Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(CN2CCCCC\C=C\C3CC3(NC(=O)C3CC(CN3C2=O)OC2=CC(=NC3=C2C=CC(OC)=C3)C2=NC(=CS2)C(C)C)C(O)=O)C=C1

InChIKey

InChIKey=YSSODYUHHYPDAJ-CSKARUKUSA-N

Formula

C41H47N5O7S

Mass

753.92

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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 or derivatives - Quinoline - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - 2,4-disubstituted 1,3-thiazole - Alkyl aryl ether - Cyclopropanecarboxylic acid or derivatives - Monocyclic benzene moiety - Benzenoid - Cyclopropanecarboxylic acid - Pyridine - Heteroaromatic compound - Azole - Thiazole - Pyrrolidine - Carboxamide group - Lactam - Secondary carboxylic acid amide - Urea - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Ether - Carbonyl group - Organic oxygen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - 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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