CAS 36190-95-1

4H-1-Benzopyran-4-one,5,7-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-

Description:

4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxy-3-methoxyphenyl), commonly referred to as a flavonoid compound, exhibits several notable characteristics. This compound features a chromone backbone, which is a fused benzopyran structure, and is substituted with hydroxyl and methoxy groups that contribute to its chemical reactivity and biological activity. The presence of multiple hydroxyl groups enhances its potential as an antioxidant, allowing it to scavenge free radicals and mitigate oxidative stress. Additionally, the methoxy group can influence its solubility and interaction with biological systems. This compound is often studied for its pharmacological properties, including anti-inflammatory, antimicrobial, and anticancer activities. Its structural complexity allows for various interactions with biological targets, making it a subject of interest in medicinal chemistry and natural product research. Overall, the unique arrangement of functional groups in this flavonoid contributes to its diverse biological effects and potential therapeutic applications.

Formula: C₁₆H₁₂O₆

3''-METHOXYOROBOL

CAS: 36190-95-1

Formula: C₁₆H₁₂O₆

Purity: 98.0%

Molecular weight: 300.2629

Ref: IN-DA00CHSJ

3'-O-Methylorobol

CAS: 36190-95-1

3'-O-Methylorobol: moderate antioxidant, potential analgesic, boosts osteoblast differentiation.

Formula: C₁₆H₁₂O₆

Purity: 98%

Color and Shape: Solid

Molecular weight: 300.26

Ref: TM-TN1265

3'-O-Methylorobol

CAS: 36190-95-1

Formula: C₁₆H₁₂O₆

Purity: 95%~99%

Molecular weight: 300.266

Ref: BP-SBP01790

Orobol-3'-methyl ether

CAS: 36190-95-1

Orobol-3'-methyl ether is a synthetic flavonoid compound, which is derived from natural flavonoids that are typically extracted from plants. Flavonoids like Orobol-3'-methyl ether are important due to their roles in various biological processes. This compound operates primarily by interacting with enzymes, potentially inhibiting or modifying their activity. The methyl ether modification can enhance its biological activity or stability, making it a valuable tool in biochemical research.

Formula: C₁₆H₁₂O₆

Purity: Min. 98 Area-%

Molecular weight: 300.26 g/mol

Ref: 3D-FO65483

3'-Methoxy-4',5,7-trihydroxyisoflavone

Controlled Product

CAS: 36190-95-1

Applications 3'-Methoxy-4',5,7-trihydroxyisoflavone is a derivative of Genistein (G350000); a compound that exhibits specific inhibitory activity against tyrosine kinases, including autophosphorylation of epidermal growth factor receptor kinase (IC50 - 2.6uM). Also inhibits other protein kinases through competitive inhibition of ATP. Inhibits tumor cell proliferation and induces tumor cell differentiation. Produces cell-cycle arrest and apoptosis in Jurat T-leukemia cells. However, it prevents anti-CD3 monoclonal antibody-induced thymic apoptosis. Genistein also inhibits topoisomerase II activity in vitro. Genistein has also been shown to inhibit the action of GABA on recombinant GABAA receptors 2.
References Akiyama, T., et al.: J. Biol. Chem., 262, 5592 (1987); O'Dell, T.J., et al.: Nature, 353, 588 (1991); Aharonovits, O., et al.: Biochim Biophys. Acta, 1112, 181 (1992); Platanias, L.C., et al.: J. Biol. Chem., 267, 24053 (1992); Yoshida, H., et al.: Biochim. Biophys. Acta, 1137, 321 (1992); Uckun, F.M., et al.: Science, 267, 886 (1995); Merck Index 12th ed. 4395, Huang, R.Q.; Fang, M.J.; Dillon, G.H., Mol. Brain Res. 67: 177-183 (1999)

Formula: C₁₆H₁₂O₆

Color and Shape: Neat

Molecular weight: 300.26

Ref: TR-M269675