Structure Information
Structure

Compound Identification

SMILES

CC(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N1[C@@H](CCCN)C(=O)N2CCC[C@H]2C(=O)N[C@H](CC2CCCCC2)C(=O)N[C@@H](CC2=CNC3=CC=CC=C23)C(=O)N[C@@H](CCCN=C(N)N)C1=O

InChIKey

InChIKey=INHDUQICVUFVQI-YZBIKCAPSA-N

Formula

C47H65N11O7

Mass

896.107

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Macrolactams

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Macrolactams

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Macrolactam - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Amphetamine or derivatives - 3-alkylindole - Indole - Indole or derivatives - Monocyclic benzene moiety - Carboxylic acid imide, n-substituted - Substituted pyrrole - Benzenoid - Carboxylic acid imide - Dicarboximide - Heteroaromatic compound - Acetamide - Pyrrole - Pyrrolidine - Tertiary carboxylic acid amide - Secondary carboxylic acid amide - Amino acid or derivatives - Lactam - Carboxamide group - Guanidine - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Amine - Carbonyl group - Primary amine - Organic oxide - Primary aliphatic amine - Organonitrogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.

External Descriptors

Not available

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