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CAS RN: 520-34-3 | Product Number: D4441
Diosmetin
Purity: >98.0%(T)(HPLC)
- 3',5,7-Trihydroxy-4'-methoxyflavone
- Luteolin 4'-Methyl Ether
- 5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-chromen-4-one
Size | Unit Price | Philadelphia, PA | Portland, OR | Japan* | Quantity |
---|---|---|---|---|---|
5G |
$81.00
|
1 | 1 | 33 |
|
* Items in stock locally ship in 1-2 business days. Items from Japan stock are able to ship from a US warehouse within 2 weeks. Please contact TCI for lead times on items not in stock. Excludes regulated items and items that ship on ice.
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Product Number | D4441 |
Purity / Analysis Method | >98.0%(T)(HPLC) |
Molecular Formula / Molecular Weight | C__1__6H__1__2O__6 = 300.27 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Refrigerated (0-10°C) |
Condition to Avoid | Light Sensitive,Heat Sensitive |
CAS RN | 520-34-3 |
Reaxys Registry Number | 294492 |
PubChem Substance ID | 468591266 |
MDL Number | MFCD00017425 |
Appearance | White to Light yellow to Light orange powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Neutralization titration) | min. 98.0 % |
Melting point | 260.0 to 264.0 °C |
Melting Point | 262 °C |
Maximum Absorption Wavelength | 348(MeOH) nm |
Solubility (soluble in) | Acetone, Chloroform, dichloromethane |
RTECS# | DJ2984400 |
HS Number | 2932.99.9090 |
References
- 1) Intracellular Antioxidant Detoxifying Effects of Diosmetin on 2,2-Azobis(2-amidinopropane) Dihydrochloride (AAPH)-Induced Oxidative Stress through Inhibition of Reactive Oxygen Species Generation
- 2) Diosmetin exerts anti-oxidative, anti-inflammatory and anti-apoptotic effects to protect against endotoxin-induced acute hepatic failure in mice.
- 3) A review on pharmacological and analytical aspects of diosmetin: A concise report
- 4) Diosmetin inhibits tumor development and block tumor angiogenesis in skin cancer
- 5) Comparative CYP1A1 and CYP1B1 substrate and inhibitor profile of dietary flavonoids
- 6) Simultaneous determination of diosmin and diosmetin in human plasma by ion trap liquid chromatography-atmospheric pressure chemical ionization tandem mass spectrometry: Application to a clinical pharmacokinetic study
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