Diterpenoid derivatives of Kenyan croton sylvaticus
dc.contributor.author | Ndunda, BE | |
dc.contributor.author | Langat, MK | |
dc.contributor.author | Midiwo, JO | |
dc.contributor.author | Omosa, LK. | |
dc.date.accessioned | 2015-04-24T07:28:19Z | |
dc.date.available | 2015-04-24T07:28:19Z | |
dc.date.issued | 2015 | |
dc.identifier.citation | Ndunda BE, Langat MK, Midiwo JO, Omosa LK. "Diterpenoid Derivatives of Kenyan Croton sylvaticus." NPC. 2015;10(4):557-558 | en_US |
dc.identifier.uri | http://hdl.handle.net/11295/82019 | |
dc.identifier.uri | http://europepmc.org/abstract/med/25973474 | |
dc.description.abstract | Kenyan 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.iso | en | en_US |
dc.publisher | University of Nairobi | en_US |
dc.title | Diterpenoid derivatives of Kenyan croton sylvaticus | en_US |
dc.type | Article | en_US |
dc.type.material | es | en_US |
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