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dc.contributor.authorNdunda, BE
dc.contributor.authorLangat, MK
dc.contributor.authorMidiwo, JO
dc.contributor.authorOmosa, LK.
dc.date.accessioned2015-04-24T07:28:19Z
dc.date.available2015-04-24T07:28:19Z
dc.date.issued2015
dc.identifier.citationNdunda BE, Langat MK, Midiwo JO, Omosa LK. "Diterpenoid Derivatives of Kenyan Croton sylvaticus." NPC. 2015;10(4):557-558en_US
dc.identifier.urihttp://hdl.handle.net/11295/82019
dc.identifier.urihttp://europepmc.org/abstract/med/25973474
dc.description.abstractKenyan Croton sylvaticus Hochst. ex Krauss gave four clerodane diterpenoids, the new ent-3,13E-clerodadiene-15-formate (1), the known 15-acetoxy-ent-3,13E-clerodadiene (2), ent-3,13E-clerodadien-15-ol (3) and hardwickiic acid (4), two known halimane diterpenoids, penduliflaworosin (5) and crotohalimaneic acid (6) and one labdane diterpenoid, labda-13E-ene-8a,15-diol (7). The compounds, when tested for their anti-microbial activities against Bacillus subtilis, Xanthomonas campestris and Candida albicans, were found to be inactive.
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.titleDiterpenoid derivatives of Kenyan croton sylvaticusen_US
dc.typeArticleen_US
dc.type.materialesen_US


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