Structure Information
Structure

Compound Identification

SMILES

Cl.CO[C@H]1C[C@H](C)CC2=C(NCC=C)C(=O)C=C(NC(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@H]1OC(=O)CCCN(C)C)C2=O

InChIKey

InChIKey=FHCZAFGHXVBKPO-LZUWHGTKSA-N

Formula

C37H55ClN4O9

Mass

735.32

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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

Aliphatic heteropolycyclic compounds

Substituents

Macrolactam - Fatty acid ester - Fatty acyl - Vinylogous amide - Carbamic acid ester - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - Ketone - Lactam - Cyclic ketone - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Enamine - Ether - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Secondary amine - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Hydrochloride - Organic oxide - Amine - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aliphatic 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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