Structure Information
Structure

Compound Identification

SMILES

COC1\C=C/OC2(C)OC3=C(C2=O)C2=C(OCC(O)=O)C=C(NC(=O)\C(C)=C/C=C\C(C)(O)C(=O)C(C)C(O)C(C)C(OC(C)=O)C1C)C(O)=C2C(O)=C3C

InChIKey

InChIKey=WVPVVIOXGMSGRF-AYDMIGIISA-N

Formula

C39H47NO15

Mass

769.797

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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

Naphthofuran - Macrolactam - 1-naphthol - Phenoxyacetate - Naphthalene - Benzofuran - Coumaran - Aryl ketone - Aryl alkyl ketone - Alkyl aryl ether - Ketal - Acyloin - Benzenoid - Dicarboxylic acid or derivatives - Tertiary alcohol - Lactam - Cyclic ketone - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid ester - Carboxamide group - Ketone - Acetal - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Oxacycle - Ether - Azacycle - Organoheterocyclic compound - Polyol - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Organic oxide - Organic nitrogen compound - Organooxygen compound - Organonitrogen 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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