Structure Information
Structure

Compound Identification

SMILES

CO[C@@H](C(=O)O[C@H](C)CC(=O)[C@@H](OC)C1=C2NC(=O)\C(C)=C\CC[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@@H](O)[C@H](C[C@H](C)CC(C2=O)=C(OC)C1=O)OC)C1=CC=CC=C1

InChIKey

InChIKey=VYPYPBNEMZGFTE-ICMBXAMCSA-N

Formula

C44H60N2O14

Mass

840.964

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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 - Benzylether - Monocyclic benzene moiety - Benzenoid - Carbamic acid ester - Vinylogous amide - Vinylogous ester - Carboxamide group - Carboxylic acid ester - Ketone - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Cyclic ketone - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Carbonyl group - Alcohol - Hydrocarbon derivative - 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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