53735-73-2 Usage
Description
(3beta,5beta,16beta)-3-((2,6-Dideoxy-beta-D-ribo-hexopyranosyl)oxy)-14,16-dihydroxycard-20(22)-enolide 16-formate is a complex organic molecule with a steroid structure, characterized by its unique configuration at the 3beta, 5beta, and 16beta positions. It features a 2,6-dideoxy-beta-D-ribo-hexopyranosyl group attached to the 3 position, 14 and 16 hydroxyl groups, a 20(22) double bond, and a formate group at the 16 position. This distinctive molecular architecture suggests potential pharmaceutical or biological applications.
Uses
Used in Pharmaceutical Industry:
(3beta,5beta,16beta)-3-((2,6-Dideoxy-beta-D-ribo-hexopyranosyl)oxy)-14,16-dihydroxycard-20(22)-enolide 16-formate is used as a potential pharmaceutical compound for its unique structure and functional groups, which may offer novel therapeutic benefits in the treatment of various diseases.
Used in Biomedical Research:
In the field of biomedical research, (3beta,5beta,16beta)-3-((2,6-Dideoxy-beta-D-ribo-hexopyranosyl)oxy)-14,16-dihydroxycard-20(22)-enolide 16-formate can be utilized as a molecular probe to study the interactions and mechanisms of steroidal compounds in biological systems, potentially leading to the discovery of new therapeutic targets and treatments.
Used in Drug Delivery Systems:
(3beta,5beta,16beta)-3-((2,6-Dideoxy-beta-D-ribo-hexopyranosyl)oxy)-14,16-dihydroxycard-20(22)-enolide 16-formate may be employed in the development of innovative drug delivery systems, leveraging its unique structural features to improve the targeting, bioavailability, and efficacy of therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 53735-73-2 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 53735-73:
(7*5)+(6*3)+(5*7)+(4*3)+(3*5)+(2*7)+(1*3)=132
132 % 10 = 2
So 53735-73-2 is a valid CAS Registry Number.
53735-73-2Relevant 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.
