Structure Information
Structure

Compound Identification

SMILES

CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H]3[C@@H]2SC(=NCC2CCCO2)N3C)[C@@](C)(C[C@@H](C)C(=O)N[C@H](C)[C@@H](O)[C@]1(C)O)OC

InChIKey

InChIKey=MCJDKAOPCMZLPR-QGXQVZRTSA-N

Formula

C43H75N3O13S

Mass

874.14

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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

Aliphatic heteropolycyclic compounds

Substituents

Macrolactam - Macrolide - Glycosyl compound - O-glycosyl compound - Monosaccharide - Oxane - Thiazolidine - Tertiary alcohol - Oxolane - Carboxamide group - Carboxylic acid ester - Isothiourea - Lactam - Lactone - Secondary carboxylic acid amide - Secondary alcohol - Acetal - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Hydrocarbon derivative - Organic nitrogen compound - Alcohol - Organic oxygen compound - Carbonyl group - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - Aliphatic 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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