Scaffold hopping from (5-hydroxymethyl) isophthalates to multisubstituted pyrimidines diminishes binding affinity to the C1 domain of protein kinase C
Author:
Funder
Suomen Kulttuurirahasto
Magnus Ehrnroothin Säätiö
Jane ja Aatos Erkon Säätiö
Academy of Finland
Sydäntutkimussäätiö
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
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