Compound Identification
SMILES
CC(=O)OC1(CCC2C3C(O)C(F)C4=CC(=O)CCC4(C)C3CCC12C)C(C)=O
InChIKey
InChIKey=BESLOANVNUVACC-UHFFFAOYSA-N
Formula
C23H31FO5
Mass
406.494
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 3-oxo delta-4-steroids 7-hydroxysteroids Halogenated steroids Delta-4-steroids Alpha-acyloxy ketones Cyclohexenones Cyclic alcohols and derivatives Carboxylic acid esters Secondary alcohols Fluorohydrins Monocarboxylic acids and derivatives Organofluorides Alkyl fluorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic homopolycyclic compounds
Substituents
Progestogin-skeleton - Steroid ester - 20-oxosteroid - 3-oxo-delta-4-steroid - 3-oxosteroid - 7-hydroxysteroid - Oxosteroid - 6-halo-steroid - Halo-steroid - Hydroxysteroid - Delta-4-steroid - Cyclohexenone - Alpha-acyloxy ketone - Cyclic alcohol - Carboxylic acid ester - Cyclic ketone - Fluorohydrin - Secondary alcohol - Halohydrin - Ketone - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Alcohol - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organooxygen compound - Organofluoride - Alkyl fluoride - Organohalogen compound - Alkyl halide - 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