Compound Identification
SMILES
CC(=O)[C@H]1CC[C@@]2(O)[C@@]1(C)[C@@H](C[C@@H]1[C@@]3(C)CC[C@@H](O)C[C@@H]3CC[C@]21O)OC(=O)C1=CN=CC=C1
InChIKey
InChIKey=LGUCVWJGAXRCTH-DMSQALJESA-N
Formula
C27H37NO6
Mass
471.594
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 3-alpha-hydroxysteroids 14-hydroxysteroids Pyridinecarboxylic acids Tertiary alcohols Heteroaromatic compounds Secondary alcohols Ketones Cyclic alcohols and derivatives Carboxylic acid esters Polyols Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Progestogin-skeleton - 20-oxosteroid - 3-alpha-hydroxysteroid - Oxosteroid - Hydroxysteroid - 14-hydroxysteroid - 3-hydroxysteroid - Pyridine carboxylic acid or derivatives - Pyridine carboxylic acid - Pyridine - Heteroaromatic compound - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Ketone - Carboxylic acid ester - Azacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Alcohol - Aromatic 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