| Literature DB >> 26158859 |
Mohamed El Hattab1, Grégory Genta-Jouve2,3, Naïma Bouzidi1, Annick Ortalo-Magné4, Claire Hellio5, Jean-Philippe Maréchal6, Louis Piovetti4, Olivier P Thomas2, Gérald Culioli2,4.
Abstract
Cystophloroketals A-E (1-5), five new phloroglucinol-meroditerpenoid hybrids, have been isolated together with their putative biosynthetic precursor, the monocyclic meroditerpenoid 6, from the Mediterranean brown alga Cystoseira tamariscifolia. They represent the first examples of meroditerpenoids linked to a phloroglucinol through a 2,7-dioxabicyclo[3.2.1]octane moiety. The chemical structures, including absolute configurations, were elucidated on the basis of extensive spectroscopic analysis (HR-ESIMS, 1D and 2D NMR, and ECD) and TDDFT ECD calculations. Compounds 1-6 were tested for their antifouling activity against several marine colonizing species (bacteria, fungi, invertebrates, micro- and macroalgae). Compound 6 showed high potency for the inhibition of macrofoulers (invertebrates and macroalgae), while cystophloroketals B (2) and D (4) displayed strong inhibition of the germination of the two macroalgae tested and moderate antimicrobial activities (bacteria, microalgae, and fungi).Entities:
Mesh:
Substances:
Year: 2015 PMID: 26158859 DOI: 10.1021/acs.jnatprod.5b00264
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050