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]([C@H]2OC(=O)OCC2=CC=CC=C2)N(C)C(=O)OCC2=CC=CC=C2)[C@](C)(O)C[C@@H](C)\C(=N/OCC2=CC=CC=C2)[C@H](C)[C@@H](OC)[C@]1(C)O

InChIKey

InChIKey=MBPQOXXIVGHUSW-MTLLPFODSA-N

Formula

C60H86N2O17

Mass

1107.345

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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 heteromonocyclic compounds

Substituents

Macrolide - Glycosyl compound - O-glycosyl compound - Benzyloxycarbonyl - Amino saccharide - Monocyclic benzene moiety - Carbonic acid diester - Monosaccharide - Benzenoid - Oxane - Carbamic acid ester - Tertiary alcohol - Carboxylic acid ester - Lactone - Carbonic acid derivative - Secondary alcohol - Oxime ether - Organoheterocyclic compound - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Acetal - Dialkyl ether - Ether - Organic oxygen compound - Organic oxide - Alcohol - Hydrocarbon derivative - Carbonyl group - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aromatic 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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