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Development in the Inhibition of Dengue Proteases as Drug Targets.

Muhammad AkramShehryar HameedAbbas HassanKhalid Khan
Published in: Current medicinal chemistry (2023)
Different classes of compounds have been reported against DENV, such as nitrogen-containing heterocycles (i.e., imidazole, pyridine, triazoles quinazolines, quinoline, and indole), oxygen-containing heterocycles (i.e., coumarins), and some are mixed heterocyclic compounds of S, N (thiazole, benzothiazine, and thiazolidinediones), and N, O (i.e., oxadiazole). There have been reports of computationally designed compounds to impede the molecular functions of specific structural and non-structural proteins as potential therapeutic targets. This review summarized the current progress in developing dengue protease inhibitors.
Keyphrases
  • dengue virus
  • zika virus
  • aedes aegypti
  • adverse drug
  • emergency department
  • molecular docking
  • human health
  • drug induced