Compound Identification
SMILES
CC(OC(=O)C=Cc1ccccc1)C1(O)CCC2(O)C1(C)C(CC1C3(C)CCC(O)CC3=CCC21O)OC(=O)C=Cc1ccccc1
InChIKey
InChIKey=NPKKRSHVJIQBKU-UHFFFAOYSA-N
Formula
C39H46O8
Mass
642.789
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 14-hydroxysteroids 17-hydroxysteroids 3-hydroxy delta-5-steroids Delta-5-steroids Cinnamic acid esters Styrenes Dicarboxylic acids and derivatives Tertiary alcohols Enoate esters Cyclic alcohols and derivatives Secondary alcohols Polyols Organic oxides Carbonyl compounds Hydrocarbon derivatives
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
Progestogin-skeleton - Steroid ester - 3-hydroxy-delta-5-steroid - 3-hydroxysteroid - 14-hydroxysteroid - Hydroxysteroid - 17-hydroxysteroid - Delta-5-steroid - Cinnamic acid ester - Cinnamic acid or derivatives - Styrene - Monocyclic benzene moiety - Benzenoid - Dicarboxylic acid or derivatives - Tertiary alcohol - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Cyclic alcohol - Secondary alcohol - Carboxylic acid ester - Polyol - Carboxylic acid derivative - Organic oxide - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Aromatic 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