Compound Identification
SMILES
C[Co]C1CC(O)=C(O)C(O)=C1c1c(O)c(O)c(O)cc1[Co]C
InChIKey
InChIKey=HDGCLDHFMQTHRW-UHFFFAOYSA-N
Formula
C14H16Co2O6
Mass
398.142
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
-
Class
Tannins
- Subclass Hydrolyzable tannins
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Class
Tannins
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Tannins
Subclass
Hydrolyzable tannins
Intermediate Tree Nodes
Not available
Direct Parent
Hydrolyzable tannins
Alternative Parents
Pyrogallols and derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Metal aryls Benzene and substituted derivatives Enediols Polyols Organic transition metal salts Enols Transition metal alkyls Organotransition metal compounds Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Hydrolyzable tannin - Pyrogallol derivative - Benzenetriol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Metal aryl - Benzenoid - Monocyclic benzene moiety - Enediol - Organic transition metal salt - Polyol - Enol - Organic oxygen compound - Transition metal alkyl - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organometallic compound - Organic transition metal moeity - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.
External Descriptors
Not available