Compound Identification
SMILES
OCC1OC(Oc2cccc3oc(=O)[nH]c23)C(O)C(O)C1O.OCC1OC(Oc2cccc3oc(=O)[nH]c23)C(O)C(O)C1O
InChIKey
InChIKey=QHABZALVNCQWSD-UHFFFAOYSA-N
Formula
C26H30N2O16
Mass
626.524
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
Hexoses O-glycosyl compounds Benzoxazolones Benzenoids Oxanes Heteroaromatic compounds Oxazoles Secondary alcohols Azacyclic compounds Polyols Acetals Oxacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Primary alcohols Organopnictogen compounds
Molecular Framework
Not available
Substituents
Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Benzoxazolone - Benzoxazole - Monosaccharide - Oxane - Benzenoid - Azole - Heteroaromatic compound - Oxazole - Secondary alcohol - Acetal - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Alcohol - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organic nitrogen compound - Primary alcohol - Organopnictogen 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