Structure Information
Structure

Compound Identification

SMILES

C[C@@H](CO)N1C[C@H](C)[C@H](CN(C)C(=O)NC2=CC=C(C=C2)C(F)(F)F)OCCCC[C@H](C)OC2=C(C=C(NC(=O)NC3=C(C)ON=C3C)C=C2)C1=O

InChIKey

InChIKey=GHGHRYAYLVHQLP-YEVBJSIWSA-N

Formula

C36H47F3N6O7

Mass

732.802

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