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Synthesis and molecular docking study of ethyl piperidine-1-carboxylate derivative Schiff bases   
Yazarlar (1)
Dr. Öğr. Üyesi Sertan AYTAÇ Dr. Öğr. Üyesi Sertan AYTAÇ
Kırşehir Ahi Evran Üniversitesi, Türkiye
Devamını Göster
Özet
In the present study, new Schiff bases (14-16) were obtained from the condensation reaction of Ethyl 4-aminopiperidine-1-carboxylate and 2/3/4-pyridine carboxyaldehyde compounds. Desired compounds were successfully synthesized with high yields in a short time. Chemical characterization (1H-NMR, 13C-NMR and elemental analysis) and molecular docking studies of the synthesized compounds were performed against the 7XN1 structure (human acetylcholinesterase in complex with tacrine) and reference drug (Donepezil and Tacrine). It was determined that compound 16 (-7.52) had higher binding energy than Tacrine (-7.48), and compounds 14 (-7.34) and 15 (-7.41) showed values close to Tacrine (-7.48). The synthesized compounds can be potent inhibitors for hAChE.
Anahtar Kelimeler
Makale Türü Özgün Makale
Makale Alt Türü ESCI dergilerinde yayınlanan tam makale
Dergi Adı Organic Communications
Dergi ISSN 1307-6175 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler ESCI
Makale Dili Türkçe
Basım Tarihi 03-2025
Cilt No 18
Sayı 1
Sayfalar 28 / 37
Doi Numarası 10.25135/acg.oc.182.2503.3450
Makale Linki https://doi.org/10.25135/acg.oc.182.2503.3450
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Synthesis and molecular docking study of ethyl piperidine-1-carboxylate derivative Schiff bases

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