Factory Supply Amentoflavone Pharmaceutical Grade Grade Amentoflavone
Prouct Description
Product Details
| Product Name |
Amentoflavone |
| Apperance |
Yellow powder |
| CAS |
1617-53-4 |
| MF |
C30H18O10 |
| MW |
538.464 |
In Selaginella, diflavonoids from Metasequoia can also be extracted. The efficacy of flavonoids is multi-faceted. It is a powerful antioxidant that can effectively eliminate oxygen free radicals in the body. For instance, anthocyanins and anthocyanins can inhibit the full-stage overflow of oily peroxides. This ability to prevent oxidation is more than ten times that of vitamin E. This antioxidant effect can prevent cell degeneration and aging. It can also prevent the occurrence of cancer.
Application&Function
Purpose
Taxus chinensis' Double Yellow 'possesses a variety of biological activities such as anti-inflammation, anti-oxidation, anti-viral, anti-tumor, hypoglycemic and vasodilation. It is an inhibitor of cyclooxygenase and xanthopterin oxidase. Meanwhile, it is also a disodium acetate inhibitor, which has a good inhibitory effect on Coxsackievirus and vesicular virus type in vitro.
The diflavonoids of Metasequoia glyptostroboides have the effects of anti-tumor, scavenging free radicals, dilating blood vessels and lowering blood sugar.
1. The diflavonoids of Metasequoia glyptostroboides have the effects of anti-tumor, scavenging free radicals, dilating blood vessels and lowering blood sugar.
2. A bioflavonoid with antiviral and anti-inflammatory effects. Amentoflavone is a bioflavonoid that has anti-viral and anti-inflammatory properties. The compound has been observed to inhibit the expression of INOS, LPS-induced activation of NFκB p50 (NF-κ B), translocation of p65 by LPS and block IKKα(I-κ B α) degradation in macrophages. Amentoflavone has been shown to up-regulate PPAR-γ and block the induction of COX-2. It is a negative modulator of the GABAA receptor at the binding site. The compound has demonstrated anti-viral activity against respiratory syncytial virus (RSV), with an IC50 of 5.5 μg/ml. Amentoflavone also pronounced inhibition at an IC50 = 14.9 +/- 1.9 nM of binding in vitro.
Specification
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