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RHOIFOLIN

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RHOIFOLIN Basic information

Product Name:
RHOIFOLIN
Synonyms:
  • APIGENIN-7-NEOHESPERIDOSIDE
  • APIGENIN 7-O-NEOHESPERIDOSIDE
  • APIGENIN-7-RHAMNOGLUCOSIDE
  • RHOIFOLIN
  • 7-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-5-hydroxy-2-(4-hydroxyphenyl)-4H-benzopyran-4-one
  • Rhoifolin, 98%, from Turpinia montana
  • RHOIFOLIN WITH HPLC
  • apigenin 7-O-hesperidoside
CAS:
17306-46-6
MF:
C27H30O14
MW:
578.52
EINECS:
241-335-4
Product Categories:
  • Inhibitors
  • reagent
  • Tri-substituted Flavones
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
Mol File:
17306-46-6.mol
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RHOIFOLIN Chemical Properties

Melting point:
250-265 °C(Solv: ethyl acetate (141-78-6))
Boiling point:
916.5±65.0 °C(Predicted)
Density 
1.69±0.1 g/cm3(Predicted)
storage temp. 
0-6°C
solubility 
Soluble in methan
form 
powder
pka
6.11±0.40(Predicted)
color 
Yellow
LogP
-0.060 (est)
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Safety Information

Hazard Codes 
Xi
Safety Statements 
24/25
WGK Germany 
3
HS Code 
29399990

MSDS

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RHOIFOLIN Usage And Synthesis

Uses

antiinflammatory

Uses

Rhoifolin is a flavone, a type of flavonoid, a new natural glycoside of apigenin, has been obtained from the green leaves of Rhus succedanea. Rhoifolin has been shown to be an apigenin-7-rhamnoglucosi de. Rhoifolin apparently is identical with the apigenin-7-rhamnoglucoside obtained by the bromination and dehydrobromination of Naringin (N378980).

Uses

Rhoifolin is a flavone, a type of flavonoid, a new natural glycoside of apigenin, has been obtained from the green leaves of Rhus succedanea. Rhoifolin has been shown to be an apigenin-7-rhamnoglucoside. Rhoifolin apparently is identical with the apigenin-7-rhamnoglucoside obtained by the bromination and dehydrobromination of Naringin (N378980).

Definition

ChEBI: Apigenin 7-O-neohesperidoside is an apigenin derivative having an alpha-(1->2)-L-rhamnopyranosyl)-beta-D-glucopyranosyl moiety attached to the 7-hydroxy group. It has a role as a metabolite. It is a neohesperidoside, a dihydroxyflavone and a glycosyloxyflavone. It is functionally related to an apigenin.

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