3466-23-7 Usage
General Description
Dehydrodeguelin is a natural product belonging to the rotenoid class of compounds, found in the plant species Tephrosia vogelii. It is known for its potential pharmacological activities, including anti-cancer, anti-inflammatory, and anti-oxidant properties. Dehydrodeguelin has been shown to possess inhibitory effects on various cancer cell lines, making it a promising candidate for cancer therapy. Additionally, it exhibits anti-inflammatory activity by inhibiting the production of inflammatory mediators and reducing the expression of inflammatory genes. Its anti-oxidant properties help to protect cells from oxidative damage and promote overall cellular health. Overall, dehydrodeguelin shows potential for various therapeutic applications and continues to be a subject of research in the field of natural products and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 3466-23-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3466-23:
(6*3)+(5*4)+(4*6)+(3*6)+(2*2)+(1*3)=87
87 % 10 = 7
So 3466-23-7 is a valid CAS Registry Number.
InChI:InChI=1/C23H20O6/c1-23(2)8-7-12-15(29-23)6-5-13-21(24)20-14-9-17(25-3)18(26-4)10-16(14)27-11-19(20)28-22(12)13/h5-10H,11H2,1-4H3
3466-23-7Relevant articles and documents
Structural elucidation and chemical conversion of amorphispironone, a novel spironone from Amorpha fruticosa, to rotenoids
Terada,Kokumai,Konoshima,Kozuka,Haruna,Ito,Estes,Li,Wang,Lee
, p. 187 - 190 (2007/10/02)
To search for possible antitumor promoters, we carried out an investigation of the leaves of Amorpha fruticosa L. (Leguminosae). The novel spironone type rotenoid, amorphispironone (1), was isolated together with four known rotenoids, tephrosin (2), amorphigenin (3), 12a-hydroxyamorphigenin (4) and 12a-hydroxydalpanol (5). Some of these compounds were inhibitors of Epstein-Barr virus early antigen activation induced by 12-O-tetradecanoylphorbol-13-acetate. The structure of 1 was determined from 2D-NMR spectral data and difference NOE experiments. Amorphispironone (1) was also converted to known rotenoids in order to confirm the proposed structure.
