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Structure Information
Structure

Compound Identification

SMILES

CC[C@@H](CO)N1[C@H]2C(=O)N(C\C=C/CCC(=O)OC[C@H](NC(=O)[C@@H]3[C@H]4O[C@]2(C=C4)[C@H]3C1=O)C1=CC=CC=C1)C1=C(C)C=CC=C1Cl

InChIKey

InChIKey=WHBFAXPRWDMODQ-FDEQSECHSA-N

Formula

C35H38ClN3O7

Mass

648.15

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