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dc.contributor.authorGuantai, Eric M.
dc.contributor.authorChibale, Kelly
dc.contributor.authorRenate, H. Hans
dc.contributor.authorCarmen, Lategan
dc.contributor.authorSmith, peter J.
dc.contributor.authorBaojie, Wan
dc.contributor.authorFranzblau, Jiri Gut
dc.contributor.authorRosenthal, Philip J.
dc.date.accessioned2013-04-22T13:33:10Z
dc.date.available2013-04-22T13:33:10Z
dc.date.issued2010-02
dc.identifier.citationBioorganic & Medicinal Chemistry Lettersen
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S0960894X09017855#
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/16509
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/20045640
dc.description.abstractA series of acetylenic chalcones were evaluated for antimalarial and antitubercular activity. The antimalarial data for this series suggests that growth inhibition of the W2 strain of Plasmodium falciparum can be imparted by the introduction of a methoxy group ortho to the acetylenic group. Most compounds were more active against non-replicating than replicating cultures of Mycobacterium tuberculosis H37Rv, an unusual pattern with respect to existing anti-TB agentsen
dc.language.isoenen
dc.relation.ispartofseriesVol. 20, Issue 3, 2010, Pages 942-944;
dc.titleSynthesis, antimalarial and antitubercular activity of acetylenic chalconesen
dc.typeArticleen
local.publisherDepartment of Medicine. College of Health Sciences. University of Nairobien


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