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Biorxiv : the Preprint Server for Biology|June 10, 2024
Discovery of Potent Degraders of the Dengue Virus Envelope ProteinZhengnian Li, Han-Yuan Liu, Zhixiang He, et al.Bioorganic & Medicinal Chemistry Letters|March 10, 2006
Design and synthesis of 7H-pyrrolo[2,3-d]pyrimidines as focal adhesion kinase inhibitors. Part 2Ha-Soon Choi, Zhicheng Wang, Wendy Richmond, et al.Nature Communications|October 12, 2022
Differential ABC transporter expression during hematopoiesis contributes to neutrophil-biased toxicity of Aurora kinase inhibitorsDavid B Chou, Brooke A Furlong, Ryan R Posey, et al.RSC Chemical Biology|September 21, 2022
Cereblon covalent modulation through structure-based design of histidine targeting chemical probesJustin T Cruite, Geoffrey P Dann, Jianwei Che, et al.Cell Chemical Biology|September 7, 2022
Exploring the target scope of KEAP1 E3 ligase-based PROTACsGuangyan Du, Jie Jiang, Nathaniel J Henning, et al.Molecular Cell|January 20, 2009
A conserved salt bridge in the G loop of multiple protein kinases is important for catalysis and for in vivo Lyn functionRina Barouch-Bentov, Jianwei Che, Christian C Lee, et al.Chembiochem : a European Journal of Chemical Biology|April 23, 2023
Development and Characterization of Selective FAK Inhibitors and PROTACs with In Vivo ActivityEriko Koide, Mikaela L Mohardt, Zainab M Doctor, et al.Journal of Medicinal Chemistry|April 10, 2023
Catalytic Degraders Effectively Address Kinase Site Mutations in EML4-ALK Oncogenic FusionsYang Gao, Baishan Jiang, Hellen Kim, et al.Nature Communications|July 24, 2025
Unveiling the hidden interactome of CRBN molecular gluesKheewoong Baek, Rebecca J Metivier, Shourya S Roy Burman, et al.Journal of Medicinal Chemistry|March 22, 2023
Structure-Based Design of Y-Shaped Covalent TEAD InhibitorsWenchao Lu, Mengyang Fan, Wenzhi Ji, et al.Pageof 8