| 1 | [SID24828847] | Active | Potency | 1.2589 | qHTS for inhibitors of ROR gamma transcriptional activity [AID2551, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | Potency | 1.2589 [uM] | | BioAssay | qHTS for inhibitors of ROR gamma transcriptional activity | | AID | 2551 | | BioAssay type | confirmatory | | Target | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] | | PubMed | | | Data Table |  |
|
| 2 | [SID24828847] | Active | EC50 | 2.351 | Luminescence Cell-Based/Microorganism Dose Confirmation HTS to Identify Inhibitors of T.Cruzi Replication. [AID2044, Type: confirmatory] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | EC50 | 2.351 [uM] | | BioAssay | Luminescence Cell-Based/Microorganism Dose Confirmation HTS to Identify Inhibitors of T.Cruzi Replication. | | AID | 2044 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 3 | [SID24828847] | Active | Potency | 2.5929 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | Potency | 2.5929 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 4 | [SID24828847] | Active | Potency | 2.5929 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | Potency | 2.5929 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 5 | [SID24828847] | Active | Potency | 2.5929 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | Potency | 2.5929 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 6 | [SID24828847] | Active | EC50 | 4.76 | Luminescence-based cell-based high throughput dose response assay for activators of the Aryl Hydrocarbon Receptor (AHR) [AID463088, Type: confirmatory] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | EC50 | 4.76 [uM] | | BioAssay | Luminescence-based cell-based high throughput dose response assay for activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 463088 | | BioAssay type | confirmatory | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
|
| 7 | [SID24828847] | Active | EC50 | 4.76 | Luminescence-based cell-based high throughput dose response assay for activators of the Aryl Hydrocarbon Receptor (AHR) [AID463088, Type: confirmatory] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | EC50 | 4.76 [uM] | | BioAssay | Luminescence-based cell-based high throughput dose response assay for activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 463088 | | BioAssay type | confirmatory | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
|
| 8 | [SID24828847] | Active | EC50 | 4.76 | Luminescence-based cell-based high throughput dose response assay for activators of the Aryl Hydrocarbon Receptor (AHR) [AID463088, Type: confirmatory] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | EC50 | 4.76 [uM] | | BioAssay | Luminescence-based cell-based high throughput dose response assay for activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 463088 | | BioAssay type | confirmatory | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
|
| 9 | [SID24828847] | Active | Potency | 5.1735 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | Potency | 5.1735 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 10 | [SID24828847] | Active | Potency | 5.1735 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | Potency | 5.1735 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 11 | [SID24828847] | Active | Potency | 5.1735 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | Potency | 5.1735 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 12 | [SID24828847] | Active | | | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID1822, Type: screening] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 1822 | | BioAssay type | screening | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
|
| 13 | [SID24828847] | Active | | | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID1822, Type: screening] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 1822 | | BioAssay type | screening | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
|
| 14 | [SID24828847] | Active | | | Screen for inhibitors of the SWI/SNF chromatin remodeling complex (esBAF) in mouse embryonic stem cells with Luciferase reporter assay Measured in Cell-Based System Using Plate Reader - 2141-01_Inhibitor_SinglePoint_HTS_Activity [AID602393, Type: screening] | transcription activator BRG1 isoform 1 [Mus musculus] [gi:291463269] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Screen for inhibitors of the SWI/SNF chromatin remodeling complex (esBAF) in mouse embryonic stem cells with Luciferase reporter assay Measured in Cell-Based System Using Plate Reader - 2141-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 602393 | | BioAssay type | screening | | Target | transcription activator BRG1 isoform 1 [Mus musculus] [gi:291463269] | | PubMed | | | Data Table |  |
|
| 15 | [SID24828847] | Active | | | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Secondary Assay 3 with KCC2 cells [AID1714, Type: other] | electroneutral potassium-chloride cotransporter KCC2 [Homo sapiens] [gi:12003227] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Secondary Assay 3 with KCC2 cells | | AID | 1714 | | BioAssay type | other | | Target | electroneutral potassium-chloride cotransporter KCC2 [Homo sapiens] [gi:12003227] | | PubMed | | | Data Table |  |
|
| 16 | [SID24828847] | Active | | | Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis [AID588726, Type: screening] | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis | | AID | 588726 | | BioAssay type | screening | | Target | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] | | PubMed | | | Data Table |  |
|
| 17 | [SID24828847] | Active | | | Fluorescence-based biochemical high throughput confirmation assay for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis [AID651616, Type: screening] | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical high throughput confirmation assay for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis | | AID | 651616 | | BioAssay type | screening | | Target | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] | | PubMed | | | Data Table |  |
|
| 18 | [SID24828847] | Active | | | uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent assay [AID463190, Type: screening] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent assay | | AID | 463190 | | BioAssay type | screening | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
|
| 19 | [SID24828847] | Active | | | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Primary Screen [AID1456, Type: other] | electroneutral potassium-chloride cotransporter KCC2 [Homo sapiens] [gi:12003227] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Primary Screen | | AID | 1456 | | BioAssay type | other | | Target | electroneutral potassium-chloride cotransporter KCC2 [Homo sapiens] [gi:12003227] | | PubMed | | | Data Table |  |
|
| 20 | [SID24828847] | Active | | | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) [AID2796, Type: screening] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 2796 | | BioAssay type | screening | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
|
| 21 | [SID24828847] | Active | | | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) [AID2796, Type: screening] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 2796 | | BioAssay type | screening | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
|
| 22 | [SID24828847] | Active | | | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) [AID2796, Type: screening] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 2796 | | BioAssay type | screening | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
|
| 23 | [SID24828847] | Active | | | Luminescence-based cell-based high throughput confirmation assay for activators of the Aryl Hydrocarbon Receptor (AHR) [AID2845, Type: screening] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Luminescence-based cell-based high throughput confirmation assay for activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 2845 | | BioAssay type | screening | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
|
| 24 | [SID24828847] | Active | | | Luminescence-based cell-based high throughput confirmation assay for activators of the Aryl Hydrocarbon Receptor (AHR) [AID2845, Type: screening] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Luminescence-based cell-based high throughput confirmation assay for activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 2845 | | BioAssay type | screening | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
|
| 25 | [SID24828847] | Active | | | Luminescence-based cell-based high throughput confirmation assay for activators of the Aryl Hydrocarbon Receptor (AHR) [AID2845, Type: screening] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Luminescence-based cell-based high throughput confirmation assay for activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 2845 | | BioAssay type | screening | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
|
| 26 | [SID24828847] | Active | | | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Counterscreen with HEK cells [AID1716, Type: other] | |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Counterscreen with HEK cells | | AID | 1716 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 27 | [SID24828847] | Active | | | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Retesting of KCC2 cells with Ouabain [AID1717, Type: other] | |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Retesting of KCC2 cells with Ouabain | | AID | 1717 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 28 | [SID24828847] | Active | | | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Counterscreen 2 with HEK cells [AID1718, Type: other] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Counterscreen 2 with HEK cells | | AID | 1718 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 29 | [SID24828847] | Active | | | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - activators [AID1814, Type: screening] | |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - activators | | AID | 1814 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 30 | [SID24828847] | Active | | | Luminescence Cell-Based/Microorganism Primary HTS to Identify Inhibitors of T.Cruzi Replication [AID1885, Type: screening] | |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Luminescence Cell-Based/Microorganism Primary HTS to Identify Inhibitors of T.Cruzi Replication | | AID | 1885 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 31 | [SID24828847] | Active | | | Cycloheximide Counterscreen for Small Molecule Inhibitors of Shiga Toxin [AID2314, Type: screening] | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Cycloheximide Counterscreen for Small Molecule Inhibitors of Shiga Toxin | | AID | 2314 | | BioAssay type | screening | | Target | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | | PubMed | | | Data Table |  |
|
| 32 | [SID24828847] | Active | | | High Throughput Screen to Identify Compounds that Inhibit Class II HMG-CoA Reductases - Primary Screen [AID1066, Type: screening] | acetyl-CoA acetyltransferase/HMG-CoA reductase [Enterococcus faecalis] [gi:9937384] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | High Throughput Screen to Identify Compounds that Inhibit Class II HMG-CoA Reductases - Primary Screen | | AID | 1066 | | BioAssay type | screening | | Target | acetyl-CoA acetyltransferase/HMG-CoA reductase [Enterococcus faecalis] [gi:9937384] | | PubMed | | | Data Table |  |
|
| 33 | [SID24828847] | Active | | | Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis: Fluroescence-based biochemical high throughput Glycerophosphate Dehydrogenase-Triosephosphate Isomerase (GDH-TPI) assay to identify assay artifacts [AID652141, Type: screening] | |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis: Fluroescence-based biochemical high throughput Glycerophosphate Dehydrogenase-Triosephosphate Isomerase (GDH-TPI) assay to identify assay artifacts | | AID | 652141 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 34 | [SID24828847] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 35 | [SID24828847] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 36 | [SID24828847] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 37 | [SID24828847] | Active | | | Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) [AID631, Type: screening] | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | | AID | 631 | | BioAssay type | screening | | Target | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] | | PubMed | | | Data Table |  |
|
| 38 | [SID24828847] | Active | | | Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) [AID631, Type: screening] | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | | AID | 631 | | BioAssay type | screening | | Target | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] | | PubMed | | | Data Table |  |
|
| 39 | [SID24828847] | Active | | | Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) [AID631, Type: screening] | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | | AID | 631 | | BioAssay type | screening | | Target | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] | | PubMed | | | Data Table |  |
|
| 40 | [SID24828847] | Active | | | Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) [AID631, Type: screening] | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Active | | BioAssay | Primary biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | | AID | 631 | | BioAssay type | screening | | Target | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] | | PubMed | | | Data Table |  |
|
| 41 | [SID24828847] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
|
| 42 | [SID24828847] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
|
| 43 | [SID24828847] | Inactive | Potency | 6.3096 | qHTS for Inhibitors of Glutaminase (GLS) [AID624170, Type: confirmatory] | GLS protein [Homo sapiens] [gi:71051501] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Inactive | | Potency | 6.3096 [uM] | | BioAssay | qHTS for Inhibitors of Glutaminase (GLS) | | AID | 624170 | | BioAssay type | confirmatory | | Target | GLS protein [Homo sapiens] [gi:71051501] | | PubMed | | | Data Table |  |
|
| 44 | [SID24828847] | Inactive | Potency | 35.4813 | qHTS Assay for Identification of Novel General Anesthetics [AID485281, Type: confirmatory] | Chain A, Horse Spleen Apoferritin [gi:254220970] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Inactive | | Potency | 35.4813 [uM] | | BioAssay | qHTS Assay for Identification of Novel General Anesthetics | | AID | 485281 | | BioAssay type | confirmatory | | Target | Chain A, Horse Spleen Apoferritin [gi:254220970] | | PubMed | | | Data Table |  |
|
| 45 | [SID24828847] | Inactive | EC50 | 60 | Luminescence Cell-Based Dose Response HTS Screen to Identify Cytotoxic Compounds of NIH3T3 cells. [AID2010, Type: confirmatory] | |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Inactive | | EC50 | 60 [uM] | | BioAssay | Luminescence Cell-Based Dose Response HTS Screen to Identify Cytotoxic Compounds of NIH3T3 cells. | | AID | 2010 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 46 | [SID24828847] | Inactive | EC50 | 79.37 | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) [AID1319, Type: confirmatory] | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Inactive | | EC50 | 79.37 [uM] | | BioAssay | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | | AID | 1319 | | BioAssay type | confirmatory | | Target | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] | | PubMed | | | Data Table |  |
|
| 47 | [SID24828847] | Inactive | EC50 | 79.37 | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) [AID1319, Type: confirmatory] | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Inactive | | EC50 | 79.37 [uM] | | BioAssay | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | | AID | 1319 | | BioAssay type | confirmatory | | Target | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] | | PubMed | | | Data Table |  |
|
| 48 | [SID24828847] | Inactive | EC50 | 79.37 | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) [AID1319, Type: confirmatory] | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Inactive | | EC50 | 79.37 [uM] | | BioAssay | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | | AID | 1319 | | BioAssay type | confirmatory | | Target | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] | | PubMed | | | Data Table |  |
|
| 49 | [SID24828847] | Inactive | EC50 | 79.37 | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) [AID1319, Type: confirmatory] | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Inactive | | EC50 | 79.37 [uM] | | BioAssay | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | | AID | 1319 | | BioAssay type | confirmatory | | Target | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] | | PubMed | | | Data Table |  |
|
| 50 | [SID24828847] | Inactive | EC50 | 79.37 | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 2 (SRC-2) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) [AID1323, Type: confirmatory] | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 24828847 | | CID | 16241391 | | Outcome | Inactive | | EC50 | 79.37 [uM] | | BioAssay | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 2 (SRC-2) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | | AID | 1323 | | BioAssay type | confirmatory | | Target | peroxisome proliferator-activated receptor gamma isoform 2 [Homo sapiens] [gi:20336229] | | PubMed | | | Data Table |  |
|