CC(C)[C@@H]1O[C@]2(CC[C@@H]1C)C[C@@H]1C[C@@H](C\C=C(C)\[C@H](OS(C)(=O)=O)[C@@H](C)\C=C\C=C3/CO[C@@H]4C(O[Si](C)(C)C(C)(C)C)C(C)=C[C@@H](C(=O)O1)[C@]34O[Si](C)(C)C)O2

InChIKey=RIZDNYCCXMEACQ-ZFDYXECQSA-N

C43H72O10SSi2

837.27

Organic compounds

Phenylpropanoids and polyketides

Macrolides and analogues

Milbemycins

Not available

Milbemycins

Ketals Organosulfonic acid esters Sulfonic acid esters Oxanes Trialkylheterosilanes Methanesulfonates Sulfonyls Oxolanes Carboxylic acid esters Lactones Silyl ethers Organic metalloid salts Monocarboxylic acids and derivatives Dialkyl ethers Oxacyclic compounds Organic oxides Carbonyl compounds Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Milbemycin - Ketal - Oxane - Sulfonic acid ester - Organosulfonic acid ester - Methanesulfonate - Trialkylheterosilane - Oxolane - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Carboxylic acid ester - Silyl ether - Lactone - Dialkyl ether - Oxacycle - Organoheterosilane - Carboxylic acid derivative - Organic metalloid salt - Organoheterocyclic compound - Ether - Monocarboxylic acid or derivatives - Acetal - Hydrocarbon derivative - Organic oxygen compound - Organic metalloid moeity - Organooxygen compound - Organosilicon compound - Organosulfur compound - Carbonyl group - Organic oxide - Aliphatic 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