CAS 478-01-3: Nobiletin
Formula:C21H22O8
InChI:InChI=1S/C21H22O8/c1-23-13-8-7-11(9-15(13)24-2)14-10-12(22)16-17(25-3)19(26-4)21(28-6)20(27-5)18(16)29-14/h7-10H,1-6H3
InChI key:InChIKey=MRIAQLRQZPPODS-UHFFFAOYSA-N
SMILES:O(C)C1=C2C(=C(OC)C(OC)=C1OC)OC(=CC2=O)C3=CC(OC)=C(OC)C=C3
Synonyms:- 2-(3,4-Dimethoxyphenyl)-5,6,7,8-tetramethoxy-4H-1-benzopyran-4-one
- 2-(3,4-Dimethoxyphenyl)-5,6,7,8-tetramethoxychromen-4-one
- 2-(3,4-dimethoxyphenyl)-5,6,7,8-tetramethoxy-4H-chromen-4-one
- 3′,4′,5,6,7,8-Hexamethoxyflavone
- 4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5,6,7,8-tetramethoxy-
- 5,6,7,8,3′,4′-Hexamethoxyflavone
- Ccris 9012
- Flavone, 3′,4′,5,6,7,8-hexamethoxy-
- Hexamethoxyflavone
- NSC 618903
- Nsc 76751
- See more synonyms
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Found 14 products.
Nobiletin
CAS:Controlled ProductStability Light Sensitive Applications Nobiletin is an O-methylated flavone, a flavonoid isolated from citrus peels like in tangerine. It is a potent antioxidant with good bioavailability. Nobiletin directly inhibits the ATP-binding cassette proteins P-glycoprotein and breast cancer resistance protein. References Shen, C., et al.: J. Nutr. Biochem. 23, 1367 (2012); Pick, A., et al.: Bioorg. Med. Chem., 19, 2090 (2011); Wang, E., et al.: Chem. Res. Toxicol., 14, 1596 (2001)Formula:C21H22O8Color and Shape:NeatMolecular weight:402.39Nobiletin
CAS:Nobiletin, a citrus flavonoid isolated from citrus peels like in tangerine, which has anti-inflammatory and anti-tumor activities, it could be a potential protective agent for the prevention and treatment of restenosis after angioplasty. Nobiletin downregulated the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase 2 (COX-2), suppressed cell viability through AKT pathways.Formula:C21H22O8Purity:95%~99%Molecular weight:402.399Nobiletin, 98%
CAS:Formula:C21H22O8Purity:≥ 98.0%Color and Shape:White, off-white or light-yellow powderMolecular weight:402.39Nobiletin (2-(3,4-Dimethoxyphenyl)-5,6,7,8-tetramethoxy-4H-chromen-4-one)
CAS:Aromatic pesticides with oxygen heteroFormula:C21H22O8Color and Shape:PowderMolecular weight:402.13147Nobiletin
CAS:Nobiletin: a citrus-derived flavone with anti-inflammatory and anti-cancer properties; water-insoluble, very weak acid.Formula:C21H22O8Purity:98.78% - 99.76%Color and Shape:SolidMolecular weight:402.39Ref: TM-T2834
5mg57.00€10mg88.00€25mg124.00€50mg168.00€100mg265.00€200mg393.00€500mg653.00€1mL*10mM (DMSO)59.00€Nobiletin
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C21H22O8Color and Shape:White to light yellow, PowderMolecular weight:402.40Nobiletin
CAS:Oxygen-heterocyclic compoundFormula:C21H22O8Purity:≥ 98.0 % (HPLC)Color and Shape:PowderMolecular weight:402.4Nobiletin, 95%
CAS:Formula:C21H22O8Purity:≥ 95.0% (dried basis)Color and Shape:White, off-white or light-yellow powderMolecular weight:402.39Nobiletin
CAS:Formula:C21H22O8Purity:>95.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:402.40Nobiletin
CAS:Nobiletin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C21H22O8Purity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:402.43',4',5,6,7,8-Hexamethoxyflavone
CAS:3',4',5,6,7,8-Hexamethoxyflavone is a polymethoxylated flavone, which is a type of specialized chemical compound known as a flavonoid. It naturally occurs in certain plants, particularly those within the citrus family, serving as a secondary metabolite. Polymethoxylated flavones like this one are of interest due to their potential interaction with various biological pathways. The mode of action of 3',4',5,6,7,8-Hexamethoxyflavone is linked to its ability to modulate enzyme activity and receptor signaling. It may exhibit antioxidant properties, potentially inhibiting oxidative stress, and has been studied for its role in modulating inflammatory pathways. These actions suggest a potential for influencing physiological responses at the cellular level. This compound has been explored for a range of applications in scientific research, particularly in the fields of pharmacology and biochemistry. Researchers study its effects on cellular models to understand its potential therapeutic roles. Due to its bioactive properties, it may be valuable in investigating treatments for conditions associated with oxidative stress and inflammation. Through a deeper understanding of its mechanisms, 3',4',5,6,7,8-Hexamethoxyflavone could contribute to the development of novel therapeutic strategies.Formula:C21H22O8Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:402.39 g/mol
