Structure Information
Structure

Compound Identification

SMILES

C[C@@H](CO)N1C[C@@H](C)[C@H](CN(C)CC2=CC=NC=C2)OCCCC[C@H](C)OC2=C(C=C(NC(=O)NC3=CC=C(F)C=C3)C=C2)C1=O

InChIKey

InChIKey=LYRCZWJWHIAWAE-FYZNHFMZSA-N

Formula

C35H46FN5O5

Mass

635.781

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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 heteropolycyclic compounds

Substituents

Macrolactam - N-phenylurea - Alkyl aryl ether - Fluorobenzene - Halobenzene - Aralkylamine - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Pyridine - Heteroaromatic compound - Tertiary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Lactam - Urea - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid derivative - Dialkyl ether - Organoheterocyclic compound - Ether - Azacycle - Oxacycle - Organic oxygen compound - Amine - Alcohol - Organohalogen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organofluoride - Organonitrogen compound - Organooxygen compound - Primary alcohol - Aromatic 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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