Abstract
Microbial transformation of psiadiarabin and its 6-desmethoxy analogue 5,3' dihydroxy-7,2',4',5'-tetramethoxyflavone by Cunninghamella elegans NRRL 1392 gave the 3'-glucoside conjugates of the two flavones. Structural elucidation of these two new metabolites was achieved using 1D and 2D NMR spectroscopy and CIMS.
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APA
Ibrahim, A. R. S., Galal, A. M., Mossa, J. S., & El-Feraly, F. S. (1997). Glucose-conjugation of the flavones of Psiadia arabica by Cunninghamella elegans. Phytochemistry, 46(7), 1193–1195. https://doi.org/10.1016/S0031-9422(97)80010-6
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