Silvia C Teguh

Substituted Pyridazin-3(2 H)-ones as Highly Potent and Biased Formyl Peptide Receptor Agonists.

L. May, J. Baell, R. Ritchie, 2019, Journal of medicinal chemistry.

Novel conjugated quinoline-indoles compromise Plasmodium falciparum mitochondrial function and show promising antimalarial activity.

J. Baell, L. Tilley, N. Klonis, 2013, Journal of medicinal chemistry.

3,3'-Disubstituted 5,5'-Bi(1,2,4-triazine) Derivatives with Potent in Vitro and in Vivo Antimalarial Activity.

Jayme L. Dahlin, R. Price, S. Ralph, 2019, Journal of medicinal chemistry.

Discovery of Acylsulfonohydrazide-Derived Lysine Acetyltransferase (KAT6A) Inhibitors as Potent Senescence-Inducing Anti-Cancer Agents.

Jayme L. Dahlin, David M. Shackleford, J. Baell, 2020, Journal of medicinal chemistry.

Haemoglobin degradation underpins the sensitivity of early ring stage Plasmodium falciparum to artemisinins

L. Tilley, E. Hanssen, N. Klonis, 2016, Journal of Cell Science.

Discovery of benzoylsulfonohydrazides as potent inhibitors of the histone acetyltransferase KAT6A.

Jayme L. Dahlin, J. Baell, M. Walters, 2019, Journal of medicinal chemistry.

Synthesis and structure-activity relationship study of pyrrolidine-oxadiazoles as anthelmintics against Haemonchus contortus.

J. Baell, A. Hofmann, R. Gasser, 2020, European journal of medicinal chemistry.

Haemoglobin degradation underpins the sensitivity of early ring stage Plasmodium falciparum to artemisinins

L. Tilley, E. Hanssen, N. Klonis, 2016, Journal of Cell Science.