Compound Identification
SMILES
CC(=O)N1[C@@H]2CC3C4CC=C5C[C@@H](O)CC[C@]5(C)C4CC[C@]3(C)[C@]12C(C)=O
InChIKey
InChIKey=ZEXKBKAYWZMNJG-SUZOORIFSA-N
Formula
C23H33NO3
Mass
371.521
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Steroids and steroid derivatives
Subclass
Pregnane steroids
Intermediate Tree Nodes
Not available
Direct Parent
Gluco/mineralocorticoids, progestogins and derivatives
Alternative Parents
20-oxosteroids 17-oxosteroids 3-beta-hydroxy delta-5-steroids 3-beta-hydroxysteroids Delta-5-steroids N-acylpiperidines Tertiary carboxylic acid amides Acetamides Cyclic alcohols and derivatives Secondary alcohols Ketones Aziridines Azacyclic compounds Organic oxides Organonitrogen compounds Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Progestogin-skeleton - 20-oxosteroid - 3-hydroxy-delta-5-steroid - 3-hydroxysteroid - Hydroxysteroid - 15-oxosteroid - 17-oxosteroid - Oxosteroid - 3-beta-hydroxy-delta-5-steroid - 3-beta-hydroxysteroid - Delta-5-steroid - N-acyl-piperidine - Piperidine - Tertiary carboxylic acid amide - Acetamide - Cyclic alcohol - Secondary alcohol - Carboxamide group - Ketone - Azacycle - Aziridine - Organoheterocyclic compound - Carboxylic acid derivative - Organopnictogen compound - Organic nitrogen compound - Alcohol - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as gluco/mineralocorticoids, progestogins and derivatives. These are steroids with a structure based on a hydroxylated prostane moiety.
External Descriptors
Not available