CAS 4569-98-6
:Isoprunetin
Description:
Isoprunetin, with the CAS number 4569-98-6, is a flavonoid compound that belongs to the class of substances known for their antioxidant properties. It is primarily found in various plants and is associated with potential health benefits, including anti-inflammatory and anti-cancer effects. Isoprunetin exhibits a structure characterized by a flavone backbone, which contributes to its biological activity. The compound is soluble in organic solvents and has limited solubility in water, which is typical for many flavonoids. Its chemical properties include the ability to undergo various reactions, such as oxidation and glycosylation, which can influence its bioavailability and efficacy in biological systems. Research into isoprunetin is ongoing, with studies focusing on its pharmacological effects and potential applications in nutraceuticals and pharmaceuticals. As with many natural compounds, the specific characteristics and effects of isoprunetin can vary based on its source and the conditions under which it is studied.
Formula:C16H12O5
InChI:InChI=1S/C16H12O5/c1-20-13-6-11(18)7-14-15(13)16(19)12(8-21-14)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3
InChI key:InChIKey=YSINCDVRUMTOPK-UHFFFAOYSA-N
SMILES:O=C1C=2C(=CC(O)=CC2OC)OC=C1C3=CC=C(O)C=C3
Synonyms:- 4H-1-Benzopyran-4-one, 7-hydroxy-3-(4-hydroxyphenyl)-5-methoxy-
- Isoprunetin
- Isoflavone, 4′,7-dihydroxy-5-methoxy-
- 7-Hydroxy-3-(4-hydroxyphenyl)-5-methoxy-4H-1-benzopyran-4-one
- 5-O-Methylgenistein
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Found 3 products.
4H-1-Benzopyran-4-one, 7-hydroxy-3-(4-hydroxyphenyl)-5-methoxy-
CAS:Formula:C16H12O5Purity:98.0%Molecular weight:284.26355-O-Methylgenistein
CAS:5-O-Methylgenistein could have antioxidant and potential liver protection effects against CCl4-induced toxicity.Formula:C16H12O5Purity:98%Color and Shape:SolidMolecular weight:284.265-O-Methylgenistein
CAS:5-O-Methylgenistein is an isoflavone compound, which is a type of flavonoid. It is derived primarily from leguminous plants, particularly soybeans and other related species. As a naturally occurring compound, 5-O-Methylgenistein exhibits biological activity through its interaction with estrogen receptors, functioning as a phytoestrogen. This unique mode of action enables it to modulate various signaling pathways that influence cellular processes, such as proliferation and apoptosis.Formula:C16H12O5Purity:Min. 95%Color and Shape:PowderMolecular weight:284.26 g/mol


