Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1C2OC(C)(C)OC(C2C)C(C)\C=C/C=C(C)/C(=O)NC2=C(C)C(OC(C)=O)=C3C(=C(O)C(C)=C4OCOC(=C34)\C(C)=C\C(C)(O)C(O)C(C)C1O)C2=O

InChIKey

InChIKey=NNEZEAVYFDRHAT-LEPLVDGDSA-N

Formula

C43H55NO14

Mass

809.906

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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 - Benzo-m-dioxin - Aryl ketone - Beta-hydroxy acid - Ketal - Meta-dioxane - Dicarboxylic acid or derivatives - Hydroxy acid - Benzenoid - Tertiary alcohol - Enol ester - Vinylogous acid - Methyl ester - Carboxylic acid ester - Secondary carboxylic acid amide - Secondary alcohol - Ketone - Lactam - Carboxamide group - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Carbonyl group - Alcohol - Organic oxygen compound - Organopnictogen 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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