A Pregnane Steroid from Aglaia Lawii and Structure Confirmation of Cabraleadiol Monoacetate by X-ray Crystallography
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The pregnane steroid, (E)-aglawone, along with four known triterpenes, and a known sterol mixture were isolated from the bark of Aglaia lawii (Wight) Saldanha ex Ramamoorty (Meliaceae). The structural determination/identification was accomplished by a combination of 1D- and 2D-NMR spectroscopic techniques. The relative stereochemistry of the known triterpene, 20S,24S-epoxydammarane-3alpha,25-diol acetate, was also unequivocally determined for the first time by X-ray crystallography. The isolates were not active against various human cancer cell lines.
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Dong J, Liu H, Wang H, Lou H, Pan W, Li J Molecules. 2024; 29(1).
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Fun H, Chantrapromma S, Supriadin A, Harneti D, Supratman U Acta Crystallogr Sect E Struct Rep Online. 2013; 68(Pt 11):o3089-90.
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