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J Antibiot (Tokyo) ; 57(1): 10-6, 2004 Jan.
Article in English | MEDLINE | ID: mdl-15032480

ABSTRACT

Vertihemipterin A, the ascochlorin glycoside, and its aglycone, 4',5'-dihydro-4'-hydroxyascochlorin, were isolated from the insect pathogenic fungus Verticillium hemipterigenum BCC 2370. A new analog, 8'-hydroxyascochlorin, and five known compounds, ascochlorin, LL-Z1272delta, 8',9'-dehydroascochlorin, ascofuranone and ascofuranol, were also isolated from the same fermentation broth. Structures of these compounds were elucidated by spectroscopic methods. Stereochemistry of the known compound, 4',5'-dihydro-4'-hydroxyascochlorin, was addressed by NMR spectral analyses and the modified Mosher's method. Antiviral (HSV-1) and cytotoxic activities of these ascochlorin analogs were evaluated.


Subject(s)
Alkenes/isolation & purification , Glycosides/isolation & purification , Phenols/isolation & purification , Verticillium/chemistry , Alkenes/chemistry , Alkenes/pharmacology , Animals , Antiviral Agents/chemistry , Antiviral Agents/isolation & purification , Antiviral Agents/pharmacology , Cell Line, Tumor , Chlorocebus aethiops , Chromatography, Gel , Fermentation , Glycosides/chemistry , Glycosides/pharmacology , Inhibitory Concentration 50 , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Phenols/chemistry , Phenols/pharmacology , Simplexvirus/metabolism , Spectrometry, Mass, Electrospray Ionization , Spectrophotometry, Infrared , Spectrophotometry, Ultraviolet , Stereoisomerism , Vero Cells , Verticillium/metabolism
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