MX2022013006A - Inhibidor de bcl-2. - Google Patents
Inhibidor de bcl-2.Info
- Publication number
- MX2022013006A MX2022013006A MX2022013006A MX2022013006A MX2022013006A MX 2022013006 A MX2022013006 A MX 2022013006A MX 2022013006 A MX2022013006 A MX 2022013006A MX 2022013006 A MX2022013006 A MX 2022013006A MX 2022013006 A MX2022013006 A MX 2022013006A
- Authority
- MX
- Mexico
- Prior art keywords
- bcl
- inhibitor
- compound
- disclosed
- inhibiting
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
- A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
-
- 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
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur 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
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/05—Isotopically modified compounds, e.g. labelled
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
En la presente se describe un compuesto de la Fórmula (I) para inhibir tanto Bcl-2 de tipo silvestre como Bcl-2 mutado, en particular, Bcl-2 G101V y D103Y, y un método para usar el compuesto divulgado en la presente para el tratamiento contra enfermedades apoptóticas no reguladas.
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2020084992 | 2020-04-15 | ||
| CN2020100472 | 2020-07-06 | ||
| CN2020125580 | 2020-10-30 | ||
| CN2021075831 | 2021-02-07 | ||
| CN2021086189 | 2021-04-09 | ||
| PCT/CN2021/087225 WO2021208963A1 (en) | 2020-04-15 | 2021-04-14 | Bcl-2 inhibitor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2022013006A true MX2022013006A (es) | 2023-01-11 |
Family
ID=78083530
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2022013006A MX2022013006A (es) | 2020-04-15 | 2021-04-14 | Inhibidor de bcl-2. |
Country Status (13)
| Country | Link |
|---|---|
| US (3) | US12286430B2 (es) |
| EP (1) | EP4136084A4 (es) |
| JP (1) | JP2023520843A (es) |
| KR (1) | KR20230002419A (es) |
| CN (3) | CN116802179A (es) |
| AU (1) | AU2021256580A1 (es) |
| BR (1) | BR112022019525A2 (es) |
| CA (1) | CA3172478A1 (es) |
| IL (1) | IL296582A (es) |
| MX (1) | MX2022013006A (es) |
| TW (1) | TW202200574A (es) |
| WO (1) | WO2021208963A1 (es) |
| ZA (1) | ZA202209891B (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL296582A (en) * | 2020-04-15 | 2022-11-01 | Beigene Ltd | bcl-2 inhibitor |
| WO2022213335A1 (en) * | 2021-04-09 | 2022-10-13 | Beigene (Beijing) Co., Ltd. | Method for preparing intermediate of bcl-2 inhibitor |
| WO2023078398A1 (en) * | 2021-11-05 | 2023-05-11 | Fochon Pharmaceuticals, Ltd. | Compounds as bcl-2 inhibitors |
| JP2024540590A (ja) * | 2021-11-20 | 2024-10-31 | フォチョン・バイオサイエンシーズ・リミテッド | Bcl-2阻害剤としての化合物 |
| KR20240135747A (ko) * | 2021-12-06 | 2024-09-12 | 항저우 힐젠 테라퓨틱스 컴퍼니 리미티드 | 항-세포사멸 단백질 bcl-2 억제제, 약학적 조성물 및 이의 응용 |
| WO2023122000A1 (en) * | 2021-12-20 | 2023-06-29 | Newave Pharmaceutical Inc. | Bcl-2 inhibitors |
| CN114292192A (zh) * | 2022-01-17 | 2022-04-08 | 山东泓瑞医药科技股份公司 | 一种3,4-二甲氧基苯甲酸甲酯的合成方法 |
| KR20240161147A (ko) | 2022-03-14 | 2024-11-12 | 슬랩 파마슈티컬스 엘엘씨 | 다중 사이클릭 화합물 |
| WO2023231777A1 (en) * | 2022-06-01 | 2023-12-07 | Fochon Pharmaceuticals, Ltd. | Compounds as bcl-2 inhibitors |
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| AR031130A1 (es) | 2000-09-20 | 2003-09-10 | Abbott Lab | N-acilsulfonamidas promotoras de la apoptosis |
| US20020055631A1 (en) | 2000-09-20 | 2002-05-09 | Augeri David J. | N-acylsulfonamide apoptosis promoters |
| WO2005049593A2 (en) | 2003-11-13 | 2005-06-02 | Abbott Laboratories | N-acylsulfonamide apoptosis promoters |
| AU2005277223C1 (en) | 2004-08-20 | 2009-05-21 | The Regents Of The University Of Michigan | Small molecule inhibitors of anti-apoptotic Bcl-2 family members and the uses thereof |
| EP1888550B1 (en) | 2005-05-12 | 2014-06-25 | AbbVie Bahamas Ltd. | Apoptosis promoters |
| MX2007014783A (es) | 2005-05-24 | 2008-02-19 | Abbott Lab | Activadores de apoptosis. |
| WO2008030836A2 (en) | 2006-09-05 | 2008-03-13 | Abbott Laboratories | Bcl inhibitors treating platelet excess |
| WO2009036051A1 (en) | 2007-09-10 | 2009-03-19 | Curis, Inc. | Bcl-2 inhibitors containing a zinc binding moiety |
| ATE540026T1 (de) | 2008-06-09 | 2012-01-15 | Bristol Myers Squibb Co | Hydroxyphenylsulfonsäureamide als antiapoptotische bcl-inhibitoren |
| US8168784B2 (en) | 2008-06-20 | 2012-05-01 | Abbott Laboratories | Processes to make apoptosis promoters |
| UA108193C2 (uk) | 2008-12-04 | 2015-04-10 | Апоптозіндукуючий засіб для лікування раку і імунних і аутоімунних захворювань | |
| US8563735B2 (en) | 2008-12-05 | 2013-10-22 | Abbvie Inc. | Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases |
| CA2744711C (en) | 2008-12-05 | 2017-06-27 | Abbott Laboratories | Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases |
| EP2373629B1 (en) | 2008-12-08 | 2013-04-10 | Boehringer Ingelheim International Gmbh | Compounds for treating cancer |
| PL2511264T3 (pl) | 2009-01-19 | 2015-08-31 | Abbvie Inc | Środki indukujące apoptozę do leczenia raka oraz chorób immunologicznych i autoimmunologicznych |
| AU2010204555B2 (en) | 2009-01-19 | 2013-03-07 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| US8546399B2 (en) | 2009-05-26 | 2013-10-01 | Abbvie Inc. | Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases |
| PE20120345A1 (es) | 2009-05-26 | 2012-05-17 | Abbvie Bahamas Ltd | Derivados de 2-(1h-pirrolo[2,3-b]piridin-5-iloxi)-n-fenilsulfonilbenzamida como inhibidores de proteinas anti-apoptoticas |
| CN102498111A (zh) | 2009-09-10 | 2012-06-13 | 诺瓦提斯公司 | 作为Bcl-2家族蛋白抑制剂用于癌症的治疗的磺酰胺化合物 |
| EP2957558A3 (en) | 2010-03-25 | 2016-03-02 | AbbVie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| TWI520960B (zh) | 2010-05-26 | 2016-02-11 | 艾伯維有限公司 | 用於治療癌症及免疫及自體免疫疾病之細胞凋亡誘導劑 |
| TWI535712B (zh) | 2010-08-06 | 2016-06-01 | 阿斯特捷利康公司 | 化合物 |
| NZ608274A (en) | 2010-10-29 | 2015-05-29 | Abbvie Inc | Solid dispersions containing an apoptosis-inducing agent |
| IT1403156B1 (it) | 2010-12-01 | 2013-10-04 | Università Degli Studi Di Torino | Inibitori di fosfatidilinositol 3-chinasi, relative composizioni ed usi. |
| US8691184B2 (en) | 2011-01-25 | 2014-04-08 | The Regents Of The University Of Michigan | Bcl-2/Bcl-xL inhibitors and therapeutic methods using the same |
| EP2714681B1 (en) | 2011-05-25 | 2015-06-24 | Bristol-Myers Squibb Company | Substituted sulfonamides useful as antiapoptotic bcl inhibitors |
| WO2013053045A1 (en) | 2011-10-12 | 2013-04-18 | Beta Pharma Canada Inc. | Heterocyclic molecules as apoptosis inducers |
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| EA201491259A1 (ru) | 2011-12-23 | 2014-11-28 | Новартис Аг | Соединения и композиции для ингибирования взаимодействия bcl2 с партнерами связывания |
| MX2014007731A (es) | 2011-12-23 | 2015-01-12 | Novartis Ag | Compuestos para inhibir la interaccion de bcl2 con los componentes de enlace. |
| EA201491265A1 (ru) | 2011-12-23 | 2014-11-28 | Новартис Аг | Соединения для ингибирования взаимодействия bcl-2 с партнерами по связыванию |
| MX2014007729A (es) | 2011-12-23 | 2015-01-12 | Novartis Ag | Compuestos para inhibir la interaccion de bcl2 con los componentes de enlace. |
| WO2013185202A1 (en) | 2012-06-14 | 2013-12-19 | Beta Pharma Canada Inc | Apoptosis inducers |
| US9096625B2 (en) | 2013-01-16 | 2015-08-04 | The Regents Of The University Of Michigan | BCL-2/BCL-XL inhibitors and therapeutic methods using the same |
| US20140275082A1 (en) | 2013-03-14 | 2014-09-18 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| CN104884458B (zh) | 2013-04-25 | 2017-04-12 | 百济神州有限公司 | 作为蛋白质激酶抑制剂的稠合杂环化合物 |
| AU2014339816B2 (en) | 2013-10-25 | 2020-05-28 | Pharmacyclics Llc | Treatment using Bruton's tyrosine kinase inhibitors and immunotherapy |
| DK3179991T3 (da) | 2014-08-11 | 2021-12-06 | Acerta Pharma Bv | Terapeutiske kombinationer af en btk-inhibitor og en bcl-2-inhibitor |
| WO2017132474A1 (en) | 2016-01-30 | 2017-08-03 | Newave Pharmaceutical Inc. | Bcl-2 inhibitors |
| US20190225607A1 (en) | 2016-07-06 | 2019-07-25 | Concert Pharmaceuticals, Inc. | Deuterated Venetoclax |
| LT3494115T (lt) | 2016-08-05 | 2021-01-25 | The Regents Of The University Of Michigan | N-(fenilsulfonil)benzamido dariniai kaip bcl-2 inhibitoriai |
| CN109641897B (zh) | 2016-09-01 | 2021-12-07 | 北京赛林泰医药技术有限公司 | Bcl-2选择性抑制剂及其制备和用途 |
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| CN106749233B (zh) * | 2016-11-24 | 2020-04-21 | 中山大学 | 一类磺酰胺衍生物及其应用 |
| CN108002087B (zh) * | 2017-01-03 | 2019-05-10 | 东莞理工学院 | 一种多种宽度规格的新旧smt接料带的粘接机 |
| WO2018127130A1 (en) | 2017-01-07 | 2018-07-12 | Shanghai Fochon Pharmaceutical Co., Ltd. | Compounds as bcl-2-selective apoptosis-inducing agents |
| PT3612531T (pt) | 2017-04-18 | 2022-10-04 | Shanghai Fochon Pharmaceutical Co Ltd | Agentes indutores de apoptose |
| ES3028360T3 (en) | 2017-06-26 | 2025-06-19 | Shenzhen Targetrx Inc | Deuterated n-benzenesulfonylbenzamide compound for inhibiting bcl-2 protein and composition and use thereof |
| CN111511748B (zh) | 2017-08-23 | 2023-05-02 | 广州麓鹏制药有限公司 | Bcl-2抑制剂 |
| FR3072679B1 (fr) | 2017-10-25 | 2020-10-30 | Servier Lab | Nouveaux derives macrocycliques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| CN110143974B (zh) | 2018-02-11 | 2021-07-13 | 中国科学院上海药物研究所 | 一类新型青蒿素衍生物、合成方法及其用途 |
| US11420968B2 (en) | 2018-04-29 | 2022-08-23 | Beigene, Ltd. | Bcl-2 inhibitors |
| CN110772521A (zh) | 2018-07-31 | 2020-02-11 | 苏州亚盛药业有限公司 | Bcl-2抑制剂或Bcl-2/Bcl-xL抑制剂与BTK抑制剂的组合产品及其用途 |
| AU2019314819A1 (en) | 2018-07-31 | 2020-10-22 | Ascentage Pharma (Suzhou) Co., Ltd. | Combination product of Bcl-2 inhibitor and chemotherapeutic agent and use thereof in the prevention and/or treatment of diseases |
| WO2020140005A2 (en) * | 2018-12-29 | 2020-07-02 | Newave Pharmaceutical Inc. | Bcl-2 inhibitors |
| CN114929689B (zh) | 2019-10-28 | 2024-08-27 | 百济神州有限公司 | Bcl-2抑制剂 |
| WO2021110102A1 (en) | 2019-12-02 | 2021-06-10 | Beigene, Ltd. | Methods of cancer treatment using bcl-2 inhibitor |
| IL296582A (en) | 2020-04-15 | 2022-11-01 | Beigene Ltd | bcl-2 inhibitor |
| WO2022213335A1 (en) | 2021-04-09 | 2022-10-13 | Beigene (Beijing) Co., Ltd. | Method for preparing intermediate of bcl-2 inhibitor |
| PH12023553203A1 (en) | 2021-06-02 | 2024-02-19 | Beigene Switzerland Gmbh | Methods of treating b-cell malignancy using bcl-2 inhibitor |
| TW202328125A (zh) | 2021-08-31 | 2023-07-16 | 英屬開曼群島商百濟神州有限公司 | Bcl-2抑制劑的固體形式、製備方法及其用途 |
| TW202400163A (zh) | 2022-05-12 | 2024-01-01 | 英屬開曼群島商百濟神州有限公司 | 使用bcl-2抑制劑治療髓性惡性腫瘤之方法 |
| CA3262418A1 (en) | 2022-07-21 | 2024-01-25 | Beigene Switzerland Gmbh | METHODS OF TREATMENT OF MULTIPLE MYELOMA USING A BCL-2 INHIBITOR |
-
2021
- 2021-04-14 IL IL296582A patent/IL296582A/en unknown
- 2021-04-14 CN CN202180029718.1A patent/CN116802179A/zh active Pending
- 2021-04-14 CA CA3172478A patent/CA3172478A1/en active Pending
- 2021-04-14 CN CN202310560508.6A patent/CN116969937A/zh active Pending
- 2021-04-14 CN CN202310559385.4A patent/CN116969936A/zh active Pending
- 2021-04-14 TW TW110113455A patent/TW202200574A/zh unknown
- 2021-04-14 BR BR112022019525A patent/BR112022019525A2/pt unknown
- 2021-04-14 EP EP21789482.3A patent/EP4136084A4/en active Pending
- 2021-04-14 AU AU2021256580A patent/AU2021256580A1/en active Pending
- 2021-04-14 JP JP2022554627A patent/JP2023520843A/ja active Pending
- 2021-04-14 WO PCT/CN2021/087225 patent/WO2021208963A1/en not_active Ceased
- 2021-04-14 US US17/916,845 patent/US12286430B2/en active Active
- 2021-04-14 MX MX2022013006A patent/MX2022013006A/es unknown
- 2021-04-14 KR KR1020227035815A patent/KR20230002419A/ko active Pending
-
2022
- 2022-09-05 ZA ZA2022/09891A patent/ZA202209891B/en unknown
-
2024
- 2024-03-01 US US18/593,497 patent/US20240376097A1/en not_active Abandoned
-
2025
- 2025-01-23 US US19/035,219 patent/US20250270210A1/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| US20240376097A1 (en) | 2024-11-14 |
| BR112022019525A2 (pt) | 2023-11-14 |
| US20230159522A1 (en) | 2023-05-25 |
| ZA202209891B (en) | 2023-05-31 |
| TW202200574A (zh) | 2022-01-01 |
| AU2021256580A1 (en) | 2022-09-29 |
| IL296582A (en) | 2022-11-01 |
| US12286430B2 (en) | 2025-04-29 |
| CA3172478A1 (en) | 2021-10-21 |
| CN116969936A (zh) | 2023-10-31 |
| JP2023520843A (ja) | 2023-05-22 |
| CN116969937A (zh) | 2023-10-31 |
| CN116802179A (zh) | 2023-09-22 |
| KR20230002419A (ko) | 2023-01-05 |
| US20250270210A1 (en) | 2025-08-28 |
| WO2021208963A1 (en) | 2021-10-21 |
| EP4136084A4 (en) | 2023-11-01 |
| EP4136084A1 (en) | 2023-02-22 |
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