Compound Identification
SMILES
[Na+].NC(NC(=O)C1=C(N)N=C(N)C(Cl)=N1)=NCCCCC1=CC=C(O[C@@H]2O[C@@H]([C@H](O)[C@@H](O)[C@@H]2O)C([O-])=O)C=C1
InChIKey
InChIKey=WEQYQNBKAOVKST-AZLFDRLPSA-M
Formula
C22H27ClN7NaO8
Mass
575.94
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
Fatty acyl glycosides of mono- and disaccharides O-glucuronides Alkyl glycosides Hexoses O-glycosyl compounds Phenylbutylamines Pyrazinecarboxamides Phenol ethers Phenoxy compounds Beta hydroxy acids and derivatives Aminopyrazines Oxanes Pyrans Imidolactams Aryl chlorides Primary aromatic amines Heteroaromatic compounds Vinylogous amides Carboxylic acid salts Secondary alcohols Guanidines Amino acids Azacyclic compounds Polyols Oxacyclic compounds Acetals Carboximidamides Carboxylic acids Monocarboxylic acids and derivatives Propargyl-type 1,3-dipolar organic compounds Organic metal halides Carbonyl compounds Hydrocarbon derivatives Organic oxides Organic sodium salts Organic zwitterions Organochlorides Organopnictogen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Phenylbutylamine - Pyrazine carboxylic acid or derivatives - Pyrazinecarboxamide - Phenol ether - Phenoxy compound - Aminopyrazine - Beta-hydroxy acid - Primary aromatic amine - Pyran - Imidolactam - Monocyclic benzene moiety - Aryl halide - Benzenoid - Hydroxy acid - Monosaccharide - Oxane - Pyrazine - Fatty acyl - Aryl chloride - Heteroaromatic compound - Vinylogous amide - Amino acid or derivatives - Carboxylic acid salt - Guanidine - Amino acid - Secondary alcohol - Polyol - Azacycle - Organic alkali metal salt - Organoheterocyclic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Oxacycle - Carboxylic acid - Propargyl-type 1,3-dipolar organic compound - Organic metal halide - Monocarboxylic acid or derivatives - Carboximidamide - Acetal - Organic sodium salt - Alcohol - Organopnictogen compound - Organic salt - Organic nitrogen compound - Organic oxide - Organic zwitterion - Organonitrogen compound - Carbonyl group - Amine - Hydrocarbon derivative - Primary amine - Organohalogen compound - Organochloride - 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