Compound Identification
SMILES
CCCC(=O)O[C@@]1(CC[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@H]3C(=O)C[C@]12C)C(=O)COP(O)(O)=O
InChIKey
InChIKey=XXODBQDAKPXCDB-PNOCSVDBSA-N
Formula
C25H33O9P
Mass
508.504
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 3-oxo delta-1,4-steroids 11-oxosteroids Delta-1,4-steroids O-acylglycerone-phosphates Monoalkyl phosphates Alpha-acyloxy ketones Cyclic ketones Carboxylic acid esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic homopolycyclic compounds
Substituents
Progestogin-skeleton - 20-oxosteroid - Steroid ester - 3-oxo-delta-1,4-steroid - 3-oxosteroid - 11-oxosteroid - Oxosteroid - Delta-1,4-steroid - O-acylglycerone-phosphate - Glycerone phosphate - Monoalkyl phosphate - Alpha-acyloxy ketone - Alkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - Cyclic ketone - Carboxylic acid ester - Ketone - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic oxide - Organooxygen compound - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Aliphatic 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