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Biosci Biotechnol Biochem ; 68(4): 903-8, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15118321

ABSTRACT

Three novel lipoxygenase inhibitors, tetrapetalone B (2, C(28)H(35)NO(9)), C (3, C(26)H(34)NO(8)), and D (4, C(28)H(36)NO(10)), were isolated from a culture broth of Streptomyces sp. USF-4727 that produced a lipoxygenase inhibitor tetrapetalone A (1) simultaneously. Each chemical structure was revealed by spectroscopic evidence, this suggests that these three compounds are structurally related to 1. They had a tetracyclic skeleton and a beta-D-rhodinosyl moiety. Tetrapetalone B, C, and D inhibited soybean lipoxygenase with IC(50): 320, 360, and 340 microM respectively.


Subject(s)
Glycosides/chemistry , Heterocyclic Compounds, 4 or More Rings/chemistry , Lipoxygenase Inhibitors/chemistry , Streptomyces/chemistry , Diazomethane/pharmacology , Glycosides/isolation & purification , Glycosides/pharmacology , Heterocyclic Compounds, 4 or More Rings/isolation & purification , Heterocyclic Compounds, 4 or More Rings/pharmacology , Inhibitory Concentration 50 , Isomerism , Lipoxygenase/metabolism , Lipoxygenase Inhibitors/isolation & purification , Lipoxygenase Inhibitors/pharmacology , Magnetic Resonance Spectroscopy , Methylation/drug effects , Molecular Structure , Glycine max/enzymology
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