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

InChIKey=XKKLHLRGTFHSMD-WILIWYMNSA-N

C36H63NO13

717.894

Organic compounds

Phenylpropanoids and polyketides

Macrolides and analogues

Not available

Not available

Macrolides and analogues

O-glycosyl compounds Pyrans Oxanes Monosaccharides Tertiary alcohols Secondary alcohols Oxime ethers Carboxylic acid esters Lactones Polyols Oxacyclic compounds Acetals Monocarboxylic acids and derivatives Dialkyl ethers Hydrocarbon derivatives Organic oxides Carbonyl compounds Organopnictogen compounds

Aliphatic heteromonocyclic compounds

Macrolide - Glycosyl compound - O-glycosyl compound - Monosaccharide - Oxane - Pyran - Tertiary alcohol - Carboxylic acid ester - Lactone - Secondary alcohol - Oxime ether - Acetal - Carboxylic acid derivative - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Oxacycle - Organoheterocyclic compound - Polyol - Organopnictogen compound - Organic oxygen compound - Organic oxide - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound

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.

Not available