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(3beta,5beta)-3-([(4alpha,16xi,17R,21alpha)-17,21-dihydroxyajmalan-4-ium-4-yl]acetyloxy)-5,14-dihydroxy-19-oxocard-20(22)-enolide chloride is a complex organic compound with a unique structure that features multiple hydroxyl groups, a card-20(22)-enolide ring, and a chloride ion. It also contains an acetyl group attached to a 17,21-dihydroxyajmalan-4-ium-4-yl moiety. This intricate chemical structure suggests potential pharmacological activity and indicates its potential for use in various scientific fields, including organic chemistry, biochemistry, medicinal chemistry, and pharmacology. Further research and characterization are required to fully comprehend its properties and possible applications.

83059-99-8

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83059-99-8 Usage

Uses

Used in Pharmaceutical Research:
(3beta,5beta)-3-([(4alpha,16xi,17R,21alpha)-17,21-dihydroxyajmalan-4-ium-4-yl]acetyloxy)-5,14-dihydroxy-19-oxocard-20(22)-enolide chloride is used as a research compound for exploring its potential pharmacological properties and applications in the development of new drugs. Its unique structure may offer insights into novel mechanisms of action and therapeutic targets.
Used in Organic Chemistry:
In the field of organic chemistry, (3beta,5beta)-3-({[(4alpha,16xi,17R,21alpha)-17,21-dihydroxyajmalan-4-ium-4-yl]acetyl}oxy)-5,14-dihydroxy-19-oxocard-20(22)-enolide chloride can be used as a starting material or a synthetic intermediate for the preparation of other complex organic molecules. Its unique functional groups and structural features make it an interesting candidate for further chemical modifications and reactions.
Used in Biochemistry and Medicinal Chemistry:
(3beta,5beta)-3-([(4alpha,16xi,17R,21alpha)-17,21-dihydroxyajmalan-4-ium-4-yl]acetyloxy)-5,14-dihydroxy-19-oxocard-20(22)-enolide chloride can be employed as a tool in biochemistry and medicinal chemistry to study the interactions between biological macromolecules and small molecules. Its structural features may facilitate the investigation of molecular recognition, binding affinity, and potential biological activities.
Used in Drug Delivery Systems:
Similar to other complex organic compounds, (3beta,5beta)-3-([(4alpha,16xi,17R,21alpha)-17,21-dihydroxyajmalan-4-ium-4-yl]acetyloxy)-5,14-dihydroxy-19-oxocard-20(22)-enolide chloride may be utilized in the development of drug delivery systems. Its unique structure could be exploited to enhance the solubility, stability, and bioavailability of other therapeutic agents, potentially improving their efficacy and reducing side effects.
Used in Chemical Synthesis:
(3beta,5beta)-3-([(4alpha,16xi,17R,21alpha)-17,21-dihydroxyajmalan-4-ium-4-yl]acetyloxy)-5,14-dihydroxy-19-oxocard-20(22)-enolide chloride can also be used in chemical synthesis as a building block or a precursor for the synthesis of other complex organic molecules with potential applications in various industries, such as pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 83059-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,5 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83059-99:
(7*8)+(6*3)+(5*0)+(4*5)+(3*9)+(2*9)+(1*9)=148
148 % 10 = 8
So 83059-99-8 is a valid CAS Registry Number.

83059-99-8Downstream Products

83059-99-8Relevant academic research and scientific papers

Alkaloid cardenolides

Makarovich, I. F.,Ivanov, L. V.,Khadzhai, Ya. I.,Belokon', V. F.,Pavlova, V. V.,et al.

, p. 224 - 228 (2007/10/02)

New alkaloid cardenolides have been synthesized and their biological activity has been studied.It has been established that ajmalinocardenolides possess cardiotonic and antiarrhytmic activity with a low or moderate toxicity, while cardenolides derivatives of hyoscyamine and of scopolamine have proved to be highly toxic compounds.Using fluorescent probes it has been shown that the ajmalinocardenolides are sorbed fairly strongly on liposome membranes, and they also promote the binding of calcium ions by biological membranes.

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