12738-19-1 Usage
Description
3β-[(3-O-Methyl-2,6-dideoxy-β-D-lyxo-hexopyranosyl)oxy]-14-hydroxy-5β,14β-carda-20(22)-enolide is a complex organic compound belonging to the cardenolide class of glycosides. It is characterized by its unique chemical structure, which includes a 3β-glycosylation at the 3-O position and a 14-hydroxylation at the 14-β position. This molecule exhibits significant biological activities and has potential applications in various fields due to its unique properties.
Uses
Used in Pharmaceutical Industry:
3β-[(3-O-Methyl-2,6-dideoxy-β-D-lyxo-hexopyranosyl)oxy]-14-hydroxy-5β,14β-carda-20(22)-enolide is used as a bioactive compound for its potential therapeutic effects. The compound is known to inhibit Na+/K+-ATPase, which plays a crucial role in maintaining cellular ion balance and is often overexpressed in various diseases, including cancer. By targeting this enzyme, the compound may have applications in treating conditions related to ion imbalance and could be further investigated for its potential as an anticancer agent.
Used in Drug Development:
In the drug development sector, 3β-[(3-O-Methyl-2,6-dideoxy-β-D-lyxo-hexopyranosyl)oxy]-14-hydroxy-5β,14β-carda-20(22)-enolide is used as a lead compound for the development of novel therapeutics. Its ability to inhibit Na+/K+-ATPase and block the Na+-dependent amino acid transport makes it a promising candidate for the development of drugs targeting various diseases, including cancer and other conditions related to cellular ion imbalance.
Used in Research Applications:
3β-[(3-O-Methyl-2,6-dideoxy-β-D-lyxo-hexopyranosyl)oxy]-14-hydroxy-5β,14β-carda-20(22)-enolide is also used as a research tool in the field of biochemistry and pharmacology. Its unique chemical structure and biological activities make it an interesting subject for studying the mechanisms of action of cardenolide glycosides and their interactions with cellular targets. This research could lead to a better understanding of the molecular basis of various diseases and the development of more effective treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 12738-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,2,7,3 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 12738-19:
(7*1)+(6*2)+(5*7)+(4*3)+(3*8)+(2*1)+(1*9)=101
101 % 10 = 1
So 12738-19-1 is a valid CAS Registry Number.
InChI:InChI=1/C30H46O7/c1-17-27(32)24(34-4)15-26(36-17)37-20-7-10-28(2)19(14-20)5-6-23-22(28)8-11-29(3)21(9-12-30(23,29)33)18-13-25(31)35-16-18/h13,17,19-24,26-27,32-33H,5-12,14-16H2,1-4H3
