Structure Information
Structure

Compound Identification

SMILES

[H]C(C)(O)C([H])(N=C(O)C([H])(N)CC1=CC=C(O)C=C1)C(O)=NCC(O)=NC([H])(CC1=CNC2=CC=CC=C12)C(O)=NC([H])(CCCC)C(O)=NC([H])(CC(=O)OS(O)(=O)=O)C(O)=NC([H])(CC1=CC=CC=C1)C(O)=NC(=O)C([H])(CC(O)=O)N=C(O)C([H])(N)CCCNC(N)=N

InChIKey

InChIKey=PBHKFCLZCVGPRU-UHFFFAOYSA-N

Formula

C55H74N14O18S

Mass

1251.34

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Peptidomimetics

Subclass

Hybrid peptides

Intermediate Tree Nodes

Not available

Direct Parent

Hybrid peptides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Hybrid peptide - Aspartic acid or derivatives - N-acyl-alpha amino acid or derivatives - 3-alkylindole - Amphetamine or derivatives - Alpha-amino acid or derivatives - Indole or derivatives - Indole - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Phenol - Benzenoid - Sulfuric acid ester - Sulfuric acid monoester - Substituted pyrrole - Dicarboxylic acid or derivatives - Monocyclic benzene moiety - Heteroaromatic compound - Pyrrole - Organic sulfuric acid or derivatives - Amino acid - N-acylimine - Secondary alcohol - Guanidine - Carboxylic acid salt - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Carboxylic acid - Carboxylic acid derivative - Carboximidic acid derivative - Carboximidic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Imine - Carbonyl group - Amine - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as hybrid peptides. These are compounds containing at least two different types of amino acids (alpha, beta, gamma, delta) linked to each other through a peptide bond.

External Descriptors

Not available

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