EA201791530A1 - НОВЫЕ N-АЦИЛАРИЛСУЛЬФОНАМИДНЫЕ ПРОИЗВОДНЫЕ В КАЧЕСТВЕ ИНГИБИТОРОВ АМИНОАЦИЛ-тРНК СИНТЕТАЗЫ - Google Patents
НОВЫЕ N-АЦИЛАРИЛСУЛЬФОНАМИДНЫЕ ПРОИЗВОДНЫЕ В КАЧЕСТВЕ ИНГИБИТОРОВ АМИНОАЦИЛ-тРНК СИНТЕТАЗЫInfo
- Publication number
- EA201791530A1 EA201791530A1 EA201791530A EA201791530A EA201791530A1 EA 201791530 A1 EA201791530 A1 EA 201791530A1 EA 201791530 A EA201791530 A EA 201791530A EA 201791530 A EA201791530 A EA 201791530A EA 201791530 A1 EA201791530 A1 EA 201791530A1
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- EA
- Eurasian Patent Office
- Prior art keywords
- inhibitors
- new
- aminoacyl
- trna
- synthetasis
- Prior art date
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- C07D213/04—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
- 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
- C07D213/70—Sulfur atoms
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- C07C311/20—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
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- C07D215/04—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms
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- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
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- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
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- Orthopedic Medicine & Surgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Heart & Thoracic Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
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- Tropical Medicine & Parasitology (AREA)
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- Cardiology (AREA)
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- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Quinoline Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
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Abstract
Изобретение относится к новым N-ацилдиарисульфонамидам, выступающим в качестве ингибиторов бактериальной аминоацил-тРНК синтетазы. Указанные соединения можно применять в качестве лекарственных средств или в составе лекарственных средств для лечения бактериальных инфекций.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
LVP-15-14A LV15146B (lv) | 2015-02-13 | 2015-02-13 | N-acil-diarilsulfonamīda atvasinājumi kā aminoacil-t-RNS sintetāžu inhibitori |
LVP-16-06A LV15257A (lv) | 2016-02-10 | 2016-02-10 | Jauni N-acil-arilsulfonamīda atvasinājumi kā aminoacil-tRNS sintetāzes inhibitori |
PCT/LV2016/000001 WO2016129983A1 (en) | 2015-02-13 | 2016-02-11 | Novel n-acyl-arylsulfonamide derivatives as aminoacyl-trna synthetase inhibitors |
Publications (2)
Publication Number | Publication Date |
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EA201791530A1 true EA201791530A1 (ru) | 2018-01-31 |
EA036995B1 EA036995B1 (ru) | 2021-01-25 |
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EA201791530A EA036995B1 (ru) | 2015-02-13 | 2016-02-11 | НОВЫЕ N-АЦИЛАРИЛСУЛЬФОНАМИДНЫЕ ПРОИЗВОДНЫЕ В КАЧЕСТВЕ ИНГИБИТОРОВ АМИНОАЦИЛ-тРНК СИНТЕТАЗЫ |
Country Status (14)
Country | Link |
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US (1) | US11072581B2 (ru) |
EP (1) | EP3259250A1 (ru) |
JP (1) | JP6740256B2 (ru) |
KR (1) | KR102568859B1 (ru) |
CN (1) | CN107257789B (ru) |
AU (1) | AU2016216782C1 (ru) |
CA (1) | CA2975682A1 (ru) |
EA (1) | EA036995B1 (ru) |
IL (1) | IL253886B (ru) |
MA (1) | MA41542A (ru) |
MX (1) | MX2017010357A (ru) |
NZ (1) | NZ735398A (ru) |
WO (1) | WO2016129983A1 (ru) |
ZA (1) | ZA201706108B (ru) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
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CN107257789B (zh) | 2015-02-13 | 2021-06-29 | 牛津药物设计有限公司 | 作为氨酰-trna合成酶抑制剂的新型n-酰基-芳基磺酰胺衍生物 |
GB201617064D0 (en) * | 2016-10-07 | 2016-11-23 | Inhibox Limited And Latvian Institute Of Organic Synthesis The | Compounds and their therapeutic use |
CN107033093B (zh) * | 2017-06-07 | 2019-09-03 | 浙江工业大学 | N-取代磺酰胺类化合物及其制备方法与应用 |
TW202120490A (zh) | 2019-07-30 | 2021-06-01 | 德商拜耳動物保健有限公司 | 新穎異喹啉衍生物 |
CN112759542B (zh) * | 2019-11-04 | 2022-04-01 | 上海现代制药股份有限公司 | 一种药物中间体及其制备和应用 |
CN110950863B (zh) * | 2019-11-15 | 2021-04-02 | 中山大学 | 一种喹唑啉酮类化合物及其制备方法和应用 |
AU2020409713A1 (en) * | 2019-12-19 | 2022-06-02 | Oxford Drug Design Limited | 2-amino-N-(amino-oxo-aryl-lambda6-sulfanylidene)acetamide compounds and their therapeutic use |
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JPH05208914A (ja) | 1991-09-03 | 1993-08-20 | Fujisawa Pharmaceut Co Ltd | ペプチド化合物を含有する医薬組成物 |
US5824657A (en) | 1997-03-18 | 1998-10-20 | Cubist Pharmaceuticals, Inc. | Aminoacyl sulfamides for the treatment of hyperproliferative disorders |
US20020052370A1 (en) | 2000-07-06 | 2002-05-02 | Barber Christopher Gordon | Cyclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase |
MXPA03011197A (es) | 2001-06-06 | 2004-02-26 | Lilly Co Eli | Benzoilsufonamidas y sulfonilbenzamidinas que se usan como agentes antitumorales. |
ZA200602937B (en) | 2003-10-10 | 2007-06-27 | Vertex Pharma | Inhibitors of serine proteases, particularly HCV NS3-NS4A protease |
KR20060130027A (ko) * | 2003-10-10 | 2006-12-18 | 버텍스 파마슈티칼스 인코포레이티드 | 세린 프로테아제, 특히 hcv ns3-ns4a 프로테아제의억제제 |
EP1730165A1 (en) * | 2004-02-27 | 2006-12-13 | Schering Corporation | Inhibitors of hepatitis c virus ns3 protease |
CN101203504B (zh) * | 2005-05-03 | 2012-11-14 | 兰贝克赛实验室有限公司 | 抗微生物剂 |
CN102970867A (zh) | 2010-03-18 | 2013-03-13 | 拜耳知识产权有限责任公司 | 作为活性剂对抗非生物植物应激的芳基和杂芳基磺酰胺 |
US20130190324A1 (en) * | 2011-12-23 | 2013-07-25 | The Regents Of The University Of Colorado, A Body Corporate | Topical ocular drug delivery |
AR091858A1 (es) | 2012-07-25 | 2015-03-04 | Sova Pharmaceuticals Inc | INHIBIDORES DE CISTATIONIN-g-LIASA (CSE) |
CN107257789B (zh) | 2015-02-13 | 2021-06-29 | 牛津药物设计有限公司 | 作为氨酰-trna合成酶抑制剂的新型n-酰基-芳基磺酰胺衍生物 |
CN105198789B (zh) * | 2015-10-26 | 2018-06-05 | 山东大学 | 取代3-吲哚类Bcl-2蛋白抑制剂及制备方法和应用 |
GB201617064D0 (en) | 2016-10-07 | 2016-11-23 | Inhibox Limited And Latvian Institute Of Organic Synthesis The | Compounds and their therapeutic use |
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AU2016216782B2 (en) | 2020-07-30 |
CN107257789B (zh) | 2021-06-29 |
NZ735398A (en) | 2024-07-05 |
US20180022696A1 (en) | 2018-01-25 |
EP3259250A1 (en) | 2017-12-27 |
CN107257789A (zh) | 2017-10-17 |
CA2975682A1 (en) | 2016-08-18 |
JP2018507257A (ja) | 2018-03-15 |
AU2016216782C1 (en) | 2021-02-18 |
AU2016216782A1 (en) | 2017-09-28 |
IL253886B (en) | 2020-01-30 |
ZA201706108B (en) | 2019-02-27 |
EA036995B1 (ru) | 2021-01-25 |
JP6740256B2 (ja) | 2020-08-12 |
IL253886A0 (en) | 2017-10-31 |
WO2016129983A1 (en) | 2016-08-18 |
MA41542A (fr) | 2021-04-14 |
BR112017016977A2 (pt) | 2018-04-03 |
KR20170118106A (ko) | 2017-10-24 |
MX2017010357A (es) | 2018-04-24 |
KR102568859B1 (ko) | 2023-08-21 |
US11072581B2 (en) | 2021-07-27 |
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