Structure Information
Structure

Compound Identification

SMILES

COC1\C=C\C=C(C)\CC2=CC(N(C)C(=O)CC(OC(=O)C=CC)C3(C)OC3C(C)C3CC1(O)NC(=O)O3)=C(Cl)C(OC)=C2

InChIKey

InChIKey=DUANORXCOLMYGW-JJSUYLOMSA-N

Formula

C32H41ClN2O9

Mass

633.14

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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 - Anisole - Phenol ether - Alkyl aryl ether - Fatty acid ester - 1,3-oxazinane - Aryl chloride - Oxazinane - Aryl halide - Benzenoid - Fatty acyl - Carbamic acid ester - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Tertiary carboxylic acid amide - Lactam - Carboxylic acid ester - Carboxamide group - Alkanolamine - Oxacycle - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Dialkyl ether - Oxirane - Ether - Monocarboxylic acid or derivatives - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Organonitrogen compound - Organochloride - Organic oxygen compound - Organohalogen 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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