Structure Information
Structure

Compound Identification

SMILES

CC(C)[C@@H]1NC(=O)[C@@H](CC(=O)C(C)(C)O)CC2=CC3=C(OC4NC5=C6C=CC=C5C34C3=C(N=C1O3)C1=NC(Cl)=C(O1)C1=C(Cl)NC3=CC=CC6=C13)C=C2

InChIKey

InChIKey=HTCYSFJWWGBAOI-KBNNZNIGSA-N

Formula

C40H33Cl2N5O6

Mass

750.63

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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 - Coumaran - Indole - Indole or derivatives - Dihydroindole - Secondary aliphatic/aromatic amine - Acyloin - Aryl halide - Aryl chloride - Benzenoid - Substituted pyrrole - Alpha-hydroxy ketone - Azole - Oxazole - Pyrrole - Heteroaromatic compound - Tertiary alcohol - Lactam - Amino acid or derivatives - Ketone - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Secondary amine - Organoheterocyclic compound - Azacycle - Oxacycle - Organic nitrogen compound - Organohalogen compound - Organochloride - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Alcohol - 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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