Structure Information
Structure

Compound Identification

SMILES

OCCCN1[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=CC2=CC=CC=C2C=C1

InChIKey

InChIKey=OLROPOGBNPYJGT-POHQUNBXSA-N

Formula

C37H37N3O7

Mass

635.717

Export to:

JSON SDF CSV

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

Previous Back Next