Structure Information
Structure

Compound Identification

SMILES

OC1C(CN2CCC(O)(CC3=CC=CC=C3)CC2)OC(CC(=O)N[C@@H](CCC(O)=O)C(O)=O)C(O)C1O

InChIKey

InChIKey=DJQIBWZTLQDPNT-FVAQWDDVSA-N

Formula

C25H36N2O10

Mass

524.567

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic oxygen compounds

Class

Organooxygen compounds

Subclass

Carbohydrates and carbohydrate conjugates

Intermediate Tree Nodes

Sugar acids and derivatives - Sugar amino acids and derivatives

Direct Parent

Pyranoid amino acids and derivatives

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Glutamic acid or derivatives - Pyranoid amino acid - N-acyl-alpha-amino acid - N-acyl-l-alpha-amino acid - N-acyl-alpha amino acid or derivatives - 4-benzylpiperidine - Benzylpiperidine - C-glycosyl compound - Glycosyl compound - Alpha-amino acid or derivatives - Aralkylamine - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Monosaccharide - Oxane - Piperidine - Benzenoid - Tertiary alcohol - Secondary alcohol - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Secondary carboxylic acid amide - 1,2-diol - Carboxamide group - Amino acid - Organoheterocyclic compound - Azacycle - Polyol - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Ether - Carbonyl group - Hydrocarbon derivative - Amine - Organonitrogen compound - Alcohol - Organic oxide - Organic nitrogen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyranoid amino acids and derivatives. These are compounds containing a (hydro)pyran ring bearing unprotected amino and carboxylic acid functionalities.

External Descriptors

Not available

Previous Back Next