Compound Identification
SMILES
CNC1=C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)C=CC(=C1)[N+]([O-])=O
InChIKey
InChIKey=PUJSPPVWDMERKO-XPORZQOISA-N
Formula
C13H16N2O9
Mass
344.276
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
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Subclass
Carbohydrates and carbohydrate conjugates
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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
O-glucuronides O-glycosyl compounds Nitrobenzenes Aniline and substituted anilines Phenylalkylamines Phenoxy compounds Phenol ethers Nitroaromatic compounds Secondary alkylarylamines Beta hydroxy acids and derivatives Pyrans Oxanes Monosaccharides Secondary alcohols Amino acids Acetals Propargyl-type 1,3-dipolar organic compounds Polyols Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Organic oxoazanium compounds Carbonyl compounds Organopnictogen compounds Organic zwitterions Organic salts Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Phenolic glycoside - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Nitrobenzene - Phenol ether - Phenoxy compound - Nitroaromatic compound - Phenylalkylamine - Aniline or substituted anilines - Secondary aliphatic/aromatic amine - Beta-hydroxy acid - Pyran - Monocyclic benzene moiety - Oxane - Benzenoid - Hydroxy acid - Monosaccharide - Amino acid or derivatives - Secondary alcohol - Organic nitro compound - Amino acid - C-nitro compound - Acetal - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Secondary amine - Polyol - Organopnictogen compound - Organic salt - Organic oxide - Carbonyl group - Alcohol - Organic zwitterion - Amine - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - 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