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Nat Prod Res ; 33(10): 1518-1521, 2019 May.
Article in English | MEDLINE | ID: mdl-29363347

ABSTRACT

The biotransformation of (+)-isofraxinellone (1) by Aspergillus niger was investigated. Compound 1 was transformed to only one new compound 2. The structure of 2 was identified as (-)-(4S)-4-hydroxyisofraxinellone which was regio- and stereo-selective hydroxylated at the C-4 position by IR, EI-MS 1D and 2D NMR. Absolute configuration of hydroxyl group at the C-4 position was detected by modified Mosher's method. Antifeedant activity of compounds 1 and 2 against larvae of Spodoptera litura was assayed. These compounds showed potent antifeedant activity and ED50 (50% of effective dose) values were 3.91 and 4.43 µg/cm2, respectively.


Subject(s)
Aspergillus niger/metabolism , Insecticides/metabolism , Insecticides/pharmacology , Limonins/metabolism , Limonins/pharmacology , Spodoptera/drug effects , Animals , Biotransformation , Drug Evaluation, Preclinical/methods , Hydroxylation , Insecticides/chemistry , Larva/drug effects , Limonins/chemistry , Magnetic Resonance Spectroscopy , Molecular Structure , Spectrometry, Mass, Electrospray Ionization , Stereoisomerism
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