Structure Information
Structure

Compound Identification

SMILES

[H][C@](O)(C=CCCOC(=O)CCCCCCC)[C@]([H])(O)[C@@]1([H])OC(=O)C=CC=CC(=O)N(C(C)=O)C(=O)C=C(C)CC[C@@]2([H])O[C@]2([H])[C@@]1([H])OC(=O)N=C(C)O

InChIKey

InChIKey=MEWNUFWOAOFSNB-MVFXJRBUSA-N

Formula

C35H48N2O13

Mass

704.77

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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 - Dicarboxylic acid or derivatives - Carboxylic acid imide, n-substituted - Fatty acyl - Carboxylic acid imide - Dicarboximide - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Acetamide - Secondary alcohol - Carbonic acid derivative - Carboxylic acid ester - 1,2-diol - Lactone - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Oxacycle - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Dialkyl ether - Ether - Oxirane - Carbonyl group - Organic nitrogen compound - Alcohol - Organic oxygen compound - Organopnictogen compound - Organic oxide - Organonitrogen compound - Hydrocarbon derivative - 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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