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"Reductive dehalogenase structure suggests a mechanism for B12-dependent dehalogenation"

Finally, 100 ul of the sample was transferred to a specific glass vial for UHPLC/MS analysis

Svendsen PF, Nilas L, Nrgaard K, Jensen JE, Madsbad S

PHA-665752 is a potent, selective and ATP-competitive c-Met inhibitor, PHA-665752 inhibited c-Met tyrosine phosphorylation at the activation loop (pY1230/34/35), multifunctional docking site (pY1349), and the juxtamembrane domain (pY1003) at 0.1 M [80]