Assay ID | Title | Year | Journal | Article |
AID603411 | Clearance in Sprague-Dawley rat at 3 umol/kg, iv | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603416 | Oral bioavailability in Sprague-Dawley rat at 10 umol/kg | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID1211402 | Drug metabolism in human liver microsomes assessed as GSH-adduct formation at 10 uM by LC-MS analysis in presence of NADPH | 2012 | Drug metabolism and disposition: the biological fate of chemicals, Nov, Volume: 40, Issue:11
| Novel bioactivation mechanism of reactive metabolite formation from phenyl methyl-isoxazoles. |
AID1211400 | Intrinsic clearance in human liver microsomes assessed per mg of protein at 10 uM by LC-MS analysis in presence of NADPH | 2012 | Drug metabolism and disposition: the biological fate of chemicals, Nov, Volume: 40, Issue:11
| Novel bioactivation mechanism of reactive metabolite formation from phenyl methyl-isoxazoles. |
AID603412 | Dose normalized AUC in Sprague-Dawley rat at 10 umol/kg, po | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603403 | Inhibition of Nav1.5 by cell based whole-cell voltage clamp electrophysiology assay | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603415 | Half life in Sprague-Dawley rat at 10 umol/kg, po | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603409 | Volume of distribution at steady state in Sprague-Dawley rat at 3 umol/kg, iv | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603406 | Intrinsic clearance in rat liver microsomes | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603402 | Inhibition of Nav1.7 by cell based whole-cell voltage clamp electrophysiology assay | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603408 | Dose normalized AUC in Sprague-Dawley rat at 3 umol/kg, iv | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603407 | Intrinsic clearance in human liver microsomes | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603405 | Solubility of the compound | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603410 | Terminal half life in Sprague-Dawley rat at 3 umol/kg, iv | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603414 | Tmax in Sprague-Dawley rat at 10 umol/kg, po | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603413 | Cmax in Sprague-Dawley rat at 10 umol/kg, po | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID603404 | Inhibition of human ERG | 2011 | Bioorganic & medicinal chemistry letters, Jul-01, Volume: 21, Issue:13
| Phenyl isoxazole voltage-gated sodium channel blockers: structure and activity relationship. |
AID1296008 | Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening | 2020 | SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
| Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening. |
AID1346986 | P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5
| A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
AID1346987 | P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5
| A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
AID1347160 | Primary screen NINDS Rhodamine qHTS for Zika virus inhibitors | 2020 | Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
| Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors. |
AID1347159 | Primary screen GU Rhodamine qHTS for Zika virus inhibitors: Unlinked NS2B-NS3 protease assay | 2020 | Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
| Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors. |
AID81982 | -log of the half-maximal concentration for stimulation of GTPase in HL-60 membrane (sensitive to PTX) | 1997 | Journal of medicinal chemistry, Sep-12, Volume: 40, Issue:19
| Alkyl-substituted amino acid amides and analogous di- and triamines: new non-peptide G protein activators. |
AID81979 | Efficacy expressed as maximal stimulation of GTP hydrolysis in HL-60 membranes at a concentration 5 uM | 1997 | Journal of medicinal chemistry, Sep-12, Volume: 40, Issue:19
| Alkyl-substituted amino acid amides and analogous di- and triamines: new non-peptide G protein activators. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |