Vitexin-2''-O-rhamnoside

Modify Date: 2025-08-22 11:06:33

Vitexin-2''-O-rhamnoside Structure
Vitexin-2''-O-rhamnoside structure
Common Name Vitexin-2''-O-rhamnoside
CAS Number 64820-99-1 Molecular Weight 578.519
Density 1.7±0.1 g/cm3 Boiling Point 898.8±65.0 °C at 760 mmHg
Molecular Formula C27H30O14 Melting Point 215ºC
MSDS Chinese USA Flash Point 299.5±27.8 °C

 Use of Vitexin-2''-O-rhamnoside


Vitexin-2-O-rhamnoside, a main flavonoid glycoside of the leaves of Cratagus pinnatifida Bge, contributes to the protection against H2O2-mediated oxidative stress damage and has potential to treat cardiovascular system diseases[1].

 Names

Name vitexin 2''-O-α-L-rhamnoside
Synonym More Synonyms

 Vitexin-2''-O-rhamnoside Biological Activity

Description Vitexin-2-O-rhamnoside, a main flavonoid glycoside of the leaves of Cratagus pinnatifida Bge, contributes to the protection against H2O2-mediated oxidative stress damage and has potential to treat cardiovascular system diseases[1].
Related Catalog
References

[1]. Wei W, et al. Effects of vitexin-2"-O-rhamnoside and vitexin-4"-O-glucoside on growth and oxidative stress-induced cell apoptosis of human adipose-derived stem cells. J Pharm Pharmacol. 2014 Jul;66(7):988-97.

 Chemical & Physical Properties

Density 1.7±0.1 g/cm3
Boiling Point 898.8±65.0 °C at 760 mmHg
Melting Point 215ºC
Molecular Formula C27H30O14
Molecular Weight 578.519
Flash Point 299.5±27.8 °C
Exact Mass 578.163574
PSA 239.97000
LogP 1.86
Vapour Pressure 0.0±0.3 mmHg at 25°C
Index of Refraction 1.751
InChIKey LYGPBZVKGHHTIE-NQQFNCMQSA-N
SMILES CC1OC(OC2C(c3c(O)cc(O)c4c(=O)cc(-c5ccc(O)cc5)oc34)OC(CO)C(O)C2O)C(O)C(O)C1O

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
RIDADR NONH for all modes of transport
WGK Germany 3

 Articles1

More Articles
Structure-activity relationships of flavonoids as inhibitors of breast cancer resistance protein (BCRP).

Bioorg. Med. Chem. 19 , 2090-102, (2011)

Flavonoids are an interesting group of natural products ubiquitously present in human diet. Their consumption has been associated with various and differing beneficial health effects. However, several...

 Synonyms

(1S)-1,5-Anhydro-2-O-(6-deoxy-β-D-mannopyranosyl)-1-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol
8-[(2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-{[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}tetrahydro-2H-pyran-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one
Vitexin-2-O-rhamnoside
vitexin 2''-O-alpha-L-rhamnoside
8-[(2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxyméthyl)-3-{[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-méthyltétrahydro-2H-pyran-2-yl]oxy}tétrahydro-2H-pyran-2-yl]-5,7-dihydroxy-2-(4-hydroxyphényl)-4H-chromén-4-one
8-[(2S,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-3-{[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}tetrahydro-2H-pyran-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-on
(1S)-1,5-Anhydro-2-O-(6-désoxy-β-D-mannopyranosyl)-1-[5,7-dihydroxy-2-(4-hydroxyphényl)-4-oxo-4H-chromén-8-yl]-D-glucitol
Apigenin-8-C-glucoside-2'-rhamnoside
D-Glucitol, 1,5-anhydro-2-O-(6-deoxy-β-D-mannopyranosyl)-1-C-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-8-yl]-, (1S)-
Vitexin-2"-O-rhamnoside
8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
Vitexin 2''-O-rhamnoside
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