Structure Information
Structure

Compound Identification

SMILES

C[C@@H](CO)N1C[C@H](C)[C@@H](CN(C)S(=O)(=O)C2=CN(C)C=N2)OCCCC[C@H](C)OC2=C(C=C(NC(=O)CC3=CC=CC=C3)C=C2)C1=O

InChIKey

InChIKey=YPSMNOUBSPQRPK-WJQRCLFPSA-N

Formula

C34H47N5O7S

Mass

669.84

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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 - Phenylacetamide - N-arylamide - Alkyl aryl ether - N-substituted imidazole - Organosulfonic acid amide - Monocyclic benzene moiety - Benzenoid - Organic sulfonic acid or derivatives - Azole - Aminosulfonyl compound - Tertiary carboxylic acid amide - Sulfonyl - Organosulfonic acid or derivatives - Imidazole - Heteroaromatic compound - Secondary carboxylic acid amide - Tertiary amine - Amino acid or derivatives - Lactam - Carboxamide group - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Amine - Organic nitrogen compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organosulfur compound - Organonitrogen compound - Organooxygen 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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