Structure Information
Structure

Compound Identification

SMILES

C[C@H](CO)N1C[C@H](C)[C@H](CN(C)CC2=CC=C(C=C2)C(O)=O)OCCCC[C@H](C)OC2=C(C=C(NS(=O)(=O)C3=CC=CS3)C=C2)C1=O

InChIKey

InChIKey=YHNJHBLLPAXULX-PBANKSGMSA-N

Formula

C34H45N3O8S2

Mass

687.87

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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 - Sulfanilide - Benzoic acid or derivatives - Benzoic acid - Benzoyl - Benzylamine - Phenylmethylamine - Alkyl aryl ether - Aralkylamine - Monocyclic benzene moiety - Organosulfonic acid amide - Benzenoid - Aminosulfonyl compound - Thiophene - Tertiary carboxylic acid amide - Organic sulfonic acid or derivatives - Sulfonyl - Heteroaromatic compound - Organosulfonic acid or derivatives - Amino acid or derivatives - Amino acid - Carboxamide group - Lactam - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Ether - Azacycle - Amine - Hydrocarbon derivative - Organic nitrogen compound - Primary alcohol - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Alcohol - Organic oxide - 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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