Structure Information
Structure

Compound Identification

SMILES

CC(=O)N(CCCCCNC(=O)CC(O)(CC(=O)NCCCCCN(OCC1=CC=CC=C1)C(=O)CCC(=O)N[C@@H](C(=O)N[C@H]1[C@H]2CCC(Cl)=C(N2C1=O)C(=O)OCC1=CC=C(C=C1)[N+]([O-])=O)C1=CC=CC=C1)C(=O)OC(C)(C)C)OCC1=CC=CC=C1

InChIKey

InChIKey=AGVQKUDHWVPPDM-QJXQQOGPSA-N

Formula

C63H77ClN8O16

Mass

1237.8

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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 - Carbacephem - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Benzyloxycarbonyl - Phenylacetamide - Nitrobenzene - Nitroaromatic compound - Tetrahydropyridine - Fatty acid ester - Dicarboxylic acid or derivatives - Fatty amide - N-acyl-amine - Fatty acyl - Monocyclic benzene moiety - Benzenoid - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Vinylogous halide - Acetamide - Tertiary alcohol - Tertiary carboxylic acid amide - Beta-lactam - Azetidine - Organic nitro compound - Carboxamide group - Carboxylic acid ester - Lactam - C-nitro compound - Secondary carboxylic acid amide - Organic oxoazanium - Vinyl chloride - Allyl-type 1,3-dipolar organic compound - Vinyl halide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Chloroalkene - Organoheterocyclic compound - Haloalkene - Organohalogen compound - Organic oxide - Organic oxygen compound - Carbonyl group - Organic salt - Organic nitrogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Hydrocarbon derivative - Alcohol - 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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