Synthesis of new N ‐(3‐oxo‐1‐thia‐4‐azaspiro[4.5]decan‐4‐yl)pyridine‐3‐carboxamide derivatives and evaluation of their anti‐influenza virus and antitubercular activities

التفاصيل البيبلوغرافية
العنوان: Synthesis of new N ‐(3‐oxo‐1‐thia‐4‐azaspiro[4.5]decan‐4‐yl)pyridine‐3‐carboxamide derivatives and evaluation of their anti‐influenza virus and antitubercular activities
المؤلفون: Gökçe Cihan‑Üstündağ, Çiğdem Acar, Lieve Naesens, Gonca Erköse‑Genç, Dilek Şatana
المصدر: Archiv der Pharmazie. 355:2200224
بيانات النشر: Wiley, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Structure-Activity Relationship, Influenza A Virus, H1N1 Subtype, Pyridines, Influenza A Virus, H3N2 Subtype, Drug Discovery, Antitubercular Agents, Isoniazid, Pharmaceutical Science, Microbial Sensitivity Tests, Antiviral Agents
الوصف: We here report the synthesis, structural characterization, and evaluation of the antiviral and antitubercular activities of a novel series of hybrid spirothiazolidinone derivatives (2a-f and 3a-f) containing the nicotinohydrazide moiety, which is an isomer form of the approved antitubercular drug isoniazid. When evaluated for activity against influenza A/H1N1, A/H3N2, and B viruses, three of the new compounds proved to possess specific antiviral activity against the influenza A/H3N2 virus. The most active analog 3a, bearing a 2,8-dimethyl group at the spiro ring, displayed an antiviral EC
تدمد: 1521-4184
0365-6233
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d5f6e308f12b7a769e107c82468f09e
https://doi.org/10.1002/ardp.202200224
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....8d5f6e308f12b7a769e107c82468f09e
قاعدة البيانات: OpenAIRE