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Linarin

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Linarin Basic information

Product Name:
Linarin
Synonyms:
  • LINARIN
  • BUDDLEOSIDE
  • BUDDLOSIDE
  • ACACETIN-7-O-RUTINOSIDE
  • ACACETIN-7-RUTINOSIDE
  • 7-[[6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-5-hydroxy-4'-methoxyflavone
  • 7-[[6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-5-hydroxy-2-(4-methoxyphenyl)-4H-benzopyran-4-one
  • 7-((6-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-5-hydroxy-2-(4-methoxyphenyl)-4H-benzopyran-4-one
CAS:
480-36-4
MF:
C28H32O14
MW:
592.55
EINECS:
207-547-6
Product Categories:
  • Tri-substituted Flavones
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
Mol File:
480-36-4.mol
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Linarin Chemical Properties

Melting point:
258-260°C
Boiling point:
885.2±65.0 °C(Predicted)
Density 
1.62±0.1 g/cm3(Predicted)
storage temp. 
Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility 
Acetic Acid (Very Slightly, Heated), Acetonitrile (Slightly), DMSO (Slightly)
form 
Solid
pka
6.11±0.40(Predicted)
color 
White to Pale Beige
Stability:
Hygroscopic
InChIKey
YFVGIJBUXMQFOF-BWLJPJRBNA-N
SMILES
C12C(O)=CC(O[C@H]3[C@H](O)[C@H]([C@H](O)[C@@H](CO[C@@H]4O[C@H]([C@H](O)[C@@H](O)[C@H]4O)C)O3)O)=CC=1OC(C1C=CC(OC)=CC=1)=CC2=O |&1:6,7,9,10,12,15,17,18,20,22,r|
CAS DataBase Reference
480-36-4(CAS DataBase Reference)
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Safety Information

Safety Statements 
22-24/25
HS Code 
29389090
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Linarin Usage And Synthesis

Chemical Properties

White crystalline powder, easily soluble in methanol, almost insoluble in ether, derived from wild chrysanthemum, great thistle, and small thistle.

Uses

Linarine (Diosmin EP Impurity E) is a naturally occurring flavone glycoside that was identified to possess potential sedative and anticonvulsant properties.

in vivo

Linarin (oral administration; 50-150 mg/kg; 8 weeks) can improve bone loss in ovariectomized mice[2].

Animal Model:Ovariectomy treated female C57/BL6 mice[2]
Dosage:50 and 150 mg/kg
Administration:Oral administration (p.o.); 8 weeks
Result:Dose?dependently preserved the trabecular bone microarchitecture of ovariectomized mice.
Slightly increased BMD compared to the control OVX group.
Significantly decreased OVX-induced serum ALP and OCN levels.

IC 50

AChE

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