29362-48-9 Usage
Uses
1. Used in Pharmaceutical Industry:
[(3S,5R,8R,9S,10S,13R,16R,17S)-3-[(2R,4S,5R,6R)-4,5-bis[[(2R,4S,5R,6R)-4,5-dihydroxy-6-methyl-oxan-2-yl]oxy]-6-methyl-oxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate is used as a potential therapeutic agent for various medical conditions due to its complex structure and hydrophobic nature, which may allow it to interact with biological targets in the human body.
2. Used in Chemical Research:
[(3S,5R,8R,9S,10S,13R,16R,17S)-3-[(2R,4S,5R,6R)-4,5-bis[[(2R,4S,5R,6R) -4,5-dihydroxy-6-methyl-oxan-2-yl]oxy]-6-methyl-oxan-2-yl]oxy-14-hydro xy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15, 16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate can be used as a research tool in the field of organic chemistry, particularly in the study of steroidal compounds and their interactions with other molecules. Its unique structure may provide insights into the development of new drugs or materials with specific properties.
3. Used in Cosmetics Industry:
Due to its hydrophobic properties, [(3S,5R,8R,9S,10S,13R,16R,17S)-3-[(2R,4S,5R,6R)-4,5-bis[[(2R,4S,5R,6R)-4,5-dihydroxy-6-methyl-oxan-2-yl]oxy]-6-methyl-oxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate may be utilized in the development of cosmetics and personal care products, where its hydrophobic nature could contribute to the formulation of creams, lotions, or other products that require a stable emulsion or dispersion of ingredients.
Check Digit Verification of cas no
The CAS Registry Mumber 29362-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,3,6 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29362-48:
(7*2)+(6*9)+(5*3)+(4*6)+(3*2)+(2*4)+(1*8)=129
129 % 10 = 9
So 29362-48-9 is a valid CAS Registry Number.
29362-48-9Relevant academic research and scientific papers
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.
