Abstract
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.
MeSH Terms
Antineoplastic Agents/chemistry,isolation & purification,pharmacology
Diterpenes/chemistry,isolation & purification,pharmacology
Drug Screening Assays, Antitumor
Fiji
Humans
Macrolides/chemistry,isolation & purification,pharmacology
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Rhodophyta/chemistry
Tumor Cells, Cultured
Chemicals
Antineoplastic Agents
Diterpenes
Macrolides
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Kubanek Julia
School of Biology, Georgia Institute of Technology, Atlanta, Georgia 30332, USA. julia.kubanek@biology.gatech.edu
Prusak Anne C
Snell Terry W
Giese Rachel A
Fairchild Craig R
Aalbersberg William
Hay Mark E
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