Eleutheroside D
Names | |
---|---|
IUPAC name
(2R,3R,4S,5S,6R)-2-[4-[6-[3,5-dimethoxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
| |
Identifiers | |
| |
3D model (JSmol)
|
|
ChemSpider | |
PubChem CID
|
|
UNII | |
| |
| |
Properties | |
C34H46O18 | |
Molar mass | 742.72 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Eleutheroside D is an eleutheroside,[1] a compound found in Eleutherococcus senticosus, the Siberian ginseng. Chemically, it is a dimer of sinapyl alcohol glucoside, and is an optical isomer of .[2]
References[]
- ^ Wang, Z.; Zhang, L.; Sun, Y. (2005). "Semipreparative separation and determination of eleutheroside E in Acanthopanax giraldii Harms by high-performance liquid chromatography". Journal of Chromatographic Science. 43 (5): 249–52. doi:10.1093/chromsci/43.5.249. PMID 15975243.
- ^ Bone, Kerry; Simon Mills, Mcpp (2013). "How to use the monographs". Principles and Practice of Phytotherapy. pp. 353–961. doi:10.1016/B978-0-443-06992-5.00010-4. ISBN 9780443069925.
External links[]
- Media related to Eleutheroside D at Wikimedia Commons
- chemblink.com
Categories:
- Phenylpropanoid glucosides
- Aromatic compound stubs