Antimicrobial activity of some novel triazolo quinoline derivatives

ABSTRACT Some triazolo quinoline derivatives were synthesized and their structures were confirmed by IR, 1 H NMR, 13 C NMR and mass spectroscopy. Screening of all these synthesized compounds were done in vitro against bacteria and three fungal strains in dimethyl sulphoxide and N, N -dimethyl formamide. It is observed that N, N -dimethyl formamide is good solvent for these compounds in selected strains. Reference Lydy, J. Belden, C. Wheelock, B. Hammock, D. Denton, Challenges in regulating pesticide mixtures, Eco Soc. 9 (2004) 1-13. U. Khan, K. R. Atanasova, W. S. Krueger, A. Remirez, G. C. Fray, Epidemiology, geographical distribution and economic consequences of swine zoonoses: a narrative review, Emer. Micro. Inf. 2 (2013) 92-103. Berdy, Thoughts and facts about antibiotics: where we are know and where we are heading, J. Antibiotics, 65 (2012) 385-395. G. Daughton, I. S. Ruhoy, Lower-dose prescribing: minimizing “side effect” of pharmaceuticals on society and the environment, Sci. 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Antimicrobial activity of some novel triazolo quinoline derivatives

Authors: Asmita V. Hirapara, Shipra H. Baluja, 117 (2019) 102-121

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Antimicrobial activity of some novel triazolo quinoline derivatives

Authors: Asmita V. Hirapara, Shipra H. Baluja, 117 (2019) 102-121

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