Compound Identification
SMILES
CC(NC(=O)CC1=CC=C(Cl)C=C1)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C
InChIKey
InChIKey=OKQFSAAVRHMANH-UHFFFAOYSA-N
Formula
C29H40ClNO2
Mass
470.09
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
Pregnane-type alkaloids 3-hydroxy delta-5-steroids Azasteroids and derivatives Delta-5-steroids Phenylacetamides Alkaloids and derivatives Chlorobenzenes Aryl chlorides Secondary carboxylic acid amides Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives Carbonyl compounds Organic oxides Organochlorides Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
22-azasteroid - Progestogin-skeleton - Pregnane-type alkaloid - Steroidal alkaloid - 3-hydroxy-delta-5-steroid - 3-hydroxysteroid - Hydroxysteroid - Azasteroid - Delta-5-steroid - Phenylacetamide - Alkaloid or derivatives - Halobenzene - Chlorobenzene - Benzenoid - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Cyclic alcohol - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Carbonyl group - Organohalogen compound - Organochloride - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Organic oxide - Aromatic homopolycyclic 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