Desrhamnosyl isoacteoside
Desrhamnosyl isoacteoside Basic information
- Product Name:
- Desrhamnosyl isoacteoside
- Synonyms:
-
- DesrhaMnosyl i
- 2-(3,4-Dihydroxyphenyl)ethyl 6-O-[(E)-3-(3,4-dihydroxyphenyl)propenoyl]-β-D-glucopyranoside
- 3,4-Dihydroxyphenethyl 6-O-(3,4-dihydroxycinnamoyl)-β-D-glucopyranoside
- Calceolarioside B
- Calceorioside B
- Desrhamnosyl isoacteoside
- (E)-beta-D-Glucopyranoside, 2-(3,4-Dihydroxyphenyl)ethyl, 6-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoate]
- beta-D-Glucopyranoside, 2-(3,4-dihydroxyphenyl)ethyl, 6-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoate]
- CAS:
- 105471-98-5
- MF:
- C23H26O11
- MW:
- 478.45
- Product Categories:
-
- chemical reagent
- pharmaceutical intermediate
- phytochemical
- reference standards from Chinese medicinal herbs (TCM).
- standardized herbal extract
- Mol File:
- 105471-98-5.mol
Desrhamnosyl isoacteoside Chemical Properties
- Boiling point:
- 799.8±60.0 °C(Predicted)
- Density
- 1.58
- storage temp.
- 2-8°C
- pka
- 9.32±0.10(Predicted)
Safety Information
- Safety Statements
- 24/25
- HS Code
- 29389090
Desrhamnosyl isoacteoside Usage And Synthesis
Chemical Properties
Soluble in methanol, not easy to chloroform from Akebia quinata (Thunb.) Decne rhizome
Chemical Properties
Source: Mutongaceae plant Mutong
Extraction part: Cane
Chemical classification: Phenylethanol glycosides
Solubility: soluble in water, methanol, ethanol
Color: light Yellowish white
Appearance: powder
Storage conditions: 2-8℃, dry, dark
Uses
Calceolarioside B can be for content determination/identification/pharmacological experiments, etc. Pharmacological effects: It has various pharmacological activities such as antibacterial, anti-inflammatory, anti-viral, liver protection, cardiotonic, anti-radiation, anti-tumor, memory enhancement, immune regulation, etc.
Definition
ChEBI: Calceolarioside B is a hydroxycinnamic acid. It has a role as a metabolite.
Preparation
Method for extracting Mutong phenetoside B: pulverizing the Mutong medicinal material, placing it in an extraction tank for extraction with ethanol liquid reflux, concentrating the extract until there is no alcohol smell, adsorbing on a macroporous resin column, and sequentially using water , eluted with ethanol, collected the ethanol eluate, concentrated and dried; the dried product was repeatedly purified by preparative chromatography to give phenethyloside B.
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