MA44721A - Inhibiteurs de mcl1 macrocycliques pour le traitement du cancer - Google Patents
Inhibiteurs de mcl1 macrocycliques pour le traitement du cancerInfo
- Publication number
- MA44721A MA44721A MA044721A MA44721A MA44721A MA 44721 A MA44721 A MA 44721A MA 044721 A MA044721 A MA 044721A MA 44721 A MA44721 A MA 44721A MA 44721 A MA44721 A MA 44721A
- Authority
- MA
- Morocco
- Prior art keywords
- macrocyclic
- cancer treatment
- acid
- mcl1 inhibitors
- pentaazaheptacyclo
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D497/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D497/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D515/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D515/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains four or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
L'invention concerne un composé qui est l'acide 17-chloro-5,13,14,22-tétraméthyl-28-oxa-2,9-dithia-5,6,12,13,22-pentaazaheptacyclo[27.7.1.14,7.011,15.016,21.020,24.030,35]octatriaconta-1(37),4(38),6,11,14,16,18,20,23,29,31,33,35-tridécaène-23-carboxylique (formule 1), des énantiomères et des sels pharmaceutiquement acceptables correspondants. L'invention concerne également des compositions pharmaceutiques de l'acide 17-chloro-5,13,14,22-tétraméthyl-28-oxa-2,9-dithia-5,6,12,13,22-pentaazaheptacyclo[27.7.1.14,7.011,15.016,21.020,24.030,35]octatriaconta-1(37),4(38),6,11,14,16,18,20,23,29,31,33,35-tridécaène-23-carboxylique, et des énantiomères et des sels pharmaceutiquement acceptables correspondants, et des méthodes de traitement du cancer avec ces composés et ces compositions.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662326156P | 2016-04-22 | 2016-04-22 | |
| PCT/EP2017/059511 WO2017182625A1 (fr) | 2016-04-22 | 2017-04-21 | Inhibiteurs de mcl1 macrocycliques pour le traitement du cancer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA44721A true MA44721A (fr) | 2019-02-27 |
| MA44721B1 MA44721B1 (fr) | 2020-05-29 |
Family
ID=58664658
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA44721A MA44721B1 (fr) | 2016-04-22 | 2017-04-21 | Inhibiteurs de mcl1 macrocycliques pour le traitement du cancer |
Country Status (37)
| Country | Link |
|---|---|
| US (4) | US9840518B2 (fr) |
| EP (1) | EP3445767B1 (fr) |
| JP (1) | JP6894449B2 (fr) |
| KR (1) | KR102388208B1 (fr) |
| CN (1) | CN109071566B (fr) |
| AR (1) | AR108301A1 (fr) |
| AU (1) | AU2017252222B2 (fr) |
| BR (1) | BR112018070677B1 (fr) |
| CL (1) | CL2018002410A1 (fr) |
| CO (1) | CO2018008759A2 (fr) |
| CR (1) | CR20180499A (fr) |
| CY (1) | CY1123186T1 (fr) |
| DK (1) | DK3445767T3 (fr) |
| DO (1) | DOP2018000222A (fr) |
| EA (1) | EA036551B1 (fr) |
| ES (1) | ES2791319T3 (fr) |
| HR (1) | HRP20200673T1 (fr) |
| HU (1) | HUE049591T2 (fr) |
| IL (1) | IL262237B (fr) |
| LT (1) | LT3445767T (fr) |
| MA (1) | MA44721B1 (fr) |
| ME (1) | ME03729B (fr) |
| MX (1) | MX386103B (fr) |
| NI (1) | NI201800093A (fr) |
| PE (1) | PE20181803A1 (fr) |
| PH (1) | PH12018502227A1 (fr) |
| PL (1) | PL3445767T3 (fr) |
| PT (1) | PT3445767T (fr) |
| RS (1) | RS60257B1 (fr) |
| SG (1) | SG11201805838UA (fr) |
| SI (1) | SI3445767T1 (fr) |
| SM (1) | SMT202000249T1 (fr) |
| SV (1) | SV2018005742A (fr) |
| TN (1) | TN2018000319A1 (fr) |
| TW (1) | TWI742074B (fr) |
| WO (1) | WO2017182625A1 (fr) |
| ZA (1) | ZA201807766B (fr) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX380313B (es) | 2016-02-04 | 2025-03-12 | Univ Johns Hopkins | Rapadocinas, inhibidores de transportador 1 de nucleósido equilibrador y usos de los mismos. |
| US11066416B2 (en) | 2016-02-04 | 2021-07-20 | The Johns Hopkins University | Rapafucin derivative compounds and methods of use thereof |
| US11708391B2 (en) | 2016-02-04 | 2023-07-25 | The Johns Hopkins University | Rapaglutins, novel inhibitors of GLUT and use thereof |
| ES2791319T3 (es) | 2016-04-22 | 2020-11-03 | Astrazeneca Ab | Inhibidores de MCL1 macrocíclicos para tratar el cáncer |
| EP3458459B1 (fr) | 2016-05-19 | 2022-04-27 | Bayer Aktiengesellschaft | Derivés d'indole macrocycliques |
| TWI781996B (zh) * | 2017-03-31 | 2022-11-01 | 瑞典商阿斯特捷利康公司 | 合成mcl-1抑制劑之方法 |
| TW201904976A (zh) * | 2017-03-31 | 2019-02-01 | 瑞典商阿斯特捷利康公司 | Mcl-1抑制劑及其使用方法 |
| AU2018317828A1 (en) * | 2017-08-15 | 2020-04-02 | AbbVie Deutschland GmbH & Co. KG | Macrocyclic MCL-1 inhibitors and methods of use |
| US10676485B2 (en) | 2017-08-15 | 2020-06-09 | Abbvie Inc. | Macrocyclic MCL-1 inhibitors and methods of use |
| TWI810220B (zh) * | 2017-11-17 | 2023-08-01 | 德商拜耳廠股份有限公司 | 經取代之巨環吲哚衍生物 |
| US11286263B2 (en) | 2017-11-17 | 2022-03-29 | The Broad Institute, Inc. | Macrocyclic fluorine substituted indole derivatives |
| UY37972A (es) | 2017-11-17 | 2019-06-28 | Bayer Pharma AG | Derivados de indol macrocíclicos sustituidos con cloro |
| EP3710450A1 (fr) | 2017-11-17 | 2020-09-23 | Bayer Aktiengesellschaft | Dérivés d'indole macrocycliques substitués par du chlore |
| TW201932473A (zh) | 2017-11-17 | 2019-08-16 | 美商博德研究所有限公司 | 巨環吲哚衍生物 |
| WO2019096907A1 (fr) * | 2017-11-17 | 2019-05-23 | Bayer Aktiengesellschaft | Dérivés d'indole macrocycliques annelés aryle |
| TW202014184A (zh) * | 2018-04-30 | 2020-04-16 | 瑞典商阿斯特捷利康公司 | 用於治療癌症之組合 |
| CA3113917A1 (fr) * | 2018-09-30 | 2020-04-02 | Jiangsu Hengrui Medicine Co., Ltd. | Derive macrocyclique d'indole, son procede de preparation et son application en medecine |
| TW202344250A (zh) | 2018-11-14 | 2023-11-16 | 瑞典商阿斯特捷利康公司 | 治療癌症之方法 |
| CN111205309B (zh) * | 2018-11-21 | 2023-04-07 | 江苏恒瑞医药股份有限公司 | 吲哚类大环衍生物、其制备方法及其在医药上的应用 |
| EP3781570A4 (fr) * | 2018-11-22 | 2021-06-02 | Ascentage Pharma (Suzhou) Co., Ltd. | Indoles macrocycliques servant d'inhibiteurs de mcl-1 |
| WO2020151738A1 (fr) * | 2019-01-23 | 2020-07-30 | Ascentage Pharma (Suzhou) Co., Ltd. | Pyrrazoles fusionnés macrocycliques utilisés en tant qu'inhibiteurs de mcl-1 |
| BR112021017620A2 (pt) * | 2019-03-08 | 2021-11-09 | Zeno Man Inc | Compostos macrocíclicos |
| BR112021020257A2 (pt) | 2019-04-11 | 2021-12-07 | Bristol Myers Squibb Co | Desempenho intensificado de sólido amorfo e formulações solubilizadas para realizar concentrações de plasma terapêutico |
| CN113574058B (zh) * | 2019-04-30 | 2024-04-16 | 江苏恒瑞医药股份有限公司 | 吲哚类大环衍生物、其制备方法及其在医药上的应用 |
| BR112021022237A2 (pt) | 2019-05-10 | 2022-03-29 | Janssen Biotech Inc | Queladores macrocíclicos e métodos de uso dos mesmos |
| EP3969457B1 (fr) | 2019-05-17 | 2025-08-13 | The Broad Institute Inc. | Procédés de préparation d'indoles macrocycliques |
| KR20220024106A (ko) | 2019-05-20 | 2022-03-03 | 노파르티스 아게 | Mcl-1 억제제 항체-약물 접합체 및 사용 방법 |
| MA56505A (fr) | 2019-06-21 | 2022-04-27 | Janssen Pharmaceutica Nv | Inhibiteurs macrocycliques de mcl-1 |
| KR20220034136A (ko) | 2019-07-09 | 2022-03-17 | 얀센 파마슈티카 엔.브이. | Mcl-1 억제제로서의 거대환식 스피로사이클 유도체 |
| WO2021067405A1 (fr) * | 2019-10-01 | 2021-04-08 | The Johns Hopkins University | Composés neuroprotecteurs et leurs procédés d'utilisation |
| WO2021092053A1 (fr) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Composés macrocycliques inhibiteurs de mcl-1 destinés à être utilisées dans la gestion clinique d'états pathologiques provoqués ou induits par des cellules sénescentes ainsi que dans le traitement du cancer |
| WO2021092061A1 (fr) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Polythérapie pour le traitement de maladies associées à la sénescence |
| EP4061819A1 (fr) | 2019-11-21 | 2022-09-28 | Janssen Pharmaceutica NV | Dérivés indoles macrocycliques utilisés comme inhibiteurs de la mcl-1 |
| WO2021099580A1 (fr) | 2019-11-21 | 2021-05-27 | Janssen Pharmaceutica Nv | Dérivés de sulfonyle macrocycliques utilisés en tant qu'inhibiteurs de mcl-1 |
| JP2023510135A (ja) * | 2019-12-18 | 2023-03-13 | ゼノ マネジメント,インコーポレイテッド | 大環状化合物 |
| EP4107161A1 (fr) | 2020-02-21 | 2022-12-28 | Janssen Pharmaceutica NV | Dérivés d'indole macrocycliques en tant qu'inhibiteurs de mcl-1 |
| WO2021197295A1 (fr) * | 2020-03-30 | 2021-10-07 | 江苏恒瑞医药股份有限公司 | Forme cristalline d'un dérivé macrocyclique d'indole et son procédé de préparation |
| JP2023526985A (ja) * | 2020-05-29 | 2023-06-26 | ヤンセン ファーマシューティカ エヌ.ベー. | Mcl-1の阻害剤としての大環状7-ピラゾール-5-イル-インドール誘導体 |
| BR112022025674A2 (pt) | 2020-06-19 | 2023-01-17 | Janssen Pharmaceutica Nv | Derivados de 7-(pirazol-5-il)-indol macrocíclico n-ligado como inibidores de mcl-1 |
| WO2021255258A1 (fr) | 2020-06-19 | 2021-12-23 | Janssen Pharmaceutica Nv | Dérivés de 4-(pyrazol-5-yl)-indole macrocycliques à liaison n utiles en tant qu'inhibiteurs de mcl-1 |
| BR112023000212A2 (pt) | 2020-07-08 | 2023-01-31 | Janssen Pharmaceutica Nv | Éter macrocíclico contendo derivados de indol como inibidores de mcl-1 |
| WO2022032284A1 (fr) * | 2020-08-07 | 2022-02-10 | Zeno Management, Inc. | Composés macrocycliques |
| IL303079A (en) | 2020-11-24 | 2023-07-01 | Novartis Ag | Mcl-1 inhibitor antibody-drug conjugates and methods of use |
| CA3200758A1 (fr) | 2020-12-17 | 2022-06-23 | Janssen Pharmaceutica Nv | Derives de 4-(pyrazol-5-yl)-indole macrocycliques ramifies utilises en tant qu'inhibiteurs de mcl-1 |
| CN116848126A (zh) | 2021-02-12 | 2023-10-03 | 詹森药业有限公司 | 大环1,3-桥联的6-氯-7-吡唑-4-基-1h-吲哚-2-羧酸酯和6-氯-7-嘧啶-5-基-1h-吲哚-2-羧酸酯衍生物作为mcl-1抑制剂用于治疗癌症 |
| WO2022251247A1 (fr) * | 2021-05-28 | 2022-12-01 | Zeno Management, Inc. | Composés macrocycliques |
| TWI910028B (zh) | 2021-06-11 | 2025-12-21 | 美商基利科學股份有限公司 | Mcl-1抑制劑與抗癌劑之組合 |
| US11931424B2 (en) | 2021-06-11 | 2024-03-19 | Gilead Sciences, Inc. | Combination MCL-1 inhibitors with anti-body drug conjugates |
| CN115490708B (zh) * | 2021-06-18 | 2025-01-24 | 苏州亚盛药业有限公司 | 磺酰胺类大环衍生物及其制备方法和用途 |
| US20240401146A1 (en) | 2021-10-06 | 2024-12-05 | Institut National de la Santé et de la Recherche Médicale | Methods for predicting and improving the efficacy of mcl-1 inhibitor therapy |
| US20250387504A1 (en) | 2022-05-20 | 2025-12-25 | Novartis Ag | Antibody-drug conjugates of antineoplastic compounds and methods of use thereof |
| PY24103486A (es) | 2023-11-22 | 2025-06-06 | Servier Lab | Conjugados de anticuerpo anti-cd74-fármaco y métodos de uso de los mismos |
| AR134424A1 (es) | 2023-11-22 | 2026-01-14 | Novartis Ag | Conjugados de anticuerpo anti-cd7-fármaco y métodos de uso de los mismos |
| TW202530255A (zh) | 2023-12-15 | 2025-08-01 | 法商亞維西亞有限公司 | 抗il-1rap結合結構域及其抗體-藥物偶聯物 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2951295C (fr) | 2007-04-16 | 2020-04-28 | Abbvie Inc. | Inhibiteurs mcl-1 indole 7-non-substitues |
| MY162157A (en) * | 2007-04-16 | 2017-05-31 | Abbott Lab | Substituted indole mcl-1 inhibitors |
| BRPI0923567A2 (pt) * | 2008-12-22 | 2016-09-27 | Cubist Pharm Inc | agentes antibactericidas novos para o tratamento de infecções gram positivas |
| JP5731538B2 (ja) * | 2009-12-23 | 2015-06-10 | アイアンウッド ファーマシューティカルズ インコーポレイテッド | Crth2モジュレーター |
| PL2710018T3 (pl) * | 2011-05-19 | 2022-04-04 | Fundación Del Sector Público Estatal Centro Nacional De Investigaciones Oncológicas Carlos III (F.S.P. CNIO) | Związki makrocykliczne jako inhibitory kinaz białkowych |
| WO2014047427A2 (fr) | 2012-09-21 | 2014-03-27 | Vanderbilt University | Inhibiteurs de la mcl-1 à base de benzofurane, de benzothiophène et d'indole substitués |
| CA2922341C (fr) | 2013-08-28 | 2022-06-07 | Vanderbilt University | Inhibiteurs de mcl-1 de type indole substitue |
| EP3105236B1 (fr) * | 2014-02-12 | 2017-10-18 | ViiV Healthcare UK (No.5) Limited | Utilisation de macrocycles de benzothiazole comme qu'inhibiteurs de la réplication du virus de l'immunodéficience humaine |
| CN106456602B (zh) | 2014-03-27 | 2020-11-24 | 范德比尔特大学 | 取代的吲哚mcl-1抑制剂 |
| WO2015155197A1 (fr) * | 2014-04-11 | 2015-10-15 | Bayer Pharma Aktiengesellschaft | Nouveaux composés macrocycliques |
| US9949965B2 (en) | 2014-10-17 | 2018-04-24 | Vanderbilt University | Tricyclic indole Mcl-1 inhibitors and uses thereof |
| ES2791319T3 (es) | 2016-04-22 | 2020-11-03 | Astrazeneca Ab | Inhibidores de MCL1 macrocíclicos para tratar el cáncer |
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2017
- 2017-04-21 ES ES17720720T patent/ES2791319T3/es active Active
- 2017-04-21 MA MA44721A patent/MA44721B1/fr unknown
- 2017-04-21 AR ARP170101026A patent/AR108301A1/es active IP Right Grant
- 2017-04-21 WO PCT/EP2017/059511 patent/WO2017182625A1/fr not_active Ceased
- 2017-04-21 CN CN201780022366.0A patent/CN109071566B/zh active Active
- 2017-04-21 TW TW106113380A patent/TWI742074B/zh active
- 2017-04-21 PT PT177207206T patent/PT3445767T/pt unknown
- 2017-04-21 EA EA201892300A patent/EA036551B1/ru not_active IP Right Cessation
- 2017-04-21 CR CR20180499A patent/CR20180499A/es unknown
- 2017-04-21 EP EP17720720.6A patent/EP3445767B1/fr active Active
- 2017-04-21 PL PL17720720T patent/PL3445767T3/pl unknown
- 2017-04-21 BR BR112018070677-9A patent/BR112018070677B1/pt active IP Right Grant
- 2017-04-21 SM SM20200249T patent/SMT202000249T1/it unknown
- 2017-04-21 CO CONC2018/0008759A patent/CO2018008759A2/es unknown
- 2017-04-21 JP JP2018553226A patent/JP6894449B2/ja active Active
- 2017-04-21 HR HRP20200673TT patent/HRP20200673T1/hr unknown
- 2017-04-21 LT LTEP17720720.6T patent/LT3445767T/lt unknown
- 2017-04-21 US US15/493,210 patent/US9840518B2/en active Active
- 2017-04-21 PE PE2018001558A patent/PE20181803A1/es unknown
- 2017-04-21 DK DK17720720.6T patent/DK3445767T3/da active
- 2017-04-21 HU HUE17720720A patent/HUE049591T2/hu unknown
- 2017-04-21 SG SG11201805838UA patent/SG11201805838UA/en unknown
- 2017-04-21 ME MEP-2020-99A patent/ME03729B/fr unknown
- 2017-04-21 AU AU2017252222A patent/AU2017252222B2/en active Active
- 2017-04-21 MX MX2018012711A patent/MX386103B/es unknown
- 2017-04-21 KR KR1020187033540A patent/KR102388208B1/ko active Active
- 2017-04-21 TN TNP/2018/000319A patent/TN2018000319A1/en unknown
- 2017-04-21 SI SI201730246T patent/SI3445767T1/sl unknown
- 2017-04-21 RS RS20200549A patent/RS60257B1/sr unknown
- 2017-10-23 US US15/790,660 patent/US10196404B2/en active Active
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2018
- 2018-08-23 CL CL2018002410A patent/CL2018002410A1/es unknown
- 2018-09-12 SV SV2018005742A patent/SV2018005742A/es unknown
- 2018-09-25 NI NI201800093A patent/NI201800093A/es unknown
- 2018-10-05 DO DO2018000222A patent/DOP2018000222A/es unknown
- 2018-10-09 IL IL262237A patent/IL262237B/en unknown
- 2018-10-18 PH PH12018502227A patent/PH12018502227A1/en unknown
- 2018-11-19 ZA ZA2018/07766A patent/ZA201807766B/en unknown
- 2018-12-18 US US16/223,538 patent/US10889594B2/en active Active
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2020
- 2020-05-14 CY CY20201100443T patent/CY1123186T1/el unknown
- 2020-12-04 US US17/111,896 patent/US11472816B2/en active Active
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