67. Biological and electronic transition studies of the previously reported organotin (IV) dithiocarbamates of p-Fluoro-Nmethylbenzylaminedithiocarbamate
Pure and Applied Biology (PAB), 2019•thepab.org
Four organotin (IV) complexes of p-Fluro-N-methylbenzylaminedithiocarbamate with general
formula R 2 SnL 2 where (R= dimethyl, diphenyl and dibutyl) and R 3 SnL (R= triphenyl)
synthesized earlier in the group were tested for their bioactivity. Antibacterial assay against
four Gram-negative and Gram-positive strains including Salmonella typhi, Escherichia coli,
Pneumoniae and Staphylococcus aureus, while antifungal activity against Aspergillus Niger
of the compounds were carried out using standard procedures. The tested compounds were …
formula R 2 SnL 2 where (R= dimethyl, diphenyl and dibutyl) and R 3 SnL (R= triphenyl)
synthesized earlier in the group were tested for their bioactivity. Antibacterial assay against
four Gram-negative and Gram-positive strains including Salmonella typhi, Escherichia coli,
Pneumoniae and Staphylococcus aureus, while antifungal activity against Aspergillus Niger
of the compounds were carried out using standard procedures. The tested compounds were …
Abstract
Four organotin (IV) complexes of p-Fluro-N-methylbenzylaminedithiocarbamate with general formula R 2 SnL 2 where (R= dimethyl, diphenyl and dibutyl) and R 3 SnL (R= triphenyl) synthesized earlier in the group were tested for their bioactivity. Antibacterial assay against four Gram-negative and Gram-positive strains including Salmonella typhi, Escherichia coli, Pneumoniae and Staphylococcus aureus, while antifungal activity against Aspergillus Niger of the compounds were carried out using standard procedures. The tested compounds were found significantly active against Aspergillus Niger. Whereas, the antibacterial activity of compounds wasfound moderate as compared to their antifungal activities.
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