Compound Identification
SMILES
COC1=C(OCC[C@H]2CCC3C4[C@H](C)CC5=C(C=CC(O)=C5)C4CCC23C)C=CC(CN2CCCC2)=C1
InChIKey
InChIKey=CSWILBOAZJPOMU-LKXNSAIPSA-N
Formula
C33H45NO3
Mass
503.727
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
3-hydroxysteroids Phenanthrenes and derivatives Tetralins Anisoles Benzylamines Methoxybenzenes Phenylmethylamines Phenoxy compounds Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Aralkylamines N-alkylpyrrolidines Trialkylamines Azacyclic compounds Hydrocarbon derivatives Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Progestogin-skeleton - 3-hydroxysteroid - Hydroxysteroid - Phenanthrene - Tetralin - Anisole - Benzylamine - Phenoxy compound - Phenol ether - Phenylmethylamine - Methoxybenzene - Phenol - Aralkylamine - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - N-alkylpyrrolidine - Monocyclic benzene moiety - Benzenoid - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Ether - Hydrocarbon derivative - Amine - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - 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