CAS 22798-96-5
:Cholest-7-en-6-one,2,3,14,25-tetrahydroxy-20,22-[(1-methylethylidene)bis(oxy)]-, (2b,3b,5b,22R)-
Description:
Cholest-7-en-6-one, 2,3,14,25-tetrahydroxy-20,22-[(1-methylethylidene)bis(oxy)]-, (2b,3b,5b,22R)- is a complex steroid compound characterized by its multi-hydroxylated structure and specific stereochemistry. This substance features a steroid backbone with a double bond at the 7-position and hydroxyl groups at the 2, 3, 14, and 25 positions, contributing to its hydrophilic properties. The presence of the 20,22-[(1-methylethylidene)bis(oxy)] moiety indicates additional functionalization that may influence its biological activity and solubility. The stereochemistry, denoted by the (2b,3b,5b,22R) configuration, plays a crucial role in determining the compound's interaction with biological systems, including potential receptor binding and metabolic pathways. This compound may be of interest in biochemical research, particularly in studies related to cholesterol metabolism, steroid hormone synthesis, or as a potential therapeutic agent. Its CAS number, 22798-96-5, allows for easy identification and reference in scientific literature and databases.
Formula:C30H48O7
Synonyms:- 5b-Cholest-7-en-6-one, 2b,3b,14,20,22,25-hexahydroxy-, cyclic 20,22-acetal withacetone, (22R)- (8CI)
- 20-Hydroxyecdysone 20,22-acetonide
- 20-Hydroxyecdysone20,22-monoacetonide
- Ecdysterone 20,22-monoacetonide
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Found 4 products.
Ecdysterone 20,22-monoacetonide
CAS:Ecdysterone 20,22-monoacetonide is a natural product for research related to life sciences. The catalog number is TN3912 and the CAS number is 22798-96-5.Formula:C30H48O7Purity:98%Color and Shape:SolidMolecular weight:520.7Ecdysterone 20,22-monoacetonide
CAS:Formula:C30H48O7Purity:95%~99%Color and Shape:PowderMolecular weight:520.707Ecdysterone 20,22-monoacetonide
CAS:Ecdysterone 20,22-monoacetonide is a bioactive steroidal compound, which is a semi-synthetic derivative of ecdysteroids naturally found in certain plants and insects. It is solubilized by acetylation to enhance its stability and bioavailability. As a phytoecdysteroid, it mimics the action of natural ecdysterones involved in the molting and metamorphosis of arthropods. The primary mode of action for Ecdysterone 20,22-monoacetonide involves interaction with the ecdysteroid receptor, modulating gene expression related to protein synthesis and muscle growth without the androgenic effects typically associated with anabolic steroids.Formula:C30H48O7Purity:Min. 95%Molecular weight:520.7 g/mol




