New naphtho/thienobenzo-triazoles with interconnected anti-inflammatory and cholinesterase inhibitory activity (CROSBI ID 311971)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Podaci o odgovornosti
Mlakić, Milena ; Odak, Ilijana ; Faraho, Ivan ; Talić, Stanislava ; Bosnar, Martina ; Lasić, Kornelija ; Barić, Danijela ; Škorić, Irena
engleski
New naphtho/thienobenzo-triazoles with interconnected anti-inflammatory and cholinesterase inhibitory activity
New 1, 2, 3-triazolo(thieno)stilbenes were synthesized by Wittig reaction and photochemically transformed to corresponding substituted thienobenzo/naphtho-triazoles in high isolated yields. They were prepared to study the acetyl- and butyrylcholinesterase inhibition associated with the inhibition of TNFalpha cytokine production and anti-inflammatory activity. The best experimental results were achieved with the allyl-thienobenzotriazole and isopropyl, p- methoxybenzyl, and hydroxybutyl substituted naphthotriazoles bearing additional chloro or methoxy groups. The allyl-thienobenzotriazole photoproduct is twice as potent an inhibitor of eqBChE compared to the standard galantamine. At the same time, this compound strongly inhibited TNFalpha production in PBMCs in response to the LPS stimulus. The complexes between selected compounds with the active site of BChE and AChE are assessed by docking, providing insight into the stabilizing interactions between the potential inhibitor and the active site.
anti-inflammatory activity ; cholinesterase inhibition ; molecular docking, 1, 2, 3-triazolo(thieno)stilbenes ; naphtho/thienobenzo-triazoles
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Podaci o izdanju
241
2022.
114616
14
objavljeno
0223-5234
1768-3254
10.1016/j.ejmech.2022.114616