| Literature DB >> 12699763 |
Wen Liu1, James E Sheppeck, David A Colby, Hsien-Bin Huang, Angus C Nairn, A Richard Chamberlin.
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.Entities:
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Year: 2003 PMID: 12699763 DOI: 10.1016/s0960-894x(03)00105-7
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823