Compound Identification
SMILES
CC(NC(=O)CC1=CC(I)=CC=C1)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C
InChIKey
InChIKey=FWRCEQRTIPQTNB-UHFFFAOYSA-N
Formula
C29H40INO2
Mass
561.548
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
Pregnane-type alkaloids 3-hydroxy delta-5-steroids Azasteroids and derivatives Delta-5-steroids Phenylacetamides Alkaloids and derivatives Iodobenzenes Aryl iodides Secondary carboxylic acid amides Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives Carbonyl compounds Organic oxides Organoiodides Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
22-azasteroid - Progestogin-skeleton - Steroidal alkaloid - Pregnane-type alkaloid - 3-hydroxy-delta-5-steroid - 3-hydroxysteroid - Hydroxysteroid - Azasteroid - Delta-5-steroid - Phenylacetamide - Alkaloid or derivatives - Halobenzene - Iodobenzene - Aryl halide - Aryl iodide - Monocyclic benzene moiety - Benzenoid - Cyclic alcohol - Secondary alcohol - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Organic oxygen compound - Organooxygen compound - Carbonyl group - Organohalogen compound - Organic oxide - Organopnictogen compound - Organoiodide - Organonitrogen compound - Hydrocarbon derivative - Alcohol - Organic nitrogen 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