AR125587A1 - Inhibidores heterocíclicos de la quinasa de rip1 - Google Patents
Inhibidores heterocíclicos de la quinasa de rip1Info
- Publication number
- AR125587A1 AR125587A1 ARP220100461A ARP220100461A AR125587A1 AR 125587 A1 AR125587 A1 AR 125587A1 AR P220100461 A ARP220100461 A AR P220100461A AR P220100461 A ARP220100461 A AR P220100461A AR 125587 A1 AR125587 A1 AR 125587A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- independently
- occurrence
- heteroaryl
- heterocyclic
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 3
- 101001109145 Homo sapiens Receptor-interacting serine/threonine-protein kinase 1 Proteins 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 8
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 102100022501 Receptor-interacting serine/threonine-protein kinase 1 Human genes 0.000 abstract 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 4
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 239000008194 pharmaceutical composition Substances 0.000 abstract 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000000172 C5-C10 aryl group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 101710138589 Receptor-interacting serine/threonine-protein kinase 1 Proteins 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- -1 alkyl phosphate Chemical compound 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 229940043355 kinase inhibitor Drugs 0.000 abstract 1
- 125000005647 linker group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- 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
- A61P19/00—Drugs for skeletal disorders
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Dermatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Diabetes (AREA)
- Endocrinology (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
En la presente descripción se describen compuestos inhibidores de quinasa, tales como los compuestos inhibidores de la proteína 1 quinasa que interactúa con el receptor (RIP1), así como también composiciones farmacéuticas y combinaciones que comprenden tales compuestos inhibidores. Los compuestos, composiciones farmacéuticas y/o combinaciones descritas pueden usarse para tratar o prevenir una enfermedad o afección asociada a quinasas, particularmente una enfermedad o afección asociada a RIP1. Reivindicación 1: Un compuesto, de acuerdo con la fórmula (1), o una sal, N-óxido, solvato, tautómero o estereoisómero farmacéuticamente aceptable de estos, en donde: el anillo B es heteroarilo; cada R¹ es independientemente un halógeno o un grupo enlazador-R⁶, en donde el enlazador es una unión o Rᵃ, siempre que Rᵃ no sea H o D, y R⁶ sea heterociclilo, Rᵇ, -C(Rᶠ)₃, o -C(Rᶠ)=C(Rᶠ)₂; R² es Rᵃ; R³ es Rᵃ; si está presente, cada R⁴ es independientemente Rᵉ; L es un heteroátomo o Rᵃ, siempre que Rᵃ no sea H o D; X es CH₂ u O; Z es heteroarilo; m es 1, 2, 3 o 4; n es 0, 1, o 2; Rᵃ es independientemente para cada ocurrencia H o D, excepto para las modalidades donde L es Rᵃ, alifático C₁₋₁₀, haloalifático C₁₋₁₀, aromático C₅₋₁₀, heterocíclico C₃₋₆ o espiroheterocíclico C₃₋₁₀; Rᵇ es independiente para cada ocurrencia -OH, -SH, -ORᶜ, - SRᶜ, -NRᵈRᵈ, -Si(Rᵃ)₃, -C(O)OH, -C(O)ORᶜ, -C(O)NRᵈRᵈ, -OC(O)NRᵈRᵈ, -OC(O)alquilo C₁₋₁₀ sustituido con uno o dos NRᵈRᵈ, carboxilo, o una combinación de estos, y opcionalmente sustituido adicionalmente con una porción aromática, -SH, acilo -O o -C(O)NH₂; Rᶜ es independientemente para cada ocurrencia alquilo C₁₋₁₀, que se puede sustituir con 1, 2 o 3 Rᵉ, alquenilo C₂₋₁₀, que se puede sustituir con 1, 2 o 3 Rᵉ, alquinilo C₂₋₁₀, que se puede sustituir con 1, 2 o 3 Rᵉ, cicloalquilo C₃₋₆, que se puede sustituir con 1, 2 o 3 Rᵉ, o aromático C₅₋₁₀, que se puede sustituir con 1, 2 o 3 Rᵉ; Rᵈ es independientemente para cada ocurrencia H; alquilo C₁₋₆, que se puede sustituir con 1, 2 o 3 Rᵉ o un heterociclilo C₃₋₉; cicloalquilo C₃₋₆, que se puede sustituir con 1, 2 o 3 Rᵉ; heterocíclico C₃₋₆, que se puede sustituir con 1, 2 o 3 Rᵉ; arilo C₅₋₁₀, que se puede sustituir con 1, 2 o 3 Rᵇ; heteroarilo C₅₋₁₀, que se puede sustituir con 1, 2 o 3 Rᵉ; o dos grupos Rᵈ junto con el nitrógeno unido a ellos proporcionan un heterocíclico C₃₋₉, que se puede sustituir con uno o más Rᵉ), o un heteroarilo C₅₋₁₀, que se puede sustituir con uno o más Rᵉ; Rᵉ es independientemente para cada ocurrencia halógeno, alquilo C₁₋₆, alquenilo C₂₋₁₀, alquinilo C₂₋₁₀, haloalquilo C₁₋₆, cicloalquilo C₃₋₆, heteroarilo C₅₋₁₀ u -ORᵃ; y Rᶠ es independientemente para cada ocurrencia: fosfato de alquilo, Rᵃ, Rᵇ o Rᵉ, o dos grupos Rᶠ junto con el átomo de carbono unido a ellos proporcionan un grupo alquenilo C₂₋₆, un grupo cicloalquilo C₃₋₆, que se puede sustituir con uno o más Rᵉ, o un heterocíclico C₃₋₁₀, que se puede sustituir con uno o más Rᵉ o acilo. Reivindicación 37: Una composición farmacéutica, que comprende un compuesto de acuerdo con la reivindicación 1. Reivindicación 39: Un método, que comprende administrar a un sujeto un compuesto de acuerdo con la reivindicación 1 o una composición de este. Reivindicación 40: Un método, que comprende poner en contacto una proteína 1 quinasa que interactúa con el receptor (RIP1) con un compuesto de acuerdo con la reivindicación 1 o una composición de este.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US202163159970P | 2021-03-11 | 2021-03-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR125587A1 true AR125587A1 (es) | 2023-08-02 |
Family
ID=81327717
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP220100461A AR125587A1 (es) | 2021-03-11 | 2022-03-02 | Inhibidores heterocíclicos de la quinasa de rip1 |
Country Status (19)
Country | Link |
---|---|
US (1) | US12156880B2 (es) |
EP (1) | EP4304713A1 (es) |
JP (1) | JP2024509466A (es) |
KR (1) | KR20230144575A (es) |
CN (1) | CN117083270A (es) |
AR (1) | AR125587A1 (es) |
AU (1) | AU2022232927B2 (es) |
BR (1) | BR112023018167A2 (es) |
CA (1) | CA3211778A1 (es) |
CL (1) | CL2023002704A1 (es) |
CO (1) | CO2023012077A2 (es) |
CR (1) | CR20230438A (es) |
DO (1) | DOP2023000186A (es) |
EC (1) | ECSP23068893A (es) |
IL (1) | IL305456A (es) |
MX (1) | MX2023010624A (es) |
PE (1) | PE20240237A1 (es) |
TW (1) | TW202300490A (es) |
WO (1) | WO2022192533A1 (es) |
Family Cites Families (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4921475A (en) | 1983-08-18 | 1990-05-01 | Drug Delivery Systems Inc. | Transdermal drug patch with microtubes |
US5087240A (en) | 1983-08-18 | 1992-02-11 | Drug Delivery Systems Inc. | Transdermal drug patch with conductive fibers |
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 |
CA2031376A1 (en) | 1989-12-04 | 1991-06-05 | Bahram Farhadieh | Single layer transdermal drug administration system |
US5268164A (en) | 1990-04-23 | 1993-12-07 | Alkermes, Inc. | Increasing blood-brain barrier permeability with permeabilizer peptides |
US5112596A (en) | 1990-04-23 | 1992-05-12 | Alkermes, Inc. | Method for increasing blood-brain barrier permeability by administering a bradykinin agonist of blood-brain barrier permeability |
US5077033A (en) | 1990-08-07 | 1991-12-31 | Mediventures Inc. | Ophthalmic drug delivery with thermo-irreversible gels of polxoxyalkylene polymer and ionic polysaccharide |
EP0495421B1 (en) | 1991-01-15 | 1996-08-21 | Alcon Laboratories, Inc. | Use of carrageenans in topical ophthalmic compositions |
US5352456A (en) | 1991-10-10 | 1994-10-04 | Cygnus Therapeutic Systems | Device for administering drug transdermally which provides an initial pulse of drug |
DE69228827T2 (de) | 1991-12-18 | 1999-10-21 | Minnesota Mining And Mfg. Co., Saint Paul | Mehrschichtige sperrstrukturen |
EP0553769B1 (de) | 1992-01-29 | 1996-01-03 | FRANZ VÖLKL GmbH & CO. SKI UND TENNIS SPORTARTIKELFABRIK KG | Ballspielschläger, insbesondere Tennisschläger |
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 |
EP2192838A4 (en) | 2007-08-15 | 2011-07-27 | Harvard College | HETEROCYCLIC NEKROPTOSIS HEMMER |
US8922322B2 (en) * | 2012-08-31 | 2014-12-30 | Delta Electronics, Inc. | Combined structure of hollow bobbin and conductive sheet, hollow bobbin, and conductive sheet |
TWI638815B (zh) * | 2013-02-15 | 2018-10-21 | 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(一) |
US20160024098A1 (en) | 2013-03-15 | 2016-01-28 | President And Fellows Of Harvard College | Hybrid necroptosis inhibitors |
KR20170042595A (ko) * | 2014-08-21 | 2017-04-19 | 글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 | 의약으로서의 rip1 키나제 억제제로서의 헤테로시클릭 아미드 |
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 |
WO2017004500A1 (en) * | 2015-07-02 | 2017-01-05 | Genentech, Inc. | Bicyclic lactams and methods of use thereof |
PL3362449T3 (pl) | 2015-10-13 | 2021-12-13 | Institut National De La Santé Et De La Recherche Médicale (Inserm) | Pochodne sybiriliny do zastosowania do zapobiegania i/lub leczenia zaburzeń związanych z nekroptozą komórkową |
AU2016340527B2 (en) | 2015-10-23 | 2020-09-17 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
WO2017109724A1 (en) | 2015-12-21 | 2017-06-29 | Glaxosmithkline Intellectual Property Development Limited | Heterocyclic amides as kinase inhibitors |
WO2017136727A2 (en) * | 2016-02-05 | 2017-08-10 | Denali Therapeutics Inc. | Compounds, compositions and methods |
WO2018073193A1 (en) | 2016-10-17 | 2018-04-26 | F. Hoffmann-La Roche Ag | Bicyclic pyridone lactams and methods of use thereof |
US11072607B2 (en) | 2016-12-16 | 2021-07-27 | Genentech, Inc. | Inhibitors of RIP1 kinase and methods of use thereof |
EP3585782A1 (en) | 2017-02-27 | 2020-01-01 | GlaxoSmithKline Intellectual Property Development Limited | Heterocyclic amides as kinase inhibitors |
PL3788045T3 (pl) | 2018-05-03 | 2023-10-09 | Rigel Pharmaceuticals, Inc. | Związki hamujące rip1 oraz sposoby ich wytwarzania i wykorzystania |
CR20200581A (es) | 2018-05-03 | 2021-05-11 | Rigel Pharmaceuticals Inc | Compuestos inhibidores de rip1 y métodos para preparar y usar los mismos |
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 |
AU2020341708B2 (en) | 2019-09-06 | 2024-01-04 | Rigel Pharmaceuticals, Inc. | RIP1 inhibitory compounds and methods for making and using the same |
EP4025574A1 (en) * | 2019-09-06 | 2022-07-13 | Rigel Pharmaceuticals, Inc. | Rip1 inhibitory compounds and methods for making and using the same |
MX2022005509A (es) | 2019-11-07 | 2022-10-18 | Rigel Pharmaceuticals Inc | Compuestos inhibidores de rip1 heterociclicos. |
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 |
-
2022
- 2022-03-02 AR ARP220100461A patent/AR125587A1/es unknown
- 2022-03-02 TW TW111107595A patent/TW202300490A/zh unknown
- 2022-03-10 MX MX2023010624A patent/MX2023010624A/es unknown
- 2022-03-10 PE PE2023002567A patent/PE20240237A1/es unknown
- 2022-03-10 KR KR1020237030350A patent/KR20230144575A/ko active Pending
- 2022-03-10 IL IL305456A patent/IL305456A/en unknown
- 2022-03-10 EP EP22714650.3A patent/EP4304713A1/en active Pending
- 2022-03-10 WO PCT/US2022/019744 patent/WO2022192533A1/en active Application Filing
- 2022-03-10 AU AU2022232927A patent/AU2022232927B2/en active Active
- 2022-03-10 CR CR20230438A patent/CR20230438A/es unknown
- 2022-03-10 JP JP2023555403A patent/JP2024509466A/ja active Pending
- 2022-03-10 BR BR112023018167A patent/BR112023018167A2/pt unknown
- 2022-03-10 CA CA3211778A patent/CA3211778A1/en active Pending
- 2022-03-10 CN CN202280020689.7A patent/CN117083270A/zh active Pending
- 2022-03-10 US US17/691,596 patent/US12156880B2/en active Active
-
2023
- 2023-09-11 CL CL2023002704A patent/CL2023002704A1/es unknown
- 2023-09-11 DO DO2023000186A patent/DOP2023000186A/es unknown
- 2023-09-11 EC ECSENADI202368893A patent/ECSP23068893A/es unknown
- 2023-09-12 CO CONC2023/0012077A patent/CO2023012077A2/es unknown
Also Published As
Publication number | Publication date |
---|---|
DOP2023000186A (es) | 2023-11-30 |
CR20230438A (es) | 2024-01-16 |
CN117083270A (zh) | 2023-11-17 |
CL2023002704A1 (es) | 2024-03-22 |
CA3211778A1 (en) | 2022-09-15 |
CO2023012077A2 (es) | 2024-01-15 |
AU2022232927B2 (en) | 2025-02-27 |
PE20240237A1 (es) | 2024-02-16 |
IL305456A (en) | 2023-10-01 |
WO2022192533A1 (en) | 2022-09-15 |
BR112023018167A2 (pt) | 2023-10-31 |
AU2022232927A1 (en) | 2023-08-17 |
MX2023010624A (es) | 2023-11-28 |
US12156880B2 (en) | 2024-12-03 |
TW202300490A (zh) | 2023-01-01 |
EP4304713A1 (en) | 2024-01-17 |
JP2024509466A (ja) | 2024-03-01 |
US20220296608A1 (en) | 2022-09-22 |
ECSP23068893A (es) | 2023-10-31 |
KR20230144575A (ko) | 2023-10-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR120338A1 (es) | Piridazinonas como inhibidores de parp7 | |
AR113818A2 (es) | Pirazolo-quinazolinas como inhibidores de proteína quinasa | |
AR113964A1 (es) | Carbamoíl ciclohexil ácidos ligados a n de triazol como antagonistas de lpa | |
AR117139A1 (es) | Derivados de piridooxazinona como inhibidores de monoacilglicerol ligasa (magl) | |
AR051026A1 (es) | Derivados heterociclicos y su uso como inhibidores de la estearoil-coa desaturasa | |
AR105648A1 (es) | Métodos para la preparación de ácidos biliares y derivados de los mismos | |
AR121717A1 (es) | Inhibidores de rip1k | |
AR090191A1 (es) | Derivados del acido fenil alcanoico como agonistas gpr | |
AR103990A1 (es) | Ureas cíclicas como inhibidoras de rock | |
AR099228A1 (es) | Inhibidores macrocíclicos de fxia que tienen grupos heterocíclicos | |
AR094929A1 (es) | Derivados de fenilpirazol como inhibidores potentes de rock1 y rock2 | |
AR125425A1 (es) | Inhibidores de proteina tirosina fosfatasa y sus metodos de uso | |
AR117229A1 (es) | Compuestos heteroaromáticos como inhibidores de vanina | |
AR116905A1 (es) | Derivados de ácido pirrolidino-2-carboxílico para tratar el dolor y afecciones relacionadas con el dolor | |
AR116464A1 (es) | Dioxociclobutenilamino-3-hidroxi-picolinamidas n-sustituidas útiles como inhibidores de ccr6 | |
AR128440A1 (es) | Inhibidores de cinasas raf | |
AR096041A1 (es) | Derivados de ácido carboxílico alquilo sustituidos como agonistas rpg | |
AR111271A1 (es) | Inhibidores dobles de magl y faah | |
AR091534A1 (es) | Derivados de sulfonamida y metodos de uso de los mismos para mejorar la farmacocinetica de un farmaco | |
AR118641A1 (es) | Compuestos, composiciones y métodos | |
AR125365A1 (es) | Derivados de 1h-pirazol como ligandos sigma | |
AR125587A1 (es) | Inhibidores heterocíclicos de la quinasa de rip1 | |
AR113799A1 (es) | Derivados de alcoxiamino para tratar dolor y estados relacionados con dolor | |
AR119911A1 (es) | Inhibidores heterocíclicos de la cinasa rip1 | |
AR126733A1 (es) | Inhibidores de nicotinamida ripk1 |