
CAS 73566-30-0: 6′′-O-Acetylgenistin
Formula:C23H22O11
InChI:InChI=1S/C23H22O11/c1-10(24)31-9-17-20(28)21(29)22(30)23(34-17)33-13-6-15(26)18-16(7-13)32-8-14(19(18)27)11-2-4-12(25)5-3-11/h2-8,17,20-23,25-26,28-30H,9H2,1H3/t17-,20-,21+,22-,23-/m1/s1
InChI key:InChIKey=DXWGBJJLEDQBKS-LDBVRRDLSA-N
SMILES:O=C1C=2C(=CC(O[C@@H]3O[C@H](COC(C)=O)[C@@H](O)[C@H](O)[C@H]3O)=CC2O)OC=C1C4=CC=C(O)C=C4
Synonyms:- 4H-1-Benzopyran-4-one, 7-((6-O-acetyl-beta-D-glucopyranosyl)oxy)-5-hydroxy-3-(4-hydroxyphenyl)-
- 4H-1-Benzopyran-4-one, 7-[(6-O-acetyl-β-<span class="text-smallcaps">D</span>-glucopyranosyl)oxy]-5-hydroxy-3-(4-hydroxyphenyl)-
- 6′′-O-Acetylgenistin
- 7-[(6-O-Acetyl-β-<span class="text-smallcaps">D</span>-glucopyranosyl)oxy]-5-hydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- Acetylgenistin
- Genistin 6′′-O-acetate
- Genistin acetate
- 7-[(6-O-Acetyl-β-D-glucopyranosyl)oxy]-5-hydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- 4H-1-Benzopyran-4-one, 7-[(6-O-acetyl-β-D-glucopyranosyl)oxy]-5-hydroxy-3-(4-hydroxyphenyl)-
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Found 7 products.
6"-O-Acetylgenistin
CAS:6-O-Acetylgenistin, isolated from soy, inhibits liver lipid peroxidation with a 10.6 μM IC50.Formula:C23H22O11Purity:98%Color and Shape:SolidMolecular weight:474.416-O-Acetylgenistin
CAS:6-O-Acetylgenistin is a natural compound, classified as an acetylated isoflavone. It is sourced from soybeans, where it is naturally present as part of the plant's secondary metabolites. Isoflavones like 6-O-Acetylgenistin are known for their structural similarity to estrogens and are consequently categorized as phytoestrogens. The mode of action of 6-O-Acetylgenistin revolves around its ability to interact with estrogen receptors, which can mimic or modulate the physiological effects of estrogen. This interaction might influence various cellular pathways, potentially affecting gene expression, cell proliferation, and apoptosis. 6-O-Acetylgenistin is under investigation for its potential uses in mitigating hormone-related disorders due to its phytoestrogenic properties. It may also hold promise in cancer research, particularly concerning breast and prostate cancer, due to its potential to modulate estrogen receptor activity. Additionally, there is interest in its application in cardiovascular health and osteoporosis, given its effects on cell signaling pathways related to these conditions. Ongoing research aims to further elucidate its biological activities and potential therapeutic benefits.Formula:C23H22O11Purity:Min. 95 Area-%Color and Shape:White PowderMolecular weight:474.41 g/molGenistin 6''-O-Acetate
CAS:Controlled ProductFormula:C23H22O11Color and Shape:NeatMolecular weight:474.414