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DESCRIPTION (provided by applicant): The long term goals of this work include the development of an understanding of the role(s) of the ser/thr protein kinase Rsk family in signal transduction within the mitogen-activated protein kinase (MAPK) pathway, and the identification of new classes of potential antitumor agents. The immediate objectives include - chemical synthesis of analogues of a group of kaempferol glycosides shown to mediate highly selective inhibition of Rsk2 - synthesis of analogues of a second class of inhibitors identified from the NCI repository by in silico screening - identification of additional naturally occurring inhibitors of p90 Rsk that have different types of chemical structures and properties This work is relevant to public health in that a potent and selective Rsk inhibitor is likely to exhibit activity useful for the treatment of certain cancers, notably breast cancer.
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Biological Regulation Studied In Vitro and In Cellulo with Modified Proteins
Biological Regulation Studied In Vitro and In Cellulo with Modified Proteins
Biological Regulation Studied In Vitro and In Cellulo with Modified Proteins
Ribosomally Synthesized Proteins Incorporating Modified Dipeptides
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