Structure Information
Structure

Compound Identification

SMILES

CC[C@H]1OC(=O)C[C@@H](O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@@H](O)[C@@H]([C@H]2O)[N+](C)(C)[O-])[C@@H](CC(OC)OC)C[C@@H](C)C(=O)\C=C\C(C)(O)C(O)[C@@H]1CO[C@@H]1O[C@H](C)[C@@H](O)[C@@H](OC)[C@H]1OC

InChIKey

InChIKey=PUNPQDMFLJOQCJ-RNXYAMRLSA-N

Formula

C41H73NO18

Mass

868.024

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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

Aliphatic heteromonocyclic compounds

Substituents

Macrolide - O-glycosyl compound - Glycosyl compound - Amino saccharide - Monosaccharide - Oxane - Trialkyl amine oxide - Tertiary alcohol - Lactone - Ketone - Carboxylic acid ester - Secondary alcohol - Cyclic ketone - Dialkyl ether - Carboxylic acid derivative - Polyol - N-oxide - Monocarboxylic acid or derivatives - Trisubstituted n-oxide - Oxacycle - Acetal - Organoheterocyclic compound - Ether - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Aldehyde - Alcohol - Aliphatic heteromonocyclic 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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