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Structure Information
Structure

Compound Identification

SMILES

COC1CC(C)CC2=C(OC)C(=O)C(=CNC(C)(C)C)C(=NC(=O)C(C)=CC=CC(OC)C(OC(N)=O)C(C)=CC(C)C1O)C2=O

InChIKey

InChIKey=SVDZUQLPVCVSCL-UHFFFAOYSA-N

Formula

C34H49N3O9

Mass

643.778

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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 - M-quinomethane - O-quinomethane - Quinomethane - Cyclohexenone - Carbamic acid ester - Vinylogous ester - Vinylogous amide - Ketone - Secondary alcohol - N-acylimine - Cyclic ketone - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Enamine - Ether - Allylamine - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Amine - Carbonyl group - Alcohol - 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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