Structure Information
Structure

Compound Identification

SMILES

COC1\C=C\C=C(C)\C(OC(C)=O)C2=CC(N(C)C(=O)CC(OC(=O)C(C)N(C)C(=O)C(C)C)C3(C)OC3C(C)C3CC1(O)NC(=O)O3)=C(Cl)C(OC)=C2

InChIKey

InChIKey=YKGZBVAXZWNQKS-OCRAYANJSA-N

Formula

C38H52ClN3O12

Mass

778.29

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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

Alpha-amino acid ester - Macrolactam - Alanine or derivatives - Alpha-amino acid or derivatives - Anisole - Alkyl aryl ether - 1,3-oxazinane - Aryl chloride - Aryl halide - Dicarboxylic acid or derivatives - Oxazinane - Benzenoid - Carbamic acid ester - Tertiary carboxylic acid amide - Carbonic acid derivative - Lactam - Carboxamide group - Carboxylic acid ester - Oxacycle - Azacycle - Organoheterocyclic compound - Alkanolamine - Ether - Oxirane - Dialkyl ether - Carboxylic acid derivative - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organic oxide - Organonitrogen compound - Organooxygen 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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