Synthesis, Characterization, and Antibacterial Activity of Novel 2,3-Dihydroxyquinoxaline-5-carboxamide Derivatives

被引:3
|
作者
Srinivas, Keesari [1 ]
Kumar, Puttapaka Vijay [1 ]
Joshi, Hemangi [2 ]
Velidandi, Amarnath [3 ]
Manchal, Ravinder [3 ]
机构
[1] MSN Labs Pvt Ltd, Hyderabad 500084, Telangana, India
[2] Keshav Mem Inst Technol, Hyderabad 500029, Telangana, India
[3] Chaitanya Deemed Univ, Dept Chem, Warangal 506001, Telangana, India
关键词
2; 3-dihydroxyquinoxaline-5-carboxamides; antibacterial activity; methyl; 3-diamino benzoate; Norfloxacin; QUINOXALINE DERIVATIVES; BIOLOGICAL EVALUATION; ANTITUMOR AGENT; INHIBITORS; CHEMISTRY;
D O I
10.1134/S106816202305014X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The quinoxaline-5-carboxamide derivatives (Vq-Vu) and (VIa-Vu) were prepared using methyl-2,3-diamino benzoate as the starting material. Analytical and spectral data were used to characterize the synthesized compounds. Four bacterial strains-Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Streptococcus pyogenes-were tested with titled compounds. Fluoro-substituted, phenethyl groups, oxygenated cyclic and aliphatic, and benzonitrile are among the reported derivatives that demonstrated good inhibition for antibacterial activity, while the rest compounds shown equipotent to moderate action. Using commercially available 2,3-diamino benzoate 1 as the starting material, innovative 2,3-dimethoxyquinoxaline-5-carboxamide derivatives (Vq-Vu) and 2,3-dihydroyquinoxaline-5-carboxamide derivatives (VIa-VIu) were synthesised in five stages. The electronegative group on the quinoxaline moiety boosts the antibacterial properties of the produced compounds, according to the results of SAR.
引用
收藏
页码:1068 / 1075
页数:8
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