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Chemical Structure| 6889-78-7 Chemical Structure| 6889-78-7
Chemical Structure| 6889-78-7

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4'-Methoxyflavonol is a synthetic flavonoid/flavonol compound that interacts with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) bilayers. 4'-Methoxyflavonol exhibits antioxidant, anti-inflammatory, and anticancer activities. It works by inhibiting the NF-κB signaling pathway, reducing pro-inflammatory cytokine production. It also inhibits cancer cell proliferation and induces apoptosis by modulating the PI3K/AKT and MAPK signaling pathways.

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Product Details of 4'-Methoxyflavonol

CAS No. :6889-78-7
Formula : C16H12O4
M.W : 268.26
SMILES Code : O=C1C(O)=C(C2=CC=C(OC)C=C2)OC3=CC=CC=C13
MDL No. :MFCD00017682
InChI Key :IIBBFGMVMNZMGA-UHFFFAOYSA-N
Pubchem ID :97141

Safety of 4'-Methoxyflavonol

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
 

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Technical Information

• Appel Reaction • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Benzylic Oxidation • Birch Reduction • Blanc Chloromethylation • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chugaev Reaction • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Corey-Kim Oxidation • Dess-Martin Oxidation • Fischer Indole Synthesis • Friedel-Crafts Reaction • Grignard Reaction • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Hydrogenolysis of Benzyl Ether • Jones Oxidation • Lawesson's Reagent • Leuckart-Wallach Reaction • Martin's Sulfurane Dehydrating Reagent • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mitsunobu Reaction • Moffatt Oxidation • Nomenclature of Ethers • Oxidation of Alcohols by DMSO • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Alcohols • Preparation of Aldehydes and Ketones • Preparation of Alkylbenzene • Preparation of Amines • Preparation of Ethers • Prins Reaction • Reactions of Alcohols • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Ethers • Reactions with Organometallic Reagents • Reformatsky Reaction • Ritter Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Sharpless Olefin Synthesis • Specialized Acylation Reagents-Ketenes • Stobbe Condensation • Swern Oxidation • Tebbe Olefination • Ugi Reaction • Vilsmeier-Haack Reaction • Wittig Reaction • Wolff-Kishner Reduction

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