Preparation and evaluation of antibacterial potential of Pithecellobium dulce root extract against Gram positive and Gram negative bacteria.

In the present study hexane, benzene, ethyl acetate and ethanol extracts of Pithecellobium dulce root were prepared using soxhlet extractor. The extracts were evaluated for antibacterial activity against one Gram positive (Staphylococcus aureus) and three Gram negative (Acetobacter aceti, Acetobacter aceti, Klebsiella pneumoniae) strains. Disc diffusion method revealed promising antibacterial activity of the extracts prepared in polar solvents (ethyl acetate and ethanol) compared to non-polar solvents (hexane and benzene). Ethanolic root extract was found to be most active against Acetobacter aceti, Staphylococcus aureus, Klebsiella pneumonia and Enterobacter aerogenes bacterial strains. The zone of inhibition of ethanolic root extract against Acetobacter aceti, Staphylococcus aureus, Klebsiella pneumonia and Enterobacter aerogenes bacterial strains was 15.4, 11.0, 19.0 and 13.0 mm, respectively at 100 mg concentration. Ethyl acetate extract also exhibited good antibacterial activity against Entrobacter aerogenes, Klebsiella pneumonia and Acetobacter aceti. The zone of inhibition of ethyl acetate root extracts against Entrobacter aerogenes, Acetobacter aceti and Klebsiella pneumonia was 10.5, 18.0 and 10.0 mm, respectively. The benzene extract showed some activity against Acetobacter aceti with the zone of inhibition 10.0 mm. The antibacterial activity of Pithecellobium dulce root hexane extract was found to be negligible against all the four tested strains of bacteria. These findings suggest that ethanolic and ethyl acetate root extracts of Pithecellobium dulce has potential as effective anti-bacterial agent.

Synthesis and in vitro evaluation of 2-(((2-ether)amino)methylene)-dimedone derivatives as potential antimicrobial agents.

The study was designed with an aim to synthesize a series of 2-(((2-ether)amino)methylene)-dimedone derivatives and evaluate the synthesized compounds for antimicrobial activity. Compound library was synthesized by reaction with alkyl, alkenyl, alkynyl and alicyclic bromo-compounds. Characterization of the synthesized compounds was performed by 1H NMR, 13C NMR and mass spectral techniques. The compounds were evaluated for their antibacterial activity against Gram-positive (Staphylococcus aureus, Bacillus subtilis, Clostridium sporogenes) and Gram-negative bacteria (Pseudomonas aeruginosa, Escherichia coli). The activity of these compounds was also evaluated against fungi (Aspergillus fumigatus, Penicillium chrysogenum, Fusarium oxysporum, Candida albicans) and molds (A. niger and A. oryzae). Broth microdilution method and CLSI guidelines with minor modification were used for the determination of anti-bacterial and antifungal activity, respectively. Although four compounds (4i, 4j, 4k and 4l) showed good antibacterial activity but compound 4k was found to be most active chemotype in the series. Compound 4k was found to be active against S. aureus, B. cereus and B. subtilis bacterial strains at one dilution lower compared to the control ciprofloxacin. Antibacterial activity of compound 4k was comparable to ciprofloxacin against S. pyogenes and M. luteus. The compound 4d, 4e and 4s showed good antifungal and antimold activity compared to other chemotypes. However, in comparison to fluconazole both the compounds showed lower activity. The results merit the antimicrobial promise of the 2-(((2-ether)amino)methylene)-dimedone analogs.