EA201992120A1 - Новые ингибиторы - Google Patents

Новые ингибиторы

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Publication number
EA201992120A1
EA201992120A1 EA201992120A EA201992120A EA201992120A1 EA 201992120 A1 EA201992120 A1 EA 201992120A1 EA 201992120 A EA201992120 A EA 201992120A EA 201992120 A EA201992120 A EA 201992120A EA 201992120 A1 EA201992120 A1 EA 201992120A1
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EA
Eurasian Patent Office
Prior art keywords
heteroaryl
heterocyclyl
cycloalkyl
aryl
independently substituted
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EA201992120A
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English (en)
Inventor
Ульрих Хайзер
Торстен Хоффманн
Ингеборг Луэс
Антье Майер
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Пробайодраг Аг
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Application filed by Пробайодраг Аг filed Critical Пробайодраг Аг
Publication of EA201992120A1 publication Critical patent/EA201992120A1/ru

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    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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  • Enzymes And Modification Thereof (AREA)
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  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
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Abstract

Настоящее изобретение относится к соединению формулы (I)или его фармацевтически приемлемым соли, сольвату или полиморфу, включая все его таутомеры и стереоизомеры, где A выбран из моноциклического и бициклического гетероарила, которые могут быть независимо замещены алкилом или амино; B выбран из алкила, гетероалкила, алкиламино, арила, гетероарила, циклоалкила, гетероциклила и алкилена, где указанные группы могут быть независимо замещены алкилом; D выбран из ариламино, гетероариламино, циклоалкиламино, гетероциклила, гетероциклиламино, мочевины, тиоамида, тиомочевины, сульфонамида, сульфоксимина и сульфамоила, где указанные арильные, гетероарильные, циклоалкильные и гетероциклильные группы могут быть независимо замещены; и E выбран из арила, гетероарила, циклоалкила, гетероциклила, где указанные арильные, гетероарильные, циклоалкильные и гетероциклильные группы могут быть независимо замещены. Соединения формулы (I) представляют собой ингибиторы глутаминилциклазы (QC, EC 2.3.2.5). QC катализирует внутримолекулярную циклизацию N-концевых остатков глутамина в пироглутаминовую кислоту (5-оксопролил, pGlu*) с высвобождением аммиака и внутримолекулярную циклизацию N-концевых остатков глутамата в пироглутаминовую кислоту с высвобождением воды.
EA201992120A 2017-03-31 2018-04-03 Новые ингибиторы EA201992120A1 (ru)

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Application Number Priority Date Filing Date Title
GBGB1705263.0A GB201705263D0 (en) 2017-03-31 2017-03-31 Novel inhibitors
PCT/EP2018/058391 WO2018178384A1 (en) 2017-03-31 2018-04-03 Novel inhibitors

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EA201992120A1 true EA201992120A1 (ru) 2020-01-29

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US (2) US11339152B2 (ru)
EP (1) EP3601269A1 (ru)
JP (2) JP2020512373A (ru)
KR (1) KR20190136005A (ru)
CN (2) CN110719910B (ru)
AU (2) AU2018246382B2 (ru)
BR (1) BR112019019553A2 (ru)
CA (2) CA3057783A1 (ru)
EA (1) EA201992120A1 (ru)
GB (1) GB201705263D0 (ru)
IL (3) IL269196B2 (ru)
MX (2) MX2019011544A (ru)
NZ (1) NZ757601A (ru)
WO (1) WO2018178384A1 (ru)
ZA (1) ZA201905811B (ru)

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