Acantrifoside E

Modify Date: 2025-08-22 12:43:13

Acantrifoside E Structure
Acantrifoside E structure
Common Name Acantrifoside E
CAS Number 645414-25-1 Molecular Weight 356.37
Density 1.3±0.1 g/cm3 Boiling Point 574.8±50.0 °C at 760 mmHg
Molecular Formula C17H24O8 Melting Point 178-180℃
MSDS N/A Flash Point 301.4±30.1 °C

 Use of Acantrifoside E


Acantrifoside E (Compound 8) is a nature compound. Acantrifoside E can be isolated from the 90% ethanol extract of Salacia cochinchinensis. Acantrifoside E has none α-glucosidase inhibitory activity[1].

 Names

Name (2S,3R,4S,5S,6R)-2-(2,6-dimethoxy-4-((E)-prop-1-en-1-yl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
Synonym More Synonyms

 Acantrifoside E Biological Activity

Description Acantrifoside E (Compound 8) is a nature compound. Acantrifoside E can be isolated from the 90% ethanol extract of Salacia cochinchinensis. Acantrifoside E has none α-glucosidase inhibitory activity[1].
Related Catalog
References

[1]. You HM, et al. Bioactive glycosides from Salacia cochinchinensis. Carbohydr Res. 2019 Oct 1;484:107777.  

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 574.8±50.0 °C at 760 mmHg
Melting Point 178-180℃
Molecular Formula C17H24O8
Molecular Weight 356.37
Flash Point 301.4±30.1 °C
Exact Mass 356.147125
PSA 117.84000
LogP -0.41
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.603

 Safety Information

Hazard Codes Xi

 Synonyms

2,6-Dimethoxy-4-[(1E)-1-propen-1-yl]phenyl β-D-glucopyranoside
β-D-Glucopyranoside, 2,6-dimethoxy-4-[(1E)-1-propen-1-yl]phenyl
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here



Get all suppliers and price by the below link:

Acantrifoside E suppliers

Acantrifoside E price

Related Compounds: More...
N-[[(E)-2-methyl-1-phenyl-but-2-enylidene]amino]-2,4-dinitro-aniline
7471-94-5
4-{(E)-[1-(3,5-Dichlorophenyl)-3-methyl-2,5-dioxo-4-imidazolidiny lidene]methyl}benzonitrile
509083-46-9
(Z,E)-2-<(4-methylphenyl)methylene>-3-(2-thienylmethylene)succinic anhydride
100047-13-0
methyl (E)-3-(thiophen-3-yl)acrylate
75754-85-7
methyl (E)-3-methoxybut-2-enoate
4525-28-4
Aegeline
456-12-2
Methyl (E)4.6-dichloro3-(2-oxo-1-phenyl-pyrrolidin-3-ylidenemethyl)-1H-indole-2-carboxylate
166974-21-6
2-[[(E)-1-hydroxy-3-oxo-prop-1-en-2-yl]carbamoyl]benzoic acid
81494-51-1
5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxypyrano[2,3-h]chromen-4-one
113558-13-7
11-(4,6-Dimethoxypyrimidin-2-yl)-7,11-diazatricyclo[7.3.1.0^{2,7}]trideca-2,4-dien-6-one
2415553-60-3
N-{2-[6-oxo-3-(trifluoromethyl)-1,6-dihydropyridazin-1-yl]ethyl}-6-(trifluoromethyl)pyridine-3-carboxamide
2415623-22-0
N-methyl-N-{[1-(5-methylpyrazine-2-carbonyl)piperidin-4-yl]methyl}-4-(trifluoromethyl)pyridin-2-amine
2415553-64-7
N-{[1-(5-bromopyrimidin-2-yl)piperidin-4-yl]methyl}-N-methyl-4-(trifluoromethyl)pyridin-2-amine
2415586-34-2
1-(4-{[1-(3-Fluoro-4-methylbenzoyl)piperidin-4-yl]oxy}but-2-yn-1-yl)-4-methylpiperazine
2415568-47-5
2-(3-{[(4-Cyanopyridin-2-yl)oxy]methyl}piperidin-1-yl)pyridine-3-carbonitrile
2415466-57-6
6-(4-{[(4-Cyanopyridin-2-yl)oxy]methyl}piperidin-1-yl)pyridine-3-carbonitrile
2415621-88-2
N-(2-ethyl-1,2,3,4-tetrahydroisoquinolin-5-yl)-2-methyl-6-(trifluoromethyl)pyrimidine-4-carboxamide
2415633-09-7
N-{2-[6-oxo-3-(trifluoromethyl)-1,6-dihydropyridazin-1-yl]ethyl}-3-phenylpropanamide
2415568-51-1
4-[(3,4-Dichlorophenyl)methyl]-2-(thiomorpholine-4-carbonyl)morpholine
2415513-99-2