Author: Nar, Herbert; Schnapp, Gisela; Hucke, Oliver; Hardman, Timothy C.; Klein, Thomas
Title: Action of Dipeptidyl Peptidaseâ€4 Inhibitors on SARSâ€CoVâ€2 Main Protease Cord-id: s8ftb5uf Document date: 2021_2_17
ID: s8ftb5uf
Snippet: In a recent publication, Eleftheriou et al. proposed that inhibitors of dipeptidyl peptidaseâ€4 (DPPâ€4) are functional inhibitors of the main protease (M(pro)) of SARSâ€CoVâ€2. Their predictions prompted the authors to suggest linagliptin, a DPPâ€4 inhibitor and approved antiâ€diabetes drug, as a repurposed drug candidate against the ongoing COVIDâ€19 pandemic. We used an enzymatic assay measuring the inhibition of M(pro) catalytic activity in the presence of four different commercially
Document: In a recent publication, Eleftheriou et al. proposed that inhibitors of dipeptidyl peptidaseâ€4 (DPPâ€4) are functional inhibitors of the main protease (M(pro)) of SARSâ€CoVâ€2. Their predictions prompted the authors to suggest linagliptin, a DPPâ€4 inhibitor and approved antiâ€diabetes drug, as a repurposed drug candidate against the ongoing COVIDâ€19 pandemic. We used an enzymatic assay measuring the inhibition of M(pro) catalytic activity in the presence of four different commercially available gliptins (linagliptin, sitagliptin, alogliptin and saxagliptin) and several structural analogues of linagliptin to study the binding of DPPâ€4 inhibitors to M(pro) and their functional activity. We show here that DPPâ€4 inhibitors like linagliptin, other gliptins and structural analogues are inactive against M(pro).
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