Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5279805 | Tetrahedron Letters | 2006 | 4 Pages |
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).
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ernesto Fattorusso, Adriana Romano, Orazio Taglialatela-Scafati, Giorgio Bavestrello, Patrizia Bonelli, Barbara Calcinai,