Structure Information
Structure

Compound Identification

SMILES

CCCNC1=C2C[C@@H](C)C[C@@H](OC)[C@@H](OC(=O)CCCN)[C@H](C)\C=C(C)\[C@@H](OC(N)=O)[C@H](OC)\C=C/C=C(C)/C(=O)NC(=CC1=O)C2=O

InChIKey

InChIKey=NSJHIHVDBZBZBW-CAQRCHCXSA-N

Formula

C35H52N4O9

Mass

672.82

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