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

InChIKey=WBHMTTLDIAMPAD-QZLHXHSDSA-N

C36H52O9

628.803

Organic compounds

Phenylpropanoids and polyketides

Macrolides and analogues

Milbemycins

Not available

Milbemycins

Ketals Oxanes Monosaccharides Tetrahydrofurans Tertiary alcohols Secondary alcohols Lactones Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aliphatic heteropolycyclic compounds

Milbemycin - Ketal - Monosaccharide - Oxane - Tertiary alcohol - Tetrahydrofuran - Carboxylic acid ester - Lactone - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Acetal - Monocarboxylic acid or derivatives - Alcohol - Organic oxygen compound - Carbonyl group - Organic oxide - Organooxygen compound - Hydrocarbon derivative - 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