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ChemicalBook > Product Catalog >Natural Products >Flavonoids >NOBILETIN

NOBILETIN

NOBILETIN Suppliers list
Company Name: PNP Biotech Co. Ltd
Tel: +8618516098983
Email: sales@pnpbiotech.com
Products Intro: Product Name:Nobiletin
CAS:478-01-3
Purity:98% Package:25kg;0.00;USD
Company Name: Hebei Yanxi Chemical Co., Ltd.
Tel: +8617531190177
Email: peter@yan-xi.com
Products Intro: Product Name:Nobiletin
CAS:478-01-3
Purity:0.99 Package:1kg;40USD|1kg;40USD|1kg;40USD Remarks:Factory direct sales
Company Name: Sinoway Industrial co., ltd.
Tel: 0592-5800732; +8613806035118
Email: xie@china-sinoway.com
Products Intro: Product Name:Nobiletin
CAS:478-01-3
Purity:98% up, Package:1Kg/Bag;0.00;USD|25Kg/Bag;0.00;USD|100Kg/Bag;0.00;USD
Company Name: Hebei Kingfiner Technology Development Co.Ltd
Tel: +86-15532196582 +86-15373005021
Email: lisa@kingfinertech.com
Products Intro: Product Name:Nobiletin
CAS:478-01-3
Purity:0.99 Package:1kg;0.00;USD|25kg;0.00;USD|50kg;0.00;USD
Company Name: Chongqing Zhihe Biopharmaceutical Co., Ltd.
Tel: +86-18580541567; +8618580541567
Email: sales@zhswyy.com
Products Intro: Product Name:NOBILETIN
CAS:478-01-3
Purity:>=98% Package:1kg;|5kg;|25kg

NOBILETIN manufacturers

  • Nobiletin
  • Nobiletin pictures
  • $150.00 / 1kg
  • 2024-12-20
  • CAS:478-01-3
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 500kg
  • NOBILETIN
  • NOBILETIN pictures
  • $0.00 / 1kg
  • 2024-12-20
  • CAS:478-01-3
  • Min. Order: 1kg
  • Purity: 98% HPLC
  • Supply Ability: 1000kg
  • Nobiletin
  • Nobiletin pictures
  • $0.00 / 1Kg/Bag
  • 2024-12-20
  • CAS:478-01-3
  • Min. Order: 1Kg/Bag
  • Purity: 98% up,
  • Supply Ability: 20 tons

Related articles

  • Nobiletin benefits
  • Nobiletin has been proved biological activitys such as having antitumor, antiviral, blood sugar lowering, neuroprotective, its....
  • Dec 15,2022
NOBILETIN Basic information
Description Source Uses structure and hydrogen bonding Application
Product Name:NOBILETIN
Synonyms:Nobiletin, froM Citrus nobilis Lour.;4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5,6,7,8-tetramethoxy-;Nobiletin, >=98%;NOBILETIN;3',4',5,6,7,8-HEXAMETHOXYFLAVONE;NOBILETIN WITH HPLC;NOBILETIN, 20% (TECHNICAL GRADE);4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-
CAS:478-01-3
MF:C21H22O8
MW:402.39
EINECS:251-228-4
Product Categories:chemical reagent;pharmaceutical intermediate;Inhibitors;natural product;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Hexa-substituted Flavones;CITRIMORE;478-01-3
Mol File:478-01-3.mol
NOBILETIN Structure
NOBILETIN Chemical Properties
Melting point 136.0 to 140.0 °C
Boiling point 587.9±50.0 °C(Predicted)
density 1.244±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility Soluble in DMSO (up to 10 mg/ml)
form Solid
color White
BRN 360887
Stability:Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
InChIKeyMRIAQLRQZPPODS-UHFFFAOYSA-N
CAS DataBase Reference478-01-3(CAS DataBase Reference)
Safety Information
Safety Statements 24/25
WGK Germany 3
RTECS DJ3052200
HS Code 29329990
MSDS Information
NOBILETIN Usage And Synthesis
DescriptionNobiletin (NOB) chemically known as 5,6,7,8,3′,4′-hexamethoxyflavone is a dietary polymethoxylated flavonoid found in Citrus fruits. Nobiletin is a flavonoid isolated from citrus peels. It is an O-methylated flavone that has the activity to rescue bulbectomy-induced memory impairment.
Nobiletin
SourceNobiletin is a nonpolar polymethoxylated flavone (PMFs) found in the citrus peel of various fruits, such as tangerine. Its chemical structure is similar to tangeretin, containing the typical flavonoid structure and six methoxyl groups (one more than tangeretin).
UsesNOB is a multifunctional pharmaceutical agent. The various pharmacological activities of NOB include neuroprotection, cardiovascular protection, antimetabolic disorder, anticancer, anti-inflammation, and antioxidation.
structure and hydrogen bondingThe crystal structure study on NOB shows that the chromene and the arene rings are almost in the same plane. The C atoms of the two methoxy groups in the arene ring are also in the same plane, while the C atoms of four methoxy groups linking to the chromene ring are not in parallel. This conformational characteristic of chiral structure is indicated by the covalent bond rotation between the arene and the chromene rings and the conformational alternations of methoxy groups.
ApplicationNobiletin has been shown to exhibit antioxidant, anti-inflammatory, antitumor/cancer, and antiangiogenic activity in vitro and in vivo. Animal and in vitro data also demonstrate nobiletin's potential ability to suppress bone loss, lower cholesterol and atherosclerosis, and improve hyperglycemia and insulin resistance.
DescriptionNobiletin (478-01-3) is a natural product isolated from citrus peels.? It has recently been shown to possess circadian clock amplitude-enhancing properties and was able to prevent metabolic syndrome in mice?via?a?Clock?gene-dependent mechanism.1? Nobiletin directly bound to and activated RORα/γ.? Nobiletin has previously been shown to attenuate the effects of metabolic syndrome2, have anti-neuroinflammatory effects3, possess neurotrophic activity4, and be a cancer chemopreventative agent5.
Chemical PropertiesWhite powder
UsesNobiletin 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.
Usesmatrix metaloproteinase inhibitor; antineoplastic
DefinitionChEBI: A methoxyflavone that is flavone substituted by methoxy groups at positions 5, 6, 7, 8, 3' and 4' respectively.
benefitsNobiletin improved cognitive deficits and the pathological features of AD, such as Aβ pathology, hyperphosphorylation of tau, and oxidative stress, in animal models of AD. In addition, nobiletin improved motor and cognitive deficits in PD animal models. These observations suggest that nobiletin has the potential to become a novel drug for the treatment and prevention of neurodegenerative diseases such as AD and PD.
References1) He?et al.?(2016),?The Small Molecule Nobiletin Targets the Molecular Oscillator to Enhance Circadian Rhythms and Protect against Metabolic Syndrome; Cell Metabolism,?23?610 2) Mulvihill?et al.?(2011),?Nobiletin attenuates VLDL overproduction, dyslipidemia, and atherosclerosis in mice with diet-induced insulin resistance; Diabetes?60?1446 3) Cui?et al.?(2010),?Anti-neuroinflammatory activity of nobiletin on suppression of microglial activation; Biol. Pharm. Bull.,?33?1814 4) Nagase?et al.?(2005),?Mechanism of neurotrophic action of nobiletin in PC12D cells; Biochemistry?44?13683 5) Walle (2007),?Methoxylated flavones, a superior cancer chemopreventative flavonoid subclass?;?Semin. Cancer Biol.?17?354
Tag:NOBILETIN(478-01-3) Related Product Information
2,3-Dimethoxy-5-methyl-1,4-hydroquinone 3',4',5,7-TETRAMETHOXYFLAVONE 7,8-DIMETHOXYFLAVONE 6,7-DIMETHOXY-3',4',5-TRIHYDROXYFLAVONE 5-DEMETHYLNOBILETIN 2,3,4-Trimethoxyphenol Wogonin 3',4',7,8-TETRAHYDROXYFLAVONE GARDENIN B 2,3,4,5-Tetramethoxytoluene 5,7,8-TRIHYDROXYFLAVONE Nobiletin LYSIONOTIN 1,2,3,4-TETRAMETHOXYBENZENE 6-METHOXYLUTEOLIN NOBILETIN(P) FLAVONE PEDALITIN