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HOMOORIENTIN

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HOMOORIENTIN Basic information

Product Name:
HOMOORIENTIN
Synonyms:
  • 2-(3,4-Dihydroxyphenyl)-6-β-D-glucopyranosyl-5,7-dihydroxy-4H-1-benzopyran-4-one
  • 6-(β-D-Glucopyranosyl)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one
  • Isoorientin/HoMoorientin
  • lespecapittoside
  • 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one
  • 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]chromone
  • HoMoorientin, froM PolygonuM orientale
  • IsoorientinI
CAS:
4261-42-1
MF:
C21H20O11
MW:
448.38
Product Categories:
  • Tetra-substituted Flavones
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
Mol File:
4261-42-1.mol
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HOMOORIENTIN Chemical Properties

Melting point:
245-246°C
Boiling point:
856.7±65.0 °C(Predicted)
Density 
1.759±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
methanol: soluble5mg/mL, clear, colorless to yellow
form 
powder
pka
5.90±0.40(Predicted)
color 
yellow
Stability:
Hygroscopic
InChIKey
ODBRNZZJSYPIDI-VJXVFPJBSA-N
LogP
1.580 (est)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
HS Code 
29389090
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HOMOORIENTIN Usage And Synthesis

Chemical Properties

Pale Yellow Solid

Uses

Reference Standard in the analysis of herbal medicinal products

Uses

Isoorientin is a flavonoid compound that can be isolated from the passion flower, and several other species of plants. Isoorientin has also shown to exert antioxidant, anti-nociceptive, anti-inflammat ory and gastroprotective activities in several studies.

Definition

ChEBI: A flavone C-glycoside consisting of luteolin having a beta-D-glucosyl residue at the 6-position.

General Description

Produced and qualified by HWI pharma services GmbH.
Exact content by quantitative NMR can be found on the certificate.

Biochem/physiol Actions

C-glycosyl flavone with anti-inflammatory, antimicrobial and antioxidant properties. Induces antioxidant response through PI3K singaling.

HOMOORIENTINSupplier

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