Compound Identification
SMILES
[H][C@]1(CC2=CC(O[C@]3([H])O[C@]([H])(CO)[C@@]([H])(O)[C@]([H])(O)[C@@]3([H])O[C@]3([H])O[C@]([H])(C(O)=O)[C@@]([H])(O)[C@]([H])(O)[C@@]3([H])O)=C(O)C=C2N1C=CC1=CC(=N[C@@]([H])(C1)C(O)=O)C(O)=O)C(O)=O
InChIKey
InChIKey=HNGVOGUQLNOBKK-POBNKHOBSA-N
Formula
C30H34N2O19
Mass
726.597
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
-
Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Level 5
Glycosyl compounds
- Level 6 Phenolic glycosides
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Level 5
Glycosyl compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Class
Organooxygen compounds
-
Superclass
Organic oxygen compounds
Kingdom
Organic compounds
Superclass
Organic oxygen compounds
Class
Organooxygen compounds
Subclass
Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes
Glycosyl compounds
Direct Parent
Phenolic glycosides
Alternative Parents
O-glucuronides Tetracarboxylic acids and derivatives Indolecarboxylic acids Disaccharides O-glycosyl compounds L-alpha-amino acids Dihydropyridinecarboxylic acids and derivatives Tertiary alkylarylamines 1-hydroxy-2-unsubstituted benzenoids Aralkylamines Beta hydroxy acids and derivatives Pyrans Oxanes Secondary alcohols Amino acids Ketimines Enamines Oxacyclic compounds Polyols Carboxylic acids Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Acetals Allylamines Hydrocarbon derivatives Carbonyl compounds Primary alcohols Organopnictogen compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Tetracarboxylic acid or derivatives - Indolecarboxylic acid - Indolecarboxylic acid derivative - Disaccharide - O-glycosyl compound - Alpha-amino acid - Alpha-amino acid or derivatives - L-alpha-amino acid - Dihydropyridinecarboxylic acid derivative - Indole or derivatives - Tertiary aliphatic/aromatic amine - 1-hydroxy-2-unsubstituted benzenoid - Beta-hydroxy acid - Dihydropyridine - Aralkylamine - Pyran - Benzenoid - Oxane - Hydropyridine - Hydroxy acid - Secondary alcohol - Tertiary amine - Amino acid or derivatives - Amino acid - Ketimine - Propargyl-type 1,3-dipolar organic compound - Polyol - Organic 1,3-dipolar compound - Carboxylic acid derivative - Carboxylic acid - Enamine - Allylamine - Organoheterocyclic compound - Acetal - Azacycle - Oxacycle - Organopnictogen compound - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Alcohol - Carbonyl group - Imine - Primary alcohol - Hydrocarbon derivative - Amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.
External Descriptors
Not available