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http://hdl.handle.net/11375/21490
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DC Field | Value | Language |
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dc.contributor.advisor | Harrison, P. H. M. | - |
dc.contributor.author | Tayierjiang, Simayi | - |
dc.date.accessioned | 2017-05-25T18:15:06Z | - |
dc.date.available | 2017-05-25T18:15:06Z | - |
dc.date.issued | 2006-06 | - |
dc.identifier.uri | http://hdl.handle.net/11375/21490 | - |
dc.description.abstract | <p> Pramanicin (1) is a natural product that was first isolated as an anti-fungal agent: it possesses bioactivity against both the acapsular and capsular forms of Cryptococcus neoformans. 1 was found to act on smooth muscle in an endotheliumdependent manner. Further, studies of Ca2+ release from the endoplasmic reticulum of endothelial cells were consistent with an influence on the endothelial nitric oxide synthase (eNOS) pathway. Recently, we showed that 1 activates caspases 3 and 9. In order to determine which functional groups in 1 are required for this activity, several analogues were prepared (2~7). These included 2 and 3 prepared through fermentation and modification of 1, as well as 4-7 which were prepared by chemical synthesis. A test of bioactivity for 1-7 indicates that all compounds are active. The small differences in activity are discussed. </p> | en_US |
dc.language.iso | en | en_US |
dc.subject | Analogues | en_US |
dc.subject | Pramanicin | en_US |
dc.subject | Bioactivity Analysis | en_US |
dc.subject | bioactivity | en_US |
dc.title | Synthesis of Analogues of Pramanicin for Bioactivity Analysis | en_US |
dc.contributor.department | Chemistry | en_US |
dc.description.degreetype | Thesis | en_US |
dc.description.degree | Master of Science (MSc) | en_US |
Appears in Collections: | Digitized Open Access Dissertations and Theses |
Files in This Item:
File | Description | Size | Format | |
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Tayierjiang_Simayi_2006Jun_ Masters.pdf | 2.94 MB | Adobe PDF | View/Open |
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