Compound Identification
SMILES
CCCCCCCCCCCCC1=CC2=NC3=C(OC2=CC1=O)C=C(O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C=C3
InChIKey
InChIKey=NENHZQCKKJTMIA-HBMYTODVSA-N
Formula
C30H41NO8
Mass
543.657
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
Phenoxazines Hexoses O-glycosyl compounds Benzenoids Oxanes Heteroaromatic compounds Cyclic ketones Secondary alcohols Polyols Acetals Azacyclic compounds Oxacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - Phenoxazine - Hexose monosaccharide - O-glycosyl compound - Monosaccharide - Oxane - Benzenoid - Heteroaromatic compound - Secondary alcohol - Cyclic ketone - Acetal - Polyol - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Primary alcohol - Hydrocarbon derivative - Organonitrogen compound - Organic oxide - Organopnictogen compound - 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