Compound Identification
SMILES
OC1=CC(O)=C(OC2=CC(O)=C(OC3=C(OC4=CC(O)=C(OC5=C(OC6=CC(O)=C(OC7=C(O)C(O)=C(O)C(O)=C7)C(O)=C6)C(O)=C(O)C(O)=C5)C(O)=C4)C(O)=C(O)C(O)=C3)C(O)=C2)C(O)=C1
InChIKey
InChIKey=OSIHPIVUZCZXAX-UHFFFAOYSA-N
Formula
C42H30O25
Mass
934.677
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
Diphenylethers Diarylethers Phloroglucinols and derivatives 5-unsubstituted pyrrogallols Resorcinols Phenoxy compounds Phenol ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Polyols Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Tannin - Diphenylether - Diaryl ether - Benzenetriol - Phloroglucinol derivative - Pyrogallol derivative - 5-unsubstituted pyrrogallol - Phenoxy compound - Resorcinol - Phenol ether - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Monocyclic benzene moiety - Polyol - Ether - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic homomonocyclic 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