Five new triterpene saponins 1 ± 5 were isolated from the roots of Muraltia ononidifolia E. Mey along with the two known saponins 3 arabinopyranosyl] ester (medicagenic acid (4a,2b,3b)-2,3-dihydroxyolean-12-ene-23,28-dioic acid). Their structures were elucidated mainly by spectroscopic experiments,
Three New Medicagenic Acid Saponins from Polygala micranthaGuill. & Perr.
✍ Scribed by Turibio Kuiate Tabopda; Anne-Claire Mitaine-Offer; Tomofumi Miyamoto; Chiaki Tanaka; Bonaventure Tchaleu Ngadjui; Jean-François Mirjolet; Olivier Duchamp; Marie-Aleth Lacaille-Dubois
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- German
- Weight
- 181 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Three new medicagenic acid saponins, micranthosides A–C (1–3), were isolated from the roots of Polygala micrantha Guill. & Perr., along with six known presenegenin saponins. Their structures were elucidated on the basis of extensive 1D‐ and 2D‐NMR experiments (^1^H, ^13^C, DEPT, COSY, TOCSY, NOESY, HSQC, and HMBC) and mass spectrometry as 3‐O‐β‐D‐glucopyranosylmedicagenic acid 28‐[O‐β‐D‐galactopyranosyl‐(1→4)‐O‐β‐D‐xylopyranosyl‐(1→4)‐O‐α‐L‐rhamnopyranosyl‐(1→2)‐β‐D‐fucopyranosyl] ester (1), 3‐O‐β‐D‐glucopyranosylmedicagenic acid 28‐[O‐6‐O‐acetyl‐β‐D‐galactopyranosyl‐(1→4)‐O‐β‐D‐xylopyranosyl‐(1→4)‐O‐α‐L‐rhamnopyranosyl‐(1→2)‐β‐D‐fucopyranosyl] ester (2), and 3‐O‐{O‐β‐D‐glucopyranosyl‐(1→3)‐O‐[β‐D‐glucopyranosyl‐(1→6)]‐β‐D‐glucopyranosyl}medicagenic acid 28‐{O‐β‐D‐apiofuranosyl‐(1→3)‐O‐β‐D‐xylopyranosyl‐(1→4)‐O‐[β‐D‐apiofuranosyl‐(1→3)]‐O‐α‐L‐rhamnopyranosyl‐(1→2)‐β‐D‐fucopyranosyl} ester (3). Compounds 1–3 were evaluated against HCT 116 and HT‐29 human colon cancer cells, but they did not show any cytotoxicity.
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