7-Hydroxy-2-methylisoflavone, with the CAS number 2859-88-3, is a naturally occurring isoflavone, a class of compounds known for their structural similarity to estrogen. This compound is characterized by its phenolic structure, which contributes to its potential biological activities, including antioxidant properties and possible health benefits related to hormone regulation. It typically appears as a yellow to orange crystalline solid and is soluble in organic solvents but has limited solubility in water. The presence of hydroxyl groups in its structure enhances its reactivity and interaction with biological systems. Isoflavones like 7-hydroxy-2-methylisoflavone are often studied for their roles in plant defense mechanisms and their potential therapeutic effects in human health, particularly in relation to menopausal symptoms and cardiovascular health. Additionally, this compound may exhibit anti-inflammatory and anticancer properties, making it a subject of interest in pharmacological research. However, further studies are necessary to fully elucidate its mechanisms of action and therapeutic potential.

7-Hydroxy-2-methylisoflavone

2859-88-3: 4H-1-benzopyran-4-one, 7-hydroxy-2-methyl-3-phenyl-, 7-Hydroxy-2-methyl-3-phenyl-4H-1-benzopyran-4-one, 7-Hydroxy-2-methyl-3-phenyl-chromen-4-one, 7-Hydroxy-2-methylisoflavone, Isoflavone, 7-hydroxy-2-methyl-, NSC 108340

4H-1-Benzopyran-4-one, 7-hydroxy-2-methyl-3-phenyl-

7-Hydroxy-2-methyl-3-phenylchromen-4-one is a synthetic flavonoid that has been shown to have hepatoprotective activity. 7-Hydroxy-2-methylchromen-4-one has been found to act as an antioxidant by inhibiting the oxidation of lipids and proteins, which in turn prevents lipid peroxidation and oxidative damage to DNA. 7HMC also inhibits the growth of cancer cells and is used in the treatment of malaria. It has antiinflammatory properties and may be useful for inflammatory bowel disease or asthma. 7HMC also has antimalarial activity, as it inhibits protein synthesis in Plasmodium falciparum, the parasite that causes malaria. The molecule is converted into 7HMC by reacting with methoxy groups with hydroxyl groups on the side chain. This reaction can be catalyzed by allanrobinson reagents such as 2-(1,2,3,4,-

CAS 2859-88-3: 7-Hydroxy-2-methylisoflavone

4H-1-Benzopyran-4-one, 7-hydroxy-2-methyl-3-phenyl-

Ref: IN-DA002VRM

7-Hydroxy-2-methyl-3-phenyl-chromen-4-one

Ref: 3D-FH12892

7-hydroxy-2-methyl-3-phenyl-4H-chromen-4-one

Ref: 10-F371819