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InChiKey: QXTWSUQCXCWEHF-JXMROGBWSA-N
InChi: InChI=1S/C15H18N2O/c1-3-11-10-6-9(2)8-15(11
84 L per h per kg body weight) and high oral bioavailability (37%)
Dalcetrapib achieves 50% inhibition of CETP activity in human plasma at a concentration of 9 μM
Probes1_000047
PND-1186 Catalog No.:M9572-2 InChiKey: QXTWSUQCXCWEHF-JXMROGBWSA-NPND 1186, also known as SR 2156 and VS 4718, is a potent FAK inhibitor with a 50% inhibitory concentration (IC50) of 1. 5 nM in vitro. PND 1186 has an IC50 of ~100 nM in breast carcinoma cells. Notably, 1. 0 M PND 1186 (>5 fold above IC50) had limited effects on cell proliferation. However, under non adherent conditions as spheroids and as colonies in soft agar, 0. 1 M PND 1186 blocked FAK and p130Cas tyrosine phosphorylation, promoted caspase 3