Compound Identification
SMILES
[H][C@@](CO)(C=C)[C@]1([H])C[C@]2([H])N(CCC3=C2NC2=C3C(O[C@]3([H])O[C@]([H])(CO)[C@@]([H])(O)[C@]([H])(O)[C@@]3([H])O)=CC=C2)C=C1C(=O)OC
InChIKey
InChIKey=USUGTFYUSIJKAR-OJIXHNPSSA-N
Formula
C27H34N2O9
Mass
530.574
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organic oxygen compounds
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Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Level 5
Glycosyl compounds
- Level 6 Phenolic glycosides
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Level 5
Glycosyl compounds
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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
Beta carbolines Hexoses O-glycosyl compounds 3-alkylindoles Quinolizines Aralkylamines Tetrahydropyridines Benzenoids Oxanes Vinylogous amides Pyrroles Enoate esters Heteroaromatic compounds Methyl esters Trialkylamines Amino acids and derivatives Secondary alcohols Allylamines Enamines Acetals Azacyclic compounds Monocarboxylic acids and derivatives Polyols Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Carbonyl compounds Organic oxides Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - Beta-carboline - Pyridoindole - Hexose monosaccharide - O-glycosyl compound - Quinolizine - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Tetrahydropyridine - Monosaccharide - Oxane - Benzenoid - Enoate ester - Heteroaromatic compound - Methyl ester - Vinylogous amide - Pyrrole - Alpha,beta-unsaturated carboxylic ester - Tertiary aliphatic amine - Carboxylic acid ester - Tertiary amine - Secondary alcohol - Amino acid or derivatives - Polyol - Azacycle - Allylamine - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Acetal - Enamine - Hydrocarbon derivative - Organopnictogen compound - Alcohol - Organic oxide - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Primary alcohol - Amine - 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