Scaffold hopping from (5-hydroxymethyl) isophthalates to multisubstituted pyrimidines diminishes binding affinity to the C1 domain of protein kinase C

Riccardo Provenzani, Ilari Matti Elias Tarvainen, Giulia Brandoli, Antti Tapani Lempinen, Sanna Artes, Ainoleena Turku, Maria Helena Jäntti, Virpi Talman, Jari Tapani Yli-Kauhaluoma, Raimo Kalevi Tuominen, Per Gustav Boije af Gennäs

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