| dc.contributor.author | Kisangau, Daniel P. | |
| dc.contributor.author | Devkota, Krishna P. | |
| dc.contributor.author | Lenta, Bruno N. | |
| dc.contributor.author | Wansi, Jean D. | |
| dc.contributor.author | Choudhary, Muhammad I. | |
| dc.contributor.author | Samreen, Qamar N. | |
| dc.contributor.author | Sewald, Norbert | |
| dc.date.accessioned | 2014-11-21T06:51:34Z | |
| dc.date.available | 2014-11-21T06:51:34Z | |
| dc.date.issued | 2008 | |
| dc.identifier.citation | Journal of Natural Products 2008, 71 (8), pp 1481–1484 | en_US |
| dc.identifier.issn | 0163-3864 | |
| dc.identifier.uri | http://pubs.acs.org/doi/abs/10.1021/np800305b | |
| dc.identifier.uri | http://hdl.handle.net/123456789/107 | |
| dc.description | DOI: 10.1021/np800305b | en_US |
| dc.description.abstract | The bioassay-guided phytochemical investigation of Sarcococca hookeriana with respect to cholinesterase inhibitory properties has yielded two new 5α-pregnane-type steroidal alkaloids, hookerianamides J (1) and K (2), along with eight known compounds (3−10). The structures of 1 and 2 were elucidated by spectroscopic methods. These compounds displayed good to moderate activities in vitro against the enzymes acetylcholinesterase (IC50 8.1−48.5 μM) and butyrylcholinesterase (IC50 0.4−4.0 μM). Compounds 1−10 were also tested in vitro for their leishmanicidal activity against Leishmania major and for their antibacterial activities against Bacillus subtilis, Micrococcus luteus, Streptococcus faecalis, and Pseudomonas pallida. | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.title | Bioactive 5α-Pregnane-Type Steroidal Alkaloids from Sarcococca hookeriana | en_US |