Kobayashi Motoo, Sato Kentaro, Yoshimura Seiji, Yamaoka Makiko, Takase Shigehiro, Ohkubo Mitsuru, Fujii Takashi, Nakajima Hidenori
Exploratory Research Laboratories, Fujisawa Pharmaceutical Co Ltd, Tsukuba, Ibaraki, Japan.
J Antibiot (Tokyo). 2005 Oct;58(10):648-53. doi: 10.1038/ja.2005.89.
FR177391 produced by Serratia liquefaciens No. 1821 enhances differentiation of mouse 3T3-L1 fibroblasts to adipocytes and reduces the circulating levels of triglyceride in C57BL/KsJ-db/bd mice, an obese non-insulin-dependent diabetes mellitus animal model, although its mechanism of actions remained to be unknown. Its active derivative, 20-hydroxy FR177391, and its inactive derivative, 3-hydroxy FR177391 were produced by microbial conversion of FR177391, and biotin-labeled FR177391 was synthesized from 20-hydroxy FR177391 as an active affinity ligand to identify target molecules of FR177391 by chemical genetic approaches.