Publications

  • Structural Biology
  • Chemistry
  • Hit ID Platform

Exploiting a Cryptic Pocket in DsbA through Structure-Guided Parallel Synthesis and Direct-to-Biology Screening

Tasdan, Y. et al., J. Med. Chem. 2026

Read on ACS Publications
  • Chemistry
  • Structural Biology
  • Protein Sciences
  • Biophysics
  • Cell Biology
  • In Vivo

Structure-Based Discovery of Potent BCL-XL Inhibitors through Rescaffolding

Timari, M. P. et al., J. Med. Chem. 2026

Read on ACS Publications
  • Fragment-Based Drug Discovery
  • Structural Biology
  • Biophysics

Targeting PTPN22 at Nonorthosteric Binding Sites─A Fragment Approach

Di Lello, P. et al., ACS Omega 2026, 11, 2, 3465–3480

Read on ACS Publications
  • Chemistry
  • Cell Biology

Chemically Induced Nuclear Pore Complex Protein Degradation via TRIM21

Li, X. et al., ACS Chem. Biol. 2025

Read on ACS Publications
  • Chemistry

Enabling organometallic libraries by flow: A tale of two metals

Maddox, D. et al., React. Chem. Eng. 2024, 9, 1656–1665

Read on RSC Publishing
  • Fragment-Based Drug Discovery
  • Chemistry
  • Structural Biology

A covalent fragment-based strategy targeting a novel cysteine to inhibit activity of mutant EGFR kinase

Kuki, N. et al., RSC Med. Chem. 2023, 14, 2731–2737

Read on RSC Publishing
  • PAC-FragmentDEL
  • DEL
  • Fragment-Based Drug Discovery
  • Hit ID Platform

PAC-FragmentDEL – photoactivated covalent capture of DNA-encoded fragments for hit discovery

Ma, H. et al., RSC Med. Chem. 2022, 13, 1341–1349

Read on RSC Publishing
  • Protein Sciences
  • Structural Biology
  • Chemistry
  • Fragment-Based Drug Discovery

Design and Synthesis of Pyrrolo[2,3-d]pyrimidine-Derived Leucine-Rich Repeat Kinase 2 (LRRK2) Inhibitors Using a Checkpoint Kinase 1 (CHK1)-Derived Crystallographic Surrogate

Williamson, D. S. et al., J. Med. Chem. 2021, 64, 10312–10332

Read on ACS Publications
  • Fragment-Based Drug Discovery
  • Biophysics
  • Hit ID Platform
  • Chemistry
  • Structural Biology
  • In Vivo
  • ADME/DMPK

Fragment-Derived Selective Inhibitors of Dual-Specificity Kinases DYRK1A and DYRK1B

Walmsley, D. L. et al., J. Med. Chem. 2021, 64, 8971–8991

Read on ACS Publications
  • Fragment-Based Drug Discovery
  • Structural Biology
  • Chemistry

Structure-Guided Discovery of Potent and Selective DYRK1A Inhibitors

Weber, C. et al., J. Med. Chem. 2021, 64, 6745–6764

Read on ACS Publications

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