Compound Identification
SMILES
[2H]C1([2H])C[C@]2(C)[C@H]3CC[C@]4(C)[C@H](CCC4[C@@]33C=C[C@@]2([C@@H]2COC(=O)[C@]32[2H])C([2H])([2H])[C@H]1O)[C@H](C)\C=C\[C@H](C)C(C)C
InChIKey
InChIKey=QUCAPBIBCZWARK-GZTBZZFPSA-N
Formula
C32H48O3
Mass
485.764
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Steroids and steroid derivatives
- Subclass Ergostane steroids
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Class
Steroids and steroid derivatives
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Steroids and steroid derivatives
Subclass
Ergostane steroids
Intermediate Tree Nodes
Not available
Direct Parent
Ergostane steroids
Alternative Parents
Steroid lactones Gamma butyrolactones Oxolanes Secondary alcohols Cyclic alcohols and derivatives Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Ergostane-skeleton - Steroid lactone - Gamma butyrolactone - Cyclic alcohol - Oxolane - Carboxylic acid ester - Lactone - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organic oxygen compound - Alcohol - Carbonyl group - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as ergostane steroids. These are steroids with a structure based on the ergostane skeleton, which arises from the methylation of cholestane at the 24-position.
External Descriptors
Not available