Structure Information
Structure

Compound Identification

SMILES

COC(=O)[C@H](CC1=CN(CC2=CC=CC=C2[N+]([O-])=O)C=N1)NC(=O)[C@@H]1C[C@@]2([C@H](N1C(=O)OC(C)(C)C)N(C(=O)OC(C)(C)C)C1=CC=CC=C21)C(C)(C)C=C

InChIKey

InChIKey=VAGHFNXVDIGBOM-KYOWQHJPSA-N

Formula

C40H50N6O9

Mass

758.873

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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 heteropolycyclic compounds

Substituents

Alpha peptide - Histidine or derivatives - Alpha-amino acid ester - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Pyrroloindole - Indolecarboxylic acid derivative - Indolecarboxylic acid - Alpha-amino acid or derivatives - Nitrobenzene - Indole or derivatives - Indole - Nitroaromatic compound - Pyrrolidine-2-carboxamide - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Imidazolyl carboxylic acid derivative - Fatty acid ester - N-substituted imidazole - Benzenoid - Monocyclic benzene moiety - Fatty acyl - Azole - Heteroaromatic compound - Imidazole - Methyl ester - Pyrrole - Carbamic acid ester - Pyrrolidine - Secondary carboxylic acid amide - Carboxamide group - C-nitro compound - Carboxylic acid ester - Organic nitro compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Azacycle - Propargyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Organic oxygen compound - Carbonyl group - Organic zwitterion - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organic salt - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic 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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