Inhibition of human VAP-1 expressed in CHO cells using 14C-benzylamine as substrate preincubated for 20 mins followed by substrate addition measured after 1 hr by scintillation spectrometric analysis
Inhibition of rat VAP-1 expressed in CHO cells using 14C-benzylamine as substrate preincubated for 20 mins followed by substrate addition measured after 1 hr by scintillation spectrometric analysis
Inhibition of CYP2C19 in human liver microsomes assessed as residual activity at 5 uM using S-mephenytoin as substrate after 20 mins by LC-MS/MS analysis
Inhibition of VAP-1 in Wistar rat plasma at 1 mg/kg, po using 14C-benzylamine as substrate preincubated for 20 mins followed by substrate addition measured after 1 hr by scintillation spectrometric analysis
Inhibition of VAP-1 in Wistar rat plasma at 1 mg/kg, po using 14C-benzylamine as substrate preincubated for 20 mins followed by substrate addition measured after 6 hr by scintillation spectrometric analysis
Inhibition of VAP-1 in Wistar rat plasma at 0.3 mg/kg, po using 14C-benzylamine as substrate preincubated for 20 mins followed by substrate addition measured after 1 hr by scintillation spectrometric analysis
Inhibition of VAP-1 in Wistar rat plasma at 0.3 mg/kg, po using 14C-benzylamine as substrate preincubated for 20 mins followed by substrate addition measured after 6 hr by scintillation spectrometric analysis
In vivo inhibition of VAP-1 in STZ-induced diabetic Sprague-Dawley rat assessed as reduction in proteinuria progression at 0.3 to 1 mg/kg, po for 4 weeks measured after 24 hrs by Bradford colorimetric assay
In vivo inhibition of VAP-1 in STZ-induced diabetic Sprague-Dawley rat plasma at 0.3 to 1 mg/kg, po for 4 weeks measured after 24 hrs after final dose using 14C-benzylamine as substrate by scintillation spectrometric analysis