Structure Information
Structure

Compound Identification

SMILES

CN1C=CC=C1C1=NC2=CC=CC=C2N=C1O[C@@H]1C[C@@H]2C(C1)C(=O)[C@@H](CCCCC\C=C/C1C[C@]1(NC2=O)C(=O)NS(=O)(=O)C1CC1)NC(=O)OC(C)(C)C

InChIKey

InChIKey=UBVPTXACJCUFKK-WVMAEJJYSA-N

Formula

C40H50N6O8S

Mass

774.93

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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 - N-methylpyrrole - Pyrazine - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Aminosulfonyl compound - Carbamic acid ester - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Carboxamide group - Secondary carboxylic acid amide - Ketone - Lactam - Carboxylic acid derivative - Organoheterocyclic compound - Ether - Azacycle - Carbonyl group - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organosulfur compound - Organooxygen compound - 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

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