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Baicalin-7-diglucoside

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Baicalin-7-diglucoside Basic information

Product Name:
Baicalin-7-diglucoside
Synonyms:
  • 5,6-Dihydroxy-4-oxo-2-phenyl-4H-chromen-7-yl 6-O-β-D-glucopyranos yl-β-D-glucopyranoside
  • Baicalein 7-diglucoside
  • Baicalin-7-diglucoside
  • 7-[(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-5,6-dihydroxy-2-phenyl-4H-1-benzopyran-4-one
  • Baicalein 7-O-beta-gentiobioside
  • Baicalein 7-O-diglucoside
  • Baicalein-7-O-gentiobioside
  • Oroxin B, 98%, from Oroxylum indicum
CAS:
114482-86-9
MF:
C27H30O15
MW:
594.52
Product Categories:
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
Mol File:
114482-86-9.mol
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Baicalin-7-diglucoside Chemical Properties

Boiling point:
957.5±65.0 °C(Predicted)
Density 
1.76
storage temp. 
4°C, protect from light
solubility 
Soluble in methanol and water
form 
powder
pka
5.91±0.40(Predicted)
color 
Yellowish
InChIKey
HAYLVXFWJCKKDW-WEYZNFCFNA-N
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Safety Information

Safety Statements 
24/25
HS Code 
29389090
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Baicalin-7-diglucoside Usage And Synthesis

Chemical Properties

Soluble in methanol, ethanol, water, etc., insoluble in petroleum ether and chloroform. Derived from Oroxylum indicum, Bignoniaceae

Uses

Oroxin B is a component of the seed of O. (oroxylum) indicum and is used in traditional Chinese medicine for antiinflammatory, analgesic and other functions. It also has been observed to selectively induce tumor-suppressive ER stress and inhibits tumor-adaptive ER stress in B-lymphoma cells attenuating tumor growth.

in vivo

Oroxin B (30 mg/kg, i.p., 28 days) induces malignant lymphoma cell ER stress, and inhibits tumor growth in human lymphoma cell (Raji cell) xenograft model[2].
Oroxin B (160 μM of 10 μL, injected into the knee joints of mice) protects articular cartilage in destabilized medial meniscus (DMM) induced mice OA[3].
Oroxin B (200 mg/kg/day, oral gavage) relieves hepatic inflammation and inhibits MAFLD progression in HFD-fed rats[4].

Animal Model:Human lymphoma cell (Raji cell) xenograft model[2]
Dosage:30 mg/kg
Administration:i.p., 28 days
Result:Induced malignant lymphoma cell ER stress.
Inhibited tumor growth.
Prolonged overall survival of tumor-bearing mice.
Animal Model:HFD-fed rats[4]
Dosage:200 mg/kg/day
Administration:oral gavage
Result:Reduced the levels of plasma lipids, LPS, IL-6, and TNF-α.
Inhibited liver fibrosis by reducing collagen deposition.

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