Compound Identification
SMILES
CC(=O)OC1=CC(OC(C)=O)=C(OC2=C(OC(C)=O)C(OC(C)=O)=C3OC4=CC(OC(C)=O)=C(OC5=CC(OC(C)=O)=C(OC(C)=O)C(OC(C)=O)=C5)C(OC(C)=O)=C4OC3=C2)C(OC(C)=O)=C1
InChIKey
InChIKey=BXJZSXMTCULZLO-UHFFFAOYSA-N
Formula
C44H36O24
Mass
948.748
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Tannins
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Tannins
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Tannins
Alternative Parents
Dibenzo-p-dioxins Diarylethers Phenol esters Phenoxy compounds Phenol ethers Carboxylic acid esters Oxacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Tannin - Dibenzo-p-dioxin - Diaryl ether - Phenol ester - Phenoxy compound - Phenol ether - Monocyclic benzene moiety - Benzenoid - Carboxylic acid ester - Oxacycle - Ether - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as tannins. These are naturally occurring polyphenols which be categorized into four main classes: hydrolyzable tannin (based on ellagic acid or gallic acid), condensed tannins (made of oligomeric or polymeric proanthocyanidins), complex tannins (made of a catechin bound to a gallotannin or elagitannin), and phlorotannins (oligomers of phloroglucinol).
External Descriptors
Not available