| dc.contributor.author | Kariba R M. | |
| dc.contributor.author | Houghton P J. | |
| dc.contributor.author | Yenesew Abiy. | |
| dc.date.accessioned | 2013-06-17T07:34:09Z | |
| dc.date.available | 2013-06-17T07:34:09Z | |
| dc.date.issued | 2002-04-21 | |
| dc.identifier.citation | J. Nat. Prod., 2002, 65 (4), pp 566–569 DOI: 10.1021/np010298m Publication Date (Web): February 21, 2002. | en |
| dc.identifier.uri | http://pubs.acs.org/doi/abs/10.1021/np010298m | |
| dc.identifier.uri | http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/34726 | |
| dc.identifier.uri | http://www.ncbi.nlm.nih.gov/pubmed/11975502 | |
| dc.description.abstract | Extracts from Schizozygia coffaeoides showed antimicrobial activity against fungal and bacterial species. Alkaloids isolated using bioassay-guided fractionation were isoschizogaline, schizogynine, and a new indoline alkaloid, 7,8-dehydro-19β-hydroxyschizozygine, shown to be the most active antifungal compound. The structure of isoschizagaline, the only active antibacterial, is revised on the basis of NMR analysis. | en |
| dc.language.iso | en | en |
| dc.publisher | University of Nairobi | en |
| dc.title | Antimicrobial Activities of a New Schizozygane Indoline Alkaloid from Schizozygia coffaeoides and the Revised Structure of Isoschizogaline | en |
| dc.type | Article | en |
| local.publisher | Department of Botany and Department of Chemistry, | en |
