CC(C)\C=C(/C)[C@H]1O[C@@]2(C[C@@H]3C[C@@H](C\C=C(C)\C[C@@H](C)\C=C\C=C4/CO[C@@H]5[C@H](OC(=O)C6=CC=C(C=C6)[Si](C)(C6=CC=CC=C6)C6=CC=CC=C6)C(C)=C[C@@H](C(=O)O3)[C@]45O)O2)CC(=O)[C@@H]1C

InChIKey=SSYOFETVEPLBCS-VZZMACMDSA-N

C56H66O9Si

911.22

Organic compounds

Phenylpropanoids and polyketides

Macrolides and analogues

Milbemycins

Not available

Milbemycins

Benzoic acid esters Benzoyl derivatives Alkylarylsilanes Ketals Oxanes Dicarboxylic acids and derivatives Tertiary alcohols Oxolanes Lactones Cyclic ketones Carboxylic acid esters Oxacyclic compounds Organic metalloid salts Dialkyl ethers Hydrocarbon derivatives Alkylsilanes Organic oxides Aldehydes

Aromatic heteropolycyclic compounds

Milbemycin - Benzoate ester - Benzoic acid or derivatives - Benzoyl - Alkylarylsilane - Ketal - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Oxane - Benzenoid - Oxolane - Tertiary alcohol - Carboxylic acid ester - Lactone - Ketone - Cyclic ketone - Organic metalloid salt - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Acetal - Ether - Dialkyl ether - Organic oxygen compound - Organic metalloid moeity - Organooxygen compound - Carbonyl group - Alkylsilane - Organosilicon compound - Hydrocarbon derivative - Organic oxide - Aldehyde - Alcohol - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as milbemycins. These are a group of macrolides with a structure containing a 16-membered lactone ring fused to a 1,7-dioxaspiroundecane ring system and to either a benzofuran (or hydrogenated derivative thereof). In some cases (e.g. Milbemycin E), the tetrahydrofuranyl ring is missing. Milbemycins can be o-glycosylated at C13 to form Avermectins. Milbemycins are produced by Streptomyces species.

Not available