CAS 124590-31-4: 6'-O-MALONYLDAIDZIN
Formula:C24H22O12
InChI:InChI=1S/C24H22O12/c25-12-3-1-11(2-4-12)15-9-33-16-7-13(5-6-14(16)20(15)29)35-24-23(32)22(31)21(30)17(36-24)10-34-19(28)8-18(26)27/h1-7,9,17,21-25,30-32H,8,10H2,(H,26,27)/t17-,21-,22+,23-,24-/m1/s1
InChI key:InChIKey=MTXMHWSVSZKYBT-ASDZUOGYSA-N
SMILES:O=C1C=2C(=CC(O[C@@H]3O[C@H](COC(CC(O)=O)=O)[C@@H](O)[C@H](O)[C@H]3O)=CC2)OC=C1C4=CC=C(O)C=C4
Synonyms:- 3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-(4-hydroxyphenyl)-4-oxo-chromen-8-yl]oxy-tetrahydropyran-2-yl]methoxy]propanoic acid
- 4H-1-Benzopyran-4-one, 7-6-O-(carboxyacetyl)-.beta.-D-glucopyranosyloxy-3-(4-hydroxyphenyl)-
- 4H-1-Benzopyran-4-one, 7-[[6-O-(2-carboxyacetyl)-β-<span class="text-smallcaps">D</span>-glucopyranosyl]oxy]-3-(4-hydroxyphenyl)-
- 4H-1-Benzopyran-4-one, 7-[[6-O-(carboxyacetyl)-β-<span class="text-smallcaps">D</span>-glucopyranosyl]oxy]-3-(4-hydroxyphenyl)-
- 7-[[6-O-(2-Carboxyacetyl)-β-<span class="text-smallcaps">D</span>-glucopyranosyl]oxy]-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- Daidzin 6′′-O-malonate
- Malonyldaidzin
- Propanedioic acid, 6′-ester with 7-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- 4H-1-Benzopyran-4-one, 7-[[6-O-(2-carboxyacetyl)-β-D-glucopyranosyl]oxy]-3-(4-hydroxyphenyl)-
- 7-[[6-O-(2-Carboxyacetyl)-β-D-glucopyranosyl]oxy]-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- 6′′-O-Malonyldaidzin
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Found 7 products.
Daidzin 6''-O-Malonate
CAS:Controlled ProductFormula:C24H22O12Color and Shape:NeatMolecular weight:502.4246"-O-Malonyldaidzin
CAS:6"-O-Malonyldaidzin (Daidzin 6''-O-malonate) may have anticancer activity.Formula:C24H22O12Purity:98%Color and Shape:SolidMolecular weight:502.426-O-Malonyldaidzin free acid
CAS:6-O-Malonyldaidzin is a metabolite of the soybean isoflavone daidzein. It is an isoflavonoid that has been shown to activate estrogen receptors in vitro and in vivo. 6-O-Malonyldaidzin has been found to have a protective effect on hepatic steatosis, as well as an anti-inflammatory effect. This compound also appears to have matrix effects on plasma lipoproteins and vascular endothelial cells. 6-O-Malonyldaidzin is absorbed efficiently from the gastrointestinal tract, with its bioavailability being 70% or higher when taken orally. The chemical reaction for the synthesis of 6-O-Malonyldaidzin free acid can be carried out using acetylgenistin as a starting material. The sample preparation for this reaction solution may include distillation, recrystallization, or column chromatography. The analytical method for measuring the concentration of this compound includes UV spectroscFormula:C24H22O12Purity:Min. 95%Color and Shape:White PowderMolecular weight:502.42 g/mol
