Sara Van Poecke

Synthesis of α-substituted fosmidomycin analogues as highly potent Plasmodium falciparum growth inhibitors

Timothy Haemers, Jochen Wiesner, Sara Van Poecke et al. · Bioorganic & Medicinal Chemistry Letters · 2006 · 106 citations · Full text

Medicinal Chemistry, Biochemistry, Medicine +8

3′-[4-Aryl-(1,2,3-triazol-1-yl)]-3′-deoxythymidine Analogues as Potent and Selective Inhibitors of Human Mitochondrial Thymidine Kinase

Sara Van Poecke, Ana Negri, Federico Gago et al. · Journal of Medicinal Chemistry · 2010 · 36 citations · Full text

Enzyme Kinetics, Molecular Pharmacology, Medicinal Chemistry +14

Synthesis and inhibitory activity of thymidine analogues targeting Mycobacterium tuberculosis thymidine monophosphate kinase

Sara Van Poecke, Hélène Munier‐Lehmann, Olivier Helynck et al. · Bioorganic & Medicinal Chemistry · 2011 · 33 citations · Full text

Pulmonary Tuberculosis, Medicine, Natural Sciences +9

Synthesis, modeling and evaluation of 3′-(1-aryl-1H-tetrazol-5-ylamino)-substituted 3′-deoxythymidine derivatives as potent and selective human mitochondrial thymidine kinase inhibitors

Sara Van Poecke, Ana Negri, Jolien Janssens et al. · Organic & Biomolecular Chemistry · 2010 · 16 citations · Full text

Combinatorial Chemistry, Molecular Pharmacology, Medicinal Chemistry +14

Synthesis and P2Y2 receptor agonist activities of uridine 5′-phosphonate analogues

Sara Van Poecke, Matthew O. Barrett, T. Santhosh Kumar et al. · Bioorganic & Medicinal Chemistry · 2012 · 14 citations · Full text

Molecular Pharmacology, Biochemistry, Functional Selectivity +9