Cabozantinib-d4 is a deuterium-labeled analog of Cabozantinib, which functions as a potent inhibitor of multiple receptor tyrosine kinases (RTKs). It exhibits significant inhibition of VEGFR2, c-Met, Kit, Axl, and Flt3 with IC50 values of 0.035 nM, 1.3 nM, 4.6 nM, 7 nM, and 11.3 nM, respectively. This stabilized isotope is valuable for pharmacokinetic and metabolic studies, enabling researchers to trace and analyze the drug's metabolic pathways and interactions in biological systems.
Cabozantinib-d4 is a deuterium-labeled analog of Cabozantinib, which functions as a potent inhibitor of multiple receptor tyrosine kinases (RTKs). It exhibits significant inhibition of VEGFR2, c-Met, Kit, Axl, and Flt3 with IC50 values of 0.035 nM, 1.3 nM, 4.6 nM, 7 nM, and 11.3 nM, respectively. This stabilized isotope is valuable for pharmacokinetic and metabolic studies, enabling researchers to trace and analyze the drug's metabolic pathways and interactions in biological systems.
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