Structure Information
Structure

Compound Identification

SMILES

CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@H]1[C@@H]2NC(=O)[C@H](NC(=O)[C@H](N)C3=CC(OC4=C(Cl)C=C1C=C4)=C(O)C(OC1=C(Cl)C=C(C[C@@H](N)CO)C=C1)=C3)C1=CC(=C(O)C=C1)C1=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C(O)C=C1[C@H](NC2=O)C(O)=O

InChIKey

InChIKey=HFXLKUBBHLUNCV-UUWWHVKGSA-N

Formula

C56H60Cl2N6O23

Mass

1256.02

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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 - N-acyl-alpha-hexosamine - Phenolic glycoside - Macrolactam - Alpha-amino acid amide - O-glycosyl compound - Glycosyl compound - Diaryl ether - Alpha-amino acid or derivatives - Amphetamine or derivatives - Phenoxy compound - Phenol ether - Aralkylamine - Halobenzene - 1-hydroxy-2-unsubstituted benzenoid - Chlorobenzene - Aryl halide - Aryl chloride - Benzenoid - Oxane - Monosaccharide - Monocyclic benzene moiety - Acetamide - 1,2-aminoalcohol - Amino acid or derivatives - Amino acid - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Lactam - Polyol - Monocarboxylic acid or derivatives - Carboxylic acid - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Acetal - Organooxygen compound - Organohalogen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Alcohol - Organic oxide - Organonitrogen compound - Primary alcohol - Organochloride - Organic oxygen compound - Amine - Organopnictogen compound - Primary amine - 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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