Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C[C@H]2NC(=O)\C=C\C[C@H](OC(=O)[C@H](CC(C)C)CC(=O)CCNC2=O)[C@H](C)[C@H]2O[C@@H]2C2=CC=CC=C2)C=C1

InChIKey

InChIKey=KNGZNRBPLJJLQQ-OXMROIEVSA-N

Formula

C35H44N2O7

Mass

604.744

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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

Aromatic heteromonocyclic compounds

Substituents

Macrolactam - Macrolide - Alpha-amino acid or derivatives - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Carboxamide group - Carboxylic acid ester - Ketone - Lactam - Lactone - Secondary carboxylic acid amide - Cyclic ketone - Oxacycle - Ether - Oxirane - Dialkyl ether - Carboxylic acid derivative - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic nitrogen compound - Aromatic heteromonocyclic 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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