Structure Information
Structure

Compound Identification

SMILES

CN1CCCC\C=C/[C@@H]2C[C@]2(NC(=O)[C@@H]2C[C@H](C[C@H]2C1=O)OC1=NC(=NC2=CC=CC=C12)[N+]1=NC=CC1)C(=O)NS(=O)(=O)C1CC1

InChIKey

InChIKey=CKOYWOBHVMZMLT-HDKVXQBBSA-O

Formula

C32H38N7O6S

Mass

648.76

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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 - Quinazolinamine - Alpha-amino acid or derivatives - Quinazoline - Alkyl aryl ether - Cyclopropanecarboxylic acid or derivatives - Pyrimidine - Benzenoid - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary carboxylic acid amide - Aminosulfonyl compound - Secondary carboxylic acid amide - Amino acid or derivatives - Tertiary amine - Carboxamide group - Lactam - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Ether - Organosulfur compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxygen compound - Organic oxide - Organic cation - 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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