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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5235
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dc.contributor.authorGoudgaon N.M
dc.contributor.authorVijayalaxmi A.
dc.date.accessioned2020-06-12T15:06:35Z-
dc.date.available2020-06-12T15:06:35Z-
dc.date.issued2003
dc.identifier.citationIndian Journal of Pharmaceutical Sciences , Vol. 65 , 5 , p. 545 - 549en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5235-
dc.description.abstractVarious acylonucleoside analogs were synthesized and evaluated for antibacterial and antifungal activity. All the acyclic nucleosides exhibited good antifungal activity compared to the standard drug clotrimazole. However, none of the compounds possess broad-spectrum antibacterial activity. The structure-activity relationships of acyclic nucleosides were studied in order to develop the most potential antifungal agent for preclinical evaluation.en_US
dc.titleAntimicrobial activity and structure-activity relationship of acyclic nucleosidesen_US
dc.typeArticle
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