Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)OC(=O)N[C@@H]1CCCCC\C=C/C2C[C@]2(NC(=O)[C@@H]2C[C@H](CC2C1=O)OC1=NC2=CC=CC=C2N=C1C1=CC=CO1)C(=O)NS(=O)(=O)C1CC1

InChIKey

InChIKey=FAWLGZMCDGHMQW-BIIBEWLWSA-N

Formula

C39H47N5O9S

Mass

761.89

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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 - Alpha-amino acid amide - Alpha-amino acid or derivatives - Quinoxaline - Alkyl aryl ether - Cyclopropanecarboxylic acid or derivatives - Pyrazine - Benzenoid - Aminosulfonyl compound - Carbamic acid ester - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Furan - Carboxamide group - Secondary carboxylic acid amide - Ketone - Lactam - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Carbonyl group - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Hydrocarbon derivative - 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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