Compound Identification
SMILES
COC1C(O)C(O)COC1OC1CCC2(C)C3CCC4(C)C(C(C)CCC(=C)C(C)CO)C(O)C(O)C4C3(O)CC(O)C2C1O
InChIKey
InChIKey=NPTLRKRGQBZTCG-UHFFFAOYSA-N
Formula
C34H58O11
Mass
642.827
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
Pentahydroxy bile acids, alcohols and derivatives Steroidal glycosides 16-hydroxysteroids 6-hydroxysteroids O-glycosyl compounds Fatty alcohols Oxanes Monosaccharides Tertiary alcohols Secondary alcohols Cyclic alcohols and derivatives Polyols Acetals Dialkyl ethers Oxacyclic compounds Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Ergostane-skeleton - Pentahydroxy bile acid, alcohol, or derivatives - 26-hydroxysteroid - Steroidal glycoside - Hydroxy bile acid, alcohol, or derivatives - Bile acid, alcohol, or derivatives - 4-hydroxysteroid - 6-hydroxysteroid - 15-hydroxysteroid - 16-hydroxysteroid - Hydroxysteroid - Glycosyl compound - O-glycosyl compound - Fatty alcohol - Oxane - Fatty acyl - Monosaccharide - Cyclic alcohol - Tertiary alcohol - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Acetal - Ether - Dialkyl ether - Polyol - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organic oxygen compound - Primary alcohol - 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