Abstract
Two novel ent-isocopalane diterpenes, coelodiol (1) and coeloic acid (2), the latter characterized by an unique oxidative degradation of ring A, have been isolated from the Indonesian sponge Coelocarteria cfr. singaporensis. The stereostructure of these metabolites has been established through interpretation of NMR data and application of the exciton chirality CD method. Coelodiol (1) and coeloic acids (2) were found to inhibit the growth of MKN-45 cell line (human gastric adenocarcinoma).
Original language | English |
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Pages (from-to) | 2197-2200 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 47 |
Issue number | 13 |
DOIs | |
Publication status | Published - Mar 27 2006 |
Keywords
- Coelocarteria cfr. singaporensis
- Diterpenes
- ent-Isocopalane
- Exciton chirality
- Indonesia
- NMR
- Structure elucidation
ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery