Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)OC(=O)C[C@H]1CCCCC\C=C/[C@H]2C[C@]2(CC(=O)[C@@H]2C[C@H](CN2C1=O)OC1=NC2=CC=CC=C2N1CC1=CC=CC=C1)C(O)=O

InChIKey

InChIKey=KPOPJCWIUYOQRU-DJGNGEBSSA-N

Formula

C39H47N3O7

Mass

669.819

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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 - Benzimidazole - Alkyl aryl ether - Monocyclic benzene moiety - Cyclopropanecarboxylic acid - Cyclopropanecarboxylic acid or derivatives - Dicarboxylic acid or derivatives - Benzenoid - N-substituted imidazole - Azole - Heteroaromatic compound - Tertiary carboxylic acid amide - Imidazole - Pyrrolidine - Amino acid or derivatives - Amino acid - Carboxamide group - Carboxylic acid ester - Tertiary amine - Ketone - Lactam - Azacycle - Carboxylic acid - Carboxylic acid derivative - Organoheterocyclic compound - Ether - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Organic oxide - Amine - Organooxygen compound - Organonitrogen 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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