Structure Information
Structure

Compound Identification

SMILES

CC1C(CN2CCC3(CC2)N(CNC3=O)C2=CC=CC=C2)OC(OC1C1=CC=C(CO)C=C1)C1=CC=C(C=C1)C1=CC(CNC(=O)C(CC2=CC=CC=C2)NS(=O)(=O)C2=CC=C(C)C=C2)=CC=C1

InChIKey

InChIKey=WIFACIFZNYKJNR-UHFFFAOYSA-N

Formula

C55H59N5O7S

Mass

934.17

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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 heteropolycyclic compounds

Substituents

Phenylalanine or derivatives - Alpha-amino acid amide - Biphenyl - P-toluenesulfonamide - Phenylimidazolidine - Amphetamine or derivatives - Azaspirodecane - Benzenesulfonamide - Tosyl compound - Benzenesulfonyl group - Benzyl alcohol - Aniline or substituted anilines - Dialkylarylamine - Toluene - Aralkylamine - Benzenoid - Fatty acyl - Fatty amide - Imidazolidinone - Monocyclic benzene moiety - Meta-dioxane - Piperidine - Organosulfonic acid amide - Aminosulfonyl compound - Imidazolidine - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary amine - Tertiary aliphatic amine - Secondary carboxylic acid amide - Lactam - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Acetal - Amine - Organic nitrogen compound - Carbonyl group - Aromatic alcohol - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Primary alcohol - Organosulfur compound - Alcohol - Organic oxygen compound - Aromatic heteropolycyclic 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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