Design and synthesis of various 1,3,4-oxadiazoles as AChE and LOX enzyme inhibitors
N-Substituted-2-propanamide analogues of 1,3,4-oxadiazole have been synthesized using a multi-step synthetic protocol to explore new therapeutic anti-enzymatic agents. Herein, we have merged sulfonyl, piperidine, oxadiazole and amide into a single unit to synthesize a library of unique compounds, 8a...
| الحاوية / القاعدة: | Heterocyclic Communications |
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| المؤلف الرئيسي: | |
| التنسيق: | مقال |
| اللغة: | English |
| منشور في: |
Walter de Gruyter GmbH
2023
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| الوصول للمادة أونلاين: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85178212455&doi=10.1515%2fhc-2022-0169&partnerID=40&md5=218e9958497d44e30e5d0fb4c27b224c |