Structure Information
Structure

Compound Identification

SMILES

CC[C@H]1OC(=O)C2=CCN(C2)C(=O)C2=COC(CCC[C@H](OC(=O)CC3=CC=C(CN4CCOCC4)C=C3)\C=C(/C)\C=C\CNC(=O)CC[C@H]1C)=N2

InChIKey

InChIKey=FSWBFDGEVHBWIA-ZPVXEAKHSA-N

Formula

C40H52N4O8

Mass

716.876

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

Macrolactam - 2-heteroaryl carboxamide - Benzylamine - Phenylmethylamine - Aralkylamine - Morpholine - Monocyclic benzene moiety - Oxazinane - Benzenoid - Dicarboxylic acid or derivatives - Azole - Heteroaromatic compound - Oxazole - Pyrroline - Tertiary carboxylic acid amide - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Lactam - Secondary carboxylic acid amide - Tertiary amine - Amino acid or derivatives - Tertiary aliphatic amine - Lactone - Carboxamide group - Carboxylic acid ester - Oxacycle - Carboxylic acid derivative - Azacycle - Dialkyl ether - Organoheterocyclic compound - Ether - Organic nitrogen compound - Amine - Carbonyl group - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - 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

Previous Back Next