Structure Information
Structure

Compound Identification

SMILES

OCCN1[C@H]2C(=O)N(CCN3CCOCC3)C\C=C/CCC(=O)NC[C@H](OC(=O)[C@@H]3[C@H]4O[C@]2(C=C4)[C@H]3C1=O)C1=CC=CC=C1

InChIKey

InChIKey=FEJULCFVNGXCJH-PAVMHARSSA-N

Formula

C32H40N4O8

Mass

608.692

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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 - Isoindole or derivatives - Isoindoline - Furopyrrole - Monocyclic benzene moiety - Morpholine - Oxazinane - Pyrrolidone - 2-pyrrolidone - N-alkylpyrrolidine - Benzenoid - Pyrrolidine - Pyrrole - Furan - Oxolane - Dihydrofuran - Tertiary carboxylic acid amide - Lactam - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Lactone - Carboxylic acid ester - Alkanolamine - Carboxylic acid derivative - Oxacycle - Dialkyl ether - Azacycle - Ether - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Amine - Organic oxygen compound - Organic oxide - Primary alcohol - Organooxygen compound - Organonitrogen compound - Carbonyl group - 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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