Compound Identification
SMILES
N[C@]1(OC2=CC=CC=C2)O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O
InChIKey
InChIKey=DRCOPPOWYVNRBK-LDMBFOFVSA-N
Formula
C12H17NO6
Mass
271.269
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
Phenoxy compounds Phenol ethers Oxanes Monosaccharides Carboxylic acid amide acetals Secondary alcohols Polyols Oxacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Phenolic glycoside - Phenoxy compound - Phenol ether - Monocyclic benzene moiety - Amide acetal - Monosaccharide - Benzenoid - Oxane - Secondary alcohol - Orthocarboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Polyol - Alcohol - Primary alcohol - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Aromatic heteromonocyclic 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