Structure Information
Structure

Compound Identification

SMILES

COC1\C=C\OC2(C)OC3=C(C)C(O)=C4C(O)=C(NC(=O)\C(C)=C\C=C\C(C)C(O)C(C)C(O)C(C)C(OC(C)=O)C1C)\C(=C\NNC1C5CC6CC(C5)CC1C6)C(=O)C4=C3C2=O

InChIKey

InChIKey=BRELVUNNRDMSJN-GXLPAGIGSA-N

Formula

C48H63N3O12

Mass

874.041

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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 - Naphthofuran - 1-naphthol - Naphthalene - Benzofuran - Coumaran - O-quinomethane - Quinomethane - Aryl ketone - Aryl alkyl ketone - Ketal - Benzenoid - Vinylogous amide - Lactam - Carboxamide group - Carboxylic acid ester - Secondary alcohol - Secondary carboxylic acid amide - Ketone - Dialkyl ether - Ether - Acetal - Carboxylic acid derivative - Polyol - Oxacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Alkylhydrazine - Azacycle - Organic nitrogen compound - Hydrazine derivative - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - 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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