Weir-torn Jiaang
Miaoli, TNQ 35040, Taiwan
Last Updated: 09/26/2026
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Found 20 publications
Development of Potent and Selective Inhibitors of Methylenetetrahydrofolate Dehydrogenase 2 for Targeting Acute Myeloid Leukemia: SAR, Structural Insights, and Biological Characterization.
Journal: Journal of medicinal chemistry
Published: November 26, 2024
Advancing precision therapy for colorectal cancer: Developing clinical indications for multi-target kinase inhibitor BPR1J481 using patient-derived xenograft models.
Journal: Pharmacological research
Published: June 17, 2024
Xanthine Derivatives Reveal an Allosteric Binding Site in Methylenetetrahydrofolate Dehydrogenase 2 (MTHFD2).
Journal: Journal of medicinal chemistry
Published: August 02, 2021
DBPR108, a novel dipeptidyl peptidase-4 inhibitor with antihyperglycemic activity.
Journal: Life sciences
Published: October 29, 2020
Potent and orally active purine-based fetal hemoglobin inducers for treating β-thalassemia and sickle cell disease.
Journal: European journal of medicinal chemistry
Published: June 30, 2020
Identification of a Multitargeted Tyrosine Kinase Inhibitor for the Treatment of Gastrointestinal Stromal Tumors and Acute Myeloid Leukemia.
Journal: Journal of medicinal chemistry
Published: November 14, 2019
Identification of Novel Anti-Liver Cancer Small Molecules with Better Therapeutic Index than Sorafenib via Zebrafish Drug Screening Platform.
Journal: Cancers
Published: May 06, 2019
Discovery of Conformational Control Inhibitors Switching off the Activated c-KIT and Targeting a Broad Range of Clinically Relevant c-KIT Mutants.
Journal: Journal of medicinal chemistry
Published: April 11, 2019
Pyrazolylamine Derivatives Reveal the Conformational Switching between Type I and Type II Binding Modes of Anaplastic Lymphoma Kinase (ALK).
Journal: Journal of medicinal chemistry
Published: April 01, 2016
BPR1J373, an Oral Multiple Tyrosine Kinase Inhibitor, Targets c-KIT for the Treatment of c-KIT-Driven Myeloid Leukemia.
Journal: Molecular cancer therapeutics
Published: December 29, 2015
Identification of a potent 5-phenyl-thiazol-2-ylamine-based inhibitor of FLT3 with activity against drug resistance-conferring point mutations.
Journal: European journal of medicinal chemistry
Published: March 24, 2015
Last Updated: 09/26/2026