1. Sequestered Chemistry of the Arminacean Nudibranch Leminda millecra in Algoa Bay, South Africa
- Author
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Michael T. Davies-Coleman, Kerry L. McPhail, and John A. Starmer
- Subjects
Cnidaria ,Magnetic Resonance Spectroscopy ,Spectrophotometry, Infrared ,Coral ,Molecular Conformation ,Pharmaceutical Science ,Gas Chromatography-Mass Spectrometry ,Analytical Chemistry ,South Africa ,Drug Discovery ,Botany ,Animals ,Furans ,Chromatography, High Pressure Liquid ,Alcyonium ,Leminda millecra ,Pharmacology ,Molecular Structure ,biology ,Organic Chemistry ,Quinones ,Stereoisomerism ,Nudibranch ,Leptogorgia ,biology.organism_classification ,Gorgonian ,Complementary and alternative medicine ,Mollusca ,Molecular Medicine ,Sesquiterpenes ,Bay - Abstract
Extracts of the endemic nudibranch Leminda millecra collected in Algoa Bay, South Africa, yielded four known metabolites, millecrones A (1) and B (2), isofuranodiene (5), and (+)-8-hydroxycalamenene (9), and nine new compounds, algoafuran (7), cubebenone (8), and a series of seven triprenylquinones and hydroquinones (21-27). A subsequent GC-MS survey of extracts of 21 of L. millecra's possible octocoral prey species in Algoa Bay identified the soft coral Alcyonium fauri as the source of 1 and the gorgonian Leptogorgia palma as the species producing 2 and 8.
- Published
- 2001
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