Compound Identification
SMILES
COC1O[C@](C)(C2CCC3C4CC=C5[C@@H](O)C=CC(=O)[C@]5(C)C4CC[C@@]123)C1CC(C)=C(C)C(=O)O1
InChIKey
InChIKey=FKDPGSFHKKGFDE-JCHGPIPOSA-N
Formula
C29H38O6
Mass
482.617
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Steroids and steroid derivatives
-
Subclass
Steroid lactones
- Level 5 Withanolides and derivatives
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Subclass
Steroid lactones
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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
Steroid lactones
Intermediate Tree Nodes
Not available
Direct Parent
Withanolides and derivatives
Alternative Parents
Oxosteroids Hydroxysteroids Dihydropyranones Cyclohexenones Oxolanes Enoate esters Secondary alcohols Lactones Oxacyclic compounds Monocarboxylic acids and derivatives Acetals Organic oxides Hydrocarbon derivatives Aldehydes
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Withanolide-skeleton - 4-hydroxysteroid - Hydroxysteroid - 1-oxosteroid - Oxosteroid - Dihydropyranone - Cyclohexenone - Pyran - Oxolane - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Secondary alcohol - Lactone - Ketone - Carboxylic acid ester - Organoheterocyclic compound - Oxacycle - Acetal - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Aldehyde - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Alcohol - Organooxygen compound - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as withanolides and derivatives. These are c28 steroids structurally characterized by an ergostane skeleton usually functionalized at carbons 1, 22 and 26 to form a lactone ring.
External Descriptors
Not available