Compound Identification
SMILES
CC(C)C(C)CC[C@H](C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)OP(O)(=O)OC1C(=O)OC(C(O)CO)C1=O
InChIKey
InChIKey=IMWWZLMPBQVGBQ-IMHXVOELSA-N
Formula
C34H57O9P
Mass
640.795
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 Dialkyl phosphates Gamma butyrolactones Furanones 1,3-dicarbonyl compounds Oxolanes Secondary alcohols Cyclic ketones Carboxylic acid esters 1,2-diols Oxacyclic compounds Monocarboxylic acids and derivatives Primary alcohols Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Ergostane-skeleton - Steroid lactone - Dialkyl phosphate - 3-furanone - Gamma butyrolactone - Organic phosphoric acid derivative - Phosphoric acid ester - 1,3-dicarbonyl compound - Alkyl phosphate - Oxolane - Cyclic ketone - Carboxylic acid ester - 1,2-diol - Ketone - Lactone - Secondary alcohol - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organic oxide - Alcohol - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Primary alcohol - Organic oxygen compound - 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