Structure Information
Structure

Compound Identification

SMILES

CC(C)[C@](CC1=CC=CC=C1)(NC(=O)[C@H](CC(N)=O)NC(=O)C1=NC2=CC=CC=C2C=C1)[C@H](CNNC(=O)OC(C)(C)C)OP(O)(O)=O

InChIKey

InChIKey=XXUHZYAVYXIEIH-ZDQHWEPJSA-N

Formula

C32H43N6O9P

Mass

686.703

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Subclass

Amino acids, peptides, and analogues

Intermediate Tree Nodes

Amino acids and derivatives - Alpha amino acids and derivatives

Direct Parent

Asparagine and derivatives

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Asparagine or derivatives - N-acyl-alpha amino acid or derivatives - Quinoline-2-carboxamide - Alpha-amino acid amide - Phenylbutylamine - Amphetamine or derivatives - Quinoline - Pyridine carboxylic acid or derivatives - 2-heteroaryl carboxamide - Phosphoethanolamine - Monoalkyl phosphate - Hydrazinecarboxylic acid ester - Monocyclic benzene moiety - Fatty amide - N-acyl-amine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyridine - Fatty acyl - Alkyl phosphate - Benzenoid - Heteroaromatic compound - Carboxamide group - Primary carboxylic acid amide - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Organic oxide - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Carbonyl group - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as asparagine and derivatives. These are compounds containing asparagine or a derivative thereof resulting from reaction of asparagine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

External Descriptors

Not available

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