dc.contributor.author |
Finlayson, R |
en |
dc.contributor.author |
Pearce, Allison |
en |
dc.contributor.author |
Page, MJ |
en |
dc.contributor.author |
Kaiser, M |
en |
dc.contributor.author |
Bourguet-Kondracki, M-L |
en |
dc.contributor.author |
Harper, JL |
en |
dc.contributor.author |
Webb, VL |
en |
dc.contributor.author |
Copp, Brent |
en |
dc.coverage.spatial |
United States |
en |
dc.date.accessioned |
2017-10-19T03:43:04Z |
en |
dc.date.issued |
2011-02-24 |
en |
dc.identifier.citation |
Journal of Natural Products, 74(4):888-892, 24 Feb 2011 |
en |
dc.identifier.issn |
0163-3864 |
en |
dc.identifier.uri |
http://hdl.handle.net/2292/36166 |
en |
dc.description.abstract |
Two new indole spermidine alkaloids, didemnidines A (1) and B (2), have been isolated from the New Zealand ascidian Didemnum sp. The structures of the metabolites, determined by analysis of 2D NMR spectra and confirmed via synthesis, embody an indole-3-glyoxylamide moiety linked to the N(1) position of spermidine, the latter motif being particularly rare among marine natural products. Didemnidine B and a synthetic precursor exhibited mild in vitro growth inhibition of Plasmodium falciparum with IC(50)'s of 15 and 8.4 μM, respectively. |
en |
dc.description.uri |
https://www.ncbi.nlm.nih.gov/pubmed/21348447 |
en |
dc.language |
English |
en |
dc.publisher |
American Chemical Society |
en |
dc.relation.ispartofseries |
J Nat Prod |
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. Details obtained from http://sherpa.ac.uk/romeo/issn/0163-3864/ |
en |
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
en |
dc.subject |
Animals |
en |
dc.subject |
Antiprotozoal Agents |
en |
dc.subject |
Indole Alkaloids |
en |
dc.subject |
Leishmania donovani |
en |
dc.subject |
Molecular Structure |
en |
dc.subject |
New Zealand |
en |
dc.subject |
Nuclear Magnetic Resonance, Biomolecular |
en |
dc.subject |
Plasmodium falciparum |
en |
dc.subject |
Spermidine |
en |
dc.subject |
Structure-Activity Relationship |
en |
dc.subject |
Trypanosoma |
en |
dc.subject |
Urochordata |
en |
dc.title |
Didemnidines A and B, indole spermidine alkaloids from the New Zealand ascidian Didemnum sp. |
en |
dc.type |
Journal Article |
en |
dc.identifier.doi |
10.1021/np1008619 |
en |
pubs.issue |
4 |
en |
pubs.begin-page |
888 |
en |
pubs.volume |
74 |
en |
dc.rights.holder |
Copyright: American Chemical Society |
en |
dc.identifier.pmid |
21348447 |
en |
pubs.author-url |
http://pubs.acs.org/doi/abs/10.1021/np1008619 |
en |
pubs.end-page |
892 |
en |
pubs.publication-status |
Published |
en |
dc.rights.accessrights |
http://purl.org/eprint/accessRights/RestrictedAccess |
en |
pubs.subtype |
Article |
en |
pubs.elements-id |
206832 |
en |
pubs.org-id |
Science |
en |
pubs.org-id |
Chemistry |
en |
pubs.org-id |
Science Research |
en |
pubs.org-id |
Maurice Wilkins Centre (2010-2014) |
en |
dc.identifier.eissn |
1520-6025 |
en |
pubs.record-created-at-source-date |
2017-10-19 |
en |
pubs.dimensions-id |
21348447 |
en |