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
InChIKey ZDLGCAQIENQSSF-UHFFFAOYSA-N
SMILES CC=Cc1cc(OC)c(OC2OC(CO)C(O)C(O)C2O)c(OC)c1

 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
5-tert-butyl 4-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl) 2-methyl-2H,4H,5H,6H,7H-pyrazolo[4,3-c]pyridine-4,5-dicarboxylate
2248258-39-9
1'-tert-butyl 1-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl) 4-methyl-3-oxaspiro[bicyclo[2.1.1]hexane-2,4'-piperidine]-1,1'-dicarboxylate
2248389-73-1
1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 2-[2-methyl-4-(trifluoromethyl)furan-3-yl]acetate
2248283-42-1
1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 2-(1-methyl-1H-indazol-5-yl)acetate
2248382-24-1
1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 3-hydroxyisoquinoline-8-carboxylate
2248283-45-4
1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 4-chloro-3-(5-methyl-1H-1,2,3,4-tetrazol-1-yl)benzoate
2248310-19-0
1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 2-oxo-6-(pyridin-3-yl)-1,2-dihydropyridine-3-carboxylate
2248368-23-0
1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 2-(3,4-difluorophenyl)-1,3-thiazole-4-carboxylate
2248389-89-9
1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 2-(3,4-difluorophenyl)-1,3-thiazole-5-carboxylate
2248334-90-7
1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl (2S)-1-(phenylcarbamoyl)pyrrolidine-2-carboxylate
2248174-50-5