Structure Information
Structure

Compound Identification

SMILES

CNCC1=C(O)C2=C3C(O)=C(C)C4=C2C(=O)C(C)(O4)O\C=C\C(OC)C(C)C(OC(C)=O)C(C)C(O)C(C)C(O)C(C)\C=C\C=C(C)/C(=O)NC1=C3O

InChIKey

InChIKey=QKOQHNFJQIUIDQ-HYUMRFKVSA-N

Formula

C39H52N2O12

Mass

740.847

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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 - 1-naphthol - Naphthalene - Benzofuran - Coumaran - Aryl ketone - Hydroquinone - Aryl alkyl ketone - Ketal - Aralkylamine - Benzenoid - Ketone - Carboxylic acid ester - Secondary carboxylic acid amide - Amino acid or derivatives - Secondary alcohol - Lactam - Carboxamide group - Acetal - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Secondary amine - Polyol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organopnictogen compound - Alcohol - Organic oxide - Amine - 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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