CN106470992A - 作为pi3k抑制剂的吡啶并[1,2‑a]嘧啶酮类似物 - Google Patents
作为pi3k抑制剂的吡啶并[1,2‑a]嘧啶酮类似物 Download PDFInfo
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- CN106470992A CN106470992A CN201580027396.1A CN201580027396A CN106470992A CN 106470992 A CN106470992 A CN 106470992A CN 201580027396 A CN201580027396 A CN 201580027396A CN 106470992 A CN106470992 A CN 106470992A
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- 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
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-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
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- 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)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Abstract
公开了一类作为PI3K抑制剂的吡啶并[1,2‑a]嘧啶酮类似物,具体涉及式(I)所示化合物或其药学上可接受的盐。
Description
PCT国内申请,说明书已公开。
Claims (12)
- PCT国内申请,权利要求书已公开。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410271282.9A CN105461711B (zh) | 2014-06-17 | 2014-06-17 | 作为PI3K抑制剂的吡啶并[1,2-a]嘧啶酮类似物 |
CN2014102712829 | 2014-06-17 | ||
CN201510324348 | 2015-06-12 | ||
CN2015103243480 | 2015-06-12 | ||
PCT/CN2015/081518 WO2015192760A1 (zh) | 2014-06-17 | 2015-06-16 | 作为pi3k抑制剂的吡啶并[1,2-a]嘧啶酮类似物 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106470992A true CN106470992A (zh) | 2017-03-01 |
CN106470992B CN106470992B (zh) | 2018-11-06 |
Family
ID=54934872
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201580027396.1A Active CN106470992B (zh) | 2014-06-17 | 2015-06-16 | 作为pi3k抑制剂的吡啶并[1,2-a]嘧啶酮类似物 |
Country Status (11)
Country | Link |
---|---|
US (1) | US9856256B2 (zh) |
EP (1) | EP3159341B8 (zh) |
JP (1) | JP6680774B2 (zh) |
KR (1) | KR102495840B1 (zh) |
CN (1) | CN106470992B (zh) |
AU (1) | AU2015276699B2 (zh) |
CA (1) | CA2951971A1 (zh) |
EA (1) | EA032642B1 (zh) |
ES (1) | ES2754264T3 (zh) |
TW (1) | TWI628180B (zh) |
WO (1) | WO2015192760A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113316575A (zh) * | 2019-01-24 | 2021-08-27 | 江苏奥赛康药业有限公司 | 作为TGF-βR1激酶抑制剂的5-(4-吡啶氧基)吡唑类化合物 |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20180095565A (ko) * | 2015-12-16 | 2018-08-27 | 치아타이 티안큉 파마수티컬 그룹 주식회사 | 피리도[1,2-a]피리미돈 유사체, 이의 결정형, 이의 중간체 및 이의 제조방법 |
CN110386932A (zh) * | 2018-04-20 | 2019-10-29 | 艾科思莱德制药公司 | 用于抗肿瘤疗法中的双重atm和dna-pk抑制剂 |
MX2022006700A (es) | 2019-12-02 | 2022-09-02 | Storm Therapeutics Ltd | Compuestos poliheterociclicos como inhibidores de mettl3. |
US20230132982A1 (en) | 2020-02-10 | 2023-05-04 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Use of pyrido[1,2-a]pyrimidinone compound in treating lymphoma |
CN115135649A (zh) * | 2020-03-10 | 2022-09-30 | 正大天晴药业集团股份有限公司 | 包括吡啶并[1,2-a]嘧啶酮化合物的药物组合 |
CA3194730A1 (en) * | 2020-09-15 | 2022-03-24 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Use of pyrido[1,2-a]pyrimidinone compound in treating peripheral t cell lymphoma |
CN116761608A (zh) * | 2020-12-08 | 2023-09-15 | 正大天晴药业集团股份有限公司 | 吡啶并[1,2-a]嘧啶酮化合物的治疗妇科肿瘤的用途 |
CN118510518A (zh) * | 2022-03-09 | 2024-08-16 | 正大天晴药业集团股份有限公司 | 包括吡啶并[1,2-a]嘧啶酮化合物和EGFR抑制剂的药物组合 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100311736A1 (en) * | 2007-10-22 | 2010-12-09 | Glaxosmithkline Llc | Pyridosulfonamide derivatives as p13 kinase inhibitors |
US20110092504A1 (en) * | 2008-05-30 | 2011-04-21 | Amgen Inc. | Inhibitors of pi3 kinase |
CN103224496A (zh) * | 2011-11-17 | 2013-07-31 | 山东轩竹医药科技有限公司 | 三环类PI3K和/或mTOR抑制剂 |
CN103539777A (zh) * | 2012-07-13 | 2014-01-29 | 广东东阳光药业有限公司 | Pi3激酶调节剂及其使用方法和用途 |
WO2014022128A1 (en) * | 2012-07-29 | 2014-02-06 | Calitor Sciences, Llc | Pi3 kinase modulators and methods of use |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE602004008098T8 (de) | 2003-10-10 | 2008-04-17 | Pfizer Products Inc., Groton | Substituierte 2h-[1,2,4]triazolo[4,3-a]pyrazine als gsk-3-inhibitoren |
ES2431466T3 (es) * | 2006-06-30 | 2013-11-26 | Sunesis Pharmaceuticals, Inc. | Inhibidores de piridinonil pdk1 |
MX2012015096A (es) * | 2010-07-02 | 2013-05-28 | Gilead Sciences Inc | Compuestos heterociclicos fusionados como moduladores del canal ion. |
WO2012037108A1 (en) * | 2010-09-13 | 2012-03-22 | Glaxosmithkline Llc | Aminoquinoline derivatives as antiviral agents |
TW201443037A (zh) * | 2013-01-09 | 2014-11-16 | Gilead Sciences Inc | 治療用化合物 |
JP6386177B2 (ja) * | 2014-06-17 | 2018-09-05 | ツーセン ファーマシューティカル カンパニー リミテッド | mTOR/PI3K阻害剤としてのピリド[1,2−a]ピリミジノン類似体 |
-
2015
- 2015-06-16 CA CA2951971A patent/CA2951971A1/en active Pending
- 2015-06-16 CN CN201580027396.1A patent/CN106470992B/zh active Active
- 2015-06-16 US US15/319,726 patent/US9856256B2/en active Active
- 2015-06-16 JP JP2017518397A patent/JP6680774B2/ja active Active
- 2015-06-16 EA EA201790016A patent/EA032642B1/ru not_active IP Right Cessation
- 2015-06-16 EP EP15810067.7A patent/EP3159341B8/en active Active
- 2015-06-16 WO PCT/CN2015/081518 patent/WO2015192760A1/zh active Application Filing
- 2015-06-16 KR KR1020177000523A patent/KR102495840B1/ko active IP Right Grant
- 2015-06-16 ES ES15810067T patent/ES2754264T3/es active Active
- 2015-06-16 AU AU2015276699A patent/AU2015276699B2/en active Active
- 2015-06-17 TW TW104119646A patent/TWI628180B/zh active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100311736A1 (en) * | 2007-10-22 | 2010-12-09 | Glaxosmithkline Llc | Pyridosulfonamide derivatives as p13 kinase inhibitors |
US20110092504A1 (en) * | 2008-05-30 | 2011-04-21 | Amgen Inc. | Inhibitors of pi3 kinase |
CN103224496A (zh) * | 2011-11-17 | 2013-07-31 | 山东轩竹医药科技有限公司 | 三环类PI3K和/或mTOR抑制剂 |
CN103539777A (zh) * | 2012-07-13 | 2014-01-29 | 广东东阳光药业有限公司 | Pi3激酶调节剂及其使用方法和用途 |
WO2014022128A1 (en) * | 2012-07-29 | 2014-02-06 | Calitor Sciences, Llc | Pi3 kinase modulators and methods of use |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113316575A (zh) * | 2019-01-24 | 2021-08-27 | 江苏奥赛康药业有限公司 | 作为TGF-βR1激酶抑制剂的5-(4-吡啶氧基)吡唑类化合物 |
CN113316575B (zh) * | 2019-01-24 | 2022-03-18 | 江苏奥赛康药业有限公司 | 作为TGF-βR1激酶抑制剂的5-(4-吡啶氧基)吡唑类化合物 |
Also Published As
Publication number | Publication date |
---|---|
AU2015276699B2 (en) | 2019-10-10 |
TWI628180B (zh) | 2018-07-01 |
CA2951971A1 (en) | 2015-12-23 |
EP3159341B8 (en) | 2020-01-08 |
EP3159341A4 (en) | 2018-05-16 |
JP2017519821A (ja) | 2017-07-20 |
EP3159341A1 (en) | 2017-04-26 |
US20170137420A1 (en) | 2017-05-18 |
AU2015276699A1 (en) | 2017-01-19 |
JP6680774B2 (ja) | 2020-04-15 |
EP3159341B1 (en) | 2019-08-21 |
KR102495840B1 (ko) | 2023-02-03 |
EA032642B1 (ru) | 2019-06-28 |
CN106470992B (zh) | 2018-11-06 |
TW201625612A (zh) | 2016-07-16 |
EA201790016A1 (ru) | 2017-06-30 |
WO2015192760A1 (zh) | 2015-12-23 |
ES2754264T3 (es) | 2020-04-16 |
US9856256B2 (en) | 2018-01-02 |
KR20170016465A (ko) | 2017-02-13 |
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