Structure Information
Structure

Compound Identification

SMILES

NC(=O)OC1CCCCC\C=C\C2CC2(NC(=O)C2(CCCN2C1=O)C(N)=O)S(=O)(=O)NC1=CC=C(C=C1)C(F)(F)F

InChIKey

InChIKey=IMNCFIYXMMWPQC-QPJJXVBHSA-N

Formula

C26H32F3N5O7S

Mass

615.63

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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 - Alpha-amino acid amide - Alpha-amino acid or derivatives - Trifluoromethylbenzene - Sulfanilide - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Monocyclic benzene moiety - Benzenoid - Organic sulfonic acid amide - Organosulfonic acid amide - Pyrrolidine - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Carbamic acid ester - Organosulfonic acid or derivatives - Tertiary carboxylic acid amide - Sulfonyl - Secondary carboxylic acid amide - Primary carboxylic acid amide - Carboxamide group - Lactam - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Carbonyl group - Organofluoride - Organohalogen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Alkyl fluoride - Alkyl halide - Organic nitrogen compound - Organic oxygen compound - Organic oxide - 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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