Q4951
Quercetin
≥95% (HPLC), solid, anticancer agent
Synonym(s):
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one, 3,3′,4′,5,6-Pentahydroxyflavone
About This Item
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product name
Quercetin, ≥95% (HPLC), solid
biological source
synthetic (organic)
Assay
≥95% (HPLC)
form
solid
mp
316.5 °C
solubility
water: practically insoluble
storage temp.
room temp
SMILES string
OC1=CC(O)=C2C(OC(C3=CC=C(O)C(O)=C3)=C(O)C2=O)=C1
InChI
1S/C15H10O7/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,16-19,21H
InChI key
REFJWTPEDVJJIY-UHFFFAOYSA-N
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General description
Application
- Quercetin has been used as an antioxidant which reversed the immunosuppressive effects of high glucose and hyperglycemic sera in type 2 diabetic patients.
- It has been used as a detoxifying phytochemical in Apis mellifera.
- It has been used as a positive control in DPPH (2,2- diphenyl-1-picryhydrazyl) radical scavenging assay. It has also been used for the preparation of calibration curve to determine total flavonoid content.
Biochem/physiol Actions
Features and Benefits
Preparation Note
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Personal Protective Equipment
Certificates of Analysis (COA)
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Articles
Information on fatty acid synthesis and metabolism in cancer cells. Learn how proliferatively active cells require fatty acids for functions such as membrane generation, protein modification, and bioenergetic requirements. These fatty acids are derived either from dietary sources or are synthesized by the cell.
Protocols
Coumaric acid; Quercitrin; Myricetin; Quercetin
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