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The 3D pharmacophore modeling to explore new antischistosomal agents among US FDA approved drugs.

Leandro DobrachinskiLeonardo Luiz Gomes FerreiraMaria E CirinoAllan I Andrade-de-SiqueiraAna Carolina MafudYvonne Primerano MascarenhasAdriano Defini AndricopuloJosué de Moraes
Published in: Future medicinal chemistry (2024)
Aim: To identify potential antischistosomal agents through 3D pharmacophore-based virtual screening of US FDA approved drugs. Materials & methods: A comprehensive virtual screening was conducted on a dataset of 10,000 FDA approved drugs, employing praziquantel as a template. Promising candidates were selected and assessed for their impact on Schistosoma mansoni viability in vitro and in vivo using S. mansoni infected mice. Results & conclusion: Among the selected drugs, betamethasone and doxazosin demonstrated in vitro efficacy, with effective concentration 50% (EC 50 ) values ranging from 35 to 60 μM. In vivo studies revealed significant (>50%) reductions in worm burden for both drugs. These findings suggest that betamethasone and doxazosin hold promise for repurposing in treating schistosomiasis. Additionally, the study showcases a useful approach for identifying new antischistosomal drugs.
Keyphrases
  • molecular docking
  • metabolic syndrome
  • risk assessment
  • risk factors
  • mass spectrometry
  • skeletal muscle
  • climate change
  • single cell
  • molecularly imprinted