The chemical substance known as "(2β,3α,5α)-2-(2,2-Dimethyl-4-morpholinyl)-3-hydroxypregnane-11,20-dione," with the CAS number 167946-96-5, is a synthetic steroid derivative. It features a pregnane backbone, which is characterized by a steroid structure with a specific arrangement of hydroxyl and ketone functional groups. The presence of a morpholine ring indicates that it has potential pharmacological properties, possibly enhancing its solubility and bioavailability. The hydroxyl group at the 3-position and the ketone groups at the 11 and 20 positions suggest that it may exhibit hormonal activity, potentially influencing steroid hormone pathways. This compound may be of interest in medicinal chemistry for its potential applications in hormone replacement therapy or as a therapeutic agent in various endocrine disorders. Its specific stereochemistry, denoted by the β and α configurations, is crucial for its biological activity, as stereoisomers can exhibit significantly different effects in biological systems. Further studies would be necessary to elucidate its full pharmacological profile and therapeutic potential.

(2β,3α,5α)-2-(2,2-Dimethyl-4-morpholinyl)-3-hydroxypregnane-11,20-dione

167946-96-5: The chemical substance known as "(2β,3α,5α)-2-(2,2-Dimethyl-4-morpholinyl)-3-hydroxypregnane-11,20-dione," with the CAS number 167946-96-5, is a synthetic steroid derivative. It features a pregnane backbone, which is characterized by a steroid structure with a specific arrangement of hydroxyl and ketone functional groups. The presence of a morpholine ring indicates that it has potential pharmacological properties, possibly enhancing its solubility and bioavailability. The hydroxyl group at the 3-position and the ketone groups at the 11 and 20 positions suggest that it may exhibit hormonal activity, potentially influencing steroid hormone pathways. This compound may be of interest in medicinal chemistry for its potential applications in hormone replacement therapy or as a therapeutic agent in various endocrine disorders. Its specific stereochemistry, denoted by the β and α configurations, is crucial for its biological activity, as stereoisomers can exhibit significantly different effects in biological systems. Further studies would be necessary to elucidate its full pharmacological profile and therapeutic potential.

<p>Org-21465, a gamma-aminobutyric acid (GABA) receptor agonist, is used potentially for the use of anesthesia.</p>

CAS 167946-96-5

(2β,3α,5α)-2-(2,2-Dimethyl-4-morpholinyl)-3-hydroxypregnane-11,20-dione

Org-21465

Ref: TM-T28259