
CAS 53947-99-2: 7,3′-Dihydroxy-8,4′-dimethoxyisoflavone
Formula:C17H14O6
InChI:InChI=1S/C17H14O6/c1-21-14-6-3-9(7-13(14)19)11-8-23-16-10(15(11)20)4-5-12(18)17(16)22-2/h3-8,18-19H,1-2H3
InChI key:InChIKey=YYWSNCLFZSMGCM-UHFFFAOYSA-N
SMILES:O=C1C=2C(=C(OC)C(O)=CC2)OC=C1C3=CC(O)=C(OC)C=C3
Synonyms:- 4H-1-Benzopyran-4-one, 7-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-8-methoxy-
- 7,3′-Dihydroxy-8,4′-dimethoxyisoflavone
- 3′-Hydroxyretusin 8-methyl ether
- 7-Hydroxy-3-(3-hydroxy-4-methoxyphenyl)-8-methoxy-4H-1-benzopyran-4-one
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3'-Hydroxy-8-O-methylretusin
CAS:3'-Hydroxy-8-O-methylretusin is a naturally occurring flavonoid, which is derived from various plant sources, primarily within the Leguminosae family. It exhibits a range of bioactivities attributed to its molecular structure, characterized by hydroxylation and methylation processes that enhance its stability and reactivity. The mode of action of 3'-Hydroxy-8-O-methylretusin is primarily linked to its ability to modulate oxidative stress pathways and inhibit certain enzymes involved in inflammatory processes. By scavenging free radicals and modulating signaling pathways, it contributes to cellular protection against oxidative damage and inflammation. The uses and applications of 3'-Hydroxy-8-O-methylretusin are diverse, with ongoing research exploring its potential therapeutic roles. It is of particular interest in the fields of pharmacology and biochemistry for its antioxidant and anti-inflammatory properties, which may be beneficial in the development of treatments for conditions characterized by oxidative stress and inflammation. Additionally, its role in plant defense mechanisms is of interest in botanical studies, with implications for natural product research and agricultural sciences.Formula:C17H14O6Purity:Min. 95%Molecular weight:314.29 g/mol