Compound Identification
SMILES
C[C@]12CC[C@H]3[C@@H](CC[C@H]4C[C@H](O)[C@H](C[C@]34C)N3CCOCC3)[C@@H]1CC[C@@H]2C(=O)CCl
InChIKey
InChIKey=NZFNABGZEQPYBX-PMBZPZLSSA-N
Formula
C25H40ClNO3
Mass
438.05
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 3-alpha-hydroxysteroids Morpholines Alpha-chloroketones Trialkylamines Secondary alcohols 1,2-aminoalcohols Cyclic alcohols and derivatives Oxacyclic compounds Dialkyl ethers Azacyclic compounds Hydrocarbon derivatives Alkyl chlorides Organic oxides Organochlorides Organopnictogen compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Progestogin-skeleton - 20-oxosteroid - 3-hydroxysteroid - Hydroxysteroid - 3-alpha-hydroxysteroid - Oxosteroid - Morpholine - Oxazinane - Alpha-haloketone - Alpha-chloroketone - Cyclic alcohol - 1,2-aminoalcohol - Ketone - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organopnictogen compound - Carbonyl group - Amine - Alkyl halide - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Alkyl chloride - Aliphatic 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