| Literature DB >> 23973825 |
Jayaram Reddy Komsani1, Satish Koppireddi, Sreenivas Avula, Pranay Kumar Koochana, Rambabu Yadla.
Abstract
A new series of disubstituted alkynes was obtained by microwave induced internal splitting of the corresponding β-oxo-alkylidenetriphenylphosphoranes. The antimicrobial potential of these conjugated alkynes and phosphoranes was assayed in vitro against three Gram-positive bacteria (Staphylococcus aureus, Bacillus subtilis, Staphylococcus epidermidis), three Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae) and five fungal strains (Aspergillus niger, Candida albicans, Aspergillus flavus, Candida rugosa, Saccharomyces cerevisiae). The 3-pyridylalkyne derivatives viz., 3-(6-chloropyridin-3-yl)propynenitrile (6a), 3-(2-chloropyridin-3-yl)propynenitrile (6b), ethyl 3-(6-chloropyridin-3-yl)propiolate (6c), iso-propyl 3-(6-chloropyridin-3-yl)propiolate (6d) and 3-(2,6-dichloro-5-fluoropyridin-3-yl)propynenitrile (6e) were found to be highly potent towards all tested microorganisms except E. coli.Entities:
Keywords: Alkyl halopyridylpropynoic acid ester; Antimicrobial activity; Halopyridylpropynenitrile; iso-Propyl bromotriphenylphosphoranylacetic acid ester; α-Nicotinoyl-α-(alkoxycarbonyl)methylenetriphenylphosphoranes; β-Oxo-alkylidene-triphenylphosphoranes
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Year: 2013 PMID: 23973825 DOI: 10.1016/j.ejmech.2013.07.013
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514