SV2017005487A - Derivados de 4h-pirrol[3,2-c]piridin-4-ona - Google Patents
Derivados de 4h-pirrol[3,2-c]piridin-4-onaInfo
- Publication number
- SV2017005487A SV2017005487A SV2017005487A SV2017005487A SV2017005487A SV 2017005487 A SV2017005487 A SV 2017005487A SV 2017005487 A SV2017005487 A SV 2017005487A SV 2017005487 A SV2017005487 A SV 2017005487A SV 2017005487 A SV2017005487 A SV 2017005487A
- Authority
- SV
- El Salvador
- Prior art keywords
- pirrol
- piridin
- ona
- derivatives
- formula
- Prior art date
Links
Classifications
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/45—Non condensed piperidines, e.g. piperocaine having oxo groups directly attached to the heterocyclic ring, e.g. cycloheximide
-
- 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
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- 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
Abstract
COMPUESTOS DE FÓRMULA (I): (VER FORMULA); PROCESOS PARA SU PRODUCCIÓN Y SU USO COMO FÁRMACOS
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15152944 | 2015-01-28 | ||
| EP15200407 | 2015-12-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SV2017005487A true SV2017005487A (es) | 2019-01-17 |
Family
ID=55236350
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SV2017005487A SV2017005487A (es) | 2015-01-28 | 2017-07-28 | Derivados de 4h-pirrol[3,2-c]piridin-4-ona |
Country Status (31)
| Country | Link |
|---|---|
| US (1) | US10428063B2 (es) |
| EP (1) | EP3250567B1 (es) |
| JP (1) | JP6704398B2 (es) |
| KR (1) | KR102544847B1 (es) |
| CN (1) | CN107406417B (es) |
| AU (1) | AU2016212230B2 (es) |
| BR (1) | BR112017016193B1 (es) |
| CA (1) | CA2974853C (es) |
| CL (1) | CL2017001930A1 (es) |
| CO (1) | CO2017007663A2 (es) |
| CR (1) | CR20170345A (es) |
| CU (1) | CU20170094A7 (es) |
| DO (1) | DOP2017000176A (es) |
| EA (1) | EA032530B1 (es) |
| EC (1) | ECSP17048527A (es) |
| HK (1) | HK1244804A1 (es) |
| IL (1) | IL253284B (es) |
| JO (1) | JO3706B1 (es) |
| MX (1) | MX2017009831A (es) |
| MY (1) | MY182181A (es) |
| NI (1) | NI201700096A (es) |
| PE (1) | PE20171240A1 (es) |
| PH (1) | PH12017501340A1 (es) |
| SG (1) | SG11201705908VA (es) |
| SV (1) | SV2017005487A (es) |
| TN (1) | TN2017000329A1 (es) |
| TW (1) | TWI699359B (es) |
| UA (1) | UA122221C2 (es) |
| UY (1) | UY36544A (es) |
| WO (1) | WO2016120196A1 (es) |
| ZA (1) | ZA201705802B (es) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2952307A1 (en) | 2014-06-17 | 2015-12-23 | Bayer Pharma Aktiengesellschaft | 3-amino-1,5,6,7-tetrahydro-4h-indol-4-ones |
| JP2018522847A (ja) | 2015-06-17 | 2018-08-16 | バイエル ファーマ アクチエンゲゼルシャフト | ３−アミノ−１，５，６，７−テトラヒドロ−４ｈ−インドール−４−オン類 |
| CA2994596A1 (en) | 2015-08-05 | 2017-02-09 | Bayer Pharma Aktiengesellschaft | 1h-pyrrol-3-amines |
| EP3390395B1 (en) | 2015-12-16 | 2020-09-09 | Loxo Oncology, Inc. | Compounds useful as kinase inhibitors |
| TWI808055B (zh) | 2016-05-11 | 2023-07-11 | 美商滬亞生物國際有限公司 | Hdac 抑制劑與 pd-1 抑制劑之組合治療 |
| TWI794171B (zh) | 2016-05-11 | 2023-03-01 | 美商滬亞生物國際有限公司 | Ｈｄａｃ抑制劑與ｐｄ-ｌ１抑制劑之組合治療 |
| WO2018122168A1 (en) | 2016-12-29 | 2018-07-05 | Bayer Pharma Aktiengesellschaft | Combinations of bub1 kinase and parp inhibitors |
| WO2018158175A1 (en) | 2017-02-28 | 2018-09-07 | Bayer Pharma Aktiengesellschaft | Combination of bub1 inhibitors |
| WO2018206547A1 (en) | 2017-05-12 | 2018-11-15 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and atr inhibitors |
| WO2018215282A1 (en) | 2017-05-26 | 2018-11-29 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and pi3k inhibitors |
| KR102440006B1 (ko) | 2017-08-23 | 2022-09-05 | 현대모비스 주식회사 | 차량용 브레이크의 캘리퍼 장치 |
| US11339157B1 (en) | 2017-10-24 | 2022-05-24 | Bayer Aktiengesellschaft | 4H-pyrrolo[3,2-c]pyridin-4-one derivatives |
| KR102658602B1 (ko) | 2018-10-31 | 2024-04-19 | 길리애드 사이언시즈, 인코포레이티드 | Hpk1 억제 활성을 갖는 치환된 6-아자벤즈이미다졸 화합물 |
| TWI721623B (zh) | 2018-10-31 | 2021-03-11 | 美商基利科學股份有限公司 | 經取代之6-氮雜苯并咪唑化合物 |
| WO2020161257A1 (en) | 2019-02-07 | 2020-08-13 | Bayer Aktiengesellschaft | 3-amino-2-[2-(acylamino)pyridin-4-yl]-1,5,6,7-tetrahydro-4h-pyrrolo[3,2-c]pyridin-4-one as csnk1 inhibitors |
| CA3137611A1 (en) | 2019-04-24 | 2020-10-29 | Bayer Aktiengesellschaft | 4h-pyrrolo[3,2-c]pyridin-4-one derivatives |
| EP3959212A1 (en) | 2019-04-24 | 2022-03-02 | Bayer Aktiengesellschaft | 4h-pyrrolo[3,2-c]pyridin-4-one compounds |
| KR20220004103A (ko) | 2019-04-24 | 2022-01-11 | 바이엘 악티엔게젤샤프트 | 4H-피롤로[3,2-c]피리딘-4-온 화합물 |
| US11453681B2 (en) | 2019-05-23 | 2022-09-27 | Gilead Sciences, Inc. | Substituted eneoxindoles and uses thereof |
| EP4188928A1 (en) | 2020-07-29 | 2023-06-07 | Bayer Aktiengesellschaft | Substituted 1 h-pyrrolo[3,2-b]pyridin compounds and methods of use thereof |
| EP4188930A1 (en) | 2020-07-29 | 2023-06-07 | Bayer Aktiengesellschaft | Substituted heterocyclic compounds and therapeutic uses thereof |
| US20230365554A1 (en) | 2020-07-29 | 2023-11-16 | The Broad Institute, Inc. | Substituted pyrrolo-pyridinone derivatives and therapeutic uses thereof |
| US20230322767A1 (en) | 2020-07-29 | 2023-10-12 | Bayer Aktiengesellschaft | Aryl substituted pyrrolo-pyridinones and therapeutic uses thereof |
| CN115836070A (zh) * | 2020-08-10 | 2023-03-21 | 上海和誉生物医药科技有限公司 | 作为egfr抑制剂的稠环化合物及其制备方法和应用 |
| IL301532A (en) | 2020-09-23 | 2023-05-01 | Scorpion Therapeutics Inc | History Pyrrolo[2,3-C]pyridin-4-one is useful in cancer treatment |
| WO2022072645A2 (en) * | 2020-09-30 | 2022-04-07 | Scorpion Therapeutics, Inc. | Methods for treating cancer |
| WO2022094271A1 (en) * | 2020-10-30 | 2022-05-05 | Scorpion Therapeutics, Inc. | Methods for treating cancer |
| WO2022098992A1 (en) * | 2020-11-05 | 2022-05-12 | Scorpion Therapeutics, Inc. | Use of macrocyclic compounds in methods of treating cancer |
| WO2023147015A1 (en) * | 2022-01-27 | 2023-08-03 | The Broad Institute, Inc. | Substituted heterocyclic csnk1 inhibitors |
| WO2023183601A1 (en) | 2022-03-24 | 2023-09-28 | Scorpion Therapeutics, Inc. | Methods of synthesizing egfr inhibitors |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US3966781A (en) | 1970-12-17 | 1976-06-29 | Merck Sharp & Dohme (I.A.) Corporation | Deuteration of functional group-containing hydrocarbons |
| US5011472A (en) | 1988-09-06 | 1991-04-30 | Brown University Research Foundation | Implantable delivery system for biological factors |
| AR056560A1 (es) | 2005-10-06 | 2007-10-10 | Astrazeneca Ab | Pirrolopiridinonas como moduladores cb1 |
| US20070142414A1 (en) | 2005-12-16 | 2007-06-21 | Pharmacia Italia S.P.A. | N-substituted pyrrolopyridinones active as kinase inhibitors |
| ES2389673T3 (es) | 2007-09-28 | 2012-10-30 | Nerviano Medical Sciences S.R.L. | Derivados de pirrolopirimidina sustituidos, procedimiento para su preparación y su uso como inhibidores de quinasas |
| CA2712959C (en) * | 2008-01-22 | 2015-06-23 | Vernalis (R & D) Ltd | Indolyl-pyridone derivatives having checkpoint kinase 1 inhibitory activity |
| EP2443117B1 (en) * | 2009-06-15 | 2016-03-23 | Nerviano Medical Sciences S.r.l. | Substituted pyrimidinylpyrrolopyridinone derivatives, process for their preparation and their use as kinase inhibitors |
| EP2675440B1 (en) | 2011-02-14 | 2020-03-25 | Merck Sharp & Dohme Corp. | Cathepsin cysteine protease inhibitors |
| UA111754C2 (uk) | 2011-10-06 | 2016-06-10 | Байєр Фарма Акцієнгезелльшафт | Заміщені бензиліндазоли для застосування як інгібіторів bub1-кінази для лікування гіперпроліферативних захворювань |
| JP6063945B2 (ja) * | 2011-10-07 | 2017-01-18 | ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ | キナーゼ阻害剤としての４−アルキル置換３，４−ジヒドロピロロ［１，２−ａ］ピラジン−１（２Ｈ）−オン誘導体 |
| CN103906732A (zh) | 2011-10-28 | 2014-07-02 | 株式会社钟根堂 | 用作hdac抑制剂的异羟肟酸酯衍生物以及包含所述衍生物的药物组合物 |
| WO2013092512A1 (en) | 2011-12-21 | 2013-06-27 | Bayer Intellectual Property Gmbh | Substituted benzylpyrazoles |
| JP2015520143A (ja) | 2012-05-11 | 2015-07-16 | バイエル ファーマ アクチエンゲゼルシャフト | 癌を治療するためのｂｕｂ１阻害薬としての置換されているシクロアルケノピラゾール類 |
| WO2014022752A1 (en) | 2012-08-03 | 2014-02-06 | Amgen Inc. | Macrocycles as pim inhibitors |
| CN104870446B (zh) | 2012-11-07 | 2019-08-13 | 内尔维阿诺医学科学有限公司 | 取代的嘧啶基和吡啶基吡咯并吡啶酮类、其制备方法及其作为激酶抑制剂的用途 |
| US20160046604A1 (en) | 2013-03-21 | 2016-02-18 | Bayer Pharma Aktiengesellschaft | Heteroaryl substituted indazoles |
| CA2907592A1 (en) * | 2013-03-21 | 2014-09-25 | Bayer Pharma Aktiengesellschaft | 3-heteroaryl substituted indazoles |
| WO2014202583A1 (en) | 2013-06-21 | 2014-12-24 | Bayer Pharma Aktiengesellschaft | Substituted benzylpyrazoles |
| US20160168130A1 (en) | 2013-06-21 | 2016-06-16 | Bayer Pharma Aktiengesellschaft | Heteroaryl substituted pyrazoles |
| WO2014202590A1 (en) | 2013-06-21 | 2014-12-24 | Bayer Pharma Aktiengesellschaft | Substituted benzylpyrazoles |
| CN105452237A (zh) | 2013-06-21 | 2016-03-30 | 拜耳制药股份公司 | 杂芳基取代的吡唑 |
| EP3033342A1 (en) | 2013-08-13 | 2016-06-22 | Grünenthal GmbH | Annelated pyrroles and their use as crac inhibitors |
| CA2952307A1 (en) * | 2014-06-17 | 2015-12-23 | Bayer Pharma Aktiengesellschaft | 3-amino-1,5,6,7-tetrahydro-4h-indol-4-ones |
| JP2018522847A (ja) | 2015-06-17 | 2018-08-16 | バイエル ファーマ アクチエンゲゼルシャフト | ３−アミノ−１，５，６，７−テトラヒドロ−４ｈ−インドール−４−オン類 |
| CA2994596A1 (en) | 2015-08-05 | 2017-02-09 | Bayer Pharma Aktiengesellschaft | 1h-pyrrol-3-amines |
| JP2019504826A (ja) | 2015-12-16 | 2019-02-21 | バイエル ファーマ アクチエンゲゼルシャフト | ヘテロ−１，５，６，７−テトラヒドロ−４ｈ−インドール−４−オン類 |
-
2016
- 2016-01-25 EP EP16701600.5A patent/EP3250567B1/en active Active
- 2016-01-25 BR BR112017016193-1A patent/BR112017016193B1/pt active IP Right Grant
- 2016-01-25 JP JP2017539454A patent/JP6704398B2/ja active Active
- 2016-01-25 MY MYPI2017702724A patent/MY182181A/en unknown
- 2016-01-25 CN CN201680013096.2A patent/CN107406417B/zh active Active
- 2016-01-25 EA EA201791692A patent/EA032530B1/ru not_active IP Right Cessation
- 2016-01-25 US US15/547,032 patent/US10428063B2/en active Active
- 2016-01-25 AU AU2016212230A patent/AU2016212230B2/en active Active
- 2016-01-25 MX MX2017009831A patent/MX2017009831A/es unknown
- 2016-01-25 CU CUP2017000094A patent/CU20170094A7/es unknown
- 2016-01-25 CR CR20170345A patent/CR20170345A/es unknown
- 2016-01-25 WO PCT/EP2016/051432 patent/WO2016120196A1/en active Application Filing
- 2016-01-25 KR KR1020177023372A patent/KR102544847B1/ko active IP Right Grant
- 2016-01-25 TN TNP/2017/000329A patent/TN2017000329A1/en unknown
- 2016-01-25 PE PE2017001288A patent/PE20171240A1/es unknown
- 2016-01-25 SG SG11201705908VA patent/SG11201705908VA/en unknown
- 2016-01-25 CA CA2974853A patent/CA2974853C/en active Active
- 2016-01-25 UA UAA201708621A patent/UA122221C2/uk unknown
- 2016-01-27 JO JOP/2016/0014A patent/JO3706B1/ar active
- 2016-01-28 UY UY0001036544A patent/UY36544A/es not_active Application Discontinuation
- 2016-01-28 TW TW105102745A patent/TWI699359B/zh active
-
2017
- 2017-07-03 IL IL253284A patent/IL253284B/en active IP Right Grant
- 2017-07-25 PH PH12017501340A patent/PH12017501340A1/en unknown
- 2017-07-27 EC ECIEPI201748527A patent/ECSP17048527A/es unknown
- 2017-07-28 DO DO2017000176A patent/DOP2017000176A/es unknown
- 2017-07-28 SV SV2017005487A patent/SV2017005487A/es unknown
- 2017-07-28 NI NI201700096A patent/NI201700096A/es unknown
- 2017-07-28 CL CL2017001930A patent/CL2017001930A1/es unknown
- 2017-07-28 CO CONC2017/0007663A patent/CO2017007663A2/es unknown
- 2017-08-25 ZA ZA2017/05802A patent/ZA201705802B/en unknown
-
2018
- 2018-03-29 HK HK18104306.1A patent/HK1244804A1/zh unknown
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