| 1 | [SID14728984] | Active | EC50 | 0.2 | Counter Screen for Luciferase-based Assay Positives [AID773, Type: confirmatory] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | EC50 | 0.2 [uM] | | BioAssay | Counter Screen for Luciferase-based Assay Positives | | AID | 773 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 2 | [SID14728984] | Active | Potency | 0.5174 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 0.5174 [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 | | | PubMed | | | Data Table |  |
|
| 3 | [SID14728984] | Active | IC50 | 0.564 | Fluorescence dose response cell-based high throughput screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) [AID1692, Type: confirmatory] | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | IC50 | 0.564 [uM] | | BioAssay | Fluorescence dose response cell-based high throughput screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | | AID | 1692 | | BioAssay type | confirmatory | | Target | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] | | PubMed | | | Data Table |  |
|
| 4 | [SID14728984] | Active | IC50 | 0.564 | Fluorescence dose response cell-based high throughput screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) [AID1692, Type: confirmatory] | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | IC50 | 0.564 [uM] | | BioAssay | Fluorescence dose response cell-based high throughput screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | | AID | 1692 | | BioAssay type | confirmatory | | Target | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] | | PubMed | | | Data Table |  |
|
| 5 | [SID14728984] | Active | Potency | 0.8199 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 0.8199 [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 | | | PubMed | | | Data Table |  |
|
| 6 | [SID14728984] | Active | AbsAC40_uM | 1.24 | In vivo-based yeast HTS counterscreen to detect compounds rescuing yeast growth/survival of Saccharomyces cerevisiae SKN7-mediated toxicity Measured in Whole Organism System Using Plate Reader - 2120-02_Inhibitor_Dose_CherryPick_Activity [AID624258, Type: confirmatory] | Skn7p [Saccharomyces cerevisiae] [gi:458922] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | AbsAC40_uM | 1.24 [uM] | | BioAssay | In vivo-based yeast HTS counterscreen to detect compounds rescuing yeast growth/survival of Saccharomyces cerevisiae SKN7-mediated toxicity Measured in Whole Organism System Using Plate Reader - 2120-02_Inhibitor_Dose_CherryPick_Activity | | AID | 624258 | | BioAssay type | confirmatory | | Target | Skn7p [Saccharomyces cerevisiae] [gi:458922] | | PubMed | | | Data Table |  |
|
| 7 | [SID14728984] | Active | IC50 | 1.43 | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA [AID856, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | IC50 | 1.43 [uM] | | BioAssay | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA | | AID | 856 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 8 | [SID14728984] | Active | IC50 | 1.43 | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA [AID856, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | IC50 | 1.43 [uM] | | BioAssay | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA | | AID | 856 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 9 | [SID14728984] | Active | IC50 | 1.43 | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA [AID856, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | IC50 | 1.43 [uM] | | BioAssay | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA | | AID | 856 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 10 | [SID14728984] | Active | IC50 | 1.484 | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor [AID851, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | IC50 | 1.484 [uM] | | BioAssay | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor | | AID | 851 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 11 | [SID14728984] | Active | IC50 | 1.484 | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor [AID851, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | IC50 | 1.484 [uM] | | BioAssay | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor | | AID | 851 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 12 | [SID14728984] | Active | IC50 | 1.484 | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor [AID851, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | IC50 | 1.484 [uM] | | BioAssay | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor | | AID | 851 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 13 | [SID14728984] | Active | Potency | 2.2387 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588453, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588453 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 14 | [SID14728984] | Active | Potency | 2.2387 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588453, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588453 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 15 | [SID14728984] | Active | Potency | 2.5119 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 2.5119 [uM] | | BioAssay | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins | | AID | 485364 | | BioAssay type | confirmatory | | Target | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] | | PubMed | | | Data Table |  |
|
| 16 | [SID14728984] | Active | Potency | 2.5119 | qHTS Assay for Inhibitors of Hepatitis C Virus (HCV) [AID651820, Type: confirmatory] | |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 2.5119 [uM] | | BioAssay | qHTS Assay for Inhibitors of Hepatitis C Virus (HCV) | | AID | 651820 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 17 | [SID14728984] | Active | Potency | 2.5119 | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 2.5119 [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
|
| 18 | [SID14728984] | Active | Potency | 2.5119 | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 2.5119 [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
|
| 19 | [SID14728984] | Active | Potency | 2.5929 | A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. [AID624297, Type: confirmatory] | GMNN gene product [Homo sapiens] [gi:7705682] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 2.5929 [uM] | | BioAssay | A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. | | AID | 624297 | | BioAssay type | confirmatory | | Target | GMNN gene product [Homo sapiens] [gi:7705682] | | PubMed | | | Data Table |  |
|
| 20 | [SID14728984] | Active | EC50 | 2.71 | Fluorescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of RecA-Intein Splicing Activity [AID435010, Type: confirmatory] | DNA recombination protein RecA [Mycobacterium tuberculosis H37Rv] [gi:15609874] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | EC50 | 2.71 [uM] | | BioAssay | Fluorescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of RecA-Intein Splicing Activity | | AID | 435010 | | BioAssay type | confirmatory | | Target | DNA recombination protein RecA [Mycobacterium tuberculosis H37Rv] [gi:15609874] | | PubMed | | | Data Table |  |
|
| 21 | [SID14728984] | Active | Potency | 3.1623 | VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity [AID2546, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity | | AID | 2546 | | BioAssay type | confirmatory | | Target | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] | | PubMed | | | Data Table |  |
|
| 22 | [SID14728984] | Active | Potency | 3.9811 | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction [AID1461, Type: confirmatory] | NPSR1 gene product [Homo sapiens] [gi:46395496] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 3.9811 [uM] | | BioAssay | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction | | AID | 1461 | | BioAssay type | confirmatory | | Target | NPSR1 gene product [Homo sapiens] [gi:46395496] | | PubMed | | | Data Table |  |
|
| 23 | [SID14728984] | Active | Potency | 3.9811 | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction [AID1461, Type: confirmatory] | NPSR1 gene product [Homo sapiens] [gi:46395496] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 3.9811 [uM] | | BioAssay | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction | | AID | 1461 | | BioAssay type | confirmatory | | Target | NPSR1 gene product [Homo sapiens] [gi:46395496] | | PubMed | | | Data Table |  |
|
| 24 | [SID14728984] | Active | AC50 | 4.268 | Fluorescence Cell-Free Homogeneous Secondary Screen to Identify Inhibitors of DnaB-Intein Splicing Activity [AID449749, Type: confirmatory] | replicative DNA helicase [Mycobacterium tuberculosis H37Rv] [gi:15607200] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | AC50 | 4.268 [uM] | | BioAssay | Fluorescence Cell-Free Homogeneous Secondary Screen to Identify Inhibitors of DnaB-Intein Splicing Activity | | AID | 449749 | | BioAssay type | confirmatory | | Target | replicative DNA helicase [Mycobacterium tuberculosis H37Rv] [gi:15607200] | | PubMed | | | Data Table |  |
|
| 25 | [SID14728984] | Active | Potency | 4.4668 | qHTS for inhibitors of ROR gamma transcriptional activity [AID2551, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 4.4668 [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 |  |
|
| 26 | [SID14728984] | Active | Potency | 4.4668 | qHTS for inhibitors of binding or entry into cells for Marburg Virus [AID540276, Type: confirmatory] | gene 4 small orf - Marburg virus [gi:420597] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 4.4668 [uM] | | BioAssay | qHTS for inhibitors of binding or entry into cells for Marburg Virus | | AID | 540276 | | BioAssay type | confirmatory | | Target | gene 4 small orf - Marburg virus [gi:420597] | | PubMed | | | Data Table |  |
|
| 27 | [SID14728984] | Active | AbsAC1000_uM | 4.666 | In vivo-based yeast HTS to detect compounds rescuing yeast growth/survival of Plasmodium Falciparum HSP40-mediated toxicity Measured in Whole Organism System Using Plate Reader - 2120-01_Inhibitor_Dose_CherryPick_Activity [AID540271, Type: confirmatory] | HSP40, subfamily A, putative [Plasmodium falciparum 3D7] [gi:124809271] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | AbsAC1000_uM | 4.666 [uM] | | BioAssay | In vivo-based yeast HTS to detect compounds rescuing yeast growth/survival of Plasmodium Falciparum HSP40-mediated toxicity Measured in Whole Organism System Using Plate Reader - 2120-01_Inhibitor_Dose_CherryPick_Activity | | AID | 540271 | | BioAssay type | confirmatory | | Target | HSP40, subfamily A, putative [Plasmodium falciparum 3D7] [gi:124809271] | | PubMed | | | Data Table |  |
|
| 28 | [SID14728984] | Active | Potency | 5.6234 | qHTS for Inhibitors of TGF-b: Cytotox Counterscreen [AID588856, Type: confirmatory] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 5.6234 [uM] | | BioAssay | qHTS for Inhibitors of TGF-b: Cytotox Counterscreen | | AID | 588856 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 29 | [SID14728984] | Active | Potency | 5.8048 | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Beta-Lactamase Assay [AID602202, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 5.8048 [uM] | | BioAssay | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Beta-Lactamase Assay | | AID | 602202 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 30 | [SID14728984] | Active | Potency | 5.8048 | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Beta-Lactamase Assay [AID602202, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 5.8048 [uM] | | BioAssay | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Beta-Lactamase Assay | | AID | 602202 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 31 | [SID14728984] | Active | Potency | 5.8048 | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Beta-Lactamase Assay [AID602202, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 5.8048 [uM] | | BioAssay | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Beta-Lactamase Assay | | AID | 602202 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 32 | [SID14728984] | Active | Potency | 5.8048 | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Beta-Lactamase Assay [AID602202, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 5.8048 [uM] | | BioAssay | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Beta-Lactamase Assay | | AID | 602202 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 33 | [SID14728984] | Active | EC50 | 6.672 | Fluorescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of GFP Chromophore Formation [AID434968, Type: confirmatory] | DNA recombination protein RecA [Mycobacterium tuberculosis H37Rv] [gi:15609874] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | EC50 | 6.672 [uM] | | BioAssay | Fluorescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of GFP Chromophore Formation | | AID | 434968 | | BioAssay type | confirmatory | | Target | DNA recombination protein RecA [Mycobacterium tuberculosis H37Rv] [gi:15609874] | | PubMed | | | Data Table |  |
|
| 34 | [SID14728984] | Active | IC50 | 7.068 | Fluorescence-based counterscreen assay for S1P4 antagonists: Cell-based dose response high throughput screening assay to identify antagonists of the Sphingosine 1-Phosphate Receptor 1 (S1P1) [AID1821, Type: confirmatory] | S1PR1 gene product [Homo sapiens] [gi:13027636] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | IC50 | 7.068 [uM] | | BioAssay | Fluorescence-based counterscreen assay for S1P4 antagonists: Cell-based dose response high throughput screening assay to identify antagonists of the Sphingosine 1-Phosphate Receptor 1 (S1P1) | | AID | 1821 | | BioAssay type | confirmatory | | Target | S1PR1 gene product [Homo sapiens] [gi:13027636] | | PubMed | | | Data Table |  |
|
| 35 | [SID14728984] | Active | IC50 | 7.068 | Fluorescence-based counterscreen assay for S1P4 antagonists: Cell-based dose response high throughput screening assay to identify antagonists of the Sphingosine 1-Phosphate Receptor 1 (S1P1) [AID1821, Type: confirmatory] | S1PR1 gene product [Homo sapiens] [gi:13027636] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | IC50 | 7.068 [uM] | | BioAssay | Fluorescence-based counterscreen assay for S1P4 antagonists: Cell-based dose response high throughput screening assay to identify antagonists of the Sphingosine 1-Phosphate Receptor 1 (S1P1) | | AID | 1821 | | BioAssay type | confirmatory | | Target | S1PR1 gene product [Homo sapiens] [gi:13027636] | | PubMed | | | Data Table |  |
|
| 36 | [SID14728984] | Active | Potency | 8.1995 | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-IDH1KD cell line [AID686971, Type: confirmatory] | |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 8.1995 [uM] | | BioAssay | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-IDH1KD cell line | | AID | 686971 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 37 | [SID14728984] | Active | Potency | 8.9125 | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 8.9125 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 38 | [SID14728984] | Active | Potency | 8.9125 | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 8.9125 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 39 | [SID14728984] | Active | Potency | 8.9125 | qHTS for Inhibitors of ATXN expression [AID651635, Type: confirmatory] | ATXN2 gene product [Homo sapiens] [gi:171543895] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 8.9125 [uM] | | BioAssay | qHTS for Inhibitors of ATXN expression | | AID | 651635 | | BioAssay type | confirmatory | | Target | ATXN2 gene product [Homo sapiens] [gi:171543895] | | PubMed | | | Data Table |  |
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| 40 | [SID14728984] | Active | Potency | 12.5893 | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Fluorescein Assay [AID602200, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Fluorescein Assay | | AID | 602200 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 41 | [SID14728984] | Active | Potency | 12.5893 | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Fluorescein Assay [AID602200, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Fluorescein Assay | | AID | 602200 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 42 | [SID14728984] | Active | Potency | 12.5893 | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Fluorescein Assay [AID602200, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Fluorescein Assay | | AID | 602200 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 43 | [SID14728984] | Active | Potency | 12.5893 | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Fluorescein Assay [AID602200, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Fluorescein Assay | | AID | 602200 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 44 | [SID14728984] | Active | Potency | 14.1254 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 14.1254 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
|
| 45 | [SID14728984] | Active | Potency | 14.1254 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 14.1254 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
|
| 46 | [SID14728984] | Active | Potency | 14.1254 | qHTS for Inhibitors of binding or entry into cells for Lassa Virus [AID540256, Type: confirmatory] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 14.1254 [uM] | | BioAssay | qHTS for Inhibitors of binding or entry into cells for Lassa Virus | | AID | 540256 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 47 | [SID14728984] | Active | EC50 | 14.5 | Luminescent HTS for small molecule inhibitors of MT1-MMP transcription [AID618, Type: confirmatory] | matrix metalloproteinase 1 [Homo sapiens] [gi:6690534] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | EC50 | 14.5 [uM] | | BioAssay | Luminescent HTS for small molecule inhibitors of MT1-MMP transcription | | AID | 618 | | BioAssay type | confirmatory | | Target | matrix metalloproteinase 1 [Homo sapiens] [gi:6690534] | | PubMed | | | Data Table |  |
|
| 48 | [SID14728984] | Active | EC50 | 14.5 | Luminescent HTS for small molecule inhibitors of MT1-MMP transcription [AID618, Type: confirmatory] | matrix metalloproteinase 1 [Homo sapiens] [gi:6690534] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | EC50 | 14.5 [uM] | | BioAssay | Luminescent HTS for small molecule inhibitors of MT1-MMP transcription | | AID | 618 | | BioAssay type | confirmatory | | Target | matrix metalloproteinase 1 [Homo sapiens] [gi:6690534] | | PubMed | | | Data Table |  |
|
| 49 | [SID14728984] | Active | EC50 | 14.5 | Luminescent HTS for small molecule inhibitors of MT1-MMP transcription [AID618, Type: confirmatory] | matrix metalloproteinase 1 [Homo sapiens] [gi:6690534] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | EC50 | 14.5 [uM] | | BioAssay | Luminescent HTS for small molecule inhibitors of MT1-MMP transcription | | AID | 618 | | BioAssay type | confirmatory | | Target | matrix metalloproteinase 1 [Homo sapiens] [gi:6690534] | | PubMed | | | Data Table |  |
|
| 50 | [SID14728984] | Active | Potency | 15.8489 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 14728984 | | CID | 1475337 | | Outcome | Active | | Potency | 15.8489 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|