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Nature|September 16, 2014
Structural and mechanistic insights into the bacterial amyloid secretion channel CsgGParveen Goyal, Petya V Krasteva, Nani Van Gerven, et al.European Journal of Medicinal Chemistry|March 31, 2018
Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acidAgnese Chiara Pippione, Irene Maria Carnovale, Davide Bonanni, et al.European Journal of Medicinal Chemistry|February 26, 2017
Design, synthesis, biological evaluation and X-ray structural studies of potent human dihydroorotate dehydrogenase inhibitors based on hydroxylated azole scaffoldsStefano Sainas, Agnese C Pippione, Marta Giorgis, et al.European Journal of Medicinal Chemistry|December 12, 2018
Hydroxyazole scaffold-based Plasmodium falciparum dihydroorotate dehydrogenase inhibitors: Synthesis, biological evaluation and X-ray structural studiesAgnese C Pippione, Stefano Sainas, Parveen Goyal, et al.Journal of Medicinal Chemistry|June 26, 2018
Targeting Myeloid Differentiation Using Potent 2-Hydroxypyrazolo[1,5- a]pyridine Scaffold-Based Human Dihydroorotate Dehydrogenase InhibitorsStefano Sainas, Agnese C Pippione, Elisa Lupino, et al.Nature Communications|May 3, 2018
Substrate-bound outward-open structure of a Na+-coupled sialic acid symporter reveals a new Na+ siteWeixiao Y Wahlgren, Elin Dunevall, Rachel A North, et al.Pageof 2