Structure Information
Structure

Compound Identification

SMILES

CCC(C)C(N=C(O)C(CC(O)=O)N=C(O)C(CC1=CC=C(OS(O)(=O)=O)C=C1)N=C(O)C(N=C(O)C1CCCN1C(=O)C(N)CO)C(C)CC)C(O)=NC(CC(O)=N)C(O)=NC(CC1=CC=C(OS(O)(=O)=O)C=C1)C(O)=NC(CC1=CC=C(O)C=C1)C(O)=O

InChIKey

InChIKey=AEOQDGDXMZRJRA-UHFFFAOYSA-N

Formula

C55H74N10O23S2

Mass

1307.36

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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 heteromonocyclic compounds

Substituents

Hybrid peptide - Tyrosine or derivatives - Phenylalanine or derivatives - N-acyl-alpha amino acid or derivatives - N-acyl-alpha-amino acid - Alpha-amino acid amide - Phenylsulfate - 3-phenylpropanoic-acid - Arylsulfate - Amphetamine or derivatives - Alpha-amino acid or derivatives - Phenoxy compound - N-acylpyrrolidine - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Sulfuric acid ester - Sulfate-ester - Sulfuric acid monoester - Dicarboxylic acid or derivatives - Monocyclic benzene moiety - Tertiary carboxylic acid amide - Pyrrolidine - Organic sulfuric acid or derivatives - Amino acid - Carboxamide group - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid - Carboxylic acid derivative - Carboximidic acid derivative - Carboximidic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Alcohol - Aromatic heteromonocyclic 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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