期刊
CHEMMEDCHEM
卷 18, 期 15, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cmdc.202300211
关键词
Acyclic nucleoside phosphonates; inhibitors; hypoxanthine-guanine-(xanthine) phosphoribosyltransferase; malaria; Plasmodium falciparum
Twelve N2'-branched acyclic nucleoside phosphonates and bisphosphonates were synthesized as potential inhibitors of Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase (PfHGXPRT). The compounds showed low to modest selectivity for the parasite enzyme over human HGPRT. The effect of different chemical groups/linkers attached to N2' atom on inhibition constants and selectivity was discussed.
Twelve N2 '-branched acyclic nucleoside phosphonates and bisphosphonates were synthesized as potential inhibitors of Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase (PfHGXPRT), the key enzyme in the purine salvage pathway for production of purine nucleotides. The chemical structures were designed with the aim to study selectivity of the inhibitors for PfHGXPRT over human HGPRT. The newly prepared compounds contain 9-deazahypoxanthine connected to a phosphonate group via a five-atom-linker bearing a nitrogen atom (N2 ') as a branching point. All compounds, with the additional phosphonate group(s) in the second aliphatic linker attached to N2 ' atom, were low micromolar inhibitors of PfHGXPRT with low to modest selectivity for the parasite enzyme over human HGPRT. The effect of the addition of different chemical groups/linkers to N2 ' atom on the inhibition constants and selectivity is discussed.
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