Structure Information
Structure

Compound Identification

SMILES

CC(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC1=CNC2=CC=CC=C12)C(=O)NC1=CC=C(C=C1)C(=O)NC1=CC=C(C=C1)C(=O)NC1=CC=C(C=C1)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC1=CNC2=CC=CC=C12)C(N)=O

InChIKey

InChIKey=JJGFTSISZWFUOF-ZLAZYUONSA-N

Formula

C87H96N24O12

Mass

1669.881

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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 - Phenylalanine or derivatives - Histidine or derivatives - Benzanilide - Aromatic anilide - Acylaminobenzoic acid or derivatives - N-acyl-alpha amino acid or derivatives - Hippuric acid or derivatives - Alpha-amino acid amide - Triptan - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Amphetamine or derivatives - 3-alkylindole - Benzamide - Benzoic acid or derivatives - Indole - Indole or derivatives - Anilide - N-arylamide - Benzoyl - Monocyclic benzene moiety - Fatty amide - Fatty acyl - N-acyl-amine - Substituted pyrrole - Benzenoid - Azole - Pyrrole - Heteroaromatic compound - Acetamide - Imidazole - Secondary carboxylic acid amide - Primary carboxylic acid amide - Carboxamide group - Guanidine - Azacycle - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic 1,3-dipolar compound - Organoheterocyclic compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organic oxide - 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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