Assay ID | Title | Year | Journal | Article |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1
| High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1
| High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID504812 | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7
| A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | | | |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1
| High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID504810 | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7
| A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | | | |
AID1199876 | Activation of recombinant human ALDH3A1 using benzaldehyde as substrate at 100 uM preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
AID1199866 | Inhibition of recombinant human ALDH1A2 using propionaldehyde as substrate preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
AID1199901 | Inhibition of recombinant human ALDH1A1 using propionaldehyde as substrate preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
AID1199870 | Inhibition of recombinant human ALDH2 using propionaldehyde as substrate preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
AID1199881 | Activation of recombinant human ALDH1B1 using propionaldehyde as substrate at 20 uM preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
AID1199886 | Inhibition of human ALDH1A1 G458N mutant using propionaldehyde as substrate at 100 uM preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis relative to control | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
AID1199879 | Activation of recombinant human ALDH1A3 using propionaldehyde as substrate at 20 uM preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
AID1199868 | Inhibition of recombinant human ALDH1A3 using propionaldehyde as substrate preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
AID1199880 | Activation of recombinant human ALDH2 using propionaldehyde as substrate at 20 uM preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
AID1199872 | Inhibition of recombinant human ALDH1B1 using propionaldehyde as substrate preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
AID1199878 | Activation of recombinant human ALDH1A2 using propionaldehyde as substrate at 20 uM preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
AID1199882 | Activation of recombinant human ALDH3A1 using benzaldehyde as substrate at 20 uM preincubated for 2 mins with NAD+ followed by substrate addition by UV-Vis spectrophotometric analysis | 2015 | Journal of medicinal chemistry, Feb-26, Volume: 58, Issue:4
| Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |