6(3,5-SUBSTITUTED-2-BROMO PHENYL) 1,2,4-TRIAZINE DERIVATIVES AS ANTIMICROBIAL AND ANTICANCER AGENTS
Rajeev Kumar*, Ram Kumar Roy and Anita Singh
ABSTRACT
6-(2-Amino-3,5-substituted phenyl)-1,2,4-triazines were prepared by
refluxing semicarbazones or thiosemicarbazones in presence of basic
medium. 6(3,5-Substituted-2-bromophenyl)1,2,4-triazine derivatives
were prepared from 6-(2-amino-3,5-substituted phenyl)-1,2,4-triazine
derivatives by using sodium nitrite, hydrobromic acid and Cu2Br2. The
structures of compounds were confirmed by FT-IR and H1-NMR
spectral data. Compounds were screened for antimicrobial activity
against four bacterial strains (Escherichia coli, Bacillus pumilus,
Klebsiella pneumonia and Staphylococcus aureus) and two fungal
strains (Aspergillus niger and Candida albicans) by using agar well
diffusion test. Some compounds showed good antimicrobial activity.
The in vitro anticancer activity of compounds was also performed by NCI 60 Cell screen at a
single high dose (10–5 M) on various panel/cell lines. In this series, some compounds showed
maximum antibacterial and antifungal activities, respectively. One compound was found to
be significant active against UO-31, renal cancer cell line with 38.62 % growth inhibition.
Keywords: Antimicrobial activity, anticancer activity, percentage growth inhibition, 1,2,4-triazine derivatives.
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