Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1C[C@H](C)CC2=C(N)C(=O)C=C(N(CC(=O)C3=CC(Cl)=C(Cl)C=C3)C(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@H]1O)C2=O

InChIKey

InChIKey=IBJVZURONIIFTC-YAVWJVNQSA-N

Formula

C36H43Cl2N3O9

Mass

732.65

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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 - Alkyl-phenylketone - Phenylketone - 1,2-dichlorobenzene - Aryl ketone - Aryl alkyl ketone - Benzoyl - Halobenzene - Chlorobenzene - Monocyclic benzene moiety - Aryl halide - Benzenoid - Aryl chloride - Carbamic acid ester - Tertiary carboxylic acid amide - Vinylogous amide - Cyclic ketone - Secondary alcohol - Lactam - Amino acid or derivatives - Ketone - Carboxamide group - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Enamine - Ether - Organooxygen compound - Primary amine - Organic nitrogen compound - Amine - Carbonyl group - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organochloride - Organohalogen compound - Primary aliphatic amine - 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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