35927-38-9 Usage
Uses
Used in Pharmaceutical Industry:
Vicenin-1 is used as a therapeutic agent for its antioxidant, anti-inflammatory, and anti-cancer properties. It protects cells from oxidative stress and inflammation, and inhibits the growth of cancer cells, making it a promising candidate for the development of new drugs to treat various diseases.
Used in Nutraceutical Industry:
Vicenin-1 is used as a dietary supplement for its potential health benefits. Its antioxidant and anti-inflammatory properties can contribute to overall health and well-being, and its potential role in the treatment of diabetes and cardiovascular diseases makes it a valuable addition to nutraceutical products.
Used in Cosmetic Industry:
Vicenin-1 is used as an active ingredient in cosmetic products for its antioxidant and anti-inflammatory properties. It can help protect the skin from oxidative stress and inflammation, promoting a healthier and more youthful appearance.
Used in Food Industry:
Vicenin-1 can be used as a natural additive in food products for its health-promoting properties. Its antioxidant and anti-inflammatory effects can contribute to the overall health benefits of the food, making it an attractive option for consumers seeking healthier food choices.
Check Digit Verification of cas no
The CAS Registry Mumber 35927-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,2 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35927-38:
(7*3)+(6*5)+(5*9)+(4*2)+(3*7)+(2*3)+(1*8)=139
139 % 10 = 9
So 35927-38-9 is a valid CAS Registry Number.
35927-38-9Relevant academic research and scientific papers
Regioselective synthesis of di-C-glycosylflavones possessing anti-inflammation activities
Shie, Jiun-Jie,Chen, Chih-An,Lin, Chih-Chien,Ku, Angela Fay,Cheng, Ting-Jen R.,Fang, Jim-Min,Wong, Chi-Huey
experimental part, p. 4451 - 4462 (2010/11/05)
Three methods are utilized to synthesize a variety of 6,8-di-C- glycosylflavones bearing identical or distinct glycosyl moieties. Some C-glycosylation compounds are found to have better anti-inflammation activities than the parent flavones. Among them, 6,8-di-C-glucosylapigenin (known as vicenin-2) shows inhibition of TNF-α expression and NO production with IC50 values of 6.8 and 5.2 μM, respectively.
Synthesis of vicenin-1 and 3, 6,8- and 8,6-di-C-β-d-(glucopyranosyl- xylopyranosyl)-4′,5,7-trihydroxyflavones using two direct C-glycosylations of naringenin and phloroacetophenone with unprotected d-glucose and d-xylose in aqueous solution as the key reactions
Sato, Shingo,Koide, Tomoyuki
body text, p. 1825 - 1830 (2010/10/18)
Vicenin-3 was synthesized from naringenin via a short five-step reaction, which included two regioselective direct C-glycosylations with d-glucose and d-xylose (yields: 22% and 30%, respectively) as the key reactions for a total yield of 4.4%. Vicenin-1 was also synthesized from phloroacetophenone via a 10-step reaction, including the same glycosylation described above, for a total yield of 2.7% with a vicenin-3 yield of 1.7%.
