Structure Information
Structure

Compound Identification

SMILES

COC1=C2OC3=C(OC)C=CC(=C3)C(=O)O[C@H]3C=COC=C4[C@@H](O)[C@@]56SS[C@@]([C@@H](O)C(C=C1)=C2)(N(C)C5=O)C(=O)N6[C@H]34

InChIKey

InChIKey=BPRXOIXJSLNVCK-KCEIGVIJSA-N

Formula

C28H24N2O10S2

Mass

612.62

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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 - Diaryl ether - Alpha-amino acid or derivatives - Epipolythiodioxopiperazine - Thiodioxopiperazine - Anisole - Dioxopiperazine - Phenol ether - 2,5-dioxopiperazine - Alkyl aryl ether - N-alkylpiperazine - N-methylpiperazine - Dithiazinane - 1,4-diazinane - Piperazine - Benzenoid - Tertiary carboxylic acid amide - Pyrrolidine - Secondary alcohol - Organic disulfide - Lactone - Lactam - Carboxamide group - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Ether - Oxacycle - Carboxylic acid derivative - Organic oxide - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxygen 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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