Potent α-glucosidase and tyrosinase inhibition by thiophene-based Schiff bases: Experimental and computational evaluation
Yazarlar (5)
Öğr. Gör. Emel Ekinci Çankırı Karatekin Üniversitesi, Türkiye
Dr. Öğr. Üyesi Kübra ÖZTÜRK Kırşehir Ahi Evran Üniversitesi, Türkiye
Doç. Dr. Özlem GÜNDOĞDU AYTAÇ Kırşehir Ahi Evran Üniversitesi, Türkiye
Doç. Dr. Sertan AYTAÇ Kırşehir Ahi Evran Üniversitesi, Türkiye
Prof. Dr. Harun ÇİFTÇİ Kırşehir Ahi Evran Üniversitesi, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı LETTERS IN DRUG DESIGN & DISCOVERY (Q4)
Dergi ISSN 1570-1808 Dergi Bilgileri (2026)
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce Basım Tarihi 01-2026
Cilt / Sayı / Sayfa 23 / 1 / – DOI 10.1016/j.lddd.2026.100366
Makale Linki https://doi.org/10.1016/j.lddd.2026.100366
UAK Araştırma Alanları
Organik Kimya Biyokimya Teorik Kimya
Özet
In this study, novel thiophene-based Schiff base derivatives were synthesized, and their structures were comprehensively analyzed. The inhibitory potentials of these compounds on α-glucosidase and tyrosinase enzymes were systematically evaluated. Among the thiophene-based Schiff bases, compound 8 exhibited moderate inhibitory activity against both α-glucosidase and tyrosinase, with IC50 values of 173.29 and 69.32 µM for each, compared to the positive controls acarbose and kojic acid, respectively. The DFT approach was used to analyze the reactivity and molecular electrostatic potential maps of the compounds, and molecular docking studies for the most active compounds 4, 6, and 8 were conducted on both the fungal tyrosinase and Saccharomyces cerevisiae protein models. Furthermore, ADME (Absorption, Distribution, Metabolism, and Excretion) analyses were performed to evaluate their …
Anahtar Kelimeler
Thiophene | Schiff base | Diabetes | Hyperpigmentation | Enzyme inhibition | Molecular docking | ADME
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Web of Science 1
Google Scholar 1
Potent α-glucosidase and tyrosinase inhibition by thiophene-based Schiff bases: Experimental and computational evaluation

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