 1994-02-01 | Merck & Co., Inc. | Benzo-fused lactams promote release of growth hormone |
CA2120956A1 (fr) | 1992-09-03 | 1994-03-17 | Franz Esser | Nouveaux derives d'acides amines, methodes pour les fabriquer et compositions pharmaceutiques les renfermant |
US5583130A (en) | 1992-09-25 | 1996-12-10 | Merck & Co., Inc. | Benzo-fused lactams promote release of growth hormone |
US5317017A (en) | 1992-09-30 | 1994-05-31 | Merck & Co., Inc. | N-biphenyl-3-amido substituted benzolactams stimulate growth hormone release |
US5374721A (en) | 1992-10-14 | 1994-12-20 | Merck & Co., Inc. | Benzo-fused lactams promote release of growth hormone |
EP0619751B1 (fr) | 1992-10-16 | 2003-05-07 | Suprex Corporation | Extraction automatique de fluide surcritique |
GB2272439A (en) | 1992-11-13 | 1994-05-18 | Merck & Co Inc | Benzo-fused lactams that inhibit the release of growth hormone |
US5284841A (en) | 1993-02-04 | 1994-02-08 | Merck & Co., Inc. | Benzo-fused lactams promote release of growth hormone |
GB9307833D0 (en) | 1993-04-15 | 1993-06-02 | Glaxo Inc | Modulators of cholecystokinin and gastrin |
WO1994026718A1 (fr) | 1993-05-13 | 1994-11-24 | Yoshitomi Pharmaceutical Industries, Ltd. | Compose de 3-aminoazepine et son utilisation pharmaceutique |
US5430144A (en) | 1993-07-26 | 1995-07-04 | Merck & Co., Inc. | Benzo-fused lactams promote release of growth hormone |
ES2081747B1 (es) | 1993-09-07 | 1997-01-16 | Esteve Labor Dr | Amidas derivadas de tienopirroles, su preparacion y su aplicacion como medicamentos. |
US5606054A (en) | 1993-12-14 | 1997-02-25 | Merck & Co., Inc. | Heterocyclic-fused lactams promote release of growth hormone |
CA2186900A1 (fr) | 1994-04-14 | 1995-10-26 | Christopher Joseph Aquino | 5-heterocyclo-1,5-benzodiazepines modulant les effets de la chol ecystokinine ou de la gastrine |
CN1147260A (zh) | 1994-05-07 | 1997-04-09 | 贝林格尔·英格海姆公司 | 神经激肽(快速激肽)拮抗剂 |
IL114955A (en) | 1994-08-17 | 1999-12-22 | Novo Nordisk As | N-substituted naphthofused lactams and pharmaceutical compositions containing them |
GB9420747D0 (en) | 1994-10-14 | 1994-11-30 | Glaxo Inc | 1,5 benzodiazepine derivatives |
GB9420748D0 (en) | 1994-10-14 | 1994-11-30 | Glaxo Inc | 1,5 benzodiazepine derivatives |
GB9420763D0 (en) | 1994-10-14 | 1994-11-30 | Glaxo Inc | Acetamide derivatives |
WO1996016008A1 (fr) | 1994-11-17 | 1996-05-30 | Ciba Specialty Chemicals Holding Inc. | Monomeres reticulables et compositions et polymeres reticules |
US5587375A (en) | 1995-02-17 | 1996-12-24 | Bristol-Myers Squibb Company | Azepinone compounds useful in the inhibition of ACE and NEP |
US5691331A (en) | 1995-06-07 | 1997-11-25 | Merck & Co., Inc. | N-(2,4-Dioxo-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3yl) -3- amides |
US5700797A (en) | 1995-06-07 | 1997-12-23 | Merck & Co, Inc. | N-(2,4-dioxo-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3-yl)-3-amides |
US5726171A (en) | 1995-06-07 | 1998-03-10 | Merck & Co Inc | N-(1-alkyl-5-phenyl-2,3,4,5-tetrahydro-1H-benzo B! 1,4!diazepin-3yl)-acetamides |
ES2193241T3 (es) | 1995-06-07 | 2003-11-01 | Merck & Co Inc | Nuevas n-2-oxo2.3.4.5-tetrajodrp-1h-1,5-benzodiazepin-3-il)-3-amidas. |
EP0761680A3 (fr) | 1995-09-12 | 1999-05-06 | Ono Pharmaceutical Co., Ltd. | Composés de tétrazole ayant une activité inhibante d'enzyme convertissant l'Interleukine-1bêta |
BR9610579A (pt) | 1995-09-15 | 1999-07-06 | Sanofi Synthelabo | Derivados de quinolein-2(1H)-ona como antagonistas da serotonina |
WO1997024339A1 (fr) | 1995-12-27 | 1997-07-10 | Ono Pharmaceutical Co., Ltd. | Derives de tetrazole et medicaments les contenant a titre d'ingredients actifs |
US5747235A (en) | 1996-01-26 | 1998-05-05 | Eastman Kodak Company | Silver halide light sensitive emulsion layer having enhanced photographic sensitivity |
JPH09295996A (ja) | 1996-03-06 | 1997-11-18 | Takeda Chem Ind Ltd | システインプロテアーゼ阻害化合物 |
ATE241600T1 (de) | 1996-06-29 | 2003-06-15 | Samjin Pharm Co Ltd | Piperazin-derivate und verfahren zu ihrer herstellung |
DE19638020A1 (de) | 1996-09-18 | 1998-03-19 | Solvay Pharm Gmbh | Die gastrointestinale Durchblutung fördernde Arzneimittel |
JP4094066B2 (ja) | 1996-12-06 | 2008-06-04 | 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 | インターロイキン−1β変換酵素のインヒビター |
JPH10251295A (ja) | 1997-03-07 | 1998-09-22 | Ono Pharmaceut Co Ltd | テトラゾール誘導体 |
JP2001515842A (ja) | 1997-08-11 | 2001-09-25 | シーオーアール セラピューティクス インコーポレイテッド | 選択的Xa因子阻害剤 |
US6211174B1 (en) | 1997-10-31 | 2001-04-03 | Merck & Co., Inc. | Naphtho-fused lactams promote release of growth hormone |
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 |
DE19858253A1 (de) | 1998-12-17 | 2000-06-21 | Aventis Pharma Gmbh | Verwendung von Inhibitoren des KQt1-Kanals zur Herstellung eines Medikaments zur Behandlung von Krankheiten, die durch Helminthen und Ektoparasiten hervorgerufen werden |
JP2000256318A (ja) | 1999-03-02 | 2000-09-19 | Toa Eiyo Ltd | 縮合複素環誘導体、その製造法およびそれを含有する医薬品 |
FR2803594B1 (fr) | 2000-01-11 | 2002-07-19 | Centre Nat Rech Scient | Oligomeres de mimes contraints non peptidiques de dipeptides ou de tripeptides, et leurs utilisations |
CA2403550A1 (fr) | 2000-04-03 | 2001-10-11 | Hong Liu | Lactames cycliques utiles en tant qu'inhibiteurs de la production de proteine a-beta |
BR0107532A (pt) | 2000-04-03 | 2004-11-03 | Bristol Myers Squibb Pharma Co | Composto, uso do composto, método para o tratamento de disfunções neurológicas associadas com a produção de b-amilóide, método de inibição da atividade de y-secretase e composição farmacêutica |
WO2001079261A1 (fr) | 2000-04-14 | 2001-10-25 | Corvas International, Inc. | Derives de tetrahydro-azepinone servant d'inhibiteurs de la thrombine |
RU2002135317A (ru) | 2000-04-24 | 2004-04-10 | Вертекс Фармасьютикалз Инкорпорейтед (Us) | Способ и промежуточные соединения для получения замещенных ацеталей аспарагиновой кислоты |
GB0012671D0 (en) | 2000-05-24 | 2000-07-19 | Merck Sharp & Dohme | Therapeutic agents |
BR0106717A (pt) | 2000-06-01 | 2002-04-16 | Bristol Myers Squibb Pharma Co | Compostos, composição farmacêutica e usos dos compostos de lactama inovadora |
AUPQ969800A0 (en) | 2000-08-28 | 2000-09-21 | Fujisawa Pharmaceutical Co., Ltd. | Pyrazolopyridine compound and pharmaceutical use thereof |
AU2001288432A1 (en) | 2000-09-01 | 2002-03-22 | Icos Corporation | Materials and methods to potentiate cancer treatment |
GB0021831D0 (en) * | 2000-09-06 | 2000-10-18 | Astrazeneca Ab | Chemical compounds |
WO2003007945A1 (fr) | 2001-07-20 | 2003-01-30 | Boehringer Ingelheim (Canada) Ltd. | Inhibiteurs de polymerase virale |
EP2335700A1 (fr) | 2001-07-25 | 2011-06-22 | Boehringer Ingelheim (Canada) Ltd. | Inhibiteurs de la polymerase du virus hepatitis C avec une structure heterobicylic |
US7294457B2 (en) | 2001-08-07 | 2007-11-13 | Boehringer Ingelheim (Canada) Ltd. | Direct binding assay for identifying inhibitors of HCV polymerase |
WO2003031376A1 (fr) | 2001-10-12 | 2003-04-17 | Aventis Pharmaceuticals Inc. | Synthese en phase solide de 1,5-benzodiazepine-2-one ou 1,5-benzothiazepine-2-one substitue |
US7057046B2 (en) * | 2002-05-20 | 2006-06-06 | Bristol-Myers Squibb Company | Lactam glycogen phosphorylase inhibitors and method of use |
CN1678586A (zh) * | 2002-06-27 | 2005-10-05 | 舍林股份公司 | 取代的喹啉ccr5受体拮抗剂 |
US7098235B2 (en) | 2002-11-14 | 2006-08-29 | Bristol-Myers Squibb Co. | Triglyceride and triglyceride-like prodrugs of glycogen phosphorylase inhibiting compounds |
EP1581520A4 (fr) | 2002-12-13 | 2006-08-23 | Smithkline Beecham Corp | Composés, compositions et méthodes |
WO2004082602A2 (fr) | 2003-03-14 | 2004-09-30 | Merck & Co. Inc. | Antagonistes des recepteurs du cgrp a base de carboxamide spirohydantoine |
PE20050525A1 (es) | 2003-05-02 | 2005-09-08 | Elan Pharm Inc | Derivados de pirazol sustituido y compuestos relacionados como antagonistas del receptor de bradiquinina b1 |
JP2005035933A (ja) | 2003-07-15 | 2005-02-10 | Takeda Chem Ind Ltd | 含窒素縮合複素環化合物の製造方法 |
EP1663184A2 (fr) | 2003-08-29 | 2006-06-07 | The Brigham And Women's Hospital, Inc. | Inhibiteurs de la necrose cellulaire |
EP1692157B1 (fr) | 2003-10-10 | 2013-04-17 | Vertex Pharmaceuticals Incorporated | Inhibiteurs de serine proteases, en particulier la ns3-ns4a protease du hcv |
WO2005056577A2 (fr) | 2003-12-05 | 2005-06-23 | The Regents Of The University Of California | Inhibiteurs peptidiques de vih |
US20070010428A1 (en) | 2004-09-03 | 2007-01-11 | Mcmurray John S | Inhibitors of signal transduction and activator of transcription 3 |
US7390798B2 (en) | 2004-09-13 | 2008-06-24 | Merck & Co., Inc. | Carboxamide spirolactam CGRP receptor antagonists |
DE602005010463D1 (de) * | 2004-10-13 | 2008-11-27 | Merck & Co Inc | Cgrp-rezeptorantagonisten |
ATE507880T1 (de) | 2004-10-14 | 2011-05-15 | Merck Sharp & Dohme | Cgrp-rezeptorantagonisten |
ATE424821T1 (de) | 2004-12-02 | 2009-03-15 | Prosidion Ltd | Pyrrolopyridin-2-karbonsäureamide |
US7875627B2 (en) | 2004-12-07 | 2011-01-25 | Abbott Laboratories | Thienopyridyl compounds that inhibit vanilloid receptor subtype 1 (VR1) and uses thereof |
WO2006071775A2 (fr) | 2004-12-29 | 2006-07-06 | Elan Pharmaceuticals, Inc. | Composes utiles pour l'antagonisme du recepteur b1 de la bradykinine |
WO2006079077A2 (fr) | 2005-01-20 | 2006-07-27 | Acadia Pharmaceuticals Inc. | Composes en tant que modulateurs de recepteur de ghreline et leurs utilisations |
US20060281763A1 (en) | 2005-03-25 | 2006-12-14 | Axon Jonathan R | Carboxamide inhibitors of TGFbeta |
BRPI0607918A2 (pt) | 2005-04-01 | 2009-10-20 | Warner Lambert Co | tetraidro-piridoazepin-8-onas e compostos relacionados para o tratemento da esquizofrenia. |
EP1874753A2 (fr) | 2005-04-14 | 2008-01-09 | Smithkline Beecham Corporation | Composes, compositions et procedes |
JO2787B1 (en) | 2005-04-27 | 2014-03-15 | امجين إنك, | Alternative amide derivatives and methods of use |
CA2623541A1 (fr) | 2005-09-23 | 2007-03-29 | Coley Pharmaceutical Group, Inc. | Procede de preparation de 1h-imidazo[4,5-c]pyridines et d'analogues de ceux-ci |
JP2009518399A (ja) | 2005-12-05 | 2009-05-07 | アフィニウム ファーマシューティカルズ, インク. | Fabi阻害剤および抗菌剤としてのヘテロ環アクリルアミド化合物 |
GB0605689D0 (en) | 2006-03-21 | 2006-05-03 | Novartis Ag | Organic compounds |
WO2007126871A1 (fr) | 2006-03-29 | 2007-11-08 | Array Biopharma Inc. | Inhibiteurs de p38 et leurs méthodes d'utilisation |
AU2007258675A1 (en) | 2006-06-09 | 2007-12-21 | Merck Sharp & Dohme Corp. | Benzazepinones as sodium channel blockers |
WO2008009122A1 (fr) | 2006-07-20 | 2008-01-24 | Affinium Pharmaceuticals, Inc. | Dérivés d'acrylamide en tant qu'inhibiteurs de fab i |
ATE469895T1 (de) | 2006-07-21 | 2010-06-15 | Vertex Pharma | Cgrp-rezeptorantagonisten |
JP5616063B2 (ja) | 2006-10-04 | 2014-10-29 | ヤンセン・アールアンドデイ・アイルランド | Hcv阻害剤として有用なカルボキシアミド4−[(4−ピリジル)アミノ]ピリミジン |
ES2430821T3 (es) * | 2006-10-10 | 2013-11-21 | Amgen Inc. | Compuestos de N-arilpirazol para usar contra la diabetes |
EP1939187A1 (fr) | 2006-12-20 | 2008-07-02 | Sanofi-Aventis | Dérivés de pyridopyrimidone hétéroaryle substitués |
EP2099770B1 (fr) | 2006-12-21 | 2015-06-10 | Sloan-Kettering Institute for Cancer Research | Pyridazinones et composés furanniques |
AU2008219723A1 (en) | 2007-02-28 | 2008-09-04 | Merck Sharp & Dohme Corp. | Substituted benzodiazepinones, benzoxazepinones and benzothiazepinones as sodium channel blockers |
WO2008135525A2 (fr) | 2007-05-02 | 2008-11-13 | Boehringer Ingelheim International Gmbh | Azétidines substituées, leur préparation et leur utilisation sous forme de médicaments |
US8242150B2 (en) | 2007-06-13 | 2012-08-14 | Merck Sharp & Dohme Corp. | Triazole derivatives for treating alzheimer'S disease and related conditions |
EP2185721B1 (fr) | 2007-08-03 | 2014-04-02 | Sanofi | Sondes d'imagerie de caspase |
WO2009085256A1 (fr) | 2007-12-27 | 2009-07-09 | Panacos Pharmaceuticals, Inc. | Composés anti-vih |
EP2085399A1 (fr) | 2008-01-29 | 2009-08-05 | Sanofi-Aventis | Dérivés d'arylamide oxazépinopyrimidone substitués |
EP2090578A1 (fr) * | 2008-01-29 | 2009-08-19 | Sanofi-Aventis | Dérivés d'arylamide diazépinopyrimidone substitués pour le traitement des maladies neurodégénératives causées par une activité anormale de GSK3-beta |
JP4708443B2 (ja) | 2008-01-31 | 2011-06-22 | トヨタ自動車株式会社 | 作動制御マップおよび白線認識装置 |
WO2009105348A1 (fr) * | 2008-02-19 | 2009-08-27 | Merck & Co., Inc. | Antagonistes de récepteurs de cgrp de type imidazobenzazépine |
EP2262783A2 (fr) | 2008-02-21 | 2010-12-22 | Sanofi-Aventis | Sondes d'imagerie à liaison covalente |
CA2723617A1 (fr) | 2008-05-14 | 2009-11-19 | Amgen Inc. | Combinaisons d'inhibiteurs de vegf(r) et d'inhibiteurs du facteur de croissance d'hepatocyte (c-met) pour le traitement du cancer |
US7884074B2 (en) | 2008-05-15 | 2011-02-08 | Ikaria Development Subsidiary Two, LLC | Compounds and methods for prevention and/or treatment of inflammation using the same |
WO2010013794A1 (fr) | 2008-07-28 | 2010-02-04 | Eisai R&D Management Co., Ltd. | Dérivés de spiroaminodihydrothiazine |
DE102008037790A1 (de) | 2008-08-14 | 2010-02-18 | Merck Patent Gmbh | Bicyclische Triazolderivate |
UY32049A (es) | 2008-08-14 | 2010-03-26 | Takeda Pharmaceutical | Inhibidores de cmet |
US8088890B2 (en) | 2008-09-26 | 2012-01-03 | Fibrex Medical Research & Development Gmbh | Peptides and peptidomimetic compounds, the manufacturing thereof as well as their use for preparing a therapeutically and/or preventively active pharmaceutical composition |
WO2010045095A1 (fr) | 2008-10-14 | 2010-04-22 | Ning Xi | Composés et procédés d'utilisation |
AU2009333427A1 (en) | 2008-12-17 | 2011-07-28 | Merck Sharp & Dohme Corp. | Imidazolinone derivatives as CGRP receptor antagonists |
CN102548999A (zh) | 2009-01-20 | 2012-07-04 | 山东轩竹医药科技有限公司 | 含有取代的含氮稠杂环的头孢菌素衍生物 |
US8624063B2 (en) | 2009-06-30 | 2014-01-07 | Wisconsin Alumni Research Foundation | Non-lactone carbocyclic and heterocyclic antagonists and agonists of bacterial quorum sensing |
EP2477493A1 (fr) | 2009-09-16 | 2012-07-25 | Cylene Pharmaceuticals, Inc. | Modulateurs tricycliques inédits des protéines kinases |
EP2493888B1 (fr) | 2009-10-29 | 2016-04-06 | GlaxoSmithKline LLC | Pyridines bicycliques et analogues en tant que modulateurs de la sirtuine |
US8481541B2 (en) | 2010-03-22 | 2013-07-09 | Hoffmann-La Roche Inc. | Pyrrolopyrazine kinase inhibitors |
AU2011242465B2 (en) | 2010-04-23 | 2017-01-19 | Massachusetts Eye And Ear Infirmary | Methods and compositions for preserving photoreceptor and retinal pigment epithelial cells |
AU2011251302A1 (en) | 2010-05-11 | 2013-01-10 | 8337187 Canada, Inc. | Benzo- or pyrido-imidazole derivative |
EA201291327A1 (ru) | 2010-05-24 | 2013-05-30 | Вандербилт Юниверсити | Замещенные 6-метилникотинамиды как позитивные аллостерические модуляторы mglur5 |
US9029501B2 (en) | 2010-11-02 | 2015-05-12 | Rigel Pharmaceuticals, Inc. | Method for making macrocycles |
US9938269B2 (en) | 2011-06-30 | 2018-04-10 | Abbvie Inc. | Inhibitor compounds of phosphodiesterase type 10A |
TW201837023A (zh) | 2011-07-01 | 2018-10-16 | 美商基利科學股份有限公司 | 作為離子通道調節劑之稠合雜環化合物 |
CA2842190A1 (fr) | 2011-07-19 | 2013-01-24 | Infinity Pharmaceuticals Inc. | Composes heterocycliques et leurs utilisations |
WO2013013826A1 (fr) | 2011-07-27 | 2013-01-31 | Friedrich-Alexander-Universität Erlangen-Nürnberg | Inhibiteurs de la nécroptose pour le traitement de maladies inflammatoires du tractus gastro-intestinal |
AR087107A1 (es) | 2011-07-27 | 2014-02-12 | Lilly Co Eli | Compuesto inhibidor de la señalizacion de la trayectoria notch |
EP2773341A2 (fr) | 2011-10-21 | 2014-09-10 | Massachusetts Eye & Ear Infirmary | Compositions comprenant des inhibiteurs de la necrose, tels que des necrostatines, seuls ou en combinaison, pour la promotion de la régénération axonale et de la fonction nerveuse, ainsi pour traiter les maladies du snc |
US9062075B2 (en) | 2011-12-02 | 2015-06-23 | Aurigene Discovery Technologies Limited | Tetrahydropyridine derivatives as FabI inhibitors |
EP2785715A1 (fr) | 2011-12-02 | 2014-10-08 | Aurigene Discovery Technologies Limited | Dérivés de pyridine substitués en tant qu'inhibiteurs de fabi |
JP2015518504A (ja) | 2012-04-03 | 2015-07-02 | スリーエム イノベイティブ プロパティズ カンパニー | 光塩基発生剤を含む架橋性組成物 |
CN103958526B (zh) | 2012-06-20 | 2015-09-09 | 上海恒瑞医药有限公司 | 嘧啶二胺类衍生物、其制备方法及其在医药上的应用 |
TWI520962B (zh) | 2012-06-29 | 2016-02-11 | As the c-Met tyrosine kinase inhibitors novel fused pyridine derivatives | |
US9611224B2 (en) | 2012-07-13 | 2017-04-04 | Hoffmann-La Roche Inc. | Antiproliferative benzo [B] azepin-2-ones |
CA2877048A1 (fr) | 2012-08-09 | 2014-02-13 | F. Hoffmann-La Roche Ag | Hetero-azepinones substituees |
CN103664904A (zh) | 2012-09-07 | 2014-03-26 | 李振 | 一种γ-分泌酶抑制剂及其用途 |
WO2014072930A2 (fr) | 2012-11-09 | 2014-05-15 | Aurigene Discovery Technologies Limited | Dérivés pyridine fondus, en tant qu'agents antibactériens |
TWI648274B (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 (二) |
WO2014144547A2 (fr) | 2013-03-15 | 2014-09-18 | The Regents Of The University Of California | Dérivés d'amide d'inhibiteurs de l'amidase acide de n-acyléthanolamine à base de lactame |
FR3003860B1 (fr) | 2013-03-29 | 2015-11-27 | Oreal | Composes derives d'iridoides proteges ou non, composition les comprenant, utilisation comme colorant des fibres keratiniques et dispositifs |
WO2014170892A1 (fr) | 2013-04-15 | 2014-10-23 | Yeda Research And Development Co. Ltd. | Inhibition de rip kinases pour triater des maladies lysosomales |
WO2015027137A1 (fr) | 2013-08-23 | 2015-02-26 | University Of Tennessee Research Foundation | Synthèse perfectionnée de capuramycine et de ses analogues |
US20160326157A1 (en) | 2014-01-06 | 2016-11-10 | President And Fellows Of Harvard College | Monobactams and methods of their synthesis and use |
WO2015104677A1 (fr) | 2014-01-10 | 2015-07-16 | Piramal Enterprises Limited | Composés hétérocycliques en tant qu'inhibiteurs de ezh2 |
EP3148543B1 (fr) | 2014-05-30 | 2020-04-08 | Icahn School of Medicine at Mount Sinai | Petites molécules en tant que modulateurs de la transcription de bromodomaines |
US9616047B2 (en) | 2014-06-30 | 2017-04-11 | Regents Of University Of Minnesota | Inhibitors of beta-catenin in treatment of colorectal cancer |
US20170226514A1 (en) | 2014-08-13 | 2017-08-10 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Prevention of tumour metastasis by inhibition of necroptosis |
BR112017003546A2 (pt) | 2014-08-21 | 2017-12-05 | Glaxosmithkline Ip Dev Ltd | amidas heterocíclicas como inibidores de rip1 quinase como medicamentos |
JP6820254B2 (ja) | 2014-10-10 | 2021-01-27 | ジェネンテック, インコーポレイテッド | 治療用化合物およびその使用 |
EP3017825A1 (fr) | 2014-11-06 | 2016-05-11 | Ludwig-Maximilians-Universität München | Inhibiteur de la voie de nécrose à dépendance RIPK1 et composition pharmaceutique le contenant |
KR102596723B1 (ko) | 2014-12-24 | 2023-11-01 | 내셔널 인스티튜트 오브 바이올로지칼 사이언시스, 베이징 | 괴사 억제제 |
AU2015371822B2 (en) | 2014-12-24 | 2020-04-09 | National Institute Of Biological Sciences, Beijing | Necrosis inhibitors |
PT3245198T (pt) | 2015-01-13 | 2020-06-16 | Novartis Ag | Derivados de pirrolidina como antagonistas de angiotensina ii tipo 2 |
CA2976172A1 (fr) | 2015-02-13 | 2016-08-18 | Glaxosmithkline Intellectual Property Development Limited | Formes cristallines de (s)-5-benzyl-n-(5-methyl-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepine-3-yl)-4h-1,2,4-triazole-3-carboxamide |
TWI609687B (zh) | 2015-04-14 | 2018-01-01 | 美國禮來大藥廠 | 平滑肌肉瘤之標靶性治療 |
AU2016287581B2 (en) * | 2015-07-02 | 2019-06-06 | F. Hoffmann-La Roche Ag | Bicyclic lactams and methods of use thereof |
WO2017022962A1 (fr) | 2015-07-07 | 2017-02-09 | 가톨릭대학교 산학협력단 | Composition pour la prévention ou le traitement d'une maladie immunitaire, comprenant un inhibiteur de la rip kinase en tant que principe actif |
CA3002542C (fr) | 2015-10-23 | 2023-11-28 | Takeda Pharmaceutical Company Limited | Derives heterocycliques d'azepine substitues et compositions utiles comme inhibiteur de rip1 kinase |
US10961258B2 (en) | 2015-12-21 | 2021-03-30 | Glaxosmithkline Intellectual Property Development Limited | Heterocyclic amides as kinase inhibitors |
SG10201913587WA (en) * | 2016-02-05 | 2020-02-27 | Denali Therapeutics Inc | Inhibitors of receptor-interacting protein kinase 1 |
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