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Detection of polyhydroxyalkaloids in Lonchocarpus extracts by GC‐MS of acetylated derivatives
Author(s) -
Magalhães Aderbal F.,
Santos Celira C.,
Magalhães Eva G.,
Nogueira Marisa A.
Publication year - 2002
Publication title -
phytochemical analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 72
eISSN - 1099-1565
pISSN - 0958-0344
DOI - 10.1002/pca.645
Subject(s) - chemistry , brine shrimp , acetylation , stereochemistry , methanol , chromatography , gas chromatography–mass spectrometry , organic chemistry , mass spectrometry , traditional medicine , biochemistry , medicine , gene
The methanol extracts of the roots of Lonchocarpus cultratus, L. latifolius and L. subglaucescens , species native to Brazil, were all active in the brine shrimp lethality test. Fractions rich in polyhydroxylated alkaloids were obtained from these extracts and, following acetylation, were analysed by GC‐MS leading to the identification of acetylated derivatives of 2,5‐ trans ‐dihydroxymethyl‐3,4‐ trans ‐dihydroxypyrrolidine (1), 1‐deoxymannojirimycin, 1‐deoxynojirimycin, fagomine and homonojirimycin. Only from L. subglaucescens could a compound with the constitution and relative configuration expected for the penta‐acetate of 1 be isolated, and its molecular structure was determined for the first time through extensive spectral data analysis. Copyright © 2002 John Wiley & Sons, Ltd.

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