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Biology and Biochemistry
Switzerland
2023

D-Index & Metrics

Biology and Biochemistry

D-Index
80
Citations
21516
World Ranking
4115
National Ranking
81

Research.com Recognitions

  • 2023 - Research.com Biology and Biochemistry in Switzerland Leader Award

Overview

Pascal Furet is affiliated with Novartis in Switzerland and has contributed extensively to research in biochemistry, genetics, and molecular biology. Their publications span several specialized areas including molecular biology, cell biology, cancer research, materials chemistry, and oncology.

Their research topics focus on multiple key areas, including:

  • Hippo pathway signaling and YAP/TAZ
  • PI3K/AKT/mTOR signaling in cancer
  • Cancer, hypoxia, and metabolism
  • Fibroblast growth factor research
  • Kruppel-like factors research
  • Cancer-related molecular pathways
  • Cancer research and treatments

Furet has published in various scientific journals, with frequent contributions to the following venues:

  • Journal of Medicinal Chemistry
  • ChemMedChem
  • Nature Communications
  • Journal of Chemical Information and Modeling
  • The FASEB Journal

Their recent papers include:

  • "Discovery of Roblitinib (FGF401) as a Reversible-Covalent Inhibitor of the Kinase Activity of Fibroblast Growth Factor Receptor 4," 2020, Journal of Medicinal Chemistry
  • "p53 dynamics vary between tissues and are linked with radiation sensitivity," 2021, Nature Communications
  • "The First Class of Small Molecules Potently Disrupting the YAP-TEAD Interaction by Direct Competition," 2022, ChemMedChem
  • "Identification of NVP-CLR457 as an Orally Bioavailable Non-CNS-Penetrant pan-Class IA Phosphoinositol-3-Kinase Inhibitor," 2022, Journal of Medicinal Chemistry
  • "Leveraging Advanced In Silico Techniques in Early Drug Discovery: A Study of Potent Small-Molecule YAP-TEAD PPI Disruptors," 2023, Journal of Chemical Information and Modeling

Frequent co-authors collaborating with Pascal Furet include:

  • Markus Wartmann
  • Joerg Kallen
  • Yannick Mesrouze
  • Patrick Chêne
  • Robin A. Fairhurst

Best Publications

  • Identification and characterization of NVP-BEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity

    Sauveur-Michel Maira;Frédéric Stauffer;Josef Brueggen;Pascal Furet

  • In vivo antitumor activity of NVP-AEW541—A novel, potent, and selective inhibitor of the IGF-IR kinase

    Carlos Garcia-Echeverria;Mark Andrew Pearson;Andreas Marti;Thomas Meyer

  • Discovery of 3-(2,6-Dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (NVP-BGJ398), A Potent and Selective Inhibitor of the Fibroblast Growth Factor Receptor Family of Receptor Tyrosine Kinase

    Vito Guagnano;Pascal Furet;Carsten Spanka;Vincent Bordas

  • The allosteric inhibitor ABL001 enables dual targeting of BCR–ABL1

    Andrew A. Wylie;Joseph Schoepfer;Wolfgang Jahnke;Sandra W. Cowan-Jacob

  • Polyclonal Secondary FGFR2 Mutations Drive Acquired Resistance to FGFR Inhibition in Patients with FGFR2 Fusion-Positive Cholangiocarcinoma.

    Lipika Goyal;Supriya K. Saha;Leah Y. Liu;Giulia Siravegna

  • Characterization of the Novel and Specific PI3Kα Inhibitor NVP-BYL719 and Development of the Patient Stratification Strategy for Clinical Trials

    Christine Fritsch;Alan Huang;Christian Chatenay-Rivauday;Christian Schnell

  • Strategies Toward the Design of Novel and Selective Protein Tyrosine Kinase Inhibitors

    Peter Traxler;Pascal Furet

  • Protein kinases as targets for anticancer agents: from inhibitors to useful drugs

    Doriano Fabbro;Stephan Ruetz;Elisabeth Buchdunger;Sandra W Cowan-Jacob

  • Discovery of NVP-BYL719 a potent and selective phosphatidylinositol-3 kinase alpha inhibitor selected for clinical evaluation.

    Pascal Furet;Vito Guagnano;Robin A. Fairhurst;Patricia Imbach-Weese

  • Inhibitors of tyrosine kinases

    Werner Breitenstein;Pascal Furet;Sandra Jacob;Paul William Manley

  • Discovery of Asciminib (ABL001), an Allosteric Inhibitor of the Tyrosine Kinase Activity of BCR-ABL1.

    J. Schoepfer;W. Jahnke;G. Berellini;S. Buonamici

  • Tyrosine kinase inhibitors: From rational design to clinical trials

    Peter Traxler;Guido Bold;Elisabeth Buchdunger;Giorgio Caravatti

  • Nye Imidazokinoliner, fremgangsmåter for fremstilling av slike og farmasøytiske preparater inneholdende slike, samt anvendelse som et farmasøytiske preparat og anvendelse for fremstilling av et farmasøytisk preparat.

    Furet Pascal;Garcia-Echeverria Carlos;Stauffer Frédéric

  • Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases

    Andreas Floersheimer;Pascal Furet;Paul William Manley;Guido Bold

  • Different susceptibility of protein kinases to staurosporine inhibition Kinetic studies and molecular bases for the resistance of protein kinase CK2

    Flavio Meggio;Arianna Donella Deana;Maria Ruzzene;Anna M. Brunati

  • Discovery of potent antagonists of the interaction between human double minute 2 and tumor suppressor p53.

    Carlos García-Echeverría;Patrick Chène;Marcel J. J. Blommers;Pascal Furet

  • New Anilinophthalazines as Potent and Orally Well Absorbed Inhibitors of the VEGF Receptor Tyrosine Kinases Useful as Antagonists of Tumor-Driven Angiogenesis

    Bold G;Altmann Kh;Frei J;Lang M

  • Imatinib: a selective tyrosine kinase inhibitor.

    P.W. Manley;S.W. Cowan-Jacob;E. Buchdunger;D. Fabbro

  • Use of a pharmacophore model for the design of EGF-R tyrosine kinase inhibitors: 4-(phenylamino)pyrazolo[3,4-d]pyrimidines.

    Peter Traxler;Guido Bold;Joerg Frei;Marc Lang

  • Structural biology contributions to the discovery of drugs to treat chronic myelogenous leukaemia.

    Sandra W. Cowan-Jacob;Gabriele Fendrich;Andreas Floersheimer;Pascal Furet

Frequent Co-Authors

Stefano Ferrari
Stefano Ferrari Veneto Eye Bank Foundation
Doriano Fabbro
Doriano Fabbro Novartis (Switzerland)
Wolfgang Jahnke
Wolfgang Jahnke Novartis (Switzerland)
Wolfgang Froestl
Wolfgang Froestl AC Immune (Switzerland)
Thomas Knöpfel
Thomas Knöpfel Hong Kong Baptist University
Nathanael S. Gray
Nathanael S. Gray Stanford University
William R. Sellers
William R. Sellers Harvard University
Thomas J. Meyer
Thomas J. Meyer University of North Carolina at Chapel Hill

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