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A new steroidal glycoside from<i>Corypha taliera</i>Roxb., a globally endangered species

Mohammad Shoeb,Moniruzzaman Khondker,Nilufar Nahar-2015-07-21-Natural Product Research
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TL;DRAbstract

A new steroidal glycoside, β-sitosterol-3-O-α-L-rhamnopyranosyl-(1→4)-β-D-xylopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-glucopyranoside was isolated from the methanol extract of the pericarp of Corypha taliera Roxb. The reversed-phased HPLC analysis of the methanol extract of the pericarp of C. taliera Roxb. (Talipalm), a rare species of Arecaceae family, afforded a new steroidal glycoside, β-sitosterol-3-O-α-L-rhamnopyranosyl-(1→4)-β-D-xylopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-glucopyranoside (1). The structure of the compound was elucidated unequivocally by UV, IR, HR-ESI-MS, (1)H and (13)C NMR spectroscopic studies.

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A new steroidal glycoside, β-sitosterol-3-O-α-L-rhamnopyranosyl-(1→4)-β-D-xylopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-glucopyranoside was isolated from the methanol extract of the pericarp of Corypha taliera Roxb. The reversed-phased HPLC analysis of the methanol extract of the pericarp of C. taliera Roxb. (Talipalm), a rare species of Arecaceae family, afforded a new steroidal glycoside, β-sitosterol-3-O-α-L-rhamnopyranosyl-(1→4)-β-D-xylopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-glucopyranoside (1). The structure of the compound was elucidated unequivocally by UV, IR, HR-ESI-MS, (1)H and (13)C NMR spectroscopic studies.

Keywords

GlycosideChemistryMethanolStereochemistryTwo-dimensional nuclear magnetic resonance spectroscopyOrganic chemistry

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