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Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(C=C1)S(=O)(=O)N[C@H](CC1=CC=CC=C1)C(=O)NC1=CC=C(C=C1)[C@H]1O[C@@H](CN2CCC[C@H]2C(=O)OC(C)(C)C)C[C@H](O1)C1=CC=C(CO)C=C1

InChIKey

InChIKey=RRADKBPSVICKKU-UPQZTPITSA-N

Formula

C43H51N3O8S

Mass

769.95

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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 - Alpha-amino acid ester - Proline or derivatives - Alpha-amino acid amide - P-toluenesulfonamide - Amphetamine or derivatives - Benzenesulfonamide - Tosyl compound - Benzenesulfonyl group - Anilide - Benzyl alcohol - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - N-arylamide - Toluene - Aralkylamine - Meta-dioxane - Monocyclic benzene moiety - Fatty amide - Organosulfonic acid amide - Fatty acyl - Benzenoid - N-alkylpyrrolidine - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Pyrrolidine - Aminosulfonyl compound - Tertiary amine - Secondary carboxylic acid amide - Tertiary aliphatic amine - Carboxamide group - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Oxacycle - Acetal - Monocarboxylic acid or derivatives - Organopnictogen compound - Alcohol - Organonitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Organosulfur compound - Aromatic alcohol - Primary alcohol - Organic nitrogen compound - Amine - 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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