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Ditoxigenin 3β-formate is a chemical compound derived from the diosgenin molecule, a naturally occurring steroidal sapogenin found in various plant species, particularly in the Dioscorea genus. It is characterized by the presence of a formate group (HCOO-) attached to the 3β-hydroxyl position of the diosgenin structure. This modification can influence the compound's pharmacological properties, potentially enhancing its bioactivity or solubility. Ditoxigenin 3β-formate is of interest in pharmaceutical research due to its potential applications in the synthesis of various steroidal drugs and hormones, as well as its possible role in the development of new therapeutic agents.

1253-23-2

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1253-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1253-23-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,5 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1253-23:
(6*1)+(5*2)+(4*5)+(3*3)+(2*2)+(1*3)=52
52 % 10 = 2
So 1253-23-2 is a valid CAS Registry Number.

1253-23-2Downstream Products

1253-23-2Relevant 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.

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