C[C@H]1N2C(=O)C[C@@](CC\C(C)=C\[C@@H](O[C@@H]3CCCCO3)C(=O)\C=C\C=C/C3=CSC1=N3)([S@@]2=O)[C@@](C)(O)C(=O)SCC1=C(C)OC(=O)O1

InChIKey=ATFISCUSRDIBNV-RHNUATAFSA-N

C32H38N2O10S3

706.84

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Thiazolidinediones Carbonic acid diesters Oxanes Thiazoles Tertiary alcohols Heteroaromatic compounds Thioesters Sulfinic acids and derivatives Carbothioic S-esters Cyclic ketones Acetals Azacyclic compounds Sulfinyl compounds Sulfenyl compounds Carboxylic acids and derivatives Oxacyclic compounds Aldehydes Organopnictogen compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds

Aromatic heteropolycyclic compounds

Macrolactam - Thiazolidinedione - Carbonic acid diester - Oxane - Azole - Tertiary alcohol - Heteroaromatic compound - Thiazole - Thiazolidine - Ketone - Sulfinic acid derivative - Thiocarboxylic acid ester - Cyclic ketone - Carbothioic s-ester - Thiocarboxylic acid or derivatives - Organoheterocyclic compound - Azacycle - Oxacycle - Sulfenyl compound - Sulfinyl compound - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organosulfur compound - Organic oxide - Carbonyl group - Organic oxygen compound - Aldehyde - Alcohol - Hydrocarbon derivative - Aromatic heteropolycyclic compound

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.

Not available