Compound Identification
SMILES
CC1(C)OC2C[C@H]3[C@@H]4CCC5=CC(=O)CC(O)[C@]5(C)C4(F)CC[C@]3(C)[C@@]2(O1)C(=O)CCl
InChIKey
InChIKey=PVFYMGVKLOGHPE-JUSCNUIDSA-N
Formula
C24H32ClFO5
Mass
454.96
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 1-hydroxysteroids 3-oxo delta-4-steroids Halogenated steroids Delta-4-steroids Ketals Cyclohexenones 1,3-dioxolanes Alpha-chloroketones Secondary alcohols Oxacyclic compounds Alkyl fluorides Alkyl chlorides Aldehydes Hydrocarbon derivatives Organic oxides Organochlorides Organofluorides
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Progestogin-skeleton - 20-oxosteroid - Halo-steroid - Hydroxysteroid - 9-halo-steroid - 3-oxo-delta-4-steroid - 1-hydroxysteroid - 3-oxosteroid - Oxosteroid - Delta-4-steroid - Ketal - Cyclohexenone - Alpha-chloroketone - Alpha-haloketone - Meta-dioxolane - Ketone - Secondary alcohol - Cyclic ketone - Organoheterocyclic compound - Oxacycle - Acetal - Organic oxygen compound - Organohalogen compound - Organochloride - Organofluoride - Carbonyl group - Alkyl halide - Alkyl fluoride - Alkyl chloride - Aldehyde - 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