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Collaborative virtual screening to elaborate an imidazo[1,2-a]pyridine hit series for visceral leishmaniasis.

Yuichiro AkaoStacie CananYafeng CaoKevin CondroskiOla EngkvistSachiko ItonoRina KakiChiaki KimuraThierry KogejKazuya NagaokaAkira NaitoHiromi NakaiGarry PairaudeauConstantin RaduIeuan RobertsMitsuyuki ShimadaDavid ShumNao-Aki WatanabeHuanxu XieShuji YonezawaOsamu YoshidaRyu YoshidaCharles MowbrayBenjamin G Perry
Published in: RSC medicinal chemistry (2021)
An innovative pre-competitive virtual screening collaboration was engaged to validate and subsequently explore an imidazo[1,2-a]pyridine screening hit for visceral leishmaniasis. In silico probing of five proprietary pharmaceutical company libraries enabled rapid expansion of the hit chemotype, alleviating initial concerns about the core chemical structure while simultaneously improving antiparasitic activity and selectivity index relative to the background cell line. Subsequent hit optimization informed by the structure-activity relationship enabled by this virtual screening allowed thorough investigation of the pharmacophore, opening avenues for further improvement and optimization of the chemical series.
Keyphrases
  • structure activity relationship
  • molecular docking
  • molecular dynamics
  • single molecule
  • quality improvement