TY - JOUR
T1 - C15 acetogenins with antistaphylococcal activity from the red alga Laurencia glandulifera
AU - Kladi, Maria
AU - Vagias, Constantinos
AU - Stavri, Michael
AU - Rahman, M. Mukhlesur
AU - Gibbons, Simon
AU - Roussis, Vassilios
PY - 2008/4/15
Y1 - 2008/4/15
N2 - Five new C15 eight-membered cyclic ethers (1, 3–6) with a characteristic terminal cis ene–yne moiety, along with the previously reported acetylenic chloro diol (2) were isolated from the organic extract of the red alga Laurencia glandulifera, collected at Crete island in South Greece. Full assignment of all 1H and 13C resonances were carried out by extensive analysis of their NMR spectra. All metabolites were tested for their antistaphylococcal activity and the minimum inhibitory concentrations (MICs) of 2–5 were in the range of 8–256 μg/ml.
AB - Five new C15 eight-membered cyclic ethers (1, 3–6) with a characteristic terminal cis ene–yne moiety, along with the previously reported acetylenic chloro diol (2) were isolated from the organic extract of the red alga Laurencia glandulifera, collected at Crete island in South Greece. Full assignment of all 1H and 13C resonances were carried out by extensive analysis of their NMR spectra. All metabolites were tested for their antistaphylococcal activity and the minimum inhibitory concentrations (MICs) of 2–5 were in the range of 8–256 μg/ml.
U2 - 10.1016/j.phytol.2007.12.004
DO - 10.1016/j.phytol.2007.12.004
M3 - Article
VL - 1
SP - 31
EP - 36
JO - Phytochemistry Letters
JF - Phytochemistry Letters
SN - 1874-3900
IS - 1
ER -