Zosuquidar 10mg 10mg | Purity Not Available
Adooq Bioscience
Zosuquidar is a potent modulator of P-glycoprotein-mediated multi-drug resistance with Ki of 60 nM.
More Information Supplier PageZosuquidar is a potent modulator of P-glycoprotein-mediated multi-drug resistance with Ki of 60 nM.
More Information Supplier PageZolpidem is an inhibitory neurotransmitter, by binding to GABAA receptors at the same location as benzodiazepines.
More Information Supplier PageZolpidem is an inhibitory neurotransmitter, by binding to GABAA receptors at the same location as benzodiazepines.
More Information Supplier PageZolpidem is an inhibitory neurotransmitter, by binding to GABAA receptors at the same location as benzodiazepines.
More Information Supplier PageZM323881 is a potent and selective inhibitor of human vascular endothelial growth factor receptor 2 (VEGFR-2/KDR) with IC50 value of 2 nM.
More Information Supplier PageZM323881 is a potent and selective inhibitor of human vascular endothelial growth factor receptor 2 (VEGFR-2/KDR) with IC50 value of 2 nM.
More Information Supplier PageZM323881 is a potent and selective inhibitor of human vascular endothelial growth factor receptor 2 (VEGFR-2/KDR) with IC50 value of 2 nM.
More Information Supplier PageZiprasidone is a combined 5-HT (serotonin) and dopamine receptor antagonist which exhibits potent effects of antipsychotic activity.
More Information Supplier PageZosuquidar is a potent modulator of P-glycoprotein-mediated multi-drug resistance with Ki of 60 nM.
More Information Supplier PageAcetyl-Calpastatin (184-210) (human), selective calpain inhibitor. Strongly inhibits calpain I (Ki = 0.2 nM) and II but does not inhibit papain, trypsin and cathepsin L (Ki = 6 ??M). Increases secretion of amyoid ??-protein (A??) 42, A??40 and A??42 ratio.
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