Compound Identification
SMILES
CC(=O)OCC(=O)[C@@]1(OC(=O)C2=CC=CO2)C(=C)CC2C3CCC4=CC(=O)C=CC4(C)C3C(O)CC12C
InChIKey
InChIKey=WFCRUQAGGMXGMK-BLIOBTBFSA-N
Formula
C29H32O8
Mass
508.567
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 11-hydroxysteroids 3-oxo delta-1,4-steroids Delta-1,4-steroids Furoic acid esters Alpha-acyloxy ketones Dicarboxylic acids and derivatives Heteroaromatic compounds Secondary alcohols Carboxylic acid esters Cyclic alcohols and derivatives Cyclic ketones Oxacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Progestogin-skeleton - 20-oxosteroid - Steroid ester - 3-oxo-delta-1,4-steroid - 3-oxosteroid - Hydroxysteroid - 11-hydroxysteroid - Oxosteroid - Delta-1,4-steroid - Furoic acid ester - Furoic acid or derivatives - Alpha-acyloxy ketone - Dicarboxylic acid or derivatives - Cyclic alcohol - Heteroaromatic compound - Furan - Ketone - Carboxylic acid ester - Cyclic ketone - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Alcohol - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organooxygen 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