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ChemMedChem ; 16(9): 1425-1426, 2021 05 06.
Article in English | MEDLINE | ID: covidwho-985986

ABSTRACT

In a recent publication, Eleftheriou et al. proposed that inhibitors of dipeptidyl peptidase-4 (DPP-4) are functional inhibitors of the main protease (Mpro ) of SARS-CoV-2. Their predictions prompted the authors to suggest linagliptin, a DPP-4 inhibitor and approved anti-diabetes drug, as a repurposed drug candidate against the ongoing COVID-19 pandemic. We used an enzymatic assay measuring the inhibition of Mpro 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 DPP-4 inhibitors to Mpro and their functional activity. We show here that DPP-4 inhibitors like linagliptin, other gliptins and structural analogues are inactive against Mpro .


Subject(s)
Coronavirus 3C Proteases/antagonists & inhibitors , Dipeptidyl-Peptidase IV Inhibitors/chemistry , Drug Repositioning , Heterocyclic Compounds/chemistry , SARS-CoV-2/enzymology , Adamantane/analogs & derivatives , Adamantane/chemistry , Antiviral Agents/chemistry , Dipeptides/chemistry , Enzyme Assays , Linagliptin/chemistry , Piperidines/chemistry , Sitagliptin Phosphate/chemistry , Uracil/analogs & derivatives , Uracil/chemistry
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