Verhasselt Sigrid, Roman Bart I, De Wever Olivier, Van Hecke Kristof, Van Deun Rik, Bracke Marc E, Stevens Christian V
SynBioC Research Group, Department of Sustainable Organic Chemistry and Technology, Ghent University, Coupure Links 653, 9000 Ghent, Belgium.
Laboratory of Experimental Cancer Research, Department of Radiation Oncology and Experimental Cancer Research, Ghent University, De Pintelaan 185, 9000 Ghent, Belgium.
Org Biomol Chem. 2017 Mar 1;15(9):2104-2118. doi: 10.1039/c7ob00006e.
In search of myosin II inhibitors with superior research tool properties, a chemical optimization campaign of the blebbistatin scaffold was conducted in this paper. (S)-Blebbistatin is the best known small-molecule inhibitor of myosin II ATPase activity. Unfortunately, as a research tool this compound has several deficiencies: it is photolabile and (photo)toxic, has low water solubility, and its (fluorescent) precipitates interfere in (fluorescence) readouts. In view of obtaining tool compounds with improved properties, both enantiomers of a series of D-ring modified polar analogs were prepared. We identified (S)-3'-hydroxyblebbistatin (S)-2 and (S)-3'-aminoblebbistatin (S)-3 as two myosin II inhibitors with a 30-fold higher water solubility than (S)-blebbistatin. These molecules furthermore do not cause interference in (fluorescence) readouts. (S)-2 and (S)-3 thus are superior alternatives to (S)-blebbistatin as research tools to study myosin II.
为了寻找具有更优研究工具特性的肌球蛋白 II 抑制剂,本文开展了对 blebbistatin 骨架的化学优化研究。(S)-Blebbistatin 是最为人熟知的肌球蛋白 II ATP 酶活性小分子抑制剂。遗憾的是,作为一种研究工具,该化合物存在若干缺陷:它对光不稳定且具有(光)毒性,水溶性低,其(荧光)沉淀物会干扰(荧光)读数。鉴于要获得性能更优的工具化合物,我们制备了一系列 D 环修饰的极性类似物的两种对映体。我们确定了(S)-3'-羟基 blebbistatin(S)-2 和(S)-3'-氨基 blebbistatin(S)-3 这两种肌球蛋白 II 抑制剂,它们的水溶性比(S)-blebbistatin 高 30 倍。此外,这些分子不会干扰(荧光)读数。因此,(S)-2 和(S)-3 作为研究肌球蛋白 II 的工具,是(S)-blebbistatin 的优越替代品。