The chemical substance with the name "[4S,7R,8S,9S,13R,14S,16S(E)]-13,14-Epoxy-4,8-dihydroxy-5,5,7,9-tetramethyl-16-[2-[2-(hydroxymethyl)thiazol-4-yl]-1-methylvinyl]-1-oxacyclohexadecane-2,6-dione" and CAS number "201049-37-8" is a complex organic compound characterized by its intricate stereochemistry and functional groups. It features multiple hydroxyl groups, an epoxy group, and a thiazole moiety, indicating potential biological activity and interactions. The presence of a dione suggests it may participate in various chemical reactions, including nucleophilic attacks or redox processes. The compound's structure includes a cyclohexadecane ring, which contributes to its three-dimensional conformation and may influence its solubility and reactivity. Given its specific stereochemistry, the compound may exhibit unique pharmacological properties, making it of interest in medicinal chemistry and drug development. Its potential applications could span from therapeutic agents to biochemical probes, depending on its biological activity and interaction with target molecules. Further studies would be necessary to elucidate its full range of characteristics and applications.

[4S,7R,8S,9S,13R,14S,16S(E)]-13,14-Epoxy-4,8-dihydroxy-5,5,7,9-tetramethyl-16-[2-[2-(hydroxymethyl)thiazol-4-yl]-1-methylvinyl]-1-oxacyclohexadecane-2,6-dione

201049-37-8: (-)-Epothilone E, (1S,3S,7S,10R,11S,12S,16R)-7,11-Dihydroxy-8,8,10,12-tetramethyl-3-[(E)-2-[2-(hydroxymethyl)-4-thiazolyl]-1-methylvinyl]-4,17-dioxabicyclo[14.1.0]heptadecane-5,9-dione

Epothilone E

Epothilone E, a derivative of epothilone, functions by inhibiting microtubule protein activity, thereby halting cell division and exhibiting anti-tumor

CAS 201049-37-8: [4S,7R,8S,9S,13R,14S,16S(E)]-13,14-Epoxy-4,8-dihydroxy-5,5,7,9-tetramethyl-16-[2-[2-(hydroxymethyl)thiazol-4-yl]-1-methylvinyl]-1-oxacyclohexadecane-2,6-dione

Epothilone E

Ref: 4Z-E-119003

Epothilone E

Ref: TM-T72934

Epothilone E

Ref: TR-E589010