Structure Information
Structure

Compound Identification

SMILES

CC(C)C1NC(=O)C(CC2=CC3=C(OC4OC5=C6C=CC=C5C34C3=C(N=C1O3)C1=NC(Cl)=C(O1)C1=CN(Cl)C3=CC=CC6=C13)C(Br)=C2)NC(=O)C1=CC=C(Br)C=C1

InChIKey

InChIKey=XNUIEVSUGUXTDR-UHFFFAOYSA-N

Formula

C42H27Br2Cl2N5O6

Mass

928.42

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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 or derivatives - 4-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Benzamide - Benzoic acid or derivatives - Indole - Coumaran - Indole or derivatives - Benzoyl - Bromobenzene - Halobenzene - Monocyclic benzene moiety - Aryl halide - Aryl chloride - Aryl bromide - Benzenoid - Substituted pyrrole - Azole - Heteroaromatic compound - Oxazole - Pyrrole - Carboxamide group - Lactam - Secondary carboxylic acid amide - Carboxylic acid derivative - Oxacycle - Azacycle - Acetal - Organoheterocyclic compound - Organooxygen compound - Carbonyl group - Organic oxide - Organopnictogen compound - Hydrocarbon derivative - Organic oxygen compound - Organohalogen compound - Organobromide - Organochloride - Organonitrogen compound - Organic nitrogen compound - 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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