Compound Identification
SMILES
CC(=O)O[C@]1(C(C)=O)C(=C)C[C@H]2[C@@H]3C=C(F)C4=CC(=O)CC[C@@]4(C)[C@@H]3CC[C@]12C
InChIKey
InChIKey=XSSIGSNQDKHHLD-JBARXXBASA-N
Formula
C24H29FO4
Mass
400.49
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
Steroid esters 20-oxosteroids Halogenated steroids 3-oxosteroids Diterpenoids Cyclohexenones Alpha-acyloxy ketones Enones Acryloyl compounds Carboxylic acid esters Vinyl fluorides Monocarboxylic acids and derivatives Fluoroalkenes Organofluorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic homopolycyclic compounds
Substituents
Progestogin-skeleton - Steroid ester - 20-oxosteroid - Diterpenoid - Oxosteroid - Halo-steroid - 6-halo-steroid - 3-oxosteroid - Cyclohexenone - Alpha-acyloxy ketone - Alpha,beta-unsaturated ketone - Enone - Acryloyl-group - Cyclic ketone - Ketone - Carboxylic acid ester - Fluoroalkene - Haloalkene - Vinyl halide - Vinyl fluoride - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organofluoride - Organohalogen compound - Aliphatic 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