Key result
(S)-Blebbistatin and its analogues are valuable myosin II inhibitors, though their application in advanced biological settings is hindered by low potency, solubility, and toxicity issues.
This review summarizes the medicinal chemistry of the myosin II inhibitor (S)-blebbistatin, detailing its physicochemical limitations and providing guidance on selecting appropriate analogues for biological research.
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Limitations restrict advanced use; extends guidance for analogue selection in myosin II research.
( S)-Blebbistatin, a chiral tetrahydropyrroloquinolinone, is a widely used and well-characterized ATPase inhibitor selective for myosin II. The central role of myosin II in many normal and pathological biological processes has been revealed with the aid of this small molecule. The first part of this manuscript provides a summary of myosin II and ( S)-blebbistatin literature from a medicinal chemist's perspective. The second part of this perspective deals with the physicochemical deficiencies that trouble the use of ( S)-blebbistatin in advanced biological settings: low potency and solubility, fluorescence interference, (photo)toxicity, and stability issues. A large toolbox of analogues has been developed in which particular shortcomings have been addressed. This perspective provides a necessary overview of these developments and presents guidelines for selecting the best available analogue for a given application. As the unmet need for high-potency analogues remains, we also propose starting points for medicinal chemists in search of nanomolar myosin II inhibitors.
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Roman et al. (2018) reported a review. (S)-Blebbistatin and its derivatives was evaluated. (S)-Blebbistatin and its analogues are valuable myosin II inhibitors, though their application in advanced biological settings is hindered by low potency, solubility, and toxicity issues.
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