Source:http://linkedlifedata.com/resource/pubmed/id/20235550
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2010-4-23
|
pubmed:abstractText |
Bioassay-guided fractionation of the crude extract from the Australian marine sponge Plakortis sp. led to the isolation of two new cyclic polyketide peroxides, 11,12-didehydro-13-oxo-plakortide Q (1) and 10-carboxy-11,12,13,14-tetranor-plakortide Q (2). Antitrypanosomal studies showed that compound 1 had an IC(50) value of 49 nM against Trypanosoma brucei brucei, and compound 2, where a carboxylic acid is present in the side chain, had a 20-fold reduction of activity. 11,12-Didehydro-13-oxo-plakortide Q (1) is the most active peroxide isolated so far against T. b. brucei, and it indicates the potential therapeutic value of this class of compounds.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
1520-6025
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:day |
23
|
pubmed:volume |
73
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
716-9
|
pubmed:meshHeading |
pubmed-meshheading:20235550-Animals,
pubmed-meshheading:20235550-Australia,
pubmed-meshheading:20235550-Dioxanes,
pubmed-meshheading:20235550-Humans,
pubmed-meshheading:20235550-Marine Biology,
pubmed-meshheading:20235550-Molecular Structure,
pubmed-meshheading:20235550-Plakortis,
pubmed-meshheading:20235550-Trypanocidal Agents,
pubmed-meshheading:20235550-Trypanosoma brucei brucei
|
pubmed:year |
2010
|
pubmed:articleTitle |
Antitrypanosomal cyclic polyketide peroxides from the Australian marine sponge Plakortis sp.
|
pubmed:affiliation |
Eskitis Institute, Griffith University, Brisbane, QLD 4111, Australia.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|