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Scaffold hopping from (5-hydroxymethyl) isophthalates to multisubstituted pyrimidines diminishes binding affinity to the C1 domain of protein kinase C
Provenzani R,
Tarvainen I,
Brandoli G,
Lempinen A,
Artes S,
et al.
(2018)
Scaffold hopping from (5-hydroxymethyl) isophthalates to multisubstituted pyrimidines diminishes binding affinity to the C1 domain of protein kinase C.
PLOS ONE 13(4): e0195668.
https://doi.org/10.1371/journal.pone.0195668