Structure Information
Structure

Compound Identification

SMILES

CC(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](CC2=CNC3=CC=CC=C23)NC(=O)[C@@H](CCCN=C(N)N)NC(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@@H](CC2=CN=CN2)NC(=O)[C@H](CCC(O)=O)NC1=O)C(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@@H]1C(N)=O

InChIKey

InChIKey=FMZPUKORONKIFF-DTOBWKGJSA-N

Formula

C56H77N17O12S2

Mass

1244.46

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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

Peptides

Direct Parent

Oligopeptides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Alpha-oligopeptide - Cyclic alpha peptide - Macrolactam - Proline or derivatives - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - 3-alkylindole - Indole or derivatives - Indole - Pyrrolidine-2-carboxamide - N-acylpyrrolidine - Pyrrolidine carboxylic acid or derivatives - Imidazolyl carboxylic acid derivative - Substituted pyrrole - Monocyclic benzene moiety - Benzenoid - Azole - Heteroaromatic compound - Acetamide - Pyrrole - Imidazole - Pyrrolidine - Tertiary carboxylic acid amide - Carboxamide group - Primary carboxylic acid amide - Amino acid or derivatives - Guanidine - Organic disulfide - Lactam - Secondary carboxylic acid amide - Amino acid - Azacycle - Organoheterocyclic compound - Carboxylic acid - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Monocarboxylic acid or derivatives - Organic oxide - Amine - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

External Descriptors

Not available

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