Structure Information
Structure

Compound Identification

SMILES

CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)N[C@@H](CC1=CSC(N)=N1)C(=O)NC(=O)[C@H](CC1=CC=CC=C1)NS(=O)(=O)N1CCOCC1

InChIKey

InChIKey=IYMYORIPWWCOOB-VFFRCKCKSA-N

Formula

C33H52N6O7S2

Mass

708.93

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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 amide - Amphetamine or derivatives - 2,4-disubstituted 1,3-thiazole - Aralkylamine - Monocyclic benzene moiety - Morpholine - Sulfuric acid diamide - Oxazinane - Benzenoid - 1,3-thiazol-2-amine - Carboxylic acid imide - Dicarboximide - Carboxylic acid imide, n-unsubstituted - 1,3-aminoalcohol - Organic sulfuric acid or derivatives - Azole - Thiazole - Heteroaromatic compound - 1,2-aminoalcohol - Secondary alcohol - 1,2-diol - Secondary aliphatic amine - Ether - Organoheterocyclic compound - Azacycle - Oxacycle - Secondary amine - Dialkyl ether - Alcohol - Carbonyl group - Organonitrogen compound - Organic oxide - Amine - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Primary 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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