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JDQ443 is a covalent inhibitor of K-RasG12C, a mutant form of K-Ras that accumulates in cancer cells.1 It decreases K-RasG12C-induced phosphorylation of ERK in NCI H358 non-small cell lung cancer (NSCLC) cells (IC50 = 0.020 µM). JDQ443 selectively inhibits the growth of NCI H358 cells, which express K-RasG12C, over NCI H1437 NSCLC cells expressing wild-type K-Ras and the constitutively active mutant MEKQ56P (GI50s = 0.018 and 4.4 µM, respectively). It reduces blood levels of free K-RasG12C at three, six, and 24 hours in a MiaPaCa-2 pancreatic cancer mouse xenograft model when administered at a dose of 30 mg/kg and inhibits tumor growth and decreases tumor volume in the same model at 10 and 30 mg/kg per day.
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1. JDQ443, a structurally novel, pyrazole-