Compound Identification
SMILES
CC(C)=CC(=C(C)C)C(=O)OCC(O)COC(=O)CCSC(C)=CC(OC(=O)C(CS(O)(=O)=O)CS(O)(=O)=O)=C(C)C
InChIKey
InChIKey=YORRIFFEIWODAG-UHFFFAOYSA-N
Formula
C26H40O13S3
Mass
656.77
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Glycerolipids
-
Subclass
Diradylglycerols
-
Level 5
Diacylglycerols
- Level 6 1,3-diacylglycerols
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Level 5
Diacylglycerols
-
Subclass
Diradylglycerols
-
Class
Glycerolipids
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Glycerolipids
Subclass
Diradylglycerols
Intermediate Tree Nodes
Diacylglycerols
Direct Parent
1,3-diacylglycerols
Alternative Parents
Tricarboxylic acids and derivatives Fatty acid esters Sulfonyls Organosulfonic acids Enol esters Enoate esters Alkanesulfonic acids Thioenol ethers Secondary alcohols Sulfenyl compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
1,3-acyl-sn-glycerol - Tricarboxylic acid or derivatives - Fatty acid ester - Fatty acyl - Enol ester - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Alkanesulfonic acid - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Secondary alcohol - Thioenolether - Carboxylic acid ester - Carboxylic acid derivative - Sulfenyl compound - Alcohol - Organosulfur compound - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as 1,3-diacylglycerols. These are diacylglycerols containing a glycerol acylated at positions 1 and 3.
External Descriptors
Not available