1986Journal of Heterocyclic ChemistryRequires access

Synthesis, 13C‐NMR characterization and antimicrobial properties of a novel series of 3‐(N‐Substituted thiocarbamoyl)hydrazino‐1,2,4‐triazino‐[5,6‐b]indole derivatives

A.‐M. M. E. OMAR, N. H. ESHBA, Hamida Abou-Shleib

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Abstract

Abstract A series of 3‐(N‐substituted thiocarbamoyl)hydrazino‐1,2,4‐triazino[5,6‐b]indole derivatives 3–22 has been synthesized and evaluated for in vitro antimicrobial activity. Although some of the products displayed significant activity against Staphylococcus aureus, Escherichia coli and Candida albicans, their bactericidal and bacterostatic potencies were lower than that of penicillin G. The structure of the products was assigned upon the basis of their infrared, 1H‐nmr and 13C‐nmr spectra.

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Abstract A series of 3‐(N‐substituted thiocarbamoyl)hydrazino‐1,2,4‐triazino[5,6‐b]indole derivatives 3–22 has been synthesized and evaluated for in vitro antimicrobial activity. Although some of the products displayed significant activity against Staphylococcus aureus, Escherichia coli and Candida albicans, their bactericidal and bacterostatic potencies were lower than that of penicillin G. The structure of the products was assigned upon the basis of their infrared, 1H‐nmr and 13C‐nmr spectra.

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Available abstract

Abstract A series of 3‐(N‐substituted thiocarbamoyl)hydrazino‐1,2,4‐triazino[5,6‐b]indole derivatives 3–22 has been synthesized and evaluated for in vitro antimicrobial activity. Although some of the products displayed significant activity against Staphylococcus aureus, Escherichia coli and Candida albicans, their bactericidal and bacterostatic potencies were lower than that of penicillin G. The structure of the products was assigned upon the basis of their infrared, 1H‐nmr and 13C‐nmr spectra.

Key concepts: Chemistry, Antimicrobial, Indole test, Candida albicans, Escherichia coli, Proton NMR, Carbon-13 NMR, Penicillin

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