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5355-48-6

Card-20(22)-enolide,3-[(O-4-O-acetyl-2,6-dideoxy-b-D-ribo-hexopyranosyl-(1?4)-O-2,6-dideoxy-b-D-ribo-hexopyranosyl-(1?4)-2,6-dideoxy-b-D-ribo-hexopyranosyl)oxy]-12,14-dihydroxy-, (3b,5b,12b)-

Catalog#: AR01CC44  |   CAS#: 5355-48-6  |   MDL#:  |   MF:  |   MW:

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Catalog Number AR01CC44
Chemical Name Card-20(22)-enolide,3-[(O-4-O-acetyl-2,6-dideoxy-b-D-ribo-hexopyranosyl-(1?4)-O-2,6-dideoxy-b-D-ribo-hexopyranosyl-(1?4)-2,6-dideoxy-b-D-ribo-hexopyranosyl)oxy]-12,14-dihydroxy-, (3b,5b,12b)-
CAS Number 5355-48-6

As a professional chemist, I can provide you with information regarding the application of β-Acetyldigoxin in chemical synthesis. β-Acetyldigoxin, a derivative of the natural cardiac glycoside digoxin, is a compound that holds significance in organic chemistry. In chemical synthesis, β-Acetyldigoxin can be utilized as a starting material for the preparation of various digoxin analogs with potentially altered biological activities. During the synthetic process, β-Acetyldigoxin can serve as a key intermediate for the modification of the digoxin molecule to introduce specific functional groups or structural alterations. By strategically incorporating different chemical moieties, researchers can explore the effects of these modifications on the pharmacological properties of the resulting analogs. This approach allows for the creation of analogs with improved potency, altered pharmacokinetic profiles, or enhanced selectivity, contributing to the development of novel therapeutic agents in the field of medicinal chemistry. Additionally, the synthetic manipulation of β-Acetyldigoxin can enable the production of labeled compounds for use in studies involving drug metabolism, pharmacokinetics, and drug-target interactions. The versatility of β-Acetyldigoxin in chemical synthesis underscores its role as a valuable tool for expanding the scope of research and innovation in the development of bioactive compounds with potential applications in pharmaceuticals and biotechnology.
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