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MA52488B1 - Composés inhibiteurs de rip1 et leurs procédés de fabrication et d'utilisation - Google Patents

Composés inhibiteurs de rip1 et leurs procédés de fabrication et d'utilisation

Info

Publication number
MA52488B1
MA52488B1 MA52488A MA52488A MA52488B1 MA 52488 B1 MA52488 B1 MA 52488B1 MA 52488 A MA52488 A MA 52488A MA 52488 A MA52488 A MA 52488A MA 52488 B1 MA52488 B1 MA 52488B1
Authority
MA
Morocco
Prior art keywords
rip1
making
methods
inhibitory compounds
compounds
Prior art date
Application number
MA52488A
Other languages
English (en)
Other versions
MA52488A (fr
Inventor
Somasekhar Bhamidipati
Esteban Masuda
Simon Shaw
Vanessa Taylor
Original Assignee
Rigel Pharmaceuticals Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Rigel Pharmaceuticals Inc filed Critical Rigel Pharmaceuticals Inc
Publication of MA52488A publication Critical patent/MA52488A/fr
Publication of MA52488B1 publication Critical patent/MA52488B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D267/02—Seven-membered rings
    • C07D267/08—Seven-membered rings having the hetero atoms in positions 1 and 4
    • C07D267/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D267/14—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/06—Antipsoriatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0803—Compounds with Si-C or Si-Si linkages
    • C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

L'invention concerne des composés inhibiteurs de kinase, tels qu'un composé inhibiteur de la protéine-1 interagissant avec le récepteur (rip1), ainsi que des compositions pharmaceutiques et des combinaisons comprenant de tels composés inhibiteurs. Les composés décrits, les compositions pharmaceutiques et/ou les combinaisons peuvent être utilisés pour traiter ou prévenir une maladie ou un état associé à une kinase, en particulier une maladie ou un état associé à rip1.
MA52488A 2018-05-03 2019-05-02 Composés inhibiteurs de rip1 et leurs procédés de fabrication et d'utilisation MA52488B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201862666462P 2018-05-03 2018-05-03
PCT/US2019/030476 WO2019213447A1 (fr) 2018-05-03 2019-05-02 Composés inhibiteurs de rip1 et leurs procédés de fabrication et d'utilisation

Publications (2)

Publication Number Publication Date
MA52488A MA52488A (fr) 2021-03-10
MA52488B1 true MA52488B1 (fr) 2023-11-30

Family

ID=66530556

Family Applications (1)

Application Number Title Priority Date Filing Date
MA52488A MA52488B1 (fr) 2018-05-03 2019-05-02 Composés inhibiteurs de rip1 et leurs procédés de fabrication et d'utilisation

Country Status (38)

Country Link
US (8) US10815206B2 (fr)
EP (2) EP3788044B1 (fr)
JP (4) JP2021523226A (fr)
KR (1) KR102808215B1 (fr)
CN (4) CN120535514A (fr)
AU (2) AU2019262144B2 (fr)
BR (1) BR112020022420A2 (fr)
CA (1) CA3099037A1 (fr)
CL (1) CL2020002841A1 (fr)
CO (1) CO2020015156A2 (fr)
CR (1) CR20200581A (fr)
DK (1) DK3788044T3 (fr)
DO (2) DOP2020000198A (fr)
EA (1) EA202092580A1 (fr)
EC (1) ECSP20078326A (fr)
ES (1) ES2956087T3 (fr)
FI (1) FI3788044T3 (fr)
HR (1) HRP20231381T1 (fr)
HU (1) HUE063896T2 (fr)
IL (2) IL299784B2 (fr)
JO (1) JOP20200278A1 (fr)
LT (1) LT3788044T (fr)
MA (1) MA52488B1 (fr)
MD (1) MD3788044T2 (fr)
MX (1) MX2020011621A (fr)
MY (1) MY208132A (fr)
PE (1) PE20211383A1 (fr)
PH (1) PH12020551847A1 (fr)
PL (1) PL3788044T3 (fr)
PT (1) PT3788044T (fr)
RS (1) RS64736B1 (fr)
SA (1) SA520420468B1 (fr)
SG (1) SG11202010915XA (fr)
SI (1) SI3788044T1 (fr)
SM (1) SMT202300313T1 (fr)
UA (1) UA128369C2 (fr)
WO (1) WO2019213447A1 (fr)
ZA (2) ZA202007486B (fr)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112020022423A2 (pt) 2018-05-03 2021-02-02 Rigel Pharmaceuticals, Inc. composto, composição farmacêutica, método, método para tratar uma doença em um indivíduo e método para fabricar o composto
KR102808215B1 (ko) * 2018-05-03 2025-05-19 리겔 파마슈티칼스, 인크. Rip1 억제 화합물 및 이를 제조하고 사용하는 방법
JP7045526B2 (ja) * 2018-11-02 2022-03-31 中国科学院上海薬物研究所 Ｒｉｐ１キナーゼを阻害する複素環状アミド及びその使用
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
US12365695B2 (en) * 2019-08-09 2025-07-22 Bisichem Co., Ltd. Fused ring heteroaryl compounds as RIPK1 inhibitors
JOP20220056A1 (ar) * 2019-09-06 2023-01-30 Rigel Pharmaceuticals Inc مركبات rip1 تثبيطية وطرق عملها واستخدامها
PH12022550536A1 (en) 2019-09-06 2023-07-31 Rigel Pharmaceuticals Inc Rip1 inhibitory compounds and methods for making and using the same.
WO2021046515A1 (fr) 2019-09-06 2021-03-11 Board Of Regents, The University Of Texas System Inhibiteurs de la protéine kinase i interagissant avec le récepteur pour le traitement d'une maladie
IL291665B2 (en) 2019-09-27 2025-07-01 Univ Texas Inhibitors of receptor interacting protein kinase i for the treatment of disease
WO2021080757A1 (fr) 2019-10-21 2021-04-29 Google Llc Consentement vérifiable permettant la protection de la vie privée
LT4055021T (lt) 2019-11-07 2026-01-12 Rigel Pharmaceuticals, Inc. Heterocikliniai junginiai, slopinantys 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
EP4110765A4 (fr) * 2020-02-28 2024-03-06 Board of Regents, The University of Texas System Inhibiteurs de la protéine kinase i interagissant avec le récepteur pour le traitement d'une maladie
AR121717A1 (es) * 2020-04-02 2022-06-29 Rigel Pharmaceuticals Inc Inhibidores de rip1k
AR122703A1 (es) 2020-07-01 2022-09-28 Rigel Pharmaceuticals Inc Inhibidores de rip1k
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
AR125587A1 (es) 2021-03-11 2023-08-02 Rigel Pharmaceuticals Inc Inhibidores heterocíclicos de la quinasa de rip1
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
MX2023014817A (es) 2021-08-10 2024-01-12 Abbvie Inc Inhibidores de ripk1 de nicotinamida.
WO2023114061A1 (fr) 2021-12-16 2023-06-22 Rigel Pharmaceuticals, Inc. Formes cristallines d'un inhibiteur de ripk1
WO2023138317A1 (fr) * 2022-01-21 2023-07-27 中国科学院上海药物研究所 Composé ayant une activité inhibitrice de ripk1, son procédé de préparation et son utilisation
US20250197390A1 (en) * 2022-03-16 2025-06-19 Jiangsu Hengrui Pharmaceuticals Co., Ltd. Fused heterocyclic compound, and preparation method therefor and medical use thereof
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
CN115353513A (zh) * 2022-07-29 2022-11-18 中国人民解放军海军军医大学 一种抑制程序性细胞坏死的硫代七元环衍生物及其应用
WO2025006250A1 (fr) 2023-06-26 2025-01-02 Eli Lilly And Company Schémas posologiques pour le traitement de maladies auto-immunes et inflammatoires à l'aide de ly3871801

Family Cites Families (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5087240A (en) 1983-08-18 1992-02-11 Drug Delivery Systems Inc. Transdermal drug patch with conductive fibers
US4921475A (en) 1983-08-18 1990-05-01 Drug Delivery Systems Inc. Transdermal drug patch with microtubes
US4738851A (en) 1985-09-27 1988-04-19 University Of Iowa Research Foundation, Inc. Controlled release ophthalmic gel formulation
US5163899A (en) 1987-03-20 1992-11-17 Drug Delivery Systems Inc. Transdermal drug delivery system
US5312325A (en) 1987-05-28 1994-05-17 Drug Delivery Systems Inc Pulsating transdermal drug delivery system
GB8804164D0 (en) 1988-02-23 1988-03-23 Tucker J M Bandage for administering physiologically active compound
US4882150A (en) 1988-06-03 1989-11-21 Kaufman Herbert E Drug delivery system
US5008110A (en) 1988-11-10 1991-04-16 The Procter & Gamble Company Storage-stable transdermal patch
US5088977A (en) 1988-12-21 1992-02-18 Drug Delivery Systems Inc. Electrical transdermal drug applicator with counteractor and method of drug delivery
US5521222A (en) 1989-09-28 1996-05-28 Alcon Laboratories, Inc. Topical ophthalmic pharmaceutical vehicles
ES2055280T3 (es) 1989-12-04 1994-08-16 Searle & Co Sistema monocapa para la administracion transdermica de farmacos.
US5077033A (en) 1990-08-07 1991-12-31 Mediventures Inc. Ophthalmic drug delivery with thermo-irreversible gels of polxoxyalkylene polymer and ionic polysaccharide
EP0495421B1 (fr) 1991-01-15 1996-08-21 Alcon Laboratories, Inc. Utilisation de carragheenane dans des compositions ophthalmologiques topiques
US5352456A (en) 1991-10-10 1994-10-04 Cygnus Therapeutic Systems Device for administering drug transdermally which provides an initial pulse of drug
EP0617665B1 (fr) 1991-12-18 1999-03-31 Minnesota Mining And Manufacturing Company Structures d'arret stratifiees
EP0553769B1 (fr) 1992-01-29 1996-01-03 FRANZ VÖLKL GmbH & CO. SKI UND TENNIS SPORTARTIKELFABRIK KG Raquette, en particulier raquette de tennis
IL114193A (en) 1994-06-20 2000-02-29 Teva Pharma Ophthalmic pharmaceutical compositions based on sodium alginate
ES2094688B1 (es) 1994-08-08 1997-08-01 Cusi Lab Manoemulsion del tipo de aceite en agua, util como vehiculo oftalmico y procedimiento para su preparacion.
IT1283911B1 (it) 1996-02-05 1998-05-07 Farmigea Spa Soluzioni oftalmiche viscosizzate con polisaccaridi della gomma di tamarindo
US5800807A (en) 1997-01-29 1998-09-01 Bausch & Lomb Incorporated Ophthalmic compositions including glycerin and propylene glycol
US6261547B1 (en) 1998-04-07 2001-07-17 Alcon Manufacturing, Ltd. Gelling ophthalmic compositions containing xanthan gum
US6197934B1 (en) 1998-05-22 2001-03-06 Collagenesis, Inc. Compound delivery using rapidly dissolving collagen film
WO2009023272A1 (fr) 2007-08-15 2009-02-19 President And Fellows Of Harvard College Inhibiteurs hétérocycliques de la nécroptose
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）
EP2968276A4 (fr) 2013-03-15 2017-02-15 President and Fellows of Harvard College Inhibiteurs hybrides de la nécroptose
WO2016027253A1 (fr) * 2014-08-21 2016-02-25 Glaxosmithkline Intellectual Property Development Limited Amides hétérocycliques utilisés comme inhibiteurs de la rip1 kinase en tant que médicaments
JP2018505199A (ja) 2015-02-13 2018-02-22 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 （Ｓ）−５−ベンジル−Ｎ−（５−メチル−４−オキソ−２，３，４，５テトラヒドロベンゾ［ｂ］［１，４］オキサゼピン−３−イル）−４Ｈ−１，２，４−トリアゾール−３−カルボキサミドの結晶形
RU2716136C2 (ru) 2015-07-02 2020-03-06 Ф. Хоффманн-Ля Рош Аг Бициклические лактамы и способы их применения
DK3362449T3 (da) 2015-10-13 2021-07-19 Inst Nat Sante Rech Med Sibirilin-derivater til anvendelse til at forebygge og/eller behandle lidelser associeret med cellulær nekroptose
AU2016340527B2 (en) 2015-10-23 2020-09-17 Takeda Pharmaceutical Company Limited Heterocyclic compound
WO2017109724A1 (fr) 2015-12-21 2017-06-29 Glaxosmithkline Intellectual Property Development Limited Amides hétérocycliques utilisés en tant qu'inhibiteurs de kinase
JP6974331B2 (ja) 2016-02-05 2021-12-01 デナリ セラピューティクス インコーポレイテッドDenali Therapeutics Inc. 化合物、組成物及び方法
WO2018073193A1 (fr) 2016-10-17 2018-04-26 F. Hoffmann-La Roche Ag Lactames de pyridone bicycliques et leurs méthodes d'utilisation
US11072607B2 (en) 2016-12-16 2021-07-27 Genentech, Inc. Inhibitors of RIP1 kinase and methods of use thereof
CA3052767A1 (fr) 2017-02-27 2018-08-30 Glaxosmithkline Intellectual Property Development Limited Amides heterocycliques en tant qu'inhibiteurs de kinase
BR112020022423A2 (pt) * 2018-05-03 2021-02-02 Rigel Pharmaceuticals, Inc. composto, composição farmacêutica, método, método para tratar uma doença em um indivíduo e método para fabricar o composto
KR102808215B1 (ko) * 2018-05-03 2025-05-19 리겔 파마슈티칼스, 인크. Rip1 억제 화합물 및 이를 제조하고 사용하는 방법
CA3104757A1 (fr) 2018-06-26 2020-01-02 Shanghai Institute Of Organic Chemistry, Chinese Academy Of Sciences Inhibiteur de necrose cellulaire, son procede de preparation et son utilisation
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
JP7045526B2 (ja) 2018-11-02 2022-03-31 中国科学院上海薬物研究所 Ｒｉｐ１キナーゼを阻害する複素環状アミド及びその使用
PH12022550536A1 (en) 2019-09-06 2023-07-31 Rigel Pharmaceuticals Inc Rip1 inhibitory compounds and methods for making and using the same.
AR121717A1 (es) 2020-04-02 2022-06-29 Rigel Pharmaceuticals Inc Inhibidores de rip1k

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Publication number Publication date
PH12020551847A1 (en) 2021-06-28
AU2019262144B2 (en) 2023-11-16
IL299784A (en) 2023-03-01
MX2020011621A (es) 2021-02-22
JOP20200278A1 (ar) 2020-11-03
KR20210005222A (ko) 2021-01-13
US20250034100A1 (en) 2025-01-30
EP3788044B1 (fr) 2023-08-09
CN120535513A (zh) 2025-08-26
US20210040053A1 (en) 2021-02-11
UA128369C2 (uk) 2024-06-26
HUE063896T2 (hu) 2024-02-28
CN112368278A (zh) 2021-02-12
SI3788044T1 (sl) 2023-12-29
US11370764B2 (en) 2022-06-28
ECSP20078326A (es) 2021-03-31
ES2956087T3 (es) 2023-12-13
EP4248975A3 (fr) 2024-03-13
EA202092580A1 (ru) 2021-04-07
US20230113841A1 (en) 2023-04-13
US20210002236A1 (en) 2021-01-07
AU2019262144A1 (en) 2020-11-26
US11472782B2 (en) 2022-10-18
FI3788044T3 (fi) 2023-09-25
US20200407332A1 (en) 2020-12-31
BR112020022420A2 (pt) 2021-03-02
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