Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1C[C@@H](CC[C@H]1O[Si](C)(C)C(C)(C)C)\C=C(/C)[C@H]1OC(=O)[C@@H]2CCCCN2C(=O)C(=O)[C@]2(O)O[C@@H]([C@H](C[C@H]2C)OC)[C@H](C[C@@H](C)C\C(C)=C/[C@@H](CC=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C)OC

InChIKey

InChIKey=KVRUABNQJVFBLO-YTQVIXAPSA-N

Formula

C55H95NO13Si2

Mass

1034.529

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Macrolide lactams

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Macrolide lactams

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Macrolide lactam - Alpha-amino acid ester - Alpha-amino acid or derivatives - Piperidine - Oxane - Trialkylheterosilane - Alpha-hydrogen aldehyde - Tertiary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Hemiacetal - Ketone - Lactam - Lactone - Cyclic ketone - Silyl ether - Organoheterosilane - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic nitrogen compound - Aldehyde - Carbonyl group - Organic oxide - Organosilicon compound - Hydrocarbon derivative - Organic metalloid moeity - Organonitrogen compound - Organooxygen compound - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as macrolide lactams. These are cyclic polyketides containing both a cyclic amide and a cyclic ester group.

External Descriptors

Not available

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