10176-66-6 Usage
Description
Nevadensin is a trimethoxyflavone, a type of flavonoid compound characterized by the presence of methoxy groups at positions 6, 8, and 4', and hydroxy groups at positions 5 and 7 on the flavone backbone. It is known for its diverse biological activities and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
Nevadensin is used as a pharmaceutical agent for its potential therapeutic effects. Its rich array of biological activities, such as anti-inflammatory, antioxidant, and anticancer properties, make it a promising candidate for the development of new drugs to treat various diseases.
Used in Cosmetic Industry:
In the cosmetic industry, nevadensin is used as an active ingredient for its skin-friendly properties. Its antioxidant and anti-inflammatory actions can contribute to skin health and protection, making it suitable for inclusion in skincare products.
Used in Nutraceutical Industry:
Nevadensin is utilized as a nutraceutical ingredient due to its health-promoting effects. It can be incorporated into dietary supplements and functional foods to provide consumers with additional health benefits, such as improved immune function and enhanced cellular protection.
Used in Agricultural Industry:
In agriculture, nevadensin may be employed as a natural pesticide or growth promoter. Its bioactive properties could potentially be harnessed to protect crops from pests or to enhance plant growth and yield, contributing to sustainable agricultural practices.
Overall, nevadensin's diverse applications across different industries highlight its versatility and potential for further research and development to maximize its benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 10176-66-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,7 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10176-66:
(7*1)+(6*0)+(5*1)+(4*7)+(3*6)+(2*6)+(1*6)=76
76 % 10 = 6
So 10176-66-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H16O7/c1-22-10-6-4-9(5-7-10)12-8-11(19)13-14(20)17(23-2)15(21)18(24-3)16(13)25-12/h4-8,20-21H,1-3H3
10176-66-6Relevant articles and documents
Nevadensin glycosides from Lysionotus pauciflorus
Liu, Yong,Wagner, Hildebert,Bauer, Rudolf
, p. 1203 - 1205 (1996)
Two new flavone glucosides, nevadensin 5-O-β-D-glucoside and nevadensin 5-O-β-D-glucosyl(1 → 6)β-D-glucoside, have been isolated from the aerial parts of Lysionotus pauciflorus. The structures have been determined by means of UV, mass spectral and one- and two-dimensional 1H and 13C NMR techniques.
Lysionotin preparation method
-
, (2017/09/05)
The invention provides a lysionotin preparation method. The lysionotin preparation method is characterized by including preparation steps: step one, adopting phloroglucinol and acetic anhydride as reaction materials, and performing Friedel-Crafts reaction under catalysis of boron trifluoride diethyl etherate to obtain 2,4,6-trihydroxyacetophone; step two, subjecting 2,4,6-trihydroxyacetophone obtained at the step one to annulation reaction with p-anisoyl chloride under catalysis of potassium carbonate to obtain 5,7-dyhydroxy-4'-methoxyflavone; step three, subjecting 5,7-dyhydroxy-4'-methoxyflavone to free radical reaction under catalysis of NBS to obtain 5,7-dyhydroxy-6,8-dibromo-4'-methoxyflavone; step four, subjecting 5,7-dyhydroxy-6,8-dibromo-4'-methoxyflavone obtained at the step three to methoxylation reaction with sodium methylate under catalysis of cuprous bromide to obtain lysionotin.