CAS 37816-20-9
:7-hydroxy-8-methoxy-3-(4-methoxyphenyl)-4H-chromen-4-one
Description:
7-Hydroxy-8-methoxy-3-(4-methoxyphenyl)-4H-chromen-4-one, also known by its CAS number 37816-20-9, is a flavonoid compound characterized by its chromone backbone, which is a fused benzopyran structure. This compound features multiple functional groups, including hydroxyl (-OH) and methoxy (-OCH3) groups, which contribute to its chemical reactivity and potential biological activity. The presence of the 4-methoxyphenyl substituent enhances its lipophilicity and may influence its interaction with biological targets. Flavonoids like this compound are often studied for their antioxidant, anti-inflammatory, and potential anticancer properties. The specific arrangement of substituents on the chromone structure can affect its solubility, stability, and overall pharmacological profile. Additionally, this compound may exhibit UV-absorbing properties, making it of interest in both pharmaceutical and cosmetic applications. As with many flavonoids, its bioactivity can be influenced by factors such as concentration, formulation, and the presence of other compounds.
Formula:C17H14O5
InChI:InChI=1/C17H14O5/c1-20-11-5-3-10(4-6-11)13-9-22-16-12(15(13)19)7-8-14(18)17(16)21-2/h3-9,18H,1-2H3
SMILES:COc1ccc(cc1)c1coc2c(ccc(c2OC)O)c1=O
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Found 2 products.
8-O-Methylretusin
CAS:<p>8-O-Methylretusin is a naturally occurring O-methylated flavonoid, which is derived from various plant sources. This compound is notable for its potential bioactive properties, including antioxidative, anti-inflammatory, and anticancer activities. The mode of action of 8-O-Methylretusin primarily involves modulation of cellular signaling pathways, such as the inhibition of reactive oxygen species and modulation of key transcription factors that regulate inflammatory and apoptotic processes.</p>Formula:C17H14O5Purity:Min. 95%Molecular weight:298.29 g/mol
