Synthesis, Structure and Antiradical Activity of Functionally Substituted Hydrazides of Isonicotinic Acid; Eurasian Chemico-Technological Journal; Vol. 25, No. 2

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Parent link:Eurasian Chemico-Technological Journal.— .— Almaty: al-Farabi KazNU
Vol. 25, No. 2.— 2023.— P. 121-128
Altri autori: Nurkenov O. A. Oralgazy Aktaevich, Fazylov S. D. Serik Drakhmetovich, Shulgau Z. T. Zarina Toktamysovna, Аbdrasilov B. S. Bolatbek Serikbaevich, Khlebnikov A. I. Andrey Ivanovich, Seylkhanov T. M. Tulegen Muratovich, Kabieva S. K. Saule Kazzhanovna, Karipova G. Zh. Gulzhanat Zhumazhanovna
Riassunto:Title screen
The purpose of this work is the synthesis of new isonicotinic acid hydrazones, the study of their structure, reactivity and biological screening of some synthesized compounds. The reactions leading to new N-arylidene(alkylidene) hydrazones via the condensation of isonicotinic acid hydrazide with various derivatives of aromatic aldehydes were studied. The structure of the new functionally substituted isonicotinic acid hydrazones was established by FTIR, 1H and 13C NMR, two-dimensional COSY (1H-1H) NMR spectroscopy and HMQC (1H-13C). The antiradical activity of the synthesized derivatives was studied using diphenylpycrylhydrazide radical (DPPH) assay. It was shown that N-(3- ethoxy-4-hydroxybenzylidene)isonicotinohydrazide possesses antiradical activity (IC50 (DPPH) 103.0 μM). The antiradical properties of compounds of phenolic nature are in agreement with the energies of homolytic O-H bond dissociation calculated with the use of density functional theory
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Lingua:inglese
Pubblicazione: 2023
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Accesso online:https://doi.org/10.18321/ectj1502
Natura: Elettronico Capitolo di libro
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=684729

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