Antioxidant CAS 480-18-2 Taxifolin Dihydroquercetin

• Certification: ISO, FDA
• Assay Method: HPLC
• Application Form: Powder
• Application: Food, Health Care Products
• State: Powder
• Extract Source: Dihydroquercetin
• Model NO.: LYPH-Dihydroquercetin
• Product Name: Dihydroquercetin
• Appearance: White or Pale Yellow
• Test Method: HPLC Tlc
• Type: Dihydroquercetin
• Other Name: Taxifolin
• Grade: Food Grade
• Brand: Lyphar
• Stock: Available
• Coa: Available
• Capacity: 90000kg/Month
• Paymnet: Credit Card/Bictoin
• Certificate: ISO;SGS;GMP
• Original: China
• MOQ: 1kg
• Transport Package: Plastic Bag
• Specification: Food Grade
• Trademark: Lyphar
• Origin: China
• Production Capacity: 9000kg/Month

Product Description

                       Antioxidant CAS 480-18-2 Taxifolin Dihydroquercetin

Products name	Dihydroquercetin
Specification	98%
Color	White or pale yellow
Free sample	Available
CAS	98006-93-0
Molecular Formula	C15H12O7
Molecular Weight	304.25

Dihydroquercetin is not mutagenic and less toxic than the related compound quercetin. It acts as a potentialchemopreventive agent by regulating genes via an ARE-dependent mechanism. Taxifolin has shown to inhibit theovarian cancer cell growth in a dose-dependent manner. There is also a strong correlation (with a correlation coefficient of 0.93) between the antiproliferative effects of dihydroquercetin (DHQ, Dihydroquercetin) derivatives on murine skin fibroblasts and human breast cancer cells.

 

The capacity of Dihydroquercetin to stimulate fibril formation and promote stabilization of fibrillar forms of collagencan be used in medicine. Also taxifolin inhibited the cellular melanogenesis as effectively as arbutin, one of the most widely used hypopigmenting agents in cosmetics. However, arbutin acts as quercetin extremely mutagenic,carcinogenic and toxic.

Dihydroquercetin enhanced also the efficacy of conventional antibiotics like levofloxacin and ceftazidime in vitro, which have potential for combinatory therapy of patients infected with methicillin-resistant Staphylococcus aureus(MRSA).

Dihydroquercetin, as well as many other flavonoids, has been found to act as a non-selective antagonist of the opioid receptors, albeit with somewhat weak affinity.