posted on 2008-07-18, 00:00authored byAngela Zampella, Valentina Sepe, Paolo Luciano, Filomena Bellotta, Maria Chiara Monti, Maria Valeria D’Auria, Trine Jepsen, Sylvain Petek, Marie-Thérèse Adeline, Olivier Laprévôte, Anne-Marie Aubertin, Cécile Debitus, Christiane Poupat, Alain Ahond
A new anti-HIV cyclodepsipeptide, homophymine A, was isolated from a New Caledonian collection of the marine sponge Homophymia sp. The structure of homophymine A was determined by interpretation of spectroscopic data, acid hydrolysis, and LC-MS analysis. Homophymine A contains 11 amino acid residues and an amide-linked 3-hydroxy-2,4,6-trimethyloctanoic acid moiety. Along with four d-, two l-, and one N-methyl amino acids, it also contains four unusual amino acid residues: (2S,3S,4R)-3,4-diMe-Gln, (2R,3R,4S)-4-amino-2,3-dihydroxy-1,7-heptandioic acid, l-ThrOMe, and (2R,3R,4R)-2-amino-3-hydroxy-4,5-dimethylhexanoic acid. In a cell-based XTT assay, homophymine A exhibited cytoprotective activity against HIV-1 infection with a IC50 of 75 nM.