Structure Information
Structure

Compound Identification

SMILES

CC(C)C[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CS)NC(=O)[C@@H](N)CO)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O

InChIKey

InChIKey=UPGRZGJMOBNXSP-PDSMTZFYSA-N

Formula

C29H50N8O12S

Mass

734.82

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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

Aliphatic heteromonocyclic compounds

Substituents

Alpha-oligopeptide - Glutamine or derivatives - Leucine or derivatives - Proline or derivatives - N-acyl-alpha amino acid or derivatives - N-acyl-alpha-amino acid - N-acyl-l-alpha-amino acid - Alpha-amino acid amide - Serine or derivatives - Cysteine or derivatives - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - N-acylpyrrolidine - Branched fatty acid - Short-chain hydroxy acid - Hydroxy fatty acid - Heterocyclic fatty acid - Beta-hydroxy acid - N-acyl-amine - Fatty amide - Hydroxy acid - Fatty acid - Fatty acyl - Tertiary carboxylic acid amide - Pyrrolidine - Amino acid or derivatives - Secondary alcohol - Secondary carboxylic acid amide - Amino acid - Primary carboxylic acid amide - Carboxamide group - Alkylthiol - Azacycle - Organoheterocyclic compound - Carboxylic acid - Monocarboxylic acid or derivatives - Primary alcohol - Organic nitrogen compound - Primary amine - Carbonyl group - Alcohol - Hydrocarbon derivative - Amine - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxygen compound - Aliphatic heteromonocyclic 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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