Structure Information
Structure

Compound Identification

SMILES

COC(=O)C(CC1=CC=CC=C1)NP(=O)(OCCC#N)OC[C@@H]1O[C@@H](C[C@H]1N=[N+]=[N-])N1C=C(C)C(=O)NC1=O

InChIKey

InChIKey=GQOOHDGGHYGHFS-HKMOIUERSA-N

Formula

C23H28N7O8P

Mass

561.492

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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

Phenylalanine and derivatives

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Phenylalanine or derivatives - Pyrimidine nucleoside - Pyrimidine 2',3'-dideoxyribonucleoside - Alpha-amino acid ester - Amphetamine or derivatives - Phosphoric diester monoamide - Fatty acid ester - Pyrimidone - Hydropyrimidine - Monocyclic benzene moiety - Benzenoid - Pyrimidine - Fatty acyl - Phosphoric acid ester - Organic phosphoric acid amide - Organic phosphoric acid derivative - Vinylogous amide - Methyl ester - Heteroaromatic compound - Oxolane - Azo compound - Azo imide - Carboxylic acid ester - Lactam - Urea - Organoheterocyclic compound - Azacycle - Monocarboxylic acid or derivatives - Carbonitrile - Nitrile - Oxacycle - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic salt - Organic oxygen compound - Organic zwitterion - Cyanide - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine 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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