| Identification | Back Directory | [Name]
irisolidone | [CAS]
2345-17-7 | [Synonyms]
irisoidone
irisolidone
4'-Methoxytectorigenin
4'-O-Methyltectorigenin
5,7-Dihydroxy-6,4'-dimethoxyisoflavon
5,7-dihydroxy-6-methoxy-3-(4-methoxyphenyl)-4H-chromen-4-one
5,7-Dihydroxy-6-methoxy-3-(4-methoxyphenyl)-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one, 5,7-dihydroxy-6-methoxy-3-(4-methoxyphenyl)- | [Molecular Formula]
C17H14O6 | [MOL File]
2345-17-7.mol | [Molecular Weight]
314.29 |
| Chemical Properties | Back Directory | [Melting point ]
190-191 °C | [Boiling point ]
565.5±50.0 °C(Predicted) | [density ]
1.402±0.06 g/cm3(Predicted) | [storage temp. ]
4°C, protect from light | [solubility ]
Chloroform (Slightly), DMSO (Slightly) | [form ]
Solid | [pka]
6.48±0.20(Predicted) | [color ]
Off-White to Pale Yellow | [InChI]
InChI=1S/C17H14O6/c1-21-10-5-3-9(4-6-10)11-8-23-13-7-12(18)17(22-2)16(20)14(13)15(11)19/h3-8,18,20H,1-2H3 | [InChIKey]
VOOFPOMXNLNEOF-UHFFFAOYSA-N | [SMILES]
C1OC2=CC(O)=C(OC)C(O)=C2C(=O)C=1C1=CC=C(OC)C=C1 |
| Hazard Information | Back Directory | [Description]
Irisolidone is a hydrolyzed product of kudzurin. Studies have shown that it can significantly dilate coronary arteries, cerebral arteries and peripheral blood vessels and microvessels, and can reduce vascular resistance, cholesterol and blood viscosity. | [Chemical Properties]
Light yellow crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, derived from kudzu. | [Uses]
Irisolidone has anti-inflammatory, antioxidant, antibacterial, anti-tumor, estrogen-like effects, and protects liver damage caused by alcoholism. | [Definition]
ChEBI: Irisolidone is a member of 4'-methoxyisoflavones. | [Biological Activity]
Irisolidone is the main isoflavone in pueraria. Irisolidone has strong hepatoprotective activity. It has a highly effective blocking effect on the anion channel VRAC. | [in vitro]
Irisolidone shows the high efficacy for Volume-regulated anion channels (VRAC) blockade with an IC 50 of 9.8 μM in HEK293 cells.
It can inhibit endothelial cell proliferation.
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