Namatame I, Tomoda H, Tabata N, Si S, Omura S
Graduate School of Pharmaceutical Sciences, Kitasato University, and Research Center for Biological Function, The Kitasato Institute, Tokyo, Japan.
J Antibiot (Tokyo). 1999 Jan;52(1):7-12. doi: 10.7164/antibiotics.52.7.
The structure of fungal beauveriolide III, an inhibitor of lipid droplet formation in mouse macrophages, was elucidated to be cyclo-[(3S,4S)-3-hydroxy-4-methyloctanoyl-L-phenylalanyl-L-alanyl- D-allo-isoleucyl] by spectral analyses and chemical degradation.