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New derivatives of the anti-inflammatory, leprostatic drug dapsone 4 are synthesized, characterized and
biologically screened by the treating the drug dapsone with chloroacetyl chloride in the presence of base. Both
amino groups are acylated to give compound 6. The symmetrical acylated product then treated with Phenol,
N-Acetyl-p-aminophenol, p-Chlorophenol, m-Chlorophenol, o-Hydroxybezoic acid and m-Hydroxybezoic acid
to give compounds 8(a-f). The antimicrobial activity was tested for the synthesized compounds; activates were
good compared to the parent drug. All the new compounds have scanned for their biological activities toward
gram ‒ve and gram +ve (M. tuberculosis, S. pneumoniae, E. coli and P. mirabilis) bacteria, the synthesized
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