Compound Identification
SMILES
COC1=CC=C(CC2=C(O[C@@H]3O[C@H]([C@H](C)O)[C@@H](O)[C@H](O)[C@H]3O)C=C(CO)C=C2F)C=C1
InChIKey
InChIKey=GBYJTHSPRXNSIP-CJZGIBHCSA-N
Formula
C22H27FO8
Mass
438.448
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
Diphenylmethanes O-glycosyl compounds Anisoles Benzyl alcohols Phenoxy compounds Methoxybenzenes Alkyl aryl ethers Fluorobenzenes Aryl fluorides Oxanes Monosaccharides Secondary alcohols Oxacyclic compounds Polyols Acetals Aromatic alcohols Hydrocarbon derivatives Organofluorides Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Phenolic glycoside - Diphenylmethane - O-glycosyl compound - Phenoxy compound - Benzyl alcohol - Methoxybenzene - Phenol ether - Anisole - Fluorobenzene - Halobenzene - Alkyl aryl ether - Benzenoid - Oxane - Aryl fluoride - Aryl halide - Monosaccharide - Monocyclic benzene moiety - Secondary alcohol - Organoheterocyclic compound - Acetal - Ether - Polyol - Oxacycle - Hydrocarbon derivative - Organohalogen compound - Organofluoride - Primary alcohol - Aromatic alcohol - Alcohol - 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