53735-71-0 Usage
Description
(3beta,5beta,16beta)-3-[(2,6-dideoxy-beta-D-ribo-hexopyranosyl)oxy]-14,16-dihydroxycard-20(22)-enolide 16-acetate is a steroid saponin derived from the oleandrigenin molecule, with a digitoxosyl residue attached at position 3. (3beta,5beta,16beta)-3-[(2,6-dideoxy-beta-D-ribo-hexopyranosyl)oxy]-14,16-dihydroxycard-20(22)-enolide 16-acetate exhibits unique structural features and potential biological activities, making it a subject of interest in various fields.
Uses
Used in Pharmaceutical Industry:
(3beta,5beta,16beta)-3-[(2,6-dideoxy-beta-D-ribo-hexopyranosyl)oxy]-14,16-dihydroxycard-20(22)-enolide 16-acetate is used as a pharmaceutical compound for its potential therapeutic applications. The specific application reason is due to its unique structural features and potential biological activities, which may contribute to the development of new drugs or treatments for various diseases.
Used in Research and Development:
In the field of research and development, (3beta,5beta,16beta)-3-[(2,6-dideoxy-beta-D-ribo-hexopyranosyl)oxy]-14,16-dihydroxycard-20(22)-enolide 16-acetate serves as a valuable compound for studying the properties and mechanisms of steroid saponins. This knowledge can be applied to the development of new drugs, understanding the interactions between these compounds and biological systems, and exploring their potential applications in various therapeutic areas.
Used in Cosmetics Industry:
(3beta,5beta,16beta)-3-[(2,6-dideoxy-beta-D-ribo-hexopyranosyl)oxy]-14,16-dihydroxycard-20(22)-enolide 16-acetate may also find applications in the cosmetics industry, where it could be used as an active ingredient in skincare products. The application reason is based on the potential benefits of this compound for skin health, such as its antioxidant, anti-inflammatory, or other properties that could contribute to improved skin condition and appearance.
Used in Agricultural Industry:
In the agricultural industry, (3beta,5beta,16beta)-3-[(2,6-dideoxy-beta-D-ribo-hexopyranosyl)oxy]-14,16-dihydroxycard-20(22)-enolide 16-acetate could be utilized as a natural pesticide or growth regulator, based on its potential biological activities and interactions with plants. The application reason is to provide an alternative to synthetic chemicals, promoting sustainable and environmentally friendly agricultural practices.
Check Digit Verification of cas no
The CAS Registry Mumber 53735-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,3 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53735-71:
(7*5)+(6*3)+(5*7)+(4*3)+(3*5)+(2*7)+(1*1)=130
130 % 10 = 0
So 53735-71-0 is a valid CAS Registry Number.
53735-71-0Relevant articles and documents
Cardiac Glycosides. 6. Gitoxigenin C16 Acetates, Formates, Methoxycarbonates, and Digitoxosides. Synthesis and Na+, K+ -ATPase Inhibitory Activities
Hashimoto, Toshihiro,Rathore, Hargovind,Satoh, Daisuke,Hong, George,Griffin, Jane F.,et al.
, p. 997 - 1003 (2007/10/02)
A series of 17 gitoxigenin 16β-formates, acetates, and methoxycarbonates was synthesized, including their 3β-acetates, formates, and digitoxosides.A 16β-formate group was generally found to increase activity 30 times, a 16β-acetate group 9-12 times, while a 16β-methoxycarbonate decreased activity by two-thirds. 3β-Formates and acetates had little effect on activity by themselves, but sometimes reduced the activity-increasing properties of 16β-formates and acetates.A 3β-digitoxoside increases the activity of ditoxigenin by 15 times, but the effect is less ifthe 16β-group is esterified.And finally, a 16-one decreases activity dramatically.These data suggest an important role for C16 esters and possibly the presence of a separate binding site on Na+, K+ -ATPase corresponding to the cardenolide C16 position.
