Structure Information
Structure

Compound Identification

SMILES

[Na+].COC1C=COC2(C)OC3=C(C2=O)C2=C([O-])C=C(NC(=O)\C(C)=C/C=C\C(C)C(O)C(C)C(O)C(C)C(C1C)C(=O)OC)C(O)=C2C(O)=C3C

InChIKey

InChIKey=LAJFQTBWGBXICV-JJMAIFDFSA-M

Formula

C37H46NNaO12

Mass

719.76

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 - Aryl ketone - Aryl alkyl ketone - Ketal - Phenoxide - Benzenoid - Methyl ester - Carboxylic acid ester - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Ketone - Lactam - Acetal - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Monocarboxylic acid or derivatives - Azacycle - Organic alkali metal salt - Organoheterocyclic compound - Polyol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Alcohol - Organic sodium salt - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Aldehyde - Organic salt - Organic zwitterion - 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