CN110914265B - 作为lsd-1抑制剂的吡咯并[2,3-c]吡啶和相关类似物 - Google Patents
作为lsd-1抑制剂的吡咯并[2,3-c]吡啶和相关类似物 Download PDFInfo
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- CN110914265B CN110914265B CN201880046207.9A CN201880046207A CN110914265B CN 110914265 B CN110914265 B CN 110914265B CN 201880046207 A CN201880046207 A CN 201880046207A CN 110914265 B CN110914265 B CN 110914265B
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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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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)
- 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)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762506349P | 2017-05-15 | 2017-05-15 | |
| US62/506,349 | 2017-05-15 | ||
| PCT/US2018/032619 WO2018213211A1 (en) | 2017-05-15 | 2018-05-15 | Pyrrolo[2,3-c]pyridines and related analogs as lsd-1 inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN110914265A CN110914265A (zh) | 2020-03-24 |
| CN110914265B true CN110914265B (zh) | 2022-12-23 |
Family
ID=62685119
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201880046207.9A Active CN110914265B (zh) | 2017-05-15 | 2018-05-15 | 作为lsd-1抑制剂的吡咯并[2,3-c]吡啶和相关类似物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US11168082B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3628044B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP7352284B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN110914265B (cg-RX-API-DMAC7.html) |
| AU (2) | AU2018269947B2 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2018213211A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112119080B (zh) * | 2018-05-15 | 2023-07-11 | 密歇根大学董事会 | 作为lsd-1抑制剂的咪唑并[4,5-c]吡啶化合物 |
| SI3941466T1 (sl) | 2019-03-20 | 2026-04-30 | Oryzon Genomics, S.A. | Vafidemstat za zdravljenje neagresivnih simptomov mejne osebnostne motnje |
| HRP20251471T1 (hr) | 2019-03-20 | 2026-01-02 | Oryzon Genomics, S.A. | Postupci liječenja poremećaja hiperaktivnosti s deficitom pažnje korištenjem inhibitora kdm1a kao što je spoj vafidemstat |
| US20220227763A1 (en) | 2019-05-29 | 2022-07-21 | Syngenta Crop Protection Ag | Microbiocidal derivatives |
| CN112451671B (zh) * | 2020-12-02 | 2021-11-02 | 武汉大学 | KDM1A在抑制RNA病毒刺激下干扰素IFNβ表达中的应用 |
| CA3231846A1 (en) | 2021-04-08 | 2022-10-13 | Tamara Maes | Combinations of lsd1 inhibitors for treating myeloid cancers |
| CN116102533A (zh) * | 2021-11-11 | 2023-05-12 | 中国科学院上海药物研究所 | 一种芳杂环类化合物及其应用 |
| JP2025503099A (ja) * | 2022-01-25 | 2025-01-30 | 成都苑▲東▼生物制▲薬▼股▲ふん▼有限公司 | ピリジン系誘導体、その製造方法及び使用 |
| US20250295660A1 (en) | 2022-05-09 | 2025-09-25 | Oryzon Genomics, S.A. | Methods of treating nf1-mutant tumors using lsd1 inhibitors |
| US20250275969A1 (en) | 2022-05-09 | 2025-09-04 | Oryzon Genomics, S.A. | Methods of treating malignant peripheral nerve sheath tumor (mpnst) using lsd1 inhibitors |
| AU2023327925A1 (en) * | 2022-08-22 | 2025-02-20 | Redx Pharma Limited | Pyrido-pyrazoles as inhibitors of ddr's for the treatment of fibrotic disorders and cancer |
| US20260151399A1 (en) | 2022-11-24 | 2026-06-04 | Oryzon Genomics, S.A. | Combinations of lsd1 inhibitors and menin inhibitors for treating cancer |
| WO2024208187A1 (zh) * | 2023-04-03 | 2024-10-10 | 上海复星医药(集团)股份有限公司 | 氮杂芳基化合物及其作为lsd1抑制剂的用途 |
| EP4784570A1 (en) * | 2023-09-28 | 2026-08-05 | The Regents of The University of Michigan | Oxygenated heterocyclic lsd-1 inhibitors and related methods of use |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002088078A2 (en) * | 2001-04-30 | 2002-11-07 | Vertex Pharmaceuticals Incorporated | INHIBITORS OF GSK-3 AND CRYSTAL STRUCTURES OF GSK-3β PROTEIN AND PROTEIN COMPLEXES |
| CN101307052A (zh) * | 2007-05-14 | 2008-11-19 | 上海恒瑞医药有限公司 | 吡咯并n杂环类衍生物的制备方法及其在医药上的应用 |
| CN101568540A (zh) * | 2006-11-01 | 2009-10-28 | 沃泰克斯药物股份有限公司 | 用作janus激酶抑制剂的三环杂芳基化合物 |
| CN101765597A (zh) * | 2007-04-12 | 2010-06-30 | 霍夫曼-拉罗奇有限公司 | 作为磷脂酰肌醇-3-激酶抑制剂的嘧啶衍生物 |
| KR20150024669A (ko) * | 2013-08-27 | 2015-03-09 | 제일모직주식회사 | 화합물, 이를 포함하는 유기발광소자 및 상기 유기발광소자를 포함하는 표시장치 |
| US20160009720A1 (en) * | 2014-07-10 | 2016-01-14 | Incyte Corporation | Imidazopyrazines as lsd1 inhibitors |
| WO2016161282A1 (en) * | 2015-04-03 | 2016-10-06 | Incyte Corporation | Heterocyclic compounds as lsd1 inhibitors |
| WO2016201266A1 (en) * | 2015-06-11 | 2016-12-15 | Usher Iii Initiative, Inc. | Methods of treating or preventing a proteopathy |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5093330A (en) | 1987-06-15 | 1992-03-03 | Ciba-Geigy Corporation | Staurosporine derivatives substituted at methylamino nitrogen |
| JP2002507996A (ja) | 1997-07-03 | 2002-03-12 | デュポン ファーマシューティカルズ カンパニー | 神経学的障害を治療するためのイミダゾピリミジン類およびイミダゾピリジン類 |
| US6365589B1 (en) | 1998-07-02 | 2002-04-02 | Bristol-Myers Squibb Pharma Company | Imidazo-pyridines, -pyridazines, and -triazines as corticotropin releasing factor antagonists |
| AU2006247322A1 (en) | 2005-05-16 | 2006-11-23 | Irm Llc | Pyrrolopyridine derivatives as protein kinase inhibitors |
| WO2007084667A2 (en) | 2006-01-19 | 2007-07-26 | Osi Pharmaceutical, Inc. | Fused heterobicyclic kinase inhibitors |
| PE20090717A1 (es) | 2007-05-18 | 2009-07-18 | Smithkline Beecham Corp | Derivados de quinolina como inhibidores de la pi3 quinasa |
| WO2009029609A1 (en) | 2007-08-27 | 2009-03-05 | Wyeth | Imidazopyridine analogs and their use as agonists of the wnt-beta-catenin cellular messaging system |
| GB201008134D0 (en) | 2010-05-14 | 2010-06-30 | Medical Res Council Technology | Compounds |
| JP5744021B2 (ja) * | 2010-06-30 | 2015-07-01 | 富士フイルム株式会社 | 新規なニコチンアミド誘導体またはその塩 |
| CA3161836A1 (en) | 2013-12-11 | 2015-06-18 | Celgene Quanticel Research, Inc. | Inhibitors of lysine specific demethylase-1 |
| LT3105218T (lt) | 2014-02-13 | 2019-12-10 | Incyte Corp | Ciklopropilaminai kaip lsd1 inhibitoriai |
| WO2015123424A1 (en) | 2014-02-13 | 2015-08-20 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
| EP3392244A1 (en) | 2014-02-13 | 2018-10-24 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
| US9527835B2 (en) | 2014-02-13 | 2016-12-27 | Incyte Corporation | Cyclopropylamines as LSD1 inhibitors |
| RU2692485C2 (ru) * | 2014-04-02 | 2019-06-25 | Интермьюн, Инк. | Противофиброзные пиридиноны |
| US9758523B2 (en) | 2014-07-10 | 2017-09-12 | Incyte Corporation | Triazolopyridines and triazolopyrazines as LSD1 inhibitors |
| WO2016007731A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Imidazopyridines and imidazopyrazines as lsd1 inhibitors |
| WO2016007722A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines and triazolopyrazines as lsd1 inhibitors |
| AR110963A1 (es) | 2017-02-07 | 2019-05-22 | Dae Woong Pharma | Compuestos heterocíclicos, su método de preparación y composición farmacéutica que los comprende |
-
2018
- 2018-05-15 JP JP2019563164A patent/JP7352284B2/ja active Active
- 2018-05-15 CN CN201880046207.9A patent/CN110914265B/zh active Active
- 2018-05-15 US US16/611,238 patent/US11168082B2/en active Active
- 2018-05-15 EP EP18733006.3A patent/EP3628044B1/en active Active
- 2018-05-15 AU AU2018269947A patent/AU2018269947B2/en active Active
- 2018-05-15 WO PCT/US2018/032619 patent/WO2018213211A1/en not_active Ceased
-
2022
- 2022-01-13 AU AU2022200197A patent/AU2022200197A1/en not_active Abandoned
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002088078A2 (en) * | 2001-04-30 | 2002-11-07 | Vertex Pharmaceuticals Incorporated | INHIBITORS OF GSK-3 AND CRYSTAL STRUCTURES OF GSK-3β PROTEIN AND PROTEIN COMPLEXES |
| CN101568540A (zh) * | 2006-11-01 | 2009-10-28 | 沃泰克斯药物股份有限公司 | 用作janus激酶抑制剂的三环杂芳基化合物 |
| CN101765597A (zh) * | 2007-04-12 | 2010-06-30 | 霍夫曼-拉罗奇有限公司 | 作为磷脂酰肌醇-3-激酶抑制剂的嘧啶衍生物 |
| CN101307052A (zh) * | 2007-05-14 | 2008-11-19 | 上海恒瑞医药有限公司 | 吡咯并n杂环类衍生物的制备方法及其在医药上的应用 |
| KR20150024669A (ko) * | 2013-08-27 | 2015-03-09 | 제일모직주식회사 | 화합물, 이를 포함하는 유기발광소자 및 상기 유기발광소자를 포함하는 표시장치 |
| US20160009720A1 (en) * | 2014-07-10 | 2016-01-14 | Incyte Corporation | Imidazopyrazines as lsd1 inhibitors |
| WO2016161282A1 (en) * | 2015-04-03 | 2016-10-06 | Incyte Corporation | Heterocyclic compounds as lsd1 inhibitors |
| WO2016201266A1 (en) * | 2015-06-11 | 2016-12-15 | Usher Iii Initiative, Inc. | Methods of treating or preventing a proteopathy |
Non-Patent Citations (2)
| Title |
|---|
| Development of 5-hydroxypyrazole derivatives as reversible inhibitors of lysine specific demethylase 1;Daniel P. Mould 等;《Bioorganic & Medicinal Chemistry Letters》;20170508;第27卷(第14期);第3190-3195页 * |
| Indoles from 3-nitropyridinium salts:an extension of the transformation method on 5-substituted indoles;Oleg D. Mitkin等;《Tetrahedron》;20010228;第57卷(第9期);第1827-1831页 * |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2018269947A1 (en) | 2019-12-19 |
| JP7352284B2 (ja) | 2023-09-28 |
| CN110914265A (zh) | 2020-03-24 |
| AU2022200197A1 (en) | 2022-02-10 |
| WO2018213211A1 (en) | 2018-11-22 |
| US11168082B2 (en) | 2021-11-09 |
| AU2018269947B2 (en) | 2021-10-14 |
| JP2020519667A (ja) | 2020-07-02 |
| EP3628044A1 (en) | 2020-04-01 |
| US20200157091A1 (en) | 2020-05-21 |
| EP3628044B1 (en) | 2023-11-22 |
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