Biological potential of novel methoxy and hydroxy substituted heteroaromatic amides designed as promising antioxidative agents: Synthesis, 3D-QSAR analysis and biological activity (CROSBI ID 267987)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Podaci o odgovornosti
Sović, Irena ; Cindrić, Maja ; Perin, Nataša ; Boček, Ida ; Novaković, Irena ; Damjanović, Ana ; Stanojković, Tatjana ; Zlatović, Mario ; Hranjec, Marijana ; Bertoša, Branimir
engleski
Biological potential of novel methoxy and hydroxy substituted heteroaromatic amides designed as promising antioxidative agents: Synthesis, 3D-QSAR analysis and biological activity
This paper discusses antioxidative and biological activity of 25 novel amidino substituted benzamides with a variety of heteroaromatic nuclei attached to the benzamide moiety and with a variable number of methoxy and/or hydroxy substituents. Targeted compounds, bearing either amidino or 2- imidazolinyl substituent, were obtained in the Pinner reaction from cyano precursors. 3D-QSAR models were generated to predict antioxidative activity of the 25 novel aromatic and heteroaromatic benzamide derivatives. The compounds were tested for antioxidative activity using in vitro spectrophotometric assays. Direct validation of 3D-QSAR approach for predicting activities of novel benzamide derivatives was carried out by comparing experimental and computationally predicted antioxidative activity. Experimentally determined activities for all novel compounds were found to be within standard deviation of error of the models. Following this, structure- activity relationships among the synthesized compounds are discussed. Furthermore, antiproliferative activity in vitro against HeLa cells as well as antibacterial and antifungal activity was tested to confirm the other biological activities of the prepared compounds.
amides ; benzimidazoles ; benzothiazoles , 3D-QSAR ; antioxidative activity ; antiproliferative activity in vitro ; antimicrobial activity
Institute of Chemistry, Technology and Metallurgy, University of Belgrade ; Faculty of Chemistry, University of Belgrade ; Institute of Oncology and Radiology
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Podaci o izdanju
32 (9)
2019.
1880-1892
objavljeno
0893-228X
1520-5010
10.1021/acs.chemrestox.9b00256
Povezanost rada
Kemija, Temeljne medicinske znanosti