Structure Information
Structure

Compound Identification

SMILES

NCCCC[C@H](NC(=O)[C@H](CS)NC(=O)[C@@H]1CCCN1)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O

InChIKey

InChIKey=UZLXNLPDLATWEN-RMIXPHLWSA-N

Formula

C38H59N11O12S

Mass

894.02

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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

Not available

Direct Parent

Peptides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Alpha peptide - Phenylalanine or derivatives - Glutamic acid or derivatives - Aspartic acid or derivatives - N-acyl-alpha-amino acid - N-acyl-l-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Proline or derivatives - Alpha-amino acid amide - Cysteine or derivatives - 3-phenylpropanoic-acid - Amphetamine or derivatives - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Tricarboxylic acid or derivatives - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Fatty acyl - Monocyclic benzene moiety - Fatty amide - N-acyl-amine - Benzenoid - Pyrrolidine - Amino acid - Amino acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Guanidine - Alkylthiol - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Carboxylic acid - Secondary aliphatic amine - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Secondary amine - Amine - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Primary aliphatic amine - Organic oxygen compound - Primary amine - Organosulfur compound - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as peptides. These are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another.

External Descriptors

Not available

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