PH12020551717A1 - Dual atm and dna-pk inhibitors for use in anti-tumor therapy - Google Patents
Dual atm and dna-pk inhibitors for use in anti-tumor therapyInfo
- Publication number
- PH12020551717A1 PH12020551717A1 PH12020551717A PH12020551717A PH12020551717A1 PH 12020551717 A1 PH12020551717 A1 PH 12020551717A1 PH 12020551717 A PH12020551717 A PH 12020551717A PH 12020551717 A PH12020551717 A PH 12020551717A PH 12020551717 A1 PH12020551717 A1 PH 12020551717A1
- Authority
- PH
- Philippines
- Prior art keywords
- inhibitors
- dna
- tumor therapy
- dual atm
- atm
- Prior art date
Links
- 230000000259 anti-tumor effect Effects 0.000 title 1
- 230000009977 dual effect Effects 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 238000002560 therapeutic procedure Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000000771 oncological effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- 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
- C07D471/10—Spiro-condensed systems
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/20—Spiro-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
- C07D491/12—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 three hetero rings
- C07D491/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Provided herein are compounds of the Formula (I), (II), and (III), as well as pharmaceutically acceptable salts thereof, wherein the substituents are those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of oncologic diseases.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201810359447.6A CN110386932A (en) | 2018-04-20 | 2018-04-20 | Dual ATM and DNA-PK inhibitors for use in antitumor therapy |
| US201862665296P | 2018-05-01 | 2018-05-01 | |
| PCT/CN2019/083104 WO2019201283A1 (en) | 2018-04-20 | 2019-04-17 | Dual atm and dna-pk inhibitors for use in anti-tumor therapy |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PH12020551717A1 true PH12020551717A1 (en) | 2021-07-12 |
Family
ID=68240416
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PH12020551717A PH12020551717A1 (en) | 2018-04-20 | 2020-10-16 | Dual atm and dna-pk inhibitors for use in anti-tumor therapy |
Country Status (2)
| Country | Link |
|---|---|
| PH (1) | PH12020551717A1 (en) |
| WO (1) | WO2019201283A1 (en) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112021005989A2 (en) * | 2018-09-30 | 2021-06-29 | Medshine Discovery Inc. | quinoline-pyrrolidin-2-one derivatives and their application |
| KR20220047290A (en) * | 2019-07-30 | 2022-04-15 | 엑스래드 테라퓨틱스, 인크. | Dual ATM and DNA-PK inhibitors for use in anti-tumor therapy |
| EP3821947A1 (en) * | 2019-11-13 | 2021-05-19 | Libra Therapeutics, Inc. | Heterocyclic trpml1 agonists |
| WO2021098734A1 (en) * | 2019-11-19 | 2021-05-27 | 南京明德新药研发有限公司 | Substituted quinolinopyrrolidone compound as atm inhibitor and application thereof |
| CN113121573A (en) * | 2019-12-31 | 2021-07-16 | 成都百裕制药股份有限公司 | Purine derivatives and their use in medicine |
| CN113121538B (en) * | 2019-12-31 | 2023-04-21 | 成都百裕制药股份有限公司 | Furan derivative and application thereof in medicine |
| US11530218B2 (en) | 2020-01-20 | 2022-12-20 | Incyte Corporation | Spiro compounds as inhibitors of KRAS |
| TWI894229B (en) * | 2020-03-16 | 2025-08-21 | 瑞士商諾華公司 | Biaryl derivatives as yap/taz-tead protein-protein interaction inhibitors |
| US20230141284A1 (en) * | 2020-04-10 | 2023-05-11 | Ono Pharmaceutical Co., Ltd. | Cancer therapeutic method |
| US11739102B2 (en) | 2020-05-13 | 2023-08-29 | Incyte Corporation | Fused pyrimidine compounds as KRAS inhibitors |
| US11691971B2 (en) | 2020-06-19 | 2023-07-04 | Incyte Corporation | Naphthyridinone compounds as JAK2 V617F inhibitors |
| WO2022006456A1 (en) | 2020-07-02 | 2022-01-06 | Incyte Corporation | Tricyclic pyridone compounds as jak2 v617f inhibitors |
| IL299612A (en) | 2020-07-02 | 2023-03-01 | Incyte Corp | Tricyclic urea compounds as jak2 v617f inhibitors |
| WO2022046989A1 (en) | 2020-08-27 | 2022-03-03 | Incyte Corporation | Tricyclic urea compounds as jak2 v617f inhibitors |
| US11999752B2 (en) | 2020-08-28 | 2024-06-04 | Incyte Corporation | Vinyl imidazole compounds as inhibitors of KRAS |
| WO2022072783A1 (en) | 2020-10-02 | 2022-04-07 | Incyte Corporation | Bicyclic dione compounds as inhibitors of kras |
| CN112279785B (en) * | 2020-10-29 | 2022-08-16 | 苏利制药科技江阴有限公司 | 3, 3-difluorocyclobutylamine hydrochloride intermediate and synthetic method thereof, and 3, 3-difluorocyclobutylamine hydrochloride synthetic method |
| EP3992191A1 (en) | 2020-11-03 | 2022-05-04 | Deutsches Krebsforschungszentrum | Imidazo[4,5-c]quinoline compounds and their use as atm kinase inhibitors |
| US11919908B2 (en) | 2020-12-21 | 2024-03-05 | Incyte Corporation | Substituted pyrrolo[2,3-d]pyrimidine compounds as JAK2 V617F inhibitors |
| US20250268873A1 (en) * | 2021-02-03 | 2025-08-28 | Xrad Therapeutics, Inc. | Combination of dual atm and dna-pk inhibitors and immunotherapeutic agents for use in cancer therapy |
| CN117015534A (en) * | 2021-02-03 | 2023-11-07 | 艾科思莱德制药公司 | Combination of dual ATM and DNA-PK inhibitors for cancer therapy and immunotherapeutic agents |
| AR125273A1 (en) | 2021-02-25 | 2023-07-05 | Incyte Corp | SPIROCYCLIC LACTAMS AS JAK2 INHIBITORS V617F |
| TW202246274A (en) * | 2021-03-16 | 2022-12-01 | 大陸商上海翰森生物醫藥科技有限公司 | Nitrogen-containing heterocyclic polycyclic compound, preparation method and application thereof |
| WO2022204112A1 (en) | 2021-03-22 | 2022-09-29 | Incyte Corporation | Imidazole and triazole kras inhibitors |
| PE20241127A1 (en) | 2021-07-07 | 2024-05-24 | Incyte Corp | TRICYCLIC COMPOUNDS AS KRAS INHIBITORS |
| EP4396187A1 (en) | 2021-08-31 | 2024-07-10 | Incyte Corporation | Naphthyridine compounds as inhibitors of kras |
| WO2023049697A1 (en) | 2021-09-21 | 2023-03-30 | Incyte Corporation | Hetero-tricyclic compounds as inhibitors of kras |
| EP4408536A1 (en) | 2021-10-01 | 2024-08-07 | Incyte Corporation | Pyrazoloquinoline kras inhibitors |
| WO2023064857A1 (en) | 2021-10-14 | 2023-04-20 | Incyte Corporation | Quinoline compounds as inhibitors of kras |
| CR20240447A (en) | 2022-03-17 | 2025-01-29 | Incyte Corp | Tricyclic urea compounds as jak2 v617f inhibitors |
| TW202508595A (en) | 2023-05-04 | 2025-03-01 | 美商銳新醫藥公司 | Combination therapy for a ras related disease or disorder |
| WO2025034702A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Rmc-6291 for use in the treatment of ras protein-related disease or disorder |
| US20250154171A1 (en) | 2023-10-12 | 2025-05-15 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025171296A1 (en) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025183591A1 (en) * | 2024-02-29 | 2025-09-04 | Федеральное государственное унитарное предприятие "Всероссийский научно-исследовательский институт автоматики им. Н.Л. Духова" (ФГУП "ВНИИА") | 2н-[1,4]oxazino- and 2h-[1,4]thiazinо[3,2-c]quinolin-3(4h)-one derivatives as atm and dna-pk kinase inhibitors |
| WO2025217307A1 (en) | 2024-04-09 | 2025-10-16 | Revolution Medicines, Inc. | Methods for predicting response to a ras(on) inhibitor and combination therapies |
| WO2025224759A1 (en) * | 2024-04-23 | 2025-10-30 | Bugworks Research India Pvt. Ltd | Indanol substituted diamino pyrimidine carboxamides as dual atm/dna-pk inhibitors |
| WO2025240847A1 (en) | 2024-05-17 | 2025-11-20 | Revolution Medicines, Inc. | Ras inhibitors |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006063149A1 (en) | 2004-12-09 | 2006-06-15 | Regents Of The University Of Minnesota | Nucleosides with antiviral and anticancer activity |
| US20110212053A1 (en) * | 2008-06-19 | 2011-09-01 | Dapeng Qian | Phosphatidylinositol 3 kinase inhibitors |
| EP2350053B1 (en) * | 2008-10-17 | 2013-12-11 | Whitehead Institute For Biomedical Research | Modulators of MTOR Complexes |
| CN102399218A (en) * | 2010-09-16 | 2012-04-04 | 和记黄埔医药(上海)有限公司 | Triheterocyclic compounds and their use as PI3K inhibitors |
| CN103936762B (en) * | 2013-01-17 | 2016-02-24 | 上海汇伦生命科技有限公司 | Morpholine quinolines, Preparation Method And The Use |
| CN103880844A (en) * | 2014-04-09 | 2014-06-25 | 彭正中 | Novel quinolinone compound and preparation method and use thereof |
| NO2714752T3 (en) * | 2014-05-08 | 2018-04-21 | ||
| CN105461711B (en) * | 2014-06-17 | 2018-11-06 | 正大天晴药业集团股份有限公司 | Pyrido [1,2-a] pyrimidinone analogues as PI3K inhibitor |
| CN105461712B (en) * | 2014-06-17 | 2019-01-29 | 上海嘉坦医药科技有限公司 | Pyrido [1,2-a] pyrimidinone analogues as mTOR/PI3K inhibitor |
| PT3560924T (en) * | 2015-04-02 | 2021-07-02 | Merck Patent Gmbh | Imidazolonyl quinolines and their use as atm kinase inhibitors |
| WO2016186453A1 (en) * | 2015-05-20 | 2016-11-24 | Kainos Medicine, Inc. | Quinoline derivatives as bromodomain inhibitors |
| GB201519406D0 (en) * | 2015-11-03 | 2015-12-16 | Astrazeneca Ab | Imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer |
| GB201519568D0 (en) | 2015-11-05 | 2015-12-23 | Astrazeneca Ab | Imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer |
| WO2017162611A1 (en) * | 2016-03-21 | 2017-09-28 | Astrazeneca Ab | Quinoline-3-carboxamide compounds and their use in treating cancer |
| GB201608227D0 (en) * | 2016-05-11 | 2016-06-22 | Astrazeneca Ab | Imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer |
| CN110386932A (en) | 2018-04-20 | 2019-10-29 | 艾科思莱德制药公司 | Dual ATM and DNA-PK inhibitors for use in antitumor therapy |
-
2019
- 2019-04-17 WO PCT/CN2019/083104 patent/WO2019201283A1/en not_active Ceased
-
2020
- 2020-10-16 PH PH12020551717A patent/PH12020551717A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2019201283A1 (en) | 2019-10-24 |
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