Journal
JOURNAL OF NATURAL PRODUCTS
Volume 69, Issue 5, Pages 731-735Publisher
AMER CHEMICAL SOC
DOI: 10.1021/np050463o
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Funding
- FIC NIH HHS [U19 TW007401, R21 TW006662, R21 TW006662-02, R21 TW006662-01, U01 TW007401-03, U01 TW007401-01, U01 TW007401, U01 TW007401-02] Funding Source: Medline
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Bromophycolides C-I ( 1-7) were isolated from extracts of the Fijian red alga Callophycus serratus and identified by NMR and mass spectral techniques. These novel natural products share a carbon skeleton and biosynthetic origin with previously identified bromophycolides A ( 8) and B ( 9), which form a rare group of diterpene-benzoate macrolides. Bromophycolides C-I ( 1-7) displayed modest antineoplastic activity against a range of human tumor cell lines.
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