The chemical substance with the name "(3alpha,5alpha,8xi,9xi,14xi,17beta)-3-(acetyloxy)-17-hydroxy-2,16-bis(1-methylpiperidinium-1-yl)androstane" and CAS number "43021-45-0" is a synthetic derivative of androstane, a steroid framework. This compound features multiple functional groups, including an acetyloxy group and a hydroxy group, which contribute to its biological activity and solubility properties. The presence of the piperidinium moieties suggests that it may exhibit quaternary ammonium characteristics, potentially influencing its interaction with biological membranes and receptors. The specific stereochemistry indicated by the nomenclature suggests a complex three-dimensional arrangement, which is crucial for its pharmacological properties. Such compounds are often investigated for their potential therapeutic applications, particularly in the fields of endocrinology and pharmacology, due to their structural similarity to natural steroid hormones. Overall, the unique combination of functional groups and stereochemistry in this compound may lead to diverse biological activities, warranting further research into its mechanisms of action and potential uses.

(3alpha,5alpha,8xi,9xi,14xi,17beta)-3-(acetyloxy)-17-hydroxy-2,16-bis(1-methylpiperidinium-1-yl)androstane

43021-45-0: The chemical substance with the name "(3alpha,5alpha,8xi,9xi,14xi,17beta)-3-(acetyloxy)-17-hydroxy-2,16-bis(1-methylpiperidinium-1-yl)androstane" and CAS number "43021-45-0" is a synthetic derivative of androstane, a steroid framework. This compound features multiple functional groups, including an acetyloxy group and a hydroxy group, which contribute to its biological activity and solubility properties. The presence of the piperidinium moieties suggests that it may exhibit quaternary ammonium characteristics, potentially influencing its interaction with biological membranes and receptors. The specific stereochemistry indicated by the nomenclature suggests a complex three-dimensional arrangement, which is crucial for its pharmacological properties. Such compounds are often investigated for their potential therapeutic applications, particularly in the fields of endocrinology and pharmacology, due to their structural similarity to natural steroid hormones. Overall, the unique combination of functional groups and stereochemistry in this compound may lead to diverse biological activities, warranting further research into its mechanisms of action and potential uses.

Dacuronium, a steroid, is 1/10 as potent as tubocurarine and 1/50 as pancuronium, with competitive neuromuscular blocking effects.

CAS 43021-45-0

(3alpha,5alpha,8xi,9xi,14xi,17beta)-3-(acetyloxy)-17-hydroxy-2,16-bis(1-methylpiperidinium-1-yl)androstane

Dacuronium

Ref: TM-T23960