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ID: ALA1130706

Journal: Bioorg Med Chem Lett

Title: Synthesis and structure-activity relationships of adenosine analogs as inhibitors of trypanosomal glyceraldehyde-3-phosphate dehydrogenase. Modifications at positions 5' and 8.

Authors: Aronov AM, Gelb MH.

Abstract: A number of 5', N6- and C8, N6-disubstituted adenosine analogs was synthesized and tested for inhibition of trypanosomal glyceraldehyde 3-phosphate dehydrogenase. The most active compound, N6-(3-methyl-2-butenyl)-8-(2-thienyl)adenosine, had Kl of 9 microM and was marginally selective for the parasite enzyme.

CiteXplore: 9934461

DOI: 10.1016/s0960-894x(98)00635-0