Structure Information
Structure

Compound Identification

SMILES

O[C@H]1[C@H](OC2=CC=CC=C2C(=O)NC2=NC=C(S2)[N+]([O-])=O)O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O

InChIKey

InChIKey=UJTOVSZPBVTOMC-QKZHPOIUSA-N

Formula

C16H15N3O10S

Mass

441.37

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Taxonomic Classification

Taxonomy Tree

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

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Phenolic glycoside - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Benzamide - Benzoic acid or derivatives - Phenoxy compound - Nitroaromatic compound - Benzoyl - Phenol ether - Nitrothiazole - 2,5-disubstituted 1,3-thiazole - Beta-hydroxy acid - Monocyclic benzene moiety - Oxane - Pyran - Benzenoid - Monosaccharide - Hydroxy acid - Heteroaromatic compound - Thiazole - Azole - Secondary alcohol - Secondary carboxylic acid amide - C-nitro compound - Organic nitro compound - Carboxamide group - Acetal - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Polyol - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Alcohol - Carbonyl group - Organonitrogen compound - Organic salt - Organic cation - 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

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