Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H](OC2=CC(=CC(=C2)[N+]([O-])=O)C(=O)NC(CN2CCOCC2)CN2CCOCC2)[C@H](O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=MCMWCTMAKPQTPI-WGNYYXNJSA-N

Formula

C24H36N4O11

Mass

556.569

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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 - Hexose monosaccharide - O-glycosyl compound - Benzamide - Benzoic acid or derivatives - Nitrobenzene - Phenol ether - Phenoxy compound - Nitroaromatic compound - Benzoyl - Oxazinane - Oxane - Monocyclic benzene moiety - Benzenoid - Morpholine - Monosaccharide - Amino acid or derivatives - Tertiary aliphatic amine - Secondary alcohol - Carboxamide group - C-nitro compound - Secondary carboxylic acid amide - Tertiary amine - Organic nitro compound - Acetal - Oxacycle - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Polyol - Organopnictogen compound - Organic oxide - Organic salt - Hydrocarbon derivative - Alcohol - Amine - Organic zwitterion - Organic nitrogen compound - Organonitrogen compound - Primary 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

CHEBI:39608 : C-nitro compound - benzamides - morpholines - oxanes

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