
Journal of Antibiotics p. 155 - 164 (2002)
Update date:2022-08-02
Topics:
Minagawa, Kazuyuki
Kouzuki, Shuichi
Yoshimoto, Jun
Kawamura, Yoshimi
Tani, Hiroyoshi
Iwata, Tatsuo
Terui, Yoshihiro
Nakai, Hiroshi
Yagi, Shigenori
Hattori, Naohiko
Fujiwara, Tamio
Kamigauchi, Toshiyuki
Two novel compounds, stachyflin and acetylstachyflin, have been isolated by solid-state fermentation of Stachybotrys sp. RF-7260. The structures of both metabolites, determined by detailed NMR analyses and X-ray crystallographic analysis, are novel with a pentacyclic moiety including cis-fused decalin. The absolute stereochemistry of stachyflins was determined by circular dichroism analysis. Stachyflin showed antiviral activity against influenza A virus (H1N1) in vitro with an IC50 value of 0.003 μM. Acetylstachyflin was about 77-fold less active than stachyflin.
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