Compound Identification
SMILES
CCCCCC[C@@H](C)\C=C(/C)\C=C\C(=O)N[C@@]1(C[C@H]2C[C@H]([C@H](C)\C=C\[C@H](C)C(C)C)[C@@]3(C)CC[C@H]4C(=C1C(=O)C1=C[C@@H](O)CC[C@]41C)[C@@]23O)C=O
InChIKey
InChIKey=TVFMBZOZGJABCW-ITNXSPAMSA-N
Formula
C45H67NO5
Mass
702.033
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
3-hydroxy delta-7-steroids Delta-7-steroids Cyclohexenones N-acyl amines Tertiary alcohols Secondary carboxylic acid amides Secondary alcohols Cyclic alcohols and derivatives Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Aldehydes
Molecular Framework
Aliphatic homopolycyclic compounds
Substituents
Ergostane-skeleton - 3-hydroxy-delta-7-steroid - Delta-7-steroid - Cyclohexenone - N-acyl-amine - Cyclic alcohol - Tertiary alcohol - Carboxamide group - Ketone - Secondary alcohol - Secondary carboxylic acid amide - Carboxylic acid derivative - Organonitrogen compound - Organic oxide - Alcohol - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Aldehyde - Hydrocarbon derivative - Aliphatic homopolycyclic 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