Compound Identification
SMILES
CC12CC(=O)C3C(CCC4=CC(=O)CCC34C)C1CCC2(O)C(=O)CN1C(=O)NC=CC1=O
InChIKey
InChIKey=XRXBEYJDVHOGHO-UHFFFAOYSA-N
Formula
C25H30N2O6
Mass
454.523
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 11-oxosteroids 17-hydroxysteroids 3-oxo delta-4-steroids Delta-4-steroids Pyrimidones Cyclohexenones Hydropyrimidines Vinylogous amides Tertiary alcohols Heteroaromatic compounds Alpha-hydroxy ketones Ureas Lactams Cyclic alcohols and derivatives Azacyclic compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Progestogin-skeleton - 20-oxosteroid - 3-oxo-delta-4-steroid - 3-oxosteroid - Hydroxysteroid - 11-oxosteroid - Oxosteroid - 17-hydroxysteroid - Delta-4-steroid - Cyclohexenone - Pyrimidone - Hydropyrimidine - Pyrimidine - Heteroaromatic compound - Cyclic alcohol - Vinylogous amide - Alpha-hydroxy ketone - Tertiary alcohol - Lactam - Ketone - Cyclic ketone - Urea - Organoheterocyclic compound - Azacycle - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Alcohol - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organopnictogen compound - Aromatic 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