In Silico Identification of Chiral Biflavonoids as Dual PI3Kα/mTOR Inhibitors

Francisca Fernanda Nunes Azevedo1, Francisca Joseli Freitas de Sousa1, Jonatas Martins Negreiro2

  • 1Postgraduate Programme in Biochemistry, Department of Biochemistry at Federal University of Ceará, Fortaleza 60440-554, CE, Brazil.

ACS Omega
|October 6, 2025
PubMed

Insights

Researchers identified four plant-derived bioflavonoids with chirality that show potential as dual inhibitors for the PI3Kα and mTOR pathways, offering new cancer therapeutic strategies.

Area of Science:

  • Medicinal Chemistry
  • Pharmacology
  • Computational Biology

Background:

  • The PI3K/AKT/mTOR pathway is vital for cell regulation and often dysregulated in cancer.
  • PI3Kα mutations are common, leading to overactivation of downstream signaling, including mTOR.
  • Current therapies targeting PI3Kα or mTOR individually have limitations; dual inhibitors are needed.

Purpose of the Study:

  • To identify novel plant-derived compounds with dual inhibitory potential against PI3Kα and mTOR.
  • To investigate the role of chirality in the binding affinity of these compounds to PI3Kα and mTOR.

Main Methods:

  • Utilized advanced computational tools for molecular docking against PI3Kα and mTOR enzymes.
  • Screened 1745 compounds from the NuBBe database of Brazilian natural products.
  • Analyzed the binding profiles and enantiomeric preferences of selected bioflavonoids.

Main Results:

  • Four chiral bioflavonoids (compounds 2-5) demonstrated selective or dual inhibitory potential.
  • Specific enantiomers showed preferential binding to either PI3Kα or mTOR.
  • (Sa)-2 preferentially bound to mTOR, (Ra)-3 to PI3Kα, and (Ra)-5 to PI3Kα while (Sa)-5 to mTOR.

Conclusions:

  • Chiral bioflavonoids are promising candidates for developing dual PI3Kα/mTOR inhibitors.
  • These findings support the rational design of novel cancer therapeutics.
  • Highlights the therapeutic potential of Brazilian natural products in medicinal chemistry.

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