Novel Cytotoxic Brominated Diterpenes from the Red Alga Laurencia obtusa
- 26 August 2003
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 68 (20), 7667-7674
- https://doi.org/10.1021/jo0342323
Abstract
Five new brominated diterpenes, along with two known, have been isolated from the organic extract of the red alga Laurencia obtusa, collected from the coastal rocks of Preveza in the Ionean Sea, Greece. The novel metabolites prevezols B−E possess two new carbon skeletons, to the best of our knowledge, unprecedented in the literature. The structures and the relative stereochemistry of the new natural products were established by means of spectral data analyses. The new metabolites were tested for their cytotoxic activity against five human cell lines. Two metabolites have exhibited significant cytotoxicity.Keywords
This publication has 8 references indexed in Scilit:
- Brasilane-Type Sesquiterpenoids from Laurencia obtusaOrganic Letters, 2002
- Halogenated sesquiterpenes from the red alga Laurencia obtusaTetrahedron, 2002
- Oxachamigrenes, New Halogenated Sesquiterpenes from Laurencia obtusaJournal of Natural Products, 2002
- C15 Acetogenins from the red alga Laurencia obtusaPhytochemistry, 2001
- Prevezols A and B: new brominated diterpenes from the red alga Laurencia obtusaTetrahedron Letters, 2001
- Rogioldiol A, a new obtusane diterpene, and rogiolal, a degraded derivative, of the red seaweedLaurencia microcladia from II rogiolo along the coast of tuscany: A Synergism in Structural ElucidationHelvetica Chimica Acta, 1997
- Okadaic acid: A proton and carbon NMR studyTetrahedron, 1991
- Brasilane-type sesquiterpenoids from the mediterranean red alga Laurencia obtusaPhytochemistry, 1991