Compound Identification
SMILES
CC1(C)O[C@H]2C[C@H]3[C@@H]4CCC5=CC(=O)CC[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@@]2(O1)C(=O)CCl
InChIKey
InChIKey=FXFIRGYQADSTIQ-JGHJVBRBSA-N
Formula
C24H33ClO5
Mass
436.97
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-oxo delta-4-steroids 11-beta-hydroxysteroids Delta-4-steroids Ketals Cyclohexenones Alpha-chloroketones 1,3-dioxolanes Secondary alcohols Cyclic alcohols and derivatives Oxacyclic compounds Organochlorides Organic oxides Hydrocarbon derivatives Alkyl chlorides
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Progestogin-skeleton - 20-oxosteroid - Hydroxysteroid - 3-oxo-delta-4-steroid - Oxosteroid - 3-oxosteroid - 11-beta-hydroxysteroid - 11-hydroxysteroid - Delta-4-steroid - Ketal - Cyclohexenone - Alpha-chloroketone - Alpha-haloketone - Cyclic alcohol - Meta-dioxolane - Secondary alcohol - Ketone - Cyclic ketone - Oxacycle - Acetal - Organoheterocyclic compound - Organic oxygen compound - Organohalogen compound - Organochloride - Carbonyl group - Alkyl halide - Alkyl chloride - Alcohol - Organooxygen compound - 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