Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1C[C@H](O[C@H]2[C@@H](C)\C=C\C=C3/CO[C@@H]4[C@H](O[Si](C)(C)C(C)(C)C)C(C)=C[C@@H](C(=O)O[C@H]5C[C@@H](C\C=C2/C)O[C@@]2(C5)O[C@H](C(C)C)[C@@H](C)C=C2)[C@]34O)O[C@@H](C)\C1=N/S(=O)C1=CC=CC=C1

InChIKey

InChIKey=YVCMAPCRZBHGBI-OXRYJGEESA-N

Formula

C52H75NO11SSi

Mass

950.31

Export to:

JSON SDF CSV

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 - Ketal - Monocyclic benzene moiety - Oxane - Pyran - Benzenoid - Trialkylheterosilane - Oxolane - Tertiary alcohol - Carboxylic acid ester - Lactone - Sulfinic acid derivative - Silyl ether - Organic metalloid salt - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Acetal - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Organoheterosilane - Sulfinyl compound - Organic metalloid moeity - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organopnictogen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Alcohol - Organosilicon compound - 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

Previous Back Next