Natural Products from New Zealand Ascidians Pseudodistoma opacum and Aplidium scabellum

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dc.contributor.advisor Copp, B en
dc.contributor.author Chan, Susanna en
dc.date.accessioned 2011-08-08T23:03:55Z en
dc.date.issued 2011 en
dc.identifier.uri http://hdl.handle.net/2292/7206 en
dc.description.abstract New Zealand has a diverse and mostly unexplored marine environment. Ascidians found in New Zealand waters are a previously documented excellent source of bioactive marine natural products. This thesis presents the results of investigation of the secondary metabolite chemistry of two species of New Zealand ascidians, Pseudodistoma opacum, collected in Maori Bay, Muriwai, Auckland and Aplidium scabellum, collected at Great Barrier Island. Four new metabolites, (-)-7-bromohomotrypargine (2.82) and opacalines A-C (2.83-2.85), all belonging to the β-carboline family, were isolated from the ascidian P. opacum. The debromo analogues of opacalines A and C were synthesized and the library was evaluated for growth inhibition properties against a range of neglected disease parasite assays. The β-carbolines tested were found to be non-cytotoxic and display mild antimalarial activity, with IC50 ranging from 5-27 μM towards Trypanosoma brucei rhodesiense and 4-12 μM towards Plasmodium falciparum. A biosynthetic pathway for the four new metabolites is proposed, with arginine and homoarginine undergoing transamination to give the respective α-keto acid precursors, followed by a Pictet-Spengler reaction to form the β- carboline skeleton. Examination of the natural product chemistry of the ascidian Aplidium scabellum led to the isolation of five new natural products, 2-geranyl-6-methoxy-1,4-hydroquinone-4- sulfate (3.57) and scabellones A-D (3.59-3.62), as well as the known chromenol, 8- methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-6-ol (3.58), and quinone, verapliquinone A (3.63). Results from biomimetic synthesis of scabellones A-D utilizing either 2-methoxy-6-geranyl-1,4-hydroquinone or 2-methoxy-6-geranyl-1,4-benzoquinone as starting material identified the latter as the species necessary for the formation of the scabellones. Unexpected products were also isolated from different biomimetic synthesis attempts, including verapliquinone C and 3-methoxy-7-prenyl-1,4-naphthoquinone. A biosynthesis route for scabellones A-D was proposed based on the results obtained from the biomimetic reactions, with 2-geranyl-1,4-benzoquinone as the starting material and scabellone A as the common intermediate to scabellones B-D. Scabellone B (3.59) was found to exhibit antimalarial properties (IC50 3.4 μM), opening the potential for structureactivity relationship studies. 2-Geranyl-6-methoxy-1,4-hydroquinone-4-sulfate (3.57) was found to inhibit the respiratory burst of human neutrophils and is non-cytotoxic, making this natural product a potential anti-inflammatory agent. In contrast, its desulfated counterpart, 2-geranyl-6-methoxy-1,4-hydroquinone, was found to be an apoptotic cytotoxin. en
dc.publisher ResearchSpace@Auckland en
dc.relation.ispartof PhD Thesis - University of Auckland en
dc.relation.isreferencedby 99231094914002091 en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.rights.uri http://creativecommons.org/licenses/by-nc-sa/3.0/nz/ en
dc.title Natural Products from New Zealand Ascidians Pseudodistoma opacum and Aplidium scabellum en
dc.type Thesis en
thesis.degree.discipline Chemistry en
thesis.degree.grantor The University of Auckland en
thesis.degree.level Doctoral en
thesis.degree.name PhD en
dc.rights.holder Copyright: The author en
pubs.elements-id 218293 en
pubs.record-created-at-source-date 2011-08-09 en


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