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Published in 2017 at "ACS medicinal chemistry letters"
DOI: 10.1021/acsmedchemlett.7b00091
Abstract: A series of 2-aminopyrimidine derivatives were designed and synthesized as highly selective FGFR4 inhibitors. One of the most promising compounds 2n tightly bound FGFR4 with a Kd value of 3.3 nM and potently inhibited its…
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Keywords:
new selective;
aminopyrimidine derivatives;
fgfr4 inhibitors;
derivatives new ... See more keywords