Butyrolactone I, one of the major secondary metabolites of fungus , is a selective cdc2 kinase inhibitor. In the present study, the metabolism of butyrolactone I in male Wistar rats was investigated by characterising metabolites excreted into faeces. Following an oral dose of 40 mg/kg butyrolactone I, two phase I metabolites were isolated from the faeces of rat. The new structure was identified on the spectroscopic data analysis. The new compound and known compound were tested for their cytotoxicity, antimicrobial and antioxidant activity. and showed significant free radical scavenging ability. also showed strong inhibitory activity against .

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http://dx.doi.org/10.1080/14786419.2019.1680668DOI Listing

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