<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>47</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Suresh Kumar *</style></author><author><style face="normal" font="default" size="100%">Sandhya Bawa</style></author><author><style face="normal" font="default" size="100%">Sushma Drabu</style></author><author><style face="normal" font="default" size="100%">B. P. Panda</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In-vitro antifungal activity of newly synthesized 2-chloro-3-(substituted phenyl/cyclohexyl/butylamino) methylquinolines.</style></title><secondary-title><style face="normal" font="default" size="100%">AICTE Sponsored National Seminar on Recent Advances in Pharmaceutical Sciences</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antifungal activity</style></keyword><keyword><style  face="normal" font="default" size="100%">quinoline</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style  face="normal" font="default" size="100%">7-9/08/2008</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">MSIP, Janakpuri, New Delhi</style></pub-location><abstract><style face="normal" font="default" size="100%">A series of 2-chloro-3-(substituted phenyl/cyclohexyl/butylamino)methylquinolines (4a-n) was synthesized and tested for in-vitro antifungal activity against Aspergillus niger (MTCC, 281), Aspergillus flavus (MTCC,277), Monascus purpureus (MTCC,369) and Penicillium citrinum (NCIM, 768)  and antibacterial activity against Escherichia coli (MTCCB, 1610), Staphylococcus aureus (MTCCB, 96) and Pseudomonas aeruginosa (MTCCB, 741) by serial plate dilutions method. Results of the preliminary screening revealed that some of the compounds mainly those with electron withdrawing groups in the phenyl ring showed promising antifungal activity. However these compounds were moderately active against bacterial strains.</style></abstract></record></records></xml>