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• W2092045986 abstract "Hypoxanthine–guanine–[xanthine] phosphoribosyltransferase (HG[X]PRT) is considered an important target for antimalarial chemotherapy as it is the only pathway for the synthesis of the purine nucleoside monophosphates required for DNA/RNA production. Thus, inhibition of this enzyme should result in cessation of replication. The aza-acyclic nucleoside phosphonates (aza-ANPs) are good inhibitors of Plasmodium falciparum HGXPRT (PfHGXPRT), with Ki values as low as 0.08 and 0.01 μM for Plasmodium vivax HGPRT (PvHGPRT). Prodrugs of these aza-ANPs exhibit antimalarial activity against Pf lines with IC50 values (0.8–6.0 μM) and have low cytotoxicity against human cells. Crystal structures of six of these compounds in complex with human HGPRT have been determined. These suggest that the different affinities of these aza-ANPs could be due to the flexibility of the loops surrounding the active site as well as the flexibility of the inhibitors, allowing them to adapt to fit into three binding pockets of the enzyme(s)." @default.
• W2092045986 created "2016-06-24" @default.
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• W2092045986 date "2014-12-24" @default.
• W2092045986 modified "2023-10-17" @default.
• W2092045986 title "Aza-acyclic Nucleoside Phosphonates Containing a Second Phosphonate Group As Inhibitors of the Human, <i>Plasmodium falciparum</i> and <i>vivax</i> 6-Oxopurine Phosphoribosyltransferases and Their Prodrugs As Antimalarial Agents" @default.
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• W2092045986 doi "https://doi.org/10.1021/jm501416t" @default.
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