Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)CC(C)(C)N1C\C=C/CCC(=O)NC[C@H](OC(=O)[C@@H]2[C@H]3O[C@]4(C=C3Br)[C@H]2C(=O)N(CCO)[C@H]4C1=O)C1=CC=CC=C1

InChIKey

InChIKey=FDUVODDDHCPWRS-VYAQPPCLSA-N

Formula

C34H44BrN3O7

Mass

686.644

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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

Macrolide - Macrolactam - Alpha-amino acid or derivatives - Isoindolone - Isoindole or derivatives - Isoindoline - Furopyrrole - Benzenoid - N-alkylpyrrolidine - 2-pyrrolidone - Pyrrolidone - Monocyclic benzene moiety - Furan - Dihydrofuran - Tertiary carboxylic acid amide - Pyrrolidine - Pyrrole - Oxolane - Carboxylic acid ester - Lactam - Secondary carboxylic acid amide - Lactone - Carboxamide group - Alkanolamine - Carboxylic acid derivative - Dialkyl ether - Oxacycle - Ether - Azacycle - Bromoalkene - Haloalkene - Organoheterocyclic compound - Vinyl halide - Vinyl bromide - Monocarboxylic acid or derivatives - Carbonyl group - Organic oxide - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organohalogen compound - Organobromide - 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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