ChemicalBook--->CAS DataBase List--->193146-53-1

193146-53-1

193146-53-1 Structure

193146-53-1 Structure
IdentificationBack Directory
[Name]

(3S,6R,7S,8S,12Z,15S,16E)-3,7,15-TRIS-{[TERT-BUTYL(DIMETHYL)SILYL]OXY}-1-HYDROXY-4,4,6,8,12,16-HEXAMETHYL-17-(2-METHYL-1,3-THIAZOL-4-YL)HEPTADECA-12,16-DIEN-5-ONE
[CAS]

193146-53-1
[Synonyms]

(3S,6R,7S,8S,12Z,15S,16E)-3,7,15-TRIS-{[TERT-BUTYL(DIMETHYL)SILYL]OXY}-1-HYDROXY-4,4,6,8,12,16-HEXAMETHYL-17-(2-METHYL-1,3-THIAZOL-4-YL)HEPTADECA-12,16-DIEN-5-ONE
[Molecular Formula]

C45H87NO5SSi3
[MDL Number]

MFCD04039707
[MOL File]

193146-53-1.mol
[Molecular Weight]

838.497
Chemical PropertiesBack Directory
[Appearance]

Colourless Oil
[solubility ]

Acetone, Dichloromethane, Ethanol, Ethyl Acetate, Methanol
[form ]

Oil
[color ]

Colourless
Hazard InformationBack Directory
[Chemical Properties]

Colourless Oil
[Uses]

An intermediate in the synthesis of Epothilones. Epothilones are polyketide natural products that inhibit cancer cells by a mechanism similar to paclitaxel, and also are effective against paclitaxel- resistant tumours. Epothilone D is in phase I clinical testing of in patients with advanced solid tumours. Epothilone D is a cytotoxic macrolide that stabilises malignant cells' microtubules and arr ests mitosis, a characteristic it shares with other epothilones. They bind to the same hepatic sites as does paclitaxel (Taxol) in a 1:1 stoichiometric ratio of a, b-tubulin heterodimers.
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