| Literature DB >> 16902873 |
Tida Dethoup1, Leka Manoch, Anake Kijjoa, Maria São Nascimento, Prapawadee Puaparoj, Artur M Silva, Graham Eaton, Werner Herz.
Abstract
The oligophenalenone dimer duclauxin and two new analogues, bacillisporins D and E, were isolated from the fungus TALAROMYCES BACILLISPORUS in addition to the previously reported bacillisporins A, B and C. Structures were established by spectroscopic studies. Duclauxin and bacillisporins A, B, C and E were evaluated for cytotoxicity against three human cancer cell lines. Bacillisporin A was strongly active against MCF-7 and NCI-H460 and moderately active against SF-268 while bacillisporins B, C and duclauxin were moderately active against all three cell lines.Entities:
Mesh：
Substances：
Year: 2006 PMID： 16902873 DOI： 10.1055/s-2006-947188
Source DB: PubMed Journal: Planta Med ISSN： 0032-0943 Impact factor: 3.352