Dedicated to Prof. I(. Hiller on the occasion of his 65th birthday (8.XII. 95) Three new saponins 1-3 were isolated from Herniaria glubra by means of prep. HPLC and TLC. The structures were established mainly by a combination of 2D-NMR techniques (COSY, TOCSY, ROESY, HMQC, and HMBC) as 0 -a -L-rhamn
Novel Triterpene Saponins from Zizyphus joazeiro
✍ Scribed by Wolfgang Schühly; Jörg Heilmann; Ihsan Çalis; Otto Sticher
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- German
- Weight
- 128 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Two dammarane-type saponins with a novel aglycone derived from the parent 16,22-epoxy-24methylidenedammarane and lotoside A, a new lotogenin derivative, were isolated from the MeOH extract of the stem bark of the Brazilian medicinal plant Zizyphus joazeiro, in addition to the known saponin 3b-{{O-
The structures of the new compounds were determined as 16,22-epoxy-3b-[(b-d-glucopyranosyl) 4) by means of 1D-and 2D-NMR spectroscopy, as well as FAB mass spectrometry. For the novel aglycone, we propose the name joazeirogenin and, for the new saponins, joazeiroside A (2) and B (3). Joazeirogenin was found to be 16,22-epoxy-24-methylidenedammarane-3b,15a,16a,20b-tetrol. a ) Arap Arabinopyranose, Araf arabinofuranose, Glcp glucopyranose, Apif apiofuranose. b ) Coupling constants not assignable due to overlapping signals.
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