AU2018269947B2 - Pyrrolo(2,3-c)pyridines and related analogs as LSD-1 inhibitors - Google Patents
Pyrrolo(2,3-c)pyridines and related analogs as LSD-1 inhibitors Download PDFInfo
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- AU2018269947B2 AU2018269947B2 AU2018269947A AU2018269947A AU2018269947B2 AU 2018269947 B2 AU2018269947 B2 AU 2018269947B2 AU 2018269947 A AU2018269947 A AU 2018269947A AU 2018269947 A AU2018269947 A AU 2018269947A AU 2018269947 B2 AU2018269947 B2 AU 2018269947B2
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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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2022200197A AU2022200197A1 (en) | 2017-05-15 | 2022-01-13 | Pyrrolo[2,3-C]pyridines and related analogs as LSD-1 inhibitors |
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 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2022200197A Division AU2022200197A1 (en) | 2017-05-15 | 2022-01-13 | Pyrrolo[2,3-C]pyridines and related analogs as LSD-1 inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2018269947A1 AU2018269947A1 (en) | 2019-12-19 |
| AU2018269947B2 true AU2018269947B2 (en) | 2021-10-14 |
Family
ID=62685119
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2018269947A Active AU2018269947B2 (en) | 2017-05-15 | 2018-05-15 | Pyrrolo(2,3-c)pyridines and related analogs as LSD-1 inhibitors |
| AU2022200197A Abandoned AU2022200197A1 (en) | 2017-05-15 | 2022-01-13 | Pyrrolo[2,3-C]pyridines and related analogs as LSD-1 inhibitors |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2022200197A Abandoned AU2022200197A1 (en) | 2017-05-15 | 2022-01-13 | Pyrrolo[2,3-C]pyridines and related analogs as LSD-1 inhibitors |
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 (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008079521A2 (en) * | 2006-11-01 | 2008-07-03 | Vertex Pharmaceuticals Incorporated | Tricyclic heteroaryl compounds useful as inhibitors of janus kinase |
| KR20150024669A (ko) * | 2013-08-27 | 2015-03-09 | 제일모직주식회사 | 화합물, 이를 포함하는 유기발광소자 및 상기 유기발광소자를 포함하는 표시장치 |
| WO2015153683A1 (en) * | 2014-04-02 | 2015-10-08 | Intermune, Inc. | Anti-fibrotic pyridinones |
| 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 |
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| 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 |
| EP2295550A3 (en) * | 2001-04-30 | 2011-12-14 | Vertex Pharmaceuticals Incorporated | Crystal structures of GSK-3beta protein and protein complexes and their use |
| 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 |
| US20100130496A1 (en) * | 2007-04-12 | 2010-05-27 | F. Hoffmann-La Roche Ag | Pyrimidine derivatives as inhibitors of phosphatidylinositol-3-kinase |
| WO2008138184A1 (fr) * | 2007-05-14 | 2008-11-20 | Shanghai Hengrui Pharmaceutical Co.Ltd. | Dérivés de pyrrolo-azacycles, leur procédé de fabrication et leur utilisation en tant qu'inhibiteurs de protéine kinases |
| 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 |
| 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 (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008079521A2 (en) * | 2006-11-01 | 2008-07-03 | Vertex Pharmaceuticals Incorporated | Tricyclic heteroaryl compounds useful as inhibitors of janus kinase |
| KR20150024669A (ko) * | 2013-08-27 | 2015-03-09 | 제일모직주식회사 | 화합물, 이를 포함하는 유기발광소자 및 상기 유기발광소자를 포함하는 표시장치 |
| WO2015153683A1 (en) * | 2014-04-02 | 2015-10-08 | Intermune, Inc. | Anti-fibrotic pyridinones |
| 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 (13)
| Title |
|---|
| CAS Registry Number 1476063-00-9; STN Entry Date 18 November 2013; 1H-Pyrrolo[2,3-c]pyridine, 4-bromo-1-[2-(1-pyrrolidinyl)ethyl]- * |
| MITKIN O D ET AL, TETRAHEDRON, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL, (2001-02-25), vol. 57, no. 9, doi:10.1016/S0040-4020(00)01162-5, ISSN 0040-4020, pages 1827 - 1831 * |
| MOULD DANIEL P ET AL, BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, PERGAMON, AMSTERDAM, NL, (2017-05-08), vol. 27, no. 14, doi:10.1016/J.BMCL.2017.05.018, ISSN 0960-894X, pages 3190 - 3195 * |
| PubChem Compound Summary for ClD 126554614 (4-(3-Fluorophenyl)-1H-pyrrolo[2,3-c]pyridine), National Center for Biotechnology Information, created on 22 April 2017 <URL: https://pubchem.ncbi.nlm.nih.gov/compound/126554614> * |
| PubChem Compound Summary for ClD 66714572 (4-(1H-pyrrolo[2,3-c]pyridin-4-yl)aniline), National Center for Biotechnology Information, created on 30 Nov 2012 <URL: https://pubchem.ncbi.nlm.nih.gov/compound/66714572> * |
| PubChem Compound Summary for ClD 68762939 (2-(1H-pyrrolo[2,3-c]pyridin-4-yl)benzonitrile), National Center for Biotechnology Information, created on 30 Nov 2012 <URL: https://pubchem.ncbi.nlm.nih.gov/compound/68762939> * |
| PubChem Compound Summary for ClD 76847332 (5-Chloro-4-fluoro-1H-pyrrolo[2,3-c]pyridine), National Center for Biotechnology Information, created on 6 August 2014 <URL: https://pubchem.ncbi.nlm.nih.gov/compound/76847332> * |
| PubChem Compound Summary for ClD 91345 (4-Chloroindole), National Center for Biotechnology Information, created on 26 March 2005 <URL: https://pubchem.ncbi.nlm.nih.gov/compound/91345> * |
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| REGISTRY, CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US, (2008-12-11), Database accession no. 1083096-61-0 * |
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 |
| JP2020519667A (ja) | 2020-07-02 |
| EP3628044A1 (en) | 2020-04-01 |
| US20200157091A1 (en) | 2020-05-21 |
| EP3628044B1 (en) | 2023-11-22 |
| CN110914265B (zh) | 2022-12-23 |
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