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10.1111/fcp.12643

http://scihub22266oqcxt.onion/10.1111/fcp.12643
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suck abstract from ncbi


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pmid33369768      Fundam+Clin+Pharmacol 2021 ; 35 (2): 432-434
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  • Remdesivir potently inhibits carboxylesterase-2 through covalent modifications: signifying strong drug-drug interactions #MMPMID33369768
  • Shen Y; Eades W; Yan B
  • Fundam Clin Pharmacol 2021[Apr]; 35 (2): 432-434 PMID33369768show ga
  • Remdesivir was recently approved to treat COVID-19. While this antiviral agent delivers clinical benefits, several safety concerns in many cases have been raised. This study reports that remdesivir at nanomolar concentrations inhibits carboxylesterase-2 (CES2) through covalent modifications. CES2 is a major drug-metabolizing enzyme. The combination of high potency with irreversible inhibition concludes that cautions must be exercised when remdesivir is used along with drugs hydrolyzed by CES2.
  • |Adenosine Monophosphate/adverse effects/*analogs & derivatives/pharmacology/therapeutic use[MESH]
  • |Alanine/adverse effects/*analogs & derivatives/pharmacology/therapeutic use[MESH]
  • |Antiviral Agents/adverse effects/*pharmacology/therapeutic use[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |Carboxylesterase/*antagonists & inhibitors/metabolism[MESH]
  • |Drug Interactions[MESH]
  • |Enzyme Inhibitors/*pharmacology[MESH]
  • |Humans[MESH]
  • |Microsomes/metabolism[MESH]
  • |Pharmaceutical Preparations/metabolism[MESH]


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