CCC(C)[C@H]1O[C@]2(CC[C@@H]1C)C[C@@H]1C[C@@H](C\C=C(C)\C(O[C@H]3C[C@H](OC)[C@@H](NC(=O)CCNC(=O)CCCCCNC(=O)CCCC[C@@H]4SCC5NC(=O)NC45)[C@H](C)O3)[C@@H](C)\C=C\C=C3/COC4[C@H](O[Si](C)(C)C(C)(C)C)C(C)=C[C@@H](C(=O)O1)[C@]34O)O2

InChIKey=ZAKLZPNOHPSEEG-CGMGKQDASA-N

C66H107N5O14SSi

1254.75

Organic compounds

Phenylpropanoids and polyketides

Macrolides and analogues

Milbemycins

Not available

Milbemycins

Biotin and derivatives Beta amino acids and derivatives Thienoimidazolidines Ketals Imidazolidinones N-acyl amines Oxanes Trialkylheterosilanes Thiophenes Thiolanes Tertiary alcohols Oxolanes Carboxylic acid esters Ureas Silyl ethers Lactones Secondary carboxylic acid amides Dialkylthioethers Monocarboxylic acids and derivatives Dialkyl ethers Organic metalloid salts Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Organonitrogen compounds Organopnictogen compounds

Aliphatic heteropolycyclic compounds

Milbemycin - Biotin_derivative - Beta amino acid or derivatives - Thienoimidazolidine - Ketal - Fatty amide - Imidazolidinone - N-acyl-amine - Oxane - Fatty acyl - Imidazolidine - Oxolane - Thiophene - Thiolane - Trialkylheterosilane - Tertiary alcohol - Carboxamide group - Carboxylic acid ester - Lactone - Silyl ether - Urea - Secondary carboxylic acid amide - Organoheterosilane - Oxacycle - Azacycle - Organic metalloid salt - Carboxylic acid derivative - Dialkyl ether - Ether - Acetal - Organoheterocyclic compound - Dialkylthioether - Monocarboxylic acid or derivatives - Thioether - Organic oxygen compound - Alcohol - Carbonyl group - Organopnictogen compound - Organic oxide - Organic metalloid moeity - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organosilicon 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