Structure Information
Structure

Compound Identification

SMILES

CC[C@@H]1[C@H](C)C[C@H]2[C@@H]3C[C@@H]4\C=C\C(=O)C5C(=O)N[C@H](CCCNC(=O)\C=C/C[C@@H]4[C@@H]3C=C[C@H]12)C5=O

InChIKey

InChIKey=ZPBFUJHHMOCPHA-XQSFWCMJSA-N

Formula

C29H38N2O4

Mass

478.633

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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 - 11-noriridane monoterpenoid - Monoterpenoid - 1,3-diketone - Pyrrolidone - 2-pyrrolidone - 3-pyrrolidone - 1,3-dicarbonyl compound - Pyrrolidine - Secondary carboxylic acid amide - Carboxamide group - Lactam - Ketone - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Carbonyl group - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - 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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