Compound Identification
SMILES
CC1(C)OC[C@H]2O[C@@H](OC3=CC=CC=C3CN)[C@H](O)[C@@H](O)[C@@H]2O1
InChIKey
InChIKey=JGJCHUQNNHFTQM-KJWHEZOQSA-N
Formula
C16H23NO6
Mass
325.361
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
Pyranodioxins Phenylmethylamines Phenoxy compounds Phenol ethers Benzylamines Ketals Aralkylamines Oxanes Monosaccharides 1,3-dioxanes Secondary alcohols 1,2-diols Oxacyclic compounds Hydrocarbon derivatives Monoalkylamines Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - Pyranodioxin - Benzylamine - Phenoxy compound - Phenol ether - Phenylmethylamine - Ketal - Aralkylamine - Meta-dioxane - Benzenoid - Monocyclic benzene moiety - Monosaccharide - Oxane - Secondary alcohol - 1,2-diol - Oxacycle - Acetal - Organoheterocyclic compound - Primary amine - Organonitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Organic nitrogen compound - Amine - 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