ES2924522T3 - Inhibidores heteroarilo de PAD4 - Google Patents
Inhibidores heteroarilo de PAD4 Download PDFInfo
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- ES2924522T3 ES2924522T3 ES17772181T ES17772181T ES2924522T3 ES 2924522 T3 ES2924522 T3 ES 2924522T3 ES 17772181 T ES17772181 T ES 17772181T ES 17772181 T ES17772181 T ES 17772181T ES 2924522 T3 ES2924522 T3 ES 2924522T3
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- dihydroquinolin
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- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
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- C07D213/647—One oxygen atom attached in position 2 or 6 and having in the molecule an acyl radical containing a saturated three-membered ring, e.g. chrysanthemumic acid esters
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
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- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- 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
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662393209P | 2016-09-12 | 2016-09-12 | |
| PCT/US2017/050886 WO2018049296A1 (en) | 2016-09-12 | 2017-09-11 | Heteroaryl inhibitors of pad4 |
Publications (1)
| Publication Number | Publication Date |
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| ES2924522T3 true ES2924522T3 (es) | 2022-10-07 |
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| WO (1) | WO2018049296A1 (enExample) |
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| EP3419969B1 (en) | 2016-02-23 | 2019-12-18 | Padlock Therapeutics, Inc. | Heteroaryl inhibitors of pad4 |
| WO2018022897A1 (en) | 2016-07-27 | 2018-02-01 | Padlock Therapeutics, Inc. | Covalent inhibitors of pad4 |
| BR112020023107A2 (pt) * | 2018-05-14 | 2021-02-02 | Ariad Pharmaceuticals, Inc. | sais farmacêuticos de derivados de pirimidina e método de tratamento de distúrbios |
| KR102089476B1 (ko) * | 2018-07-11 | 2020-03-16 | 이화여자대학교 산학협력단 | 피부 염증 질환 예방 또는 치료용 조성물 |
| EP3833440A1 (en) | 2018-08-08 | 2021-06-16 | Bristol-Myers Squibb Company | Indole and azaindole inhibitors of pad enzymes |
| CN112566916B (zh) | 2018-08-08 | 2023-10-20 | 百时美施贵宝公司 | 作为pad4抑制剂的经取代的噻吩并吡咯 |
| CN109467549B (zh) * | 2018-12-07 | 2021-02-09 | 中国药科大学 | 喹啉取代查尔酮类化合物、其制备方法及用途 |
| KR102173983B1 (ko) | 2019-04-18 | 2020-11-04 | 현대모비스 주식회사 | 전자식 유압 브레이크 장치 |
| WO2021158840A1 (en) | 2020-02-06 | 2021-08-12 | Bristol-Myers Squibb Company | Macrocyclic pad4 inhibitors useful as immunosuppressant |
| TW202140477A (zh) | 2020-02-12 | 2021-11-01 | 美商必治妥美雅史谷比公司 | 雜環pad4抑制劑 |
| PE20230488A1 (es) | 2020-04-30 | 2023-03-21 | Gilead Sciences Inc | Inhibidores macrociclicos de las peptidilarginina deiminasas |
| EP4267562A1 (en) | 2020-12-22 | 2023-11-01 | Gilead Sciences, Inc. | Inhibitors of peptidylarginine deiminases |
| US12240862B2 (en) | 2020-12-22 | 2025-03-04 | Gilead Sciences, Inc. | Inhibitors of peptidylarginine deiminases |
| WO2024112749A1 (en) * | 2022-11-23 | 2024-05-30 | The Children's Medical Center Corporation | Methods of treating heart failure |
| CN115778930B (zh) * | 2022-12-08 | 2024-02-27 | 陕西中医药大学 | 一种具有血管舒张活性的二硫缩醛类化合物在制备具有血管舒张活性药物方面的应用 |
| US11731942B1 (en) | 2023-01-12 | 2023-08-22 | King Faisal University | 3-substituted quinolin-2-one compounds as antibacterial agents |
| AR131956A1 (es) * | 2023-02-28 | 2025-05-21 | Chugai Pharmaceutical Co Ltd | Compuesto heterocíclico que contiene nitrógeno con actividad inhibidora de myt1 |
| WO2025024265A1 (en) | 2023-07-21 | 2025-01-30 | Bristol-Myers Squibb Company | Methods of assessing citrullination and activity of pad4 modulators |
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| AU2876000A (en) * | 1999-02-10 | 2000-08-29 | Trustees Of The University Of Pennsylvania, The | Tyrosine kinase inhibitors and methods of using the same |
| WO2002098425A1 (en) * | 2001-06-04 | 2002-12-12 | Cytovia, Inc. | Substituted 4-aryl-3-(3-aryl-1-oxo-2-propenyl)-2(1h)-quinolinones and analogs as activators of caspases and inducers of apoptosis and the use thereof |
| JP2002371078A (ja) * | 2001-06-12 | 2002-12-26 | Sankyo Co Ltd | キノリン誘導体及びキノロン誘導体 |
| JP4815773B2 (ja) * | 2003-09-17 | 2011-11-16 | 住友化学株式会社 | シンナモイル化合物及びその用途 |
| AU2004274328B2 (en) * | 2003-09-17 | 2011-11-10 | Sumitomo Chemical Company, Limited | Cinnamoyl compound and use of the same |
| JP2008501804A (ja) * | 2004-06-08 | 2008-01-24 | テンプル・ユニバーシティ−オブ・ザ・コモンウェルス・システム・オブ・ハイアー・エデュケイション | ヘテロアリール、スルホン及びスルホンアミド並びにそれらの治療用途 |
| JP2006273848A (ja) * | 2005-03-02 | 2006-10-12 | Sumitomo Chemical Co Ltd | シンナモイル化合物の用途 |
| AU2006219222A1 (en) * | 2005-03-02 | 2006-09-08 | Sumitomo Chemical Company, Limited | Use of cinnamoyl compound |
| CA2611608A1 (en) * | 2005-06-08 | 2006-12-14 | Temple University - Of The Commonwealth System Of Higher Education | 3-acyl coumarins, thiochromones and quinolones and therapeutic uses thereof |
| JP5642963B2 (ja) * | 2006-06-30 | 2014-12-17 | スネシス ファーマシューティカルズ,インコーポレイティド | ピリジノニルpdk1阻害剤 |
| EP1987717A1 (de) * | 2007-04-30 | 2008-11-05 | Bayer CropScience AG | Pyridoncarboxamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung und deren Verwendung |
| US20120190707A1 (en) * | 2008-04-25 | 2012-07-26 | Ronai Ze Ev | Selective inhibitors of akt and methods of using same |
| WO2014015905A1 (en) * | 2012-07-26 | 2014-01-30 | Glaxo Group Limited | 2 - (azaindol- 2 -yl) benz imidazoles as pad4 inhibitors |
| CN105315333A (zh) * | 2014-06-10 | 2016-02-10 | 首都医科大学 | 异喹啉-3-甲酰-RV-OBzl,其制备,纳米结构,活性和应用 |
| US10577349B2 (en) * | 2015-03-02 | 2020-03-03 | Sanford Burnham Prebys Medical Discovery Institute | Quinolinones as inhibitors of translation initiation complex |
| CA3199601A1 (en) | 2015-05-21 | 2016-11-24 | Glaxosmithkline Intellectual Property Development Limited | Benzoimidazole derivatives as pad4 inhibitors |
| AR107030A1 (es) | 2015-12-09 | 2018-03-14 | Padlock Therapeutics Inc | Inhibidores aza-bencimidazol de pad4 |
| AR107032A1 (es) | 2015-12-09 | 2018-03-14 | Padlock Therapeutics Inc | Inhibidores bicíclicos de pad4 |
| EP3419969B1 (en) | 2016-02-23 | 2019-12-18 | Padlock Therapeutics, Inc. | Heteroaryl inhibitors of pad4 |
| CN105820058A (zh) * | 2016-03-01 | 2016-08-03 | 南开大学 | 精氨酸脱亚氨酶4的新型抑制剂 |
| WO2018022897A1 (en) | 2016-07-27 | 2018-02-01 | Padlock Therapeutics, Inc. | Covalent inhibitors of pad4 |
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Also Published As
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| MA46193A (fr) | 2019-07-17 |
| CN110248934B (zh) | 2022-05-24 |
| WO2018049296A1 (en) | 2018-03-15 |
| EP3510025B1 (en) | 2022-06-29 |
| EP3510025A1 (en) | 2019-07-17 |
| CN110248934A (zh) | 2019-09-17 |
| US11026937B2 (en) | 2021-06-08 |
| KR102502992B1 (ko) | 2023-02-24 |
| JP2019526606A (ja) | 2019-09-19 |
| US20190358216A1 (en) | 2019-11-28 |
| KR20190045335A (ko) | 2019-05-02 |
| JP7118951B2 (ja) | 2022-08-16 |
| US20210299115A1 (en) | 2021-09-30 |
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