ECSP22077299A - Inhibidores alostéricos de cromenona del fosfoinosítido 3-quinasa (pi3k) para el tratamiento de enfermedades asociadas con modulación del pi3k - Google Patents
Inhibidores alostéricos de cromenona del fosfoinosítido 3-quinasa (pi3k) para el tratamiento de enfermedades asociadas con modulación del pi3kInfo
- Publication number
- ECSP22077299A ECSP22077299A ECSENADI202277299A ECDI202277299A ECSP22077299A EC SP22077299 A ECSP22077299 A EC SP22077299A EC SENADI202277299 A ECSENADI202277299 A EC SENADI202277299A EC DI202277299 A ECDI202277299 A EC DI202277299A EC SP22077299 A ECSP22077299 A EC SP22077299A
- Authority
- EC
- Ecuador
- Prior art keywords
- pi3k
- phosphoinositide
- kinase
- modulation
- treatment
- Prior art date
Links
Classifications
-
- 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
- C07D405/02—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 two hetero rings
- C07D405/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/4035—Isoindoles, e.g. phthalimide
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/056—Ortho-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
La descripción se refiere a los compuestos de la Fórmula (I) como inhibidores alostéricos de cromenona del fosfoinosítido 3-quinasa (PI3K) útiles en el tratamiento de enfermedades o trastornos asociados con la modulación del PI3K, Fórmula (I): o un profármaco, solvato, enantiómero, estereoisómero, tautómero o sal farmacéuticamente aceptable de este, en donde R1, R2, R3, R4, R5, R6, R7, R8, R9, W, X, Y, s, y el Anillo A son como se describen en la presente descripción.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US202063005096P | 2020-04-03 | 2020-04-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP22077299A true ECSP22077299A (es) | 2023-01-31 |
Family
ID=75674963
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ECSENADI202277299A ECSP22077299A (es) | 2020-04-03 | 2022-10-03 | Inhibidores alostéricos de cromenona del fosfoinosítido 3-quinasa (pi3k) para el tratamiento de enfermedades asociadas con modulación del pi3k |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US11649227B2 (es) |
| EP (1) | EP4126851A1 (es) |
| JP (1) | JP7505023B2 (es) |
| KR (1) | KR102857816B1 (es) |
| CN (1) | CN115956075B (es) |
| AR (1) | AR121719A1 (es) |
| AU (1) | AU2021248415B2 (es) |
| BR (1) | BR112022019918A2 (es) |
| CO (1) | CO2022014160A2 (es) |
| CR (1) | CR20220493A (es) |
| EC (1) | ECSP22077299A (es) |
| IL (1) | IL296918A (es) |
| JO (1) | JOP20220247A1 (es) |
| MX (1) | MX2022012306A (es) |
| PE (1) | PE20230824A1 (es) |
| PH (1) | PH12022552637A1 (es) |
| TW (1) | TWI794780B (es) |
| WO (1) | WO2021202964A1 (es) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR121719A1 (es) | 2020-04-03 | 2022-06-29 | Petra Pharma Corp | Inhibidores alostéricos de cromenona del fosfoinosítido 3-quinasa (pi3k) para el tratamiento de enfermedades |
| MX2023013082A (es) * | 2021-05-03 | 2024-01-08 | Petra Pharma Corp | Inhibidores alostéricos de cromenona de la fosfoinosítido 3-quinasa (pi3k) para el tratamiento de enfermedades. |
| CR20230517A (es) | 2021-05-03 | 2023-11-28 | Petra Pharma Corp | Inhibidores alostéricos de cromenona del fosfoinosítido 3-quinasa (pi3k) para el tratamiento de enfermedades |
| AU2022282380B2 (en) * | 2021-05-27 | 2025-08-14 | Petra Pharma Corporation | Allosteric chromenone inhibitors of phosphoinositide 3-kinase (pi3k) for the treatment of cancer |
| TW202329930A (zh) | 2021-09-30 | 2023-08-01 | 美商佩特拉製藥公司 | 用於治療疾病之磷酸肌醇3-激酶(pi3k)之異位色烯酮抑制劑 |
| WO2023060262A1 (en) * | 2021-10-07 | 2023-04-13 | Relay Therapeutics, Inc. | Pi3k-alpha inhibitors and methods of use thereof |
| TW202334137A (zh) * | 2021-11-03 | 2023-09-01 | 美商薩諾管理公司 | Pi3k抑制劑及治療癌症之方法 |
| WO2023104111A1 (en) * | 2021-12-08 | 2023-06-15 | Nanjing Zenshine Pharmaceuticals Co., Ltd. | Fused heterocyclic compounds as pi3kalpha inhibitors |
| CA3240772A1 (en) * | 2021-12-22 | 2023-06-29 | Kevan M. Shokat | Covalently binding inhibitors of g12s, g12d and/or g12e mutants of k-ras gtpase |
| US20240124422A1 (en) * | 2022-03-29 | 2024-04-18 | Prelude Therapeutics Incorporated | Mutant pi3k-alpha inhibitors and their use as pharmaceuticals |
| WO2023205680A1 (en) * | 2022-04-20 | 2023-10-26 | Synnovation Therapeutics, Inc. | PI3Kα INHIBITORS |
| US20250263394A1 (en) * | 2022-04-24 | 2025-08-21 | InventisBio Co., Ltd. | Compounds, preparation methods and uses thereof |
| CN119301106A (zh) * | 2022-04-29 | 2025-01-10 | 佩特拉制药公司 | 用于治疗疾病的磷酸肌醇3-激酶(pi3k)的变构苯并吡喃酮抑制剂 |
| US20250313524A1 (en) * | 2022-05-10 | 2025-10-09 | Relay Therapeutics, Inc. | Pi3k-alpha inhibitors and methods of use thereof |
| AU2023283727A1 (en) | 2022-06-08 | 2024-12-12 | Onkure, Inc. | Benzopyrimidin-4(3h)-ones as pi3k inhibitors |
| CN117384124B (zh) * | 2022-07-04 | 2025-08-01 | 安徽中医药大学 | Hdac抑制剂、组合物及其应用 |
| CN117362281A (zh) * | 2022-07-07 | 2024-01-09 | 海创药业股份有限公司 | 一种pi3k抑制剂及其制备方法和用途 |
| IL319246A (en) | 2022-09-08 | 2025-04-01 | Onkure Inc | Isoquinolones as PI3K inhibitors |
| CN119894898A (zh) * | 2022-09-09 | 2025-04-25 | 益方生物科技(上海)股份有限公司 | 化合物、其制备方法和用途 |
| WO2024064024A1 (en) | 2022-09-19 | 2024-03-28 | Onkure, Inc. | ((4-oxo-3,4-dihydroquinazolin-8-yl)methyl)amine derivatives as p13k inhibitors for the treatment of cancer |
| WO2024081345A1 (en) | 2022-10-14 | 2024-04-18 | Onkure, Inc. | Benzopyrimidin-4(3h)-ones as pi3k inhibitors |
| EP4602031A1 (en) * | 2022-10-14 | 2025-08-20 | Genesis Therapeutics, Inc. | Methods for treating cancer |
| WO2024086789A2 (en) * | 2022-10-20 | 2024-04-25 | Prelude Therapeutics Incorporated | Mutant pi3k-alpha inhibitors and their use as pharmaceuticals |
| KR20250109699A (ko) * | 2022-11-01 | 2025-07-17 | 페트라 파마 코포레이션 | 질환의 치료를 위한 포스포이노시티드 3-키나제 (pi3k)의 알로스테릭 크로메논 억제제 |
| IL320602A (en) | 2022-11-02 | 2025-07-01 | Petra Pharma Corp | Targeting allosteric and orthosteric pockets of phosphoinositide 3-kinase (pi3k) for the treatment of disease |
| KR20250097960A (ko) * | 2022-11-02 | 2025-06-30 | 페트라 파마 코포레이션 | 질환의 치료를 위한 포스포이노시티드 3-키나제 (pi3k)의 알로스테릭 크로메논 억제제 |
| WO2024099437A1 (en) * | 2022-11-11 | 2024-05-16 | Fochon Biosciences, Ltd. | Compounds as protein kinase inhibitors |
| WO2024163752A1 (en) * | 2023-02-02 | 2024-08-08 | Synnovation Therapeutics, Inc. | HETEROCYCLIC COMPOUNDS AS PI3Kα INHIBITORS |
| AU2024234319A1 (en) * | 2023-03-15 | 2025-10-02 | An2 Therapeutics, Inc. | Chemical compounds |
| WO2024211346A1 (en) * | 2023-04-03 | 2024-10-10 | Prelude Therapeutics Incorporated | Mutant pi3k-alpha inhibitors and their use as pharmaceuticals |
| KR20260005985A (ko) | 2023-05-05 | 2026-01-12 | 일라이 릴리 앤드 캄파니 | Er+ 유방암을 갖는 대상체에서 중추 신경계 (cns) 전이를 치료 및 예방하는 데 사용하기 위한 임루네스트란트 또는 그의 염 |
| WO2024260464A1 (en) * | 2023-06-21 | 2024-12-26 | Regor Pharmaceuticals, Inc. | Pi3k inhibitors and use thereof |
| WO2025007074A1 (en) * | 2023-06-30 | 2025-01-02 | Reactive Biosciences, Inc. | Chemical compounds |
| CN119431297A (zh) * | 2023-08-02 | 2025-02-14 | 郑州同源康医药有限公司 | 稠环类化合物及其用途 |
| AU2024325407A1 (en) | 2023-08-11 | 2026-02-19 | Onkure Therapeutics, Inc. | Benzopyridinones and benzopyrimidinones as pi3k inhibitors |
| WO2025042896A1 (en) * | 2023-08-22 | 2025-02-27 | Mayo Foundation For Medical Education And Research | DNA TOPOISOMERASE IIβ INHIBITORS |
| CN119874676A (zh) * | 2023-10-25 | 2025-04-25 | 海创药业股份有限公司 | 一种pi3k抑制剂及其制备方法和用途 |
| WO2025207755A1 (en) | 2024-03-29 | 2025-10-02 | Onkure, Inc. | Quinolizinones as pi3k inhibitors |
| WO2025212360A1 (en) | 2024-04-01 | 2025-10-09 | Onkure, Inc. | Isoquinolones as pi3k inhibitors |
| WO2025231052A1 (en) * | 2024-05-01 | 2025-11-06 | Petra Pharma Corporation | Solid dispersions of 6-chloro-3-[(1r)-1-[3,6-dimethyl-2-(2- methylindazol-5-yl)-4-oxo-chromen-8-yl]ethoxy]pyridine-2-carboxamide |
| WO2025231053A1 (en) * | 2024-05-01 | 2025-11-06 | Petra Pharma Corporation | Solid forms of 6-chloro-3-[(1r)-1-[3,6-dimethyl-2-(2-methylindazol-5-yl)-4-oxo-chromen-8-yl]ethoxy]pyridine-2-carboxamide |
| WO2025255233A1 (en) | 2024-06-07 | 2025-12-11 | Onkure, Inc. | Compounds containing fused tricyclic rings as pi3k inhibitors |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1190405B (it) | 1985-10-22 | 1988-02-16 | Recordati Chem Pharm | Derivati del flavone |
| IL89840A (en) | 1988-04-06 | 1996-10-31 | Lipha | Substituted flavonoid compounds and salts thereof their preparation and pharmaceutical composition containing them |
| RU2118321C1 (ru) | 1988-12-21 | 1998-08-27 | Дзе Апджон Компани | Замещенные бензопираноны и их фармацевтически приемлемые соли и гидраты |
| US5763263A (en) | 1995-11-27 | 1998-06-09 | Dehlinger; Peter J. | Method and apparatus for producing position addressable combinatorial libraries |
| AU2001230426C1 (en) | 2000-01-24 | 2006-06-22 | Astrazeneca Ab | Therapeutic morpholino-substituted compounds |
| US20030105073A1 (en) * | 2001-10-23 | 2003-06-05 | Haughan Alan Findlay | Quinolone derivatives |
| US7884127B2 (en) | 2002-07-08 | 2011-02-08 | Pirimal Life Sciences Ltd. | Inhibitors of cyclin dependent kinases and their use |
| TWI331034B (en) | 2002-07-08 | 2010-10-01 | Piramal Life Sciences Ltd | Inhibitors of cyclin-dependent kinases and their use |
| NZ538420A (en) | 2002-08-16 | 2007-06-29 | Kinacia Pty Ltd | Inhibition of phosphoinositide 3-kinase beta |
| CN101260104A (zh) * | 2002-08-16 | 2008-09-10 | 阿斯利康(瑞典)有限公司 | 抑制磷酸肌醇3-激酶β |
| CN102227420B (zh) | 2008-09-29 | 2015-06-24 | 西特里斯药业公司 | 作为沉默调节蛋白调节剂的喹唑啉酮、喹诺酮和相关的类似物 |
| US8399460B2 (en) * | 2009-10-27 | 2013-03-19 | Astrazeneca Ab | Chromenone derivatives |
| PT2496567T (pt) * | 2009-11-05 | 2017-11-15 | Rhizen Pharmaceuticals S A | Novos moduladores de quinase benzopiran |
| US8530470B2 (en) * | 2011-04-13 | 2013-09-10 | Astrazeneca Ab | Chromenone derivatives |
| CN106008479B (zh) * | 2015-03-06 | 2020-01-10 | 南京圣和药业股份有限公司 | 作为磷脂酰肌醇3-激酶δ抑制剂的取代嘧啶类化合物及其应用 |
| CA3017366A1 (en) | 2016-03-11 | 2017-09-14 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Icariin and icaritin derivatives |
| CN108299365B (zh) | 2018-01-31 | 2021-08-06 | 中南大学 | 一种黄酮衍生物及其应用 |
| AR121719A1 (es) * | 2020-04-03 | 2022-06-29 | Petra Pharma Corp | Inhibidores alostéricos de cromenona del fosfoinosítido 3-quinasa (pi3k) para el tratamiento de enfermedades |
-
2021
- 2021-03-31 AR ARP210100822A patent/AR121719A1/es not_active Application Discontinuation
- 2021-04-01 TW TW110112268A patent/TWI794780B/zh not_active IP Right Cessation
- 2021-04-02 MX MX2022012306A patent/MX2022012306A/es unknown
- 2021-04-02 KR KR1020227038553A patent/KR102857816B1/ko active Active
- 2021-04-02 EP EP21721700.9A patent/EP4126851A1/en active Pending
- 2021-04-02 US US17/221,209 patent/US11649227B2/en active Active
- 2021-04-02 CN CN202180039596.4A patent/CN115956075B/zh active Active
- 2021-04-02 PE PE2022002162A patent/PE20230824A1/es unknown
- 2021-04-02 AU AU2021248415A patent/AU2021248415B2/en active Active
- 2021-04-02 BR BR112022019918A patent/BR112022019918A2/pt not_active Application Discontinuation
- 2021-04-02 PH PH1/2022/552637A patent/PH12022552637A1/en unknown
- 2021-04-02 JP JP2022560305A patent/JP7505023B2/ja active Active
- 2021-04-02 CR CR20220493A patent/CR20220493A/es unknown
- 2021-04-02 WO PCT/US2021/025521 patent/WO2021202964A1/en not_active Ceased
- 2021-04-02 IL IL296918A patent/IL296918A/en unknown
-
2022
- 2022-10-03 CO CONC2022/0014160A patent/CO2022014160A2/es unknown
- 2022-10-03 EC ECSENADI202277299A patent/ECSP22077299A/es unknown
- 2022-10-04 JO JOP/2022/0247A patent/JOP20220247A1/ar unknown
-
2023
- 2023-04-18 US US18/302,573 patent/US20230286960A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| TW202200567A (zh) | 2022-01-01 |
| WO2021202964A1 (en) | 2021-10-07 |
| PH12022552637A1 (en) | 2023-01-16 |
| KR20220163462A (ko) | 2022-12-09 |
| CO2022014160A2 (es) | 2023-02-16 |
| JOP20220247A1 (ar) | 2023-01-30 |
| EP4126851A1 (en) | 2023-02-08 |
| US20230286960A1 (en) | 2023-09-14 |
| US20220372023A1 (en) | 2022-11-24 |
| CA3173569A1 (en) | 2021-10-07 |
| BR112022019918A2 (pt) | 2023-02-14 |
| KR102857816B1 (ko) | 2025-09-11 |
| PE20230824A1 (es) | 2023-05-19 |
| TWI794780B (zh) | 2023-03-01 |
| AR121719A1 (es) | 2022-06-29 |
| AU2021248415B2 (en) | 2024-03-21 |
| JP7505023B2 (ja) | 2024-06-24 |
| MX2022012306A (es) | 2023-01-04 |
| AU2021248415A1 (en) | 2022-10-20 |
| JP2023521321A (ja) | 2023-05-24 |
| US11649227B2 (en) | 2023-05-16 |
| CR20220493A (es) | 2022-12-15 |
| IL296918A (en) | 2022-12-01 |
| CN115956075A (zh) | 2023-04-11 |
| CN115956075B (zh) | 2025-11-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ECSP22077299A (es) | Inhibidores alostéricos de cromenona del fosfoinosítido 3-quinasa (pi3k) para el tratamiento de enfermedades asociadas con modulación del pi3k | |
| DOP2023000245A (es) | Inhibidores alostéricos de cromenona del fosfoinosítido 3-quinasa (pi3k) para el tratamiento de enfermedades | |
| MX2024003721A (es) | Inhibidores alostericos de cromenona de la fosfoinositido 3-quinasa (pi3k) para el tratamiento de enfermedades. | |
| MX2023013987A (es) | Inhibidores alostéricos de cromenona de la fosfoinosítido 3-quinasa (pi3k) para el tratamiento contra el cáncer. | |
| CL2022001739A1 (es) | Compuestos tricíclicos sustituidos | |
| DOP2025000245A (es) | Inhibidores de kras | |
| MX2023001876A (es) | Derivados de rapamicina. | |
| MX394700B (es) | Inhibidores de mnk sustituidos con piperidina y métodos relacionados con los mismos. | |
| CO2019000932A2 (es) | Nuevos compuestos sulfonimidoilpurinona 7-sustituidos y derivados para el tratamiento y la profilaxis de la infección vírica. | |
| CL2021000844A1 (es) | Compuestos de indolinona para uso como inhibidores de map4k1 | |
| UY35551A (es) | Derivados heteroarilos como inhibidores de aldosterona sintasa | |
| AR115731A1 (es) | Derivados de pirrolo[1,2-b]piridazina como inhibidores de quinasas irak4 | |
| CO2020010306A2 (es) | Compuestos de sulfonimidoilpurinona 7-sustituida y derivados para el tratamiento y profilaxis de cáncer de hígado. | |
| CL2022002975A1 (es) | Compuestos y composiciones para inhibir la actividad de hif2-alfa y sus métodos de uso | |
| CO2025003099A2 (es) | Compuestos para el tratamiento del cáncer | |
| MX2024003028A (es) | Derivados de 6 aza quinolina y usos relacionados. | |
| CO2025011377A2 (es) | Derivados de hidroquinazolina para el tratamiento de una enfermedad o un trastorno | |
| CL2025002151A1 (es) | Derivados de fenilpiperidina como inhibidores de la glutaminil-péptido ciclotransferasa y proteína similar a glutaminil-péptido ciclotransferasa | |
| MX2025005073A (es) | Inhibidores alostericos de cromenona de la fosfoinositido 3-quinasa (pi3k) para el tratamiento de enfermedades | |
| CL2022002697A1 (es) | Inhibidores alostéricos de cromenona del fosfoinosítido 3-quinasa (pi3k) para el tratamiento de enfermedades | |
| AR131413A1 (es) | Inhibidores de la proteína tirosina fosfatasa, composiciones y métodos de uso | |
| AR131414A1 (es) | Inhibidores de la proteína tirosina fosfatasa, composiciones y métodos de uso | |
| AR130937A1 (es) | Inhibidores alostéricos de cromenona del fosfoinosítido 3-quinasa (pi3k) para el tratamiento de enfermedades | |
| AR125979A1 (es) | Inhibidores alostéricos de cromenona de la fosfoinositido 3-quinasa (pi3k) para el tratamiento de enfermedades | |
| AR125742A1 (es) | Inhibidores alostéricos de cromenona de la fosfoinositida 3-quina6sa (pi3k) para el tratamiento de enfermedades |