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

InChIKey=UQENCEKCLUPKFH-UVUCKXMKSA-N

C38H60O7Si

656.976

Organic compounds

Phenylpropanoids and polyketides

Macrolides and analogues

Milbemycins

Not available

Milbemycins

Ketals Oxanes Trialkylheterosilanes Tertiary alcohols Oxolanes Silyl ethers Lactones Carboxylic acid esters Oxacyclic compounds Organic metalloid salts Monocarboxylic acids and derivatives Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aliphatic heteropolycyclic compounds

Milbemycin - Ketal - Oxane - Trialkylheterosilane - Oxolane - Tertiary alcohol - Carboxylic acid ester - Lactone - Silyl ether - Acetal - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterosilane - Monocarboxylic acid or derivatives - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Organic oxide - Organic oxygen compound - Organic metalloid moeity - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organosilicon compound - Alcohol - 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