Structure Information
Structure

Compound Identification

SMILES

COC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CC2=CC=CC=C2)N2CC3=C(O)C(CC4=CC(=CC(CN(CC5=C(O)C(CC6=CC(=CC(C2)=C6O)C(C)(C)C)=CC(=C5)C(C)(C)C)[C@@H](CC2=CC=CC=C2)C(=O)N1)=C4O)C(C)(C)C)=CC(=C3)C(C)(C)C)C(=O)OC

InChIKey

InChIKey=AMDKRVRQNSPBJE-YKDOIGRJSA-N

Formula

C72H90N4O10S2

Mass

1235.65

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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

Alpha-amino acid ester - Macrolactam - Alpha-amino acid amide - Alpha-amino acid or derivatives - Aralkylamine - Phenol - Dicarboxylic acid or derivatives - Monocyclic benzene moiety - Benzenoid - Methyl ester - Carboxylic acid ester - Amino acid or derivatives - Lactam - Organic disulfide - Tertiary amine - Secondary carboxylic acid amide - Tertiary aliphatic amine - Carboxamide group - Carboxylic acid derivative - Polyol - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Amine - Organic oxide - 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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