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Kemisk inaktivering av den E3 ubiquitin Ligase Cereblon av pomalidomid-baserade homo-PROTAC

Article DOI: 10.3791/59472-v • 10:44 min • May 15th, 2019
May 15th, 2019 •
*1, *2, 1, 2, 2, 1
1Department of Internal Medicine III, University Hospital Ulm, 2Pharmaceutical Institute, Pharmaceutical Chemistry I, University of Bonn
* These authors contributed equally

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Detta arbete beskriver syntesen och karakterisering av en pomalidomid-baserade, bifunktionella homo-PROTAC som en ny metod för att inducera ubiquitination och nedbrytning av E3 ubiquitin Ligase cereblon (CRBN), målet för talidomid analoger.

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Kemi crbn PROTAC Imid pomalidomid ubiquitin Ligase multipelt myelom proteasom
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