Structure Information
Structure

Compound Identification

SMILES

OC[C@@H](CC1=CC=CC=C1)NC(=O)C[C@H]1CC=CCC[C@H](CC2=CC=CC=C2)C(=O)OC[C@H](CSCC2=CC=CC=C2)NC1=O

InChIKey

InChIKey=SZTWYXQHLYXAEN-YFRBGRBWSA-N

Formula

C37H44N2O5S

Mass

628.83

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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 heteromonocyclic compounds

Substituents

Macrolactam - Amphetamine or derivatives - Monocyclic benzene moiety - Benzenoid - Carboxamide group - Carboxylic acid ester - Lactam - Lactone - Secondary carboxylic acid amide - Carboxylic acid derivative - Oxacycle - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Thioether - Sulfenyl compound - Dialkylthioether - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Primary alcohol - Carbonyl group - Organopnictogen compound - Alcohol - Organic oxide - Aromatic heteromonocyclic 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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