Structure Information
Structure

Compound Identification

SMILES

COC1C=COC2(C)OC3=C(C2=O)C2=C(O)C=C(NC(=O)C(C)=CC=CC(C)C(O)C(C)C(O)C(C)C(OC(O)CC(O)=O)C1C)C(O)=C2C(O)=C3C

InChIKey

InChIKey=RJCFANQNXMPQKU-UHFFFAOYSA-N

Formula

C38H49NO14

Mass

743.803

Export to:

JSON SDF CSV

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 - Naphthalene - Benzofuran - Coumaran - Hydroquinone - Aryl alkyl ketone - Aryl ketone - 1-hydroxy-2-unsubstituted benzenoid - Beta-hydroxy acid - Ketal - Hydroxy acid - Benzenoid - Secondary carboxylic acid amide - Secondary alcohol - Lactam - Ketone - Hemiacetal - Carboxamide group - Acetal - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organopnictogen compound - Alcohol - 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

Previous Back Next