Source:http://linkedlifedata.com/resource/pubmed/id/19769341
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2009-10-23
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pubmed:abstractText |
Eight drimane sesquiterpenes (1-8), six isochromane derivatives (9-14), and three known compounds, daldinin B (15), 9alpha-hydroxy-6beta-[(2E,4E,6E)-octa-2,4,6-trienoyloxy]-5alpha-drim-7-en-11,12-olide (16), and pergillin (17), were isolated from the EtOAc extract of the marine-derived fungus Aspergillus ustus 094102. The structures of the new compounds were elucidated on the basis of spectroscopic analysis. The cytotoxic effects on A549 and HL-60 cell lines were evaluated by SRB and MTT methods. Ustusorane E (13) showed significant cytotoxicity against HL-60 cells with an IC50 value of 0.13 microM. Ustusolates C (6) and E (8) exhibited moderate cytotoxicity against A549 and HL-60 cells with IC50 values of 10.5 and 9.0 microM, respectively, and ustusolate A (4) showed weak cytotoxicity against HL-60 and A549 cells with IC50 values of 20.6 and 30.0 microM, respectively.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, Phytogenic,
http://linkedlifedata.com/resource/pubmed/chemical/Benzofurans,
http://linkedlifedata.com/resource/pubmed/chemical/Chromans,
http://linkedlifedata.com/resource/pubmed/chemical/Sesquiterpenes,
http://linkedlifedata.com/resource/pubmed/chemical/drimane
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1520-6025
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
72
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1761-7
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pubmed:meshHeading |
pubmed-meshheading:19769341-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:19769341-Aspergillus,
pubmed-meshheading:19769341-Benzofurans,
pubmed-meshheading:19769341-Chromans,
pubmed-meshheading:19769341-Drug Screening Assays, Antitumor,
pubmed-meshheading:19769341-HL-60 Cells,
pubmed-meshheading:19769341-Humans,
pubmed-meshheading:19769341-Inhibitory Concentration 50,
pubmed-meshheading:19769341-Marine Biology,
pubmed-meshheading:19769341-Molecular Structure,
pubmed-meshheading:19769341-Nuclear Magnetic Resonance, Biomolecular,
pubmed-meshheading:19769341-Sesquiterpenes,
pubmed-meshheading:19769341-Stereoisomerism
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pubmed:year |
2009
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pubmed:articleTitle |
Sesquiterpenoids and benzofuranoids from the marine-derived fungus Aspergillus ustus 094102.
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pubmed:affiliation |
Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, People's Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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