2006ARKIVOCOpen access

Novel antibacterial triterpenoid from Combretum padoides [Combretaceae]

Jeremiah Eloh Angeh, Xueshi Huang, Gerry E. Swan, Ute Möllman, Isabel Sattler, J.N. Eloff

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Abstract

The dichloromethane extract of C. padoides leaves was subjected to antibacterial activity guided fractionation against Staphylococcus aureus to afford a new oleanene-type triterpenoid glycoside identified as 1α,23β-dihydroxy-12-oleanen-29-oic-acid-23β-O-α-4-acetylrhamnopyranoside (1) together with two known compounds 1,22-dihydroxy-12-oleanen-30-oic acid (2) and 24ethylcholesta-7,22,25-trien-O-β-D-glucopyranoside (3) on the basis of 1D NMR, 2D NMR and ESI-MS analysis.Compounds 1 and 2 had a reasonable antibacterial activity [MIC of 0.031 and 0.063 mg/ml] against S. aureus and Escherichia coli.All compounds were non-cytotoxic.The results indicate that pentacyclic triterpenes from C. padoides have some antibacterial activity with no cytotoxic activity.

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The dichloromethane extract of C. padoides leaves was subjected to antibacterial activity guided fractionation against Staphylococcus aureus to afford a new oleanene-type triterpenoid glycoside identified as 1α,23β-dihydroxy-12-oleanen-29-oic-acid-23β-O-α-4-acetylrhamnopyranoside (1) together with two known compounds 1,22-dihydroxy-12-oleanen-30-oic acid (2) and 24ethylcholesta-7,22,25-trien-O-β-D-glucopyranoside (3) on the basis of 1D NMR, 2D NMR and ESI-MS analysis.Compounds 1 and 2 had a reasonable antibacterial activity [MIC of 0.031 and 0.063 mg/ml] against S. aureus and Escherichia coli.All compounds were non-cytotoxic.The results indicate that pentacyclic triterpenes from C. padoides have some antibacterial activity with no cytotoxic activity.

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Available abstract

The dichloromethane extract of C. padoides leaves was subjected to antibacterial activity guided fractionation against Staphylococcus aureus to afford a new oleanene-type triterpenoid glycoside identified as 1α,23β-dihydroxy-12-oleanen-29-oic-acid-23β-O-α-4-acetylrhamnopyranoside (1) together with two known compounds 1,22-dihydroxy-12-oleanen-30-oic acid (2) and 24ethylcholesta-7,22,25-trien-O-β-D-glucopyranoside (3) on the basis of 1D NMR, 2D NMR and ESI-MS analysis.Compounds 1 and 2 had a reasonable antibacterial activity [MIC of 0.031 and 0.063 mg/ml] against S. aureus and Escherichia coli.All compounds were non-cytotoxic.The results indicate that pentacyclic triterpenes from C. padoides have some antibacterial activity with no cytotoxic activity.

Key concepts: Combretaceae, Chemistry, Traditional medicine, Triterpenoid, Stereochemistry, Medicine

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