Structure Information
Structure

Compound Identification

SMILES

COC1=C(C)C2=C(C=C1)C(O[C@H]1CCN3[C@@H](C1)C(=O)N[C@]1(C[C@@H]1\C=C\CCCCN(C)C3=O)C(=O)NS(=O)(=O)C1(C)CC1)=CC(=N2)C1=NC(=CS1)C#C

InChIKey

InChIKey=CJSPRFCEDGIRKZ-QRZZCTQLSA-N

Formula

C38H44N6O7S2

Mass

760.93

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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 - Quinoline - Anisole - Phenol ether - 2,4-disubstituted 1,3-thiazole - Alkyl aryl ether - Cyclopropanecarboxylic acid or derivatives - Benzenoid - Piperidine - Pyridine - Azole - Heteroaromatic compound - Aminosulfonyl compound - Thiazole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary amine - Amino acid or derivatives - Secondary carboxylic acid amide - Urea - Carboxamide group - Lactam - Acetylide - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Azacycle - Carbonyl group - Organic nitrogen compound - Organooxygen compound - Organic oxide - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Amine - Organosulfur 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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