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Identification of NVP-CLR457 as an Orally Bioavailable Non-CNS-Penetrant pan-Class IA Phosphoinositol-3-Kinase Inhibitor.

Robin A FairhurstPascal FuretPatricia Imbach-WeeseFrédéric StaufferHeinrich RueegerClive McCarthySebastien RipocheSusanne OswaldBertrand ArnaudAline JaryMichel MairaChristian SchnellDaniel A GuthyMarkus WartmannMichael KiffeSandrine DesrayaudFrancesca BlascoToni WidmerFrank SeilerSascha GutmannMark KnappGiorgio Caravatti
Published in: Journal of medicinal chemistry (2022)
Balanced pan-class I phosphoinositide 3-kinase inhibition as an approach to cancer treatment offers the prospect of treating a broad range of tumor types and/or a way to achieve greater efficacy with a single inhibitor. Taking buparlisib as the starting point, the balanced pan-class I PI3K inhibitor 40 (NVP-CLR457) was identified with what was considered to be a best-in-class profile. Key to the optimization to achieve this profile was eliminating a microtubule stabilizing off-target activity, balancing the pan-class I PI3K inhibition profile, minimizing CNS penetration, and developing an amorphous solid dispersion formulation. A rationale for the poor tolerability profile of 40 in a clinical study is discussed.
Keyphrases
  • blood brain barrier
  • drug delivery
  • open label
  • room temperature
  • protein kinase