Structure Information
Structure

Compound Identification

SMILES

COC1C=COC2(C)OC3=C(C)C(O)=C4C(=O)C(NC(=O)C(C)=CC=CC(C)C(O)C(C)C(O)C(C)C(OC(C)=O)C1C)=C(NCCC(=O)OC)C(=O)C4=C3C2=O

InChIKey

InChIKey=KCHFEPWTGHIDQO-UHFFFAOYSA-N

Formula

C41H52N2O14

Mass

796.867

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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 - Naphthoquinone - Beta amino acid or derivatives - Naphthalene - Benzofuran - Coumaran - Quinone - Aryl ketone - Aryl alkyl ketone - Ketal - Dicarboxylic acid or derivatives - Benzenoid - Methyl ester - Vinylogous amide - Vinylogous acid - Secondary carboxylic acid amide - Lactam - Secondary alcohol - Ketone - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - Acetal - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Oxacycle - Enamine - Ether - Azacycle - Organoheterocyclic compound - Secondary amine - Polyol - Amine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Organic oxide - Alcohol - Hydrocarbon derivative - 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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