CAS 220930-96-1

7-hydroxy-3-[4-hydroxy(3,5-~2~H_2_)phenyl](8-~2~H)-4H-chromen-4-one

Description:

7-Hydroxy-3-[4-hydroxy(3,5-~2~H_2_)phenyl](8-~2~H)-4H-chromen-4-one, with the CAS number 220930-96-1, is a synthetic organic compound belonging to the flavonoid class, characterized by its chromone backbone. This compound features multiple hydroxyl groups, which contribute to its potential antioxidant properties. The presence of deuterium (indicated by ~2~H) suggests isotopic labeling, which can be useful in studies involving metabolic pathways or pharmacokinetics. The structural complexity, including the phenolic substituents, may influence its biological activity, making it a candidate for research in medicinal chemistry. Flavonoids are known for their diverse biological activities, including anti-inflammatory, antiviral, and anticancer effects. The solubility and stability of this compound can vary depending on the solvent and environmental conditions, which is crucial for its application in biological assays. Overall, this compound's unique structure and functional groups make it a subject of interest in both synthetic and medicinal chemistry research.

Formula: C₁₅H₇D₃O₄

InChI: InChI=1/C15H10O4/c16-10-3-1-9(2-4-10)13-8-19-14-7-11(17)5-6-12(14)15(13)18/h1-8,16-17H/i3D,4D,7D

SMILES: c1c(c(c(cc1c1coc2c(c(ccc2c1=O)O)[2H])[2H])O)[2H]

Daidzein-3',5',8-d3

Controlled Product

CAS: 220930-96-1

Applications Daidzein-3',5',8-d3 is labelled Daidzein (D103500) which is an inactive analog of Genistein (Cat. #G350000). It blocks the G1 phase of the cell cycle in Swiss 3T3 cells by inhibiting casein kinase II activity.
References Jones, P., et al.: J. Biol. Chem., 274, 32008 (1999), Hassan, M., et al.: Anticancer Res., 19, 5657 (1999), Salti, G., et al.: Eur. J . Cancer, 36, 796 (2000).

Formula: C₁₅₂H₃H₇O₄

Color and Shape: Off-White To Grey

Molecular weight: 257.26

Ref: TR-D103501

Daidzein-3,5,8-d3

CAS: 220930-96-1

Formula: C₁₅H₁₀O₄

Color and Shape: Solid

Molecular weight: 257.259g/mol

Ref: IN-DA003P87