Assay ID | Title | Year | Journal | Article |
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. |
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. |
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. |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | | | |
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | | | |
AID1448716 | Inhibition of NOD1 in human PBMC-derived macrophages assessed as reduction in C12-iE-DAP-stimulated IL6 mRNA expression at 1 uM preincubated for 1 hr followed by C12-iE-DAP stimulation for 90 mins by RT-qPCR analysis | 2017 | Journal of medicinal chemistry, 06-22, Volume: 60, Issue:12
| Discovery of 1,4-Benzodiazepine-2,5-dione (BZD) Derivatives as Dual Nucleotide Binding Oligomerization Domain Containing 1/2 (NOD1/NOD2) Antagonists Sensitizing Paclitaxel (PTX) To Suppress Lewis Lung Carcinoma (LLC) Growth in Vivo. |
AID655845 | Inhibition of TNFalpha-induced NFkappaB activation in HEK293T cells after 14 hrs by luciferase reporter gene assay | 2011 | ACS medicinal chemistry letters, Oct-13, Volume: 2, Issue:10
| Identification of Inhibitors of NOD1-Induced Nuclear Factor-κB Activation. |
AID655846 | Cytotoxicity against HEK293T cells at 20 uM by alamar blue assay | 2011 | ACS medicinal chemistry letters, Oct-13, Volume: 2, Issue:10
| Identification of Inhibitors of NOD1-Induced Nuclear Factor-κB Activation. |
AID655843 | Inhibition of NOD-1 mediated NFkappaB activation in HEK293T cells assessed as inhibition of gamma-tri-DAP-induced luciferase activity after 14 hrs by reporter gene assay | 2011 | ACS medicinal chemistry letters, Oct-13, Volume: 2, Issue:10
| Identification of Inhibitors of NOD1-Induced Nuclear Factor-κB Activation. |
AID1068462 | Inhibition of human ALDH1A3 using propionaldehyde as substrate up to 100 uM preincubated for 1 min followed by substrate addition by spectrophotometric analysis | 2014 | Journal of medicinal chemistry, Jan-23, Volume: 57, Issue:2
| Selective ALDH3A1 inhibition by benzimidazole analogues increase mafosfamide sensitivity in cancer cells. |
AID1068474 | Inhibition of human ALDH3A1-mediated benzaldehyde oxidation preincubated for 1 min followed by substrate addition by spectrophotometric analysis | 2014 | Journal of medicinal chemistry, Jan-23, Volume: 57, Issue:2
| Selective ALDH3A1 inhibition by benzimidazole analogues increase mafosfamide sensitivity in cancer cells. |
AID1178166 | Inhibition of NOD1 (unknown origin) expressed in HEK293T cells coexpressing NF-kappaB driven luciferase reporter gene by HTS primary assay | 2014 | Journal of medicinal chemistry, Aug-28, Volume: 57, Issue:16
| Nucleotide-binding oligomerization domain (NOD) inhibitors: a rational approach toward inhibition of NOD signaling pathway. |
AID1178167 | Inhibition of NOD2 (unknown origin) expressed in HEK293T cells coexpressing NF-kappaB driven luciferase reporter gene by HTS primary assay | 2014 | Journal of medicinal chemistry, Aug-28, Volume: 57, Issue:16
| Nucleotide-binding oligomerization domain (NOD) inhibitors: a rational approach toward inhibition of NOD signaling pathway. |
AID1068463 | Inhibition of human ALDH1A2 using propionaldehyde as substrate up to 100 uM preincubated for 1 min followed by substrate addition by spectrophotometric analysis | 2014 | Journal of medicinal chemistry, Jan-23, Volume: 57, Issue:2
| Selective ALDH3A1 inhibition by benzimidazole analogues increase mafosfamide sensitivity in cancer cells. |
AID1068464 | Activation of human ALDH1A1 using propionaldehyde as substrate at 100 uM preincubated for 1 min followed by substrate addition by spectrophotometric analysis | 2014 | Journal of medicinal chemistry, Jan-23, Volume: 57, Issue:2
| Selective ALDH3A1 inhibition by benzimidazole analogues increase mafosfamide sensitivity in cancer cells. |
AID1068465 | Inhibition of human ALDH2 using propionaldehyde as substrate preincubated for 1 min followed by substrate addition by spectrophotometric analysis | 2014 | Journal of medicinal chemistry, Jan-23, Volume: 57, Issue:2
| Selective ALDH3A1 inhibition by benzimidazole analogues increase mafosfamide sensitivity in cancer cells. |
AID655844 | Inhibition of NOD-2 mediated NFkappaB activation in HEK293T cells assessed as inhibition of MDP-induced luciferase activity after 14 hrs by reporter gene assay | 2011 | ACS medicinal chemistry letters, Oct-13, Volume: 2, Issue:10
| Identification of Inhibitors of NOD1-Induced Nuclear Factor-κB Activation. |
AID1178168 | Selectivity ratio of IC50 for NOD2 (unknown origin) to IC50 for NOD1 (unknown origin) | 2014 | Journal of medicinal chemistry, Aug-28, Volume: 57, Issue:16
| Nucleotide-binding oligomerization domain (NOD) inhibitors: a rational approach toward inhibition of NOD signaling pathway. |
AID1068461 | Inhibition of human ALDH1B1 using propionaldehyde as substrate up to 100 uM preincubated for 1 min followed by substrate addition by spectrophotometric analysis | 2014 | Journal of medicinal chemistry, Jan-23, Volume: 57, Issue:2
| Selective ALDH3A1 inhibition by benzimidazole analogues increase mafosfamide sensitivity in cancer cells. |
AID1448717 | Inhibition of NOD1 in human PBMC-derived macrophages assessed as reduction in C12-iE-DAP-stimulated TNFalpha mRNA expression at 1 uM preincubated for 1 hr followed by C12-iE-DAP stimulation for 90 mins by RT-qPCR analysis | 2017 | Journal of medicinal chemistry, 06-22, Volume: 60, Issue:12
| Discovery of 1,4-Benzodiazepine-2,5-dione (BZD) Derivatives as Dual Nucleotide Binding Oligomerization Domain Containing 1/2 (NOD1/NOD2) Antagonists Sensitizing Paclitaxel (PTX) To Suppress Lewis Lung Carcinoma (LLC) Growth in Vivo. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |