
CAS 1195795-81-3
:Pregn-5-ene-3,21-diol, 17,20-epoxy-, (3β,20R)-
Description:
Pregn-5-ene-3,21-diol, 17,20-epoxy-, (3β,20R)- is a steroid compound characterized by its specific structural features, including a pregnane backbone, which consists of four fused carbon rings. This compound contains hydroxyl (-OH) groups at the 3 and 21 positions, contributing to its solubility and reactivity. The presence of an epoxy group at the 17 and 20 positions indicates a cyclic ether formation, which can influence its biological activity and stability. The stereochemistry, denoted by (3β,20R), specifies the orientation of substituents around the chiral centers, which is crucial for the compound's interaction with biological systems, including hormone receptors. This compound may exhibit various pharmacological properties, potentially acting as a precursor or modulator in steroid biosynthesis. Its CAS number, 1195795-81-3, allows for precise identification in chemical databases, facilitating research and application in fields such as medicinal chemistry and endocrinology. Overall, the unique structural characteristics of this compound suggest potential therapeutic applications, although further studies would be necessary to elucidate its specific biological roles.
Formula:C21H32O3
Synonyms:- Pregn-5-ene-3,21-diol, 17,20-epoxy-, (3β,20R)-
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BNN27
CAS:<p>BNN27 is an agonist of the TrkA receptor (TrkAreceptor) and the p75NTR receptor (p75NTR receptor), exhibiting neurotrophic and anti-apoptotic properties. It enhances levels of glutamate, GABA, and glutamine in the hippocampus and prefrontal cortex of rats, improving glutamate turnover. In a mouse model of amyotrophic lateral sclerosis (ALS), BNN27 demonstrates neuroprotective effects, shows anti-inflammatory properties in an experimental autoimmune encephalomyelitis (EAE) model, and exhibits retinal protection in a rat diabetes model. BNN27 also possesses blood-brain barrier permeability.</p>Formula:C21H32O3Color and Shape:SolidMolecular weight:332.477
