Structure Information
Structure

Compound Identification

SMILES

CC[Si](CC)(CC)O[C@H]1C=C2C[C@H](C[C@@H](O[Si](CC)(CC)CC)[C@@H](CC[C@H](C[C@H](CC(=O)O[C@@H](C)[C@H](C)[C@H](O[Si](CC)(CC)CC)[C@@H](C)\C=C\C=C\C=C\C=C\C=C\C=C\C=C\[C@@H](C[C@H](O2)[C@@H]1C(=O)SC1=CC=CC=N1)O[C@@H]1O[C@H](C)[C@@H](O[Si](CC)(CC)CC)[C@H](NC(=O)C(F)(F)F)[C@@H]1O[Si](CC)(CC)CC)O[Si](CC)(CC)CC)O[Si](CC)(CC)CC)O[Si](CC)(CC)CC)O[Si](CC)(CC)CC

InChIKey

InChIKey=HUJMAKINMPRFSV-AJQDRLCQSA-N

Formula

C108H199F3N2O16SSi9

Mass

2123.6

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Macrolides and analogues

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Macrolide - Glycosyl compound - O-glycosyl compound - Aryl thioether - Monosaccharide - Oxane - Pyran - Pyridine - Heteroaromatic compound - Trialkylheterosilane - Lactone - Carboxylic acid ester - Carboxamide group - Secondary carboxylic acid amide - Thiocarboxylic acid ester - Silyl ether - Carbothioic s-ester - Carboxylic acid derivative - Thiocarboxylic acid or derivatives - Monocarboxylic acid or derivatives - Oxacycle - Acetal - Sulfenyl compound - Organoheterosilane - Organoheterocyclic compound - Organic metalloid salt - Azacycle - Organosilicon compound - Organic metalloid moeity - Organohalogen compound - Organopnictogen compound - Organofluoride - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Organosulfur compound - Alkyl fluoride - Alkyl halide - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

External Descriptors

Not available

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