Structure Information
Structure

Compound Identification

SMILES

N[C@@H](C[C@@H](O)COC(O)=N)C(O)=NC(C1OC(C(O)C1O)n1cc(C=O)nc1O)C(O)=O

InChIKey

InChIKey=RQVSNRJHTPSRIL-XIMYAXABSA-N

Formula

C16H23N5O11

Mass

461.384

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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 - N-acyl-alpha amino acid or derivatives - N-acyl-alpha-amino acid - Glycosyl compound - N-glycosyl compound - Alpha-amino acid or derivatives - 1,2,4-trisubstituted-imidazole - Trisubstituted imidazole - Imidazolyl carboxylic acid derivative - Imidazole-4-carbonyl group - Aryl-aldehyde - N-substituted imidazole - 1,3-aminoalcohol - Azole - Tetrahydrofuran - Imidazole - Vinylogous amide - Heteroaromatic compound - Amino acid or derivatives - Secondary alcohol - Amino acid - Oxacycle - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Organopnictogen compound - Aldehyde - Alcohol - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Amine - Organic oxide - Imine - Primary aliphatic amine - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen 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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