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Modulation of Human Acetylthiocholine Esterase Activity by Novel Fused Pyrimidine Derivatives: In vitro, Theoretical and ADMET Studies      
Yazarlar
Zaizafoone N. Nasif
Zahraa S. Al-Garawi
Doç. Dr. Füreya Elif ÖZTÜRKKAN Doç. Dr. Füreya Elif ÖZTÜRKKAN
Kafkas Üniversitesi, Türkiye
Özet
Pyrimidine compounds have medicinal and biological activities as previously reported. In this work, two novel fused pyrimidine compounds were synthesized, fused pyrazolo–pyrimidine compound was synthesized by cyclization of 5-amino-4-cyano-1-phenyl pyrazole with propionic acid in the presence of POCl3, and the other fused pyrrole–pyrano-pyrimidine compound was synthesized by cyclization of ethyl(E)-N-(3-cyano-4-(4-(dimethylamino)phenyl)-7-methyl-4,5,6,7-tetrahydropyrano[2,3-b] pyrrole-2-yl) formimidate with hydrazine hydrate, in methanol. These fused pyrimidine compounds were characterized by FT-IR and1 H NMR. The effect of these compounds was studied on the activity of the human neurotransmission enzyme acetylthiocholine esterase AChE. Results indicated that these compounds significantly inhibited AChE activity at concentrations of 10-11 M. Michalis-Menton showed mixed noncompetitive inhibition of AChE activity. In conclusion, newly synthesized compounds could be promising derivatives for enhancing cholinergic neurotransmission. Among the other derivatives, derivative 4 formed H-bond interactions with key amino acid residues Tyr334, and Asp72, whereas the other electrostatic interactions formed with Tyr334, Phe330, Ile287, Tyr121, Arg289, Trp279, Gly335, and Phe288. In the case of derivatives 9, similar binding interactions with active pockets of 2ACE were observed due to the high homology of the binding site residues. In addition, we examined ADMET properties with the help of online databases to search for possible drug similarity of synthesized compounds 4 and 9 and revealed that both molecules were compatible with Lipinski's five rules.
Anahtar Kelimeler
AChE activity | ADMET | Fused pyrazolo–pyrimidine | Molecular docking | Noncompetitive inhibition
Makale Türü Özgün Makale
Makale Alt Türü SCOPUS dergilerinde yayımlanan tam makale
Dergi Adı Journal of the Turkish Chemical Society Section A: Chemistry
Dergi ISSN 2149-0120
Dergi Tarandığı Indeksler TR DİZİN
Makale Dili Türkçe
Basım Tarihi 06-2024
Cilt No 11
Sayı 3
Sayfalar 1197 / 1210
Doi Numarası 10.18596/jotcsa.1327285
Makale Linki http://dx.doi.org/10.18596/jotcsa.1327285