C[C@H]1CC[C@]2(C[C@@H]3C[C@@H](C\C=C(C)\[C@H](O)[C@@H](C)\C=C\C=C4/CO[C@@H]5\C(=N/O[Si](C)(C)C(C)(C)C)C(C)=C[C@@H](C(=O)O3)[C@]45O)O2)O[C@@H]1C1CCCCC1

InChIKey=NKLJQOONZLWSLJ-NNTPKQHGSA-N

C42H65NO8Si

740.066

Organic compounds

Phenylpropanoids and polyketides

Macrolides and analogues

Milbemycins

Not available

Milbemycins

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

Aliphatic heteropolycyclic compounds

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