Inhibition of SARS-CoV-2 MPro expressed in Escherichia coli BL21(DE3) using Dabcyl-KLSAVLQSGERKM-Edans as substrate at 5 uM incubated for 30 mins followed by substrate addition by FRET assay
Inhibition of SARS-CoV-2 PLpro expressed in Escherichia coli BL21(DE3) using CBZ-RLRGG-AMC as substrate at 5 uM incubated for 30 mins followed by substrate addition by FRET assay
Binding affinity to SARS-CoV-2 MPro expressed in Escherichia coli BL21(DE3) assessed as mass shift at 15 uM incubated for 4 hrs by mass spectrometry analysis
Binding affinity to SARS-CoV-2 PLpro expressed in Escherichia coli BL21(DE3) assessed as mass shift at 30 uM incubated for 4 hrs by mass spectrometry analysis
Drug metabolism in normal saline assessed as conversion of closed form to open form by measuring rate constant at equilibrium at 2 mg/ml measured at 5 hrs by RP-HPLC analysis
Covalent binding affinity to Cys145 residue of SARS-CoV-2 MPro expressed in Escherichia coli BL21(DE3) assessed as trypsin digestion mediated mass shift by mass spectrometry analysis
Covalent binding affinity to Cys111 residue of SARS-CoV-2 PLpro expressed in Escherichia coli BL21(DE3) assessed as mass shift at 3 to 15 uM incubated for 4 hrs followed by trypsin digestion by mass spectrometry analysis
Inhibition of SARS-CoV-2 MPro expressed in Escherichia coli BL21(DE3) using Dabcyl-KLSAVLQSGERKM-Edans as substrate assessed as inhibition constant measured for 30 mins by fluorimetry based microplate reader analysis
Inhibition of SARS-CoV-2 MPro expressed in Escherichia coli BL21(DE3) using Dabcyl-KLSAVLQSGERKM-Edans as substrate assessed as inactivation constant measured for 30 mins by fluorimetry based microplate reader analysis
Inhibition of SARS-CoV-2 MPro expressed in Escherichia coli BL21(DE3) using Dabcyl-KLSAVLQSGERKM-Edans as substrate assessed as Kinact/Ki measured for 30 mins by fluorimetry based microplate reader analysis
Inhibition of SARS-CoV-2 PLpro expressed in Escherichia coli BL21(DE3) using CBZ-RLRGG-AMC as substrate assessed as inhibition constant measured for 30 mins by fluorimetry based microplate reader analysis
Inhibition of SARS-CoV-2 PLpro expressed in Escherichia coli BL21(DE3) using CBZ-RLRGG-AMC as substrate assessed as inactivation constant measured for 30 mins by fluorimetry based microplate reader analysis
Inhibition of SARS-CoV-2 PLpro expressed in Escherichia coli BL21(DE3) using CBZ-RLRGG-AMC as substrate assessed as Kinact/Ki measured for 30 mins by fluorimetry based microplate reader analysis
Inhibition of native full length human thrombin using Boc-Asp(OBz1)-Pro-Arg-AMC as substrate at 5 uM incubated for 30 mins followed by substrate addition by fluorescence based analysis
Inhibition of native full length human factor 10a using Bz-Ile-Glu-Gly-Arg-pNA as substrate at 5 uM incubated for 30 mins followed by substrate addition by fluorescence based analysis
inhibition of native full length human plasmin using H-D-Val-Leu-Lys-pNA as substrate at 5 uM incubated for 30 mins followed by substrate addition by fluorescence based analysis