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AURANTIO-OBTUSIN

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AURANTIO-OBTUSIN Basic information

Product Name:
AURANTIO-OBTUSIN
Synonyms:
  • 1,3,7-Trihydroxy-2,8-diMethoxy-6-Methyl-9,10-anthracenedione
  • Aurantio-obtusifolin
  • AURANTIO-OBTUSIN
  • 1,3,7-Trihydroxy-2,8-dimethoxy-6-methylanthracene-9,10-dione
  • URANTIO-OBTUSIN
  • Aurantioobtusin, 98%, from Catsia tora Linn
  • 9,10-Anthracenedione, 1,3,7-trihydroxy-2,8-dimethoxy-6-methyl-
  • 67979-25-3 AURANTIO-OBTUSIN
CAS:
67979-25-3
MF:
C17H14O7
MW:
330.29
Product Categories:
  • chemical reagent
  • pharmaceutical intermediate
  • Intermediates & Fine Chemicals
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
  • Pharmaceuticals
Mol File:
67979-25-3.mol
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AURANTIO-OBTUSIN Chemical Properties

Melting point:
265-266 °C
Boiling point:
594.6±50.0 °C(Predicted)
Density 
1.510±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Soluble in chloroform, DMSO and methan
form 
powder
pka
6.32±0.20(Predicted)
color 
Orange
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Safety Information

Safety Statements 
24/25
HS Code 
29389090
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AURANTIO-OBTUSIN Usage And Synthesis

Description

Aurantioobtusin is an anthraquinone originally isolated from Cassia seeds with diverse biological activities. It inhibits rat lens aldose reductase (RLAR) in vitro (IC50 = 13.6 μM). Aurantioobtusin (10 and 100 μM) activates the aryl hydrocarbon receptor (AhR) in a concentration-dependent manner. It inhibits rat platelet aggregation induced by arachidonic acid (Item Nos. 90010 | 90010.1 | 10006607), ADP, and collagen. Aurantioobtusin induces vasorelaxation in isolated precontracted rat mesenteric artery rings, an effect that is inhibited by the PI3K inhibitor LY290042 or inhibition of endothelial nitric oxide synthase (eNOS). It is larvicidal against A. gambiae mosquitoes (LD50 = 10 ppm).

Uses

A compound found in herbal remedies, believed to have an effect on blood platelet aggregation and lower blood lipid count

Definition

ChEBI: A trihydroxyanthraquinone that is 1,3,7-trihydroxy-9,10-anthraquinone which is by methoxy groups at positions 2 and 8, and by a methyl group at position 6.

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