Phenethylamidediesters (2-6) were synthesized by reacting [3-ethoxy-4- (ethoxycarbonyl)phenyl]acetic acid with a series of C-protected aminoacids viz., Alanine, Proline, Phenylalanine, Tyrosine and 2-amino-5-(benzyloxy)-5-oxopentanoic aciddiesters and these compounds were hydrolyzed using sodium hydroxide to their respective diacids (7-11). The newly synthesized compounds were tested for antimicrobial activity against Escherichia coli, Staphylococcus Aureus, Pseudomonas Aeruginos,Aspergillus Flavus, ChrysosporiumKeratinophilum, Candida Albicansand antioxidant activity by DPPH method. Compounds 6, 7, 8, and 11 were most active as antimicrobials and 6, 10 and 11have shown promising antioxidant activity.
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