Pyrimidines: Molecular docking and inhibition studies on carbonic anhydrase and cholinesterases
 
Yazarlar (1)
Doç. Dr. Hatice Esra DURAN Kafkas Üniversitesi, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY (Q2)
Dergi ISSN 0885-4513 Dergi Bilgileri (2023)
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili Türkçe Basım Tarihi 02-2023
Kabul Tarihi 18-01-2022 Yayınlanma Tarihi 23-02-2022
Cilt / Sayı / Sayfa 70 / 1 / 68–82 DOI 10.1002/bab.2329
Makale Linki http://dx.doi.org/10.1002/bab.2329
UAK Araştırma Alanları
Tıbbi Biyokimya
Özet
Alzheimer's disease (AD) is a neurodegenerative disorder. The disease is characterized by dementia, memory impairment, cognitive impairment, and speech impairment. Cholinesterases (ChEs; AChE, acetylcholinesterase and BChE, butyrylcholinesterase) inhibitors and their benefits of cholinergic replacement in the treatment of AD have been researched and documented by scientists in various ways to date. Recent studies prove that human carbonic anhydrases (hCAs) are also one of the important targets in the treatment of AD. Therefore, the development of new agents that can simultaneously modulate the various mechanisms or targets involved in the AD pathway may be a powerful strategy to treat AD, the current disease. Considering these data, the effects of the pyrimidines (1–7) were investigated in this study for the discovery and development of multitargeted ChEs and hCAs inhibitors associated with AD …
Anahtar Kelimeler
biological activity | enzymes | inhibition | molecular docking | pyrimidine
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Web of Science 8
Google Scholar 12
Pyrimidines: Molecular docking and inhibition studies on carbonic anhydrase and cholinesterases

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