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Improved synthesis and comparative analysis of the tool properties of new and existing D-ring modified (S)-blebbistatin analogs.
Verhasselt, Sigrid; Roman, Bart I; Bracke, Marc E; Stevens, Christian V.
Afiliación
  • Verhasselt S; SynBioC Research Group, Department of Sustainable Organic Chemistry and Technology, Campus Coupure, Ghent University, Coupure Links 653, 9000 Ghent, Belgium.
  • Roman BI; SynBioC Research Group, Department of Sustainable Organic Chemistry and Technology, Campus Coupure, Ghent University, Coupure Links 653, 9000 Ghent, Belgium. Electronic address: bart1.roman@ugent.be.
  • Bracke ME; Laboratory of Experimental Cancer Research, Department of Radiation Oncology and Experimental Cancer Research, Ghent University, De Pintelaan 185, 9000 Ghent, Belgium.
  • Stevens CV; SynBioC Research Group, Department of Sustainable Organic Chemistry and Technology, Campus Coupure, Ghent University, Coupure Links 653, 9000 Ghent, Belgium. Electronic address: chris.stevens@ugent.be.
Eur J Med Chem ; 136: 85-103, 2017 Aug 18.
Article en En | MEDLINE | ID: mdl-28486210
(S)-Blebbistatin is a widely used research tool to study myosin II, an important regulator of many motility based diseases. Its potency is too low to be of clinical relevance, but identification of analogs with enhanced potency could deliver leads for targeted pharmacotherapeutics. This, however, requires a profound insight into the structure-activity relationship of the (S)-blebbistatin scaffold. Therefore, new D-ring modified (S)-blebbistatin derivatives were prepared to extend the existing small library of analogs. These molecules were obtained via an improved synthesis pathway and their myosin II inhibitory properties were evaluated in vitro. Finally, all new and known D-ring modified (S)-blebbistatin analogs were compared and the most potent ones underwent a screening of their physicochemical properties.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Miosina Tipo II / Inhibidores Enzimáticos / Compuestos Heterocíclicos de 4 o más Anillos Límite: Humans Idioma: En Revista: Eur J Med Chem Año: 2017 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Miosina Tipo II / Inhibidores Enzimáticos / Compuestos Heterocíclicos de 4 o más Anillos Límite: Humans Idioma: En Revista: Eur J Med Chem Año: 2017 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Francia