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ID: ALA1145771

Journal: Bioorg Med Chem Lett

Title: The selective inhibition of phosphatases by natural toxins: the anhydride domain of tautomycin is not a primary factor in controlling PP1/PP2A selectivity.

Authors: Liu W, Sheppeck JE, Colby DA, Huang HB, Nairn AC, Chamberlin AR.

Abstract: Analogues of the potent and moderately selective PP1/PP2A inhibitor tautomycin (TM) were prepared with modifications in the C1'-C7' anhydride moiety. While all retain varying degrees of activity within a 3000-fold range of potencies, they also show remarkable constancy in their IC(50) ratios, suggesting that the anhydride moiety is not critical in controlling the selectivity of inhibition.

CiteXplore: 12699763

DOI: 10.1016/s0960-894x(03)00105-7