Cakmak_2024_ACS.Omega_9_20030

Reference

Title : Synthesis of Novel Hydrazide-Hydrazone Compounds and In Vitro and In Silico Investigation of Their Biological Activities against AChE, BChE, and hCA I and II - Cakmak_2024_ACS.Omega_9_20030
Author(s) : Cakmak R , Basaran E , Sahin K , Senturk M , Durdagi S
Ref : ACS Omega , 9 :20030 , 2024
Abstract : The abnormal levels of the human carbonic anhydrase isoenzymes I and II (hCA I and II) and cholinesterase enzymes, namely, acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), are linked with various disorders including Alzheimer's disease. In this study, six new nicotinic hydrazide derivatives (7-12) were designed and synthesized for the first time, and their inhibitory profiles against hCA I, hCA II, AChE, and BChE were investigated by in vitro assays and in silico studies. The structures of novel molecules were elucidated by using spectroscopic techniques and elemental analysis. These molecules showed inhibitory activities against hCA I and II with IC(50) values ranging from 7.12 to 45.12 nM. Compared to reference drug acetazolamide (AZA), compound 8 was the most active inhibitor against hCA I and II. On the other hand, it was determined that IC(50) values of the tested molecules ranged between 21.45 and 61.37 nM for AChE and between 18.42 and 54.74 nM for BChE. Among them, compound 12 was the most potent inhibitor of AChE and BChE, with IC(50) values of 21.45 and 18.42 nM, respectively. In order to better understand the mode of action of these new compounds, state-of-the-art molecular modeling techniques were also conducted.
ESTHER : Cakmak_2024_ACS.Omega_9_20030
PubMedSearch : Cakmak_2024_ACS.Omega_9_20030
PubMedID: 38737075

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Citations formats

Cakmak R, Basaran E, Sahin K, Senturk M, Durdagi S (2024)
Synthesis of Novel Hydrazide-Hydrazone Compounds and In Vitro and In Silico Investigation of Their Biological Activities against AChE, BChE, and hCA I and II
ACS Omega 9 :20030

Cakmak R, Basaran E, Sahin K, Senturk M, Durdagi S (2024)
ACS Omega 9 :20030