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| | 4)]-alpha-L-arabinopyranosyl)oxy]-27-hydroxy-olean-12-en-28-oic acid Basic information |
| Product Name: | 4)]-alpha-L-arabinopyranosyl)oxy]-27-hydroxy-olean-12-en-28-oic acid | | Synonyms: | 4)]-alpha-L-arabinopyranosyl)oxy]-27-hydroxy-olean-12-en-28-oic acid;Raddeanoside 20;(3beta)-3-[(O-6-Deoxy-alpha-L-mannopyranosyl-(1-2)-O-[beta-D-glucopyranosyl-(1-4)]-alpha-L-arabinopyranosyl)oxy]-27-hydroxy-olean-12-en-28-oic acid;Olean-12-en-28-oic acid, 3-[(O-6-deoxy-α-L-mannopyranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→4)]-α-L-arabinopyranosyl)oxy]-27-hydroxy-, (3β)- | | CAS: | 335354-79-5 | | MF: | C47H76O17 | | MW: | 913.1 | | EINECS: | | | Product Categories: | | | Mol File: | 335354-79-5.mol | ![4)]-alpha-L-arabinopyranosyl)oxy]-27-hydroxy-olean-12-en-28-oic acid Structure](CAS/20180808/GIF/335354-79-5.gif) |
| | 4)]-alpha-L-arabinopyranosyl)oxy]-27-hydroxy-olean-12-en-28-oic acid Chemical Properties |
| Boiling point | 999.7±65.0 °C(Predicted) | | density | 1.40±0.1 g/cm3(Predicted) | | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | | form | Powder | | pka | 4.55±0.70(Predicted) | | CAS DataBase Reference | 335354-79-5 |
| | 4)]-alpha-L-arabinopyranosyl)oxy]-27-hydroxy-olean-12-en-28-oic acid Usage And Synthesis |
| Uses | Raddeanoside 20 is a triterpenoid isolated from the rhizome of Anemone raddeana. Raddeanoside 20 can suppresse superoxide generation[1]. | | Biological Activity | Raddeanoside 20 is a triterpenoid isolated from the rhizome of Anemone raddeana. It inhibits superoxide production. | | Synthesis | After crushing 4.5Kg of dried two-headed pointed herbs, the extract was refluxed with 80% ethanol (ethanol/water, the same hereinafter) for 2 times, each time for 3 hours, the extract was combined, and the solvent was recovered under reduced pressure to obtain the ethanol extracted extract of 580g. The extract was suspended in 5L of water, and then extracted with the equal amounts of petroleum ether, ethyl acetate and n-butanol, respectively, and the petroleum ether extract, ethyl acetate extract and n-butanol extract were obtained after recovering the respective portions of the solvent. The petroleum ether extract, ethyl acetate extract and n-butanol extract were obtained after recovering the solvents. The n-butanol extract was eluted with water, 10% ethanol, 30% ethanol, 50% ethanol, 70% ethanol and 95% ethanol in a gradient by AB-8 macroporous resin column, and the 50% and 70% ethanol eluent was dried to dry paste after recovering ethanol under reduced pressure, then analyzed by silica gel column chromatography with chloroform-methanol-water (8:2:1 v/v/v), and then combined into 8 portions for thin-layer chromatography detection, and then analyzed by silica gel column chromatography with chloroform-methanol-water (8:2:1 v/v). The fourth portion was then eluted by silica gel column chromatography, chloroform-methanol-water (7:3:1 v/v), and combined into 4 portions by thin-layer chromatography detection, of which the second portion was obtained by Sephadex LH20 column chromatography (60% methanol-water) to obtain Compound 1 (24mg), and the third portion was obtained by Sephadex LH20 column chromatography (60% methanol-water) to obtain Compound 2 (12mg). Compound 2 i.e. multiplied by psoralenoside 20. | | References | [1] Chen X, et al. Antiperoxidation activity of triterpenoids from rhizome of Anemone raddeana. Fitoterapia. 2009 Mar;80(2):105-11. DOI:10.1016/j.fitote.2008.11.003 |
| | 4)]-alpha-L-arabinopyranosyl)oxy]-27-hydroxy-olean-12-en-28-oic acid Preparation Products And Raw materials |
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