JP7762957B2 - Mettl3阻害化合物 - Google Patents
Mettl3阻害化合物Info
- Publication number
- JP7762957B2 JP7762957B2 JP2021560410A JP2021560410A JP7762957B2 JP 7762957 B2 JP7762957 B2 JP 7762957B2 JP 2021560410 A JP2021560410 A JP 2021560410A JP 2021560410 A JP2021560410 A JP 2021560410A JP 7762957 B2 JP7762957 B2 JP 7762957B2
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- pyridin
- imidazo
- carboxamide
- oxo
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Communicable Diseases (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1904848.7 | 2019-04-05 | ||
| GBGB1904848.7A GB201904848D0 (en) | 2019-04-05 | 2019-04-05 | Inhibitory compounds |
| GBGB1912603.6A GB201912603D0 (en) | 2019-09-02 | 2019-09-02 | Inhibitory compounds |
| GB1912603.6 | 2019-09-02 | ||
| GBGB1919095.8A GB201919095D0 (en) | 2019-12-20 | 2019-12-20 | Inhibitory compounds |
| GB1919095.8 | 2019-12-20 | ||
| PCT/GB2020/050898 WO2020201773A1 (en) | 2019-04-05 | 2020-04-03 | Mettl3 inhibitory compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2022528562A JP2022528562A (ja) | 2022-06-14 |
| JPWO2020201773A5 JPWO2020201773A5 (enExample) | 2023-04-10 |
| JP7762957B2 true JP7762957B2 (ja) | 2025-10-31 |
Family
ID=70285722
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021560410A Active JP7762957B2 (ja) | 2019-04-05 | 2020-04-03 | Mettl3阻害化合物 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US12358915B2 (enExample) |
| EP (1) | EP3946618A1 (enExample) |
| JP (1) | JP7762957B2 (enExample) |
| CN (1) | CN113905787A (enExample) |
| WO (1) | WO2020201773A1 (enExample) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018165520A1 (en) | 2017-03-10 | 2018-09-13 | Vps-3, Inc. | Metalloenzyme inhibitor compounds |
| HUE067314T2 (hu) | 2017-09-22 | 2024-10-28 | Jubilant Epipad LLC | Heterociklusos vegyületek mint PAD gátlók |
| KR102782563B1 (ko) | 2017-10-18 | 2025-03-14 | 주빌런트 에피파드 엘엘씨 | Pad 억제제로서의 이미다조-피리딘 화합물 |
| KR20200085836A (ko) | 2017-11-06 | 2020-07-15 | 주빌런트 프로델 엘엘씨 | Pd1/pd-l1 활성화 억제제로서의 피리미딘 유도체 |
| BR112020010322A2 (pt) | 2017-11-24 | 2020-11-17 | Jubilant Episcribe Llc | composto da fórmula i; composto da fórmula ia; composto da fórmula ib; processo de preparação de compostos da fórmula i; composição farmacêutica; método para o tratamento e/ou prevenção de várias doenças; uso dos compostos; método para o tratamento de câncer; e método para o tratamento e/ou prevenção de uma afecção mediada por prmt5 ou um distúrbio proliferativo ou câncer |
| SG11202008950PA (en) | 2018-03-13 | 2020-10-29 | Jubilant Prodel LLC | Bicyclic compounds as inhibitors of pd1/pd-l1 interaction/activation |
| KR20210125471A (ko) | 2018-10-05 | 2021-10-18 | 안나푸르나 바이오, 인코포레이티드 | Apj 수용체 활성과 관련된 병태를 치료하기 위한 화합물 및 조성물 |
| BR112022010561A2 (pt) | 2019-12-02 | 2022-11-16 | Storm Therapeutics Ltd | Compostos poli-heterocíclicos como inibidores de mettl3 |
| US20230391770A1 (en) * | 2020-10-06 | 2023-12-07 | Storm Therapeutics Limited | Mettl3 inhibitory compounds |
| US11944608B2 (en) * | 2020-10-26 | 2024-04-02 | New York University | Targeting RNA viruses using inhibitors of METTL3 |
| CA3219183A1 (en) * | 2021-05-17 | 2022-11-24 | Amedeo Caflisch | N6-adenosine-methyltransferase inhibitors in cancer treatment |
| GB202107905D0 (en) * | 2021-06-02 | 2021-07-14 | Storm Therapeutics Ltd | Processes for the preparation of inhibitory compounds |
| GB202107907D0 (en) * | 2021-06-02 | 2021-07-14 | Storm Therapeutics Ltd | Combination therapies |
| WO2023104209A1 (zh) * | 2021-12-10 | 2023-06-15 | 上海昂阔医药有限公司 | Mettl3抑制剂化合物 |
| CN118660890A (zh) * | 2022-02-11 | 2024-09-17 | 西藏海思科制药有限公司 | 一种mettl3抑制剂及组合物及其在医药上的应用 |
| CN114869891A (zh) * | 2022-04-28 | 2022-08-09 | 复旦大学附属中山医院 | Mettl3抑制剂在制备治疗肝癌药物中的应用 |
| WO2023217109A1 (zh) * | 2022-05-13 | 2023-11-16 | 中国科学院广州生物医药与健康研究院 | m6A RNA甲基化酶抑制剂与免疫检查点抑制剂联合治疗肿瘤 |
| JP2025530847A (ja) * | 2022-09-16 | 2025-09-17 | 北京華益健康薬物研究中心 | Mettl3阻害剤化合物、その医薬組成物及び用途 |
| WO2024107763A1 (en) * | 2022-11-16 | 2024-05-23 | University Of Zurich | N6-adenosine-methyltransferase protacs and methods of use thereof |
| GB202218672D0 (en) | 2022-12-12 | 2023-01-25 | Storm Therapeutics Ltd | Inhibitory compounds |
| CN120731203A (zh) | 2023-01-20 | 2025-09-30 | 艾匹克治疗公司 | 作为mettl3抑制剂的哌啶衍生物 |
| WO2024200835A1 (en) | 2023-03-30 | 2024-10-03 | Novalix | Novel mettl3 inhibitors and use thereof in therapy |
| GB202316683D0 (en) * | 2023-10-31 | 2023-12-13 | Storm Therapeutics Ltd | Inhibitory compounds |
| WO2025237957A1 (en) | 2024-05-14 | 2025-11-20 | Institut Curie | Composition for treatment of estrogen-dependent cancer comprising a mettl-3 inhibitor and a topoisomerase-1 inhibitor |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003506387A (ja) | 1999-08-04 | 2003-02-18 | アイカゲン インコーポレイテッド | カリウムチャンネルオープナーとしてのベンズアニリド |
| JP2004517080A (ja) | 2000-11-29 | 2004-06-10 | グラクソ グループ リミテッド | Tie−2および/またはvegfr−2の阻害剤として有用なベンゾイミダゾール誘導体 |
| JP2005509003A (ja) | 2001-11-09 | 2005-04-07 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | タンパク質キナーゼインヒビターとして有用なベンゾイミダゾール化合物 |
| WO2008016131A1 (en) | 2006-08-04 | 2008-02-07 | Takeda Pharmaceutical Company Limited | Fused heterocyclic compound |
| JP2009530233A (ja) | 2006-02-14 | 2009-08-27 | ノバルティス アーゲー | Pi−3キナーゼインヒビターおよびそれらの使用方法 |
| JP2010527909A (ja) | 2007-06-05 | 2010-08-19 | 武田薬品工業株式会社 | キナーゼ阻害剤としての二環式複素環化合物 |
| JP2011509250A (ja) | 2008-01-02 | 2011-03-24 | サノフイ−アベンテイス | N−複素環式イミダゾ[1,2−a]ピリジン−2−カルボキサミドの誘導体、この調製およびこの治療的用途 |
| WO2018169994A1 (en) | 2017-03-13 | 2018-09-20 | City Of Hope | m6A mRNA MODIFICATION IN CANCER TREATMENT |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3880874A (en) * | 1973-10-04 | 1975-04-29 | Syntex Inc | 2-Substituted -1,2,4-thiadiazolo-(2,3-a)benzimidazoles and process for their preparation |
| US3946031A (en) * | 1973-10-04 | 1976-03-23 | Syntex Inc. | 2-Substituted-1,2,4-thiadiazolo-[2,3-a]-benzimidazoles |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| PL194689B1 (pl) | 1996-02-13 | 2007-06-29 | Astrazeneca Uk Ltd | Pochodne chinazoliny, ich kompozycje farmaceutyczne oraz ich zastosowania |
| EP0885198B1 (en) | 1996-03-05 | 2001-12-19 | AstraZeneca AB | 4-anilinoquinazoline derivatives |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
| GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
| TR200500745T2 (tr) | 1999-02-10 | 2005-05-23 | Astrazeneca Ab | Damar gelişimi inhibitörleri olarak kuinazolin türevleri. |
| DE19936780A1 (de) | 1999-08-09 | 2001-02-15 | Basf Ag | Neue Antagonisten von Integrinrezeptoren |
| EP1289952A1 (en) | 2000-05-31 | 2003-03-12 | AstraZeneca AB | Indole derivatives with vascular damaging activity |
| UA73993C2 (uk) | 2000-06-06 | 2005-10-17 | Астразенека Аб | Хіназолінові похідні для лікування пухлин та фармацевтична композиція |
| WO2002008213A1 (en) | 2000-07-07 | 2002-01-31 | Angiogene Pharmaceuticals Limited | Colchinol derivatives as angiogenesis inhibitors |
| CN1255391C (zh) | 2000-07-07 | 2006-05-10 | 安吉奥金尼药品有限公司 | 作为血管破坏剂的colchinol衍生物 |
| NZ602311A (en) | 2010-03-18 | 2014-08-29 | Pasteur Institut Korea | Anti-infective compounds |
| BR112022010561A2 (pt) * | 2019-12-02 | 2022-11-16 | Storm Therapeutics Ltd | Compostos poli-heterocíclicos como inibidores de mettl3 |
-
2020
- 2020-04-03 JP JP2021560410A patent/JP7762957B2/ja active Active
- 2020-04-03 CN CN202080040641.3A patent/CN113905787A/zh active Pending
- 2020-04-03 EP EP20718757.6A patent/EP3946618A1/en active Pending
- 2020-04-03 WO PCT/GB2020/050898 patent/WO2020201773A1/en not_active Ceased
- 2020-04-03 US US17/601,292 patent/US12358915B2/en active Active
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003506387A (ja) | 1999-08-04 | 2003-02-18 | アイカゲン インコーポレイテッド | カリウムチャンネルオープナーとしてのベンズアニリド |
| JP2004517080A (ja) | 2000-11-29 | 2004-06-10 | グラクソ グループ リミテッド | Tie−2および/またはvegfr−2の阻害剤として有用なベンゾイミダゾール誘導体 |
| JP2005509003A (ja) | 2001-11-09 | 2005-04-07 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | タンパク質キナーゼインヒビターとして有用なベンゾイミダゾール化合物 |
| JP2009530233A (ja) | 2006-02-14 | 2009-08-27 | ノバルティス アーゲー | Pi−3キナーゼインヒビターおよびそれらの使用方法 |
| WO2008016131A1 (en) | 2006-08-04 | 2008-02-07 | Takeda Pharmaceutical Company Limited | Fused heterocyclic compound |
| JP2010527909A (ja) | 2007-06-05 | 2010-08-19 | 武田薬品工業株式会社 | キナーゼ阻害剤としての二環式複素環化合物 |
| JP2011509250A (ja) | 2008-01-02 | 2011-03-24 | サノフイ−アベンテイス | N−複素環式イミダゾ[1,2−a]ピリジン−2−カルボキサミドの誘導体、この調製およびこの治療的用途 |
| WO2018169994A1 (en) | 2017-03-13 | 2018-09-20 | City Of Hope | m6A mRNA MODIFICATION IN CANCER TREATMENT |
Non-Patent Citations (3)
| Title |
|---|
| Herath, Ananda et al.,Continuous-flow synthesis of highly functionalized imidazo-oxadiazoles facilitated by microfluidic extraction,Beilstein Journal of Organic Chemistry ,2017年,13,239-246 |
| REGISTRY(STN)[online],2018.03.02 [検索日 2024.02.20]CAS登録番号 2183120-12-7 ほか8件 |
| Ukhin, L.Y. et al.,Synthesis of phthalimidines linked to quinoline derivatives by an amide bridge,Russian Chemical Bulletin,2010年,59,1023-1030 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN113905787A (zh) | 2022-01-07 |
| EP3946618A1 (en) | 2022-02-09 |
| JP2022528562A (ja) | 2022-06-14 |
| US20230085408A1 (en) | 2023-03-16 |
| US12358915B2 (en) | 2025-07-15 |
| WO2020201773A1 (en) | 2020-10-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP7762957B2 (ja) | Mettl3阻害化合物 | |
| JP7765088B2 (ja) | Mettl3阻害剤としてのポリヘテロ環式化合物 | |
| JP7534379B2 (ja) | ベンズイミダゾロン由来のbcl6阻害剤 | |
| EP3630749B9 (en) | 2-quinolone derived inhibitors of bcl6 | |
| CN106459035B (zh) | N2‑苯基‑吡啶并[3,4‑d]嘧啶‑2,8‑二胺衍生物及其作为mps1抑制剂的用途 | |
| BR112015004489B1 (pt) | Composto, composição farmacêutica, e, uso de um composto | |
| EP2892890A1 (en) | Pharmacologically active compounds | |
| WO2022074379A1 (en) | Mettl3 inhibitory compounds | |
| EP4633735A1 (en) | Inhibitory compounds | |
| WO2024020419A1 (en) | Aza-quinazoline compounds and methods of use | |
| US20250388577A1 (en) | Mettl3 inhibitory compounds | |
| HK40111504A (en) | Benzimidazolone derived inhibitors of bcl6 | |
| BR112019024830B1 (pt) | Inibidores de bcl6 derivados de benzimidazolona, seus usos e composição farmacêutica | |
| HK40025715B (en) | Benzimidazolone derived inhibitors of bcl6 | |
| HK40025715A (en) | Benzimidazolone derived inhibitors of bcl6 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20230331 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20230331 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20240314 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20240416 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20240712 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20241105 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20250204 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20250401 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20250626 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20250819 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20250917 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20251014 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 7762957 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |