Lc. Chang et al., Phyllolactones A-E: new bishomoscalarane sesterterpenes from the marine sponge Phyllospongia lamellosa, TETRAHEDRON, 57(27), 2001, pp. 5731-5738
Five new bishomoscalarane sesterterpenes, phyllolactones A-E (1-5), have be
en isolated from the marine sponge Phyllospongia lamellosa. The structures
were elucidated by 1D and 2D H-1 and C-13 NMR, unambiguous assignments of o
verlapping H-1 and C-13 resonances were made by analysis of an HSQC-TOCSY s
pectrum, and relative stereochemistry established by analysis of coupling c
onstants and ROESY and NOESY spectra. A summary of previously reported carb
olactone-containing bishomoscalarane structures and the range of C-13 chemi
cal shifts arising from the various oxy substituents at C-3, C-12, C-16, C-
20 and C-24 is included. Phyllolactones A-E modestly inhibit HIV-1 envelope
-mediated fusion in vitro with IC(50)s of similar to2 muM, and show negligi
ble cytotoxicity toward the cell lines used in the fusion assay (BS-C-1 and
NIH 3T3). Published by Elsevier Science Ltd.