Compound Identification
SMILES
O[C@H]1[C@H](O)[C@@H](COC(=O)\C=C/C2=CC=C(O)C=C2)O[C@@H](OC2=C(O)C=C3C[C@@H](C([O-])=O)[N+](=C\C=C4/C[C@H](NC(=C4)C(O)=O)C(O)=O)C3=C2)[C@@H]1O
InChIKey
InChIKey=DZZRFXSVXQHJLV-DOHUEXTKSA-N
Formula
C33H32N2O15
Mass
696.618
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
-
Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
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Level 5
Glycosyl compounds
- Level 6 Phenolic glycosides
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Level 5
Glycosyl compounds
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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
Tetracarboxylic acids and derivatives Coumaric acid esters Cinnamic acid esters Coumaric acids and derivatives Indolecarboxylic acids O-glycosyl compounds L-alpha-amino acids Styrenes Tetrahydropyridines 1-hydroxy-2-unsubstituted benzenoids Fatty acid esters Oxanes Monosaccharides Enoate esters Amino acids Carboxylic acid salts Shiff bases Secondary alcohols Polyols Acetals Oxacyclic compounds Azacyclic compounds Carboxylic acids Dialkylamines Propargyl-type 1,3-dipolar organic compounds Enamines Organic salts Organic oxides Organopnictogen compounds Carbonyl compounds Organic zwitterions Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - Coumaric acid ester - Tetracarboxylic acid or derivatives - Cinnamic acid or derivatives - Coumaric acid or derivatives - Hydroxycinnamic acid or derivatives - Indolecarboxylic acid - Indolecarboxylic acid derivative - Cinnamic acid ester - O-glycosyl compound - Alpha-amino acid - Alpha-amino acid or derivatives - L-alpha-amino acid - Indole or derivatives - Styrene - 1-hydroxy-2-unsubstituted benzenoid - Fatty acid ester - Phenol - Tetrahydropyridine - Benzenoid - Monocyclic benzene moiety - Oxane - Hydropyridine - Monosaccharide - Fatty acyl - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Amino acid or derivatives - Shiff base - Secondary alcohol - Carboxylic acid ester - Carboxylic acid salt - Amino acid - Propargyl-type 1,3-dipolar organic compound - Acetal - Organic 1,3-dipolar compound - Secondary amine - Carboxylic acid derivative - Polyol - Carboxylic acid - Secondary aliphatic amine - Enamine - Organoheterocyclic compound - Oxacycle - Azacycle - Organopnictogen compound - Organic oxide - Organonitrogen compound - Organic zwitterion - Carbonyl group - Alcohol - Amine - Hydrocarbon derivative - Organic salt - Organic nitrogen compound - 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