| 1 | [SID51086417] | Active | EC50 | 0.596 | Confirmation dose response assay for compounds that activate transient receptor potential cation channel C4 (TRPC4) [AID434937, Type: confirmatory] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 0.596 [uM] | | BioAssay | Confirmation dose response assay for compounds that activate transient receptor potential cation channel C4 (TRPC4) | | AID | 434937 | | BioAssay type | confirmatory | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
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| 2 | [SID51086417] | Active | EC50 | 1.272 | Luminescence-based cell-based high throughput dose response assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors [AID588407, Type: confirmatory] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 1.272 [uM] | | BioAssay | Luminescence-based cell-based high throughput dose response assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | | AID | 588407 | | BioAssay type | confirmatory | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
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| 3 | [SID51086417] | Active | EC50 | 1.272 | Luminescence-based cell-based high throughput dose response assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors [AID588407, Type: confirmatory] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 1.272 [uM] | | BioAssay | Luminescence-based cell-based high throughput dose response assay for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | | AID | 588407 | | BioAssay type | confirmatory | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
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| 4 | [SID51086417] | Active | EC50 | 3.284 | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRM1 homodimerization [AID588435, Type: confirmatory] | OPRM1 gene product [Homo sapiens] [gi:117940060] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 3.284 [uM] | | BioAssay | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRM1 homodimerization | | AID | 588435 | | BioAssay type | confirmatory | | Target | OPRM1 gene product [Homo sapiens] [gi:117940060] | | PubMed | | | Data Table |  |
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| 5 | [SID51086417] | Active | EC50 | 3.284 | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRM1 homodimerization [AID588435, Type: confirmatory] | OPRM1 gene product [Homo sapiens] [gi:117940060] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 3.284 [uM] | | BioAssay | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRM1 homodimerization | | AID | 588435 | | BioAssay type | confirmatory | | Target | OPRM1 gene product [Homo sapiens] [gi:117940060] | | PubMed | | | Data Table |  |
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| 6 | [SID51086417] | Active | EC50 | 3.284 | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRM1 homodimerization [AID588435, Type: confirmatory] | OPRM1 gene product [Homo sapiens] [gi:117940060] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 3.284 [uM] | | BioAssay | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRM1 homodimerization | | AID | 588435 | | BioAssay type | confirmatory | | Target | OPRM1 gene product [Homo sapiens] [gi:117940060] | | PubMed | | | Data Table |  |
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| 7 | [SID51086417] | Active | EC50 | 3.284 | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRM1 homodimerization [AID588435, Type: confirmatory] | OPRM1 gene product [Homo sapiens] [gi:117940060] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 3.284 [uM] | | BioAssay | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRM1 homodimerization | | AID | 588435 | | BioAssay type | confirmatory | | Target | OPRM1 gene product [Homo sapiens] [gi:117940060] | | PubMed | | | Data Table |  |
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| 8 | [SID51086417] | Active | Potency | 4.1095 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | Potency | 4.1095 [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 |  |
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| 9 | [SID51086417] | Active | Potency | 4.6109 | A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. [AID624296, Type: confirmatory] | GMNN gene product [Homo sapiens] [gi:7705682] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | Potency | 4.6109 [uM] | | BioAssay | A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. | | AID | 624296 | | BioAssay type | confirmatory | | Target | GMNN gene product [Homo sapiens] [gi:7705682] | | PubMed | | | Data Table |  |
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| 10 | [SID51086417] | Active | Potency | 5.1735 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | Potency | 5.1735 [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 |  |
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| 11 | [SID51086417] | Active | AbsAC35_uM | 5.39 | Counterscreen for inhibitors of NLG for Luciferase Activators Measured in Cell-Based System Using Plate Reader - 2146-03_Inhibitor_Dose_CherryPick_Activity [AID624404, Type: confirmatory] | |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | AbsAC35_uM | 5.39 [uM] | | BioAssay | Counterscreen for inhibitors of NLG for Luciferase Activators Measured in Cell-Based System Using Plate Reader - 2146-03_Inhibitor_Dose_CherryPick_Activity | | AID | 624404 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 12 | [SID51086417] | Active | EC50 | 8.2 | Dose response counterscreen for uHTS small molecule activators of the adaptive arm of the Unfolded Protein Response via a luminescent-based reporter assay [AID489027, Type: confirmatory] | |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 8.2 [uM] | | BioAssay | Dose response counterscreen for uHTS small molecule activators of the adaptive arm of the Unfolded Protein Response via a luminescent-based reporter assay | | AID | 489027 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 13 | [SID51086417] | Active | Potency | 11.2202 | 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. | 13 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | Potency | 11.2202 [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 |  |
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| 14 | [SID51086417] | Active | Potency | 13.1154 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | Potency | 13.1154 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation | | AID | 504832 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 15 | [SID51086417] | Active | Potency | 16.3601 | 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. | 15 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | Potency | 16.3601 [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 |  |
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| 16 | [SID51086417] | Active | IC50 | 24.7 | Dose response confirmation of uHTS hits for Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay [AID588574, Type: confirmatory] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | IC50 | 24.7 [uM] | | BioAssay | Dose response confirmation of uHTS hits for Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay | | AID | 588574 | | BioAssay type | confirmatory | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
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| 17 | [SID51086417] | Active | IC50 | 24.7 | Dose response confirmation of uHTS hits for Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay [AID588574, Type: confirmatory] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | IC50 | 24.7 [uM] | | BioAssay | Dose response confirmation of uHTS hits for Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay | | AID | 588574 | | BioAssay type | confirmatory | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
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| 18 | [SID51086417] | Active | IC50 | 24.7 | Dose response confirmation of uHTS hits for Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay [AID588574, Type: confirmatory] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | IC50 | 24.7 [uM] | | BioAssay | Dose response confirmation of uHTS hits for Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay | | AID | 588574 | | BioAssay type | confirmatory | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
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| 19 | [SID51086417] | Active | IC50 | 24.7 | Dose response confirmation of uHTS hits for Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay [AID588574, Type: confirmatory] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | IC50 | 24.7 [uM] | | BioAssay | Dose response confirmation of uHTS hits for Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay | | AID | 588574 | | BioAssay type | confirmatory | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
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| 20 | [SID51086417] | Active | CC50 | 31.08 | An HTS Cytotoxicity Screen to evaluate New Inhibitors of Respiratory Syncytial Virus (RSV) [AID2410, Type: confirmatory] | |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | CC50 | 31.08 [uM] | | BioAssay | An HTS Cytotoxicity Screen to evaluate New Inhibitors of Respiratory Syncytial Virus (RSV) | | AID | 2410 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 21 | [SID51086417] | Active | Potency | 39.8107 | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a [AID504332, Type: confirmatory] | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a | | AID | 504332 | | BioAssay type | confirmatory | | Target | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] | | PubMed | | | Data Table |  |
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| 22 | [SID51086417] | Active | Potency | 44.6684 | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | | AID | 1490 | | BioAssay type | confirmatory | | Target | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] | | PubMed | | | Data Table |  |
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| 23 | [SID51086417] | Active | IC50 | 47.9 | Dose response confirmation of uHTS hits for Apaf-1 in a Fluorescent assay [AID588524, Type: confirmatory] | Apoptotic peptidase activating factor 1 [Homo sapiens] [gi:187952397] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | IC50 | 47.9 [uM] | | BioAssay | Dose response confirmation of uHTS hits for Apaf-1 in a Fluorescent assay | | AID | 588524 | | BioAssay type | confirmatory | | Target | Apoptotic peptidase activating factor 1 [Homo sapiens] [gi:187952397] | | PubMed | | | Data Table |  |
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| 24 | [SID51086417] | Active | EC50 | 75.25 | Luminescence Cell-Based Dose Retest to Identify Inhibitors of A1 Apoptosis [AID2765, Type: confirmatory] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 75.25 [uM] | | BioAssay | Luminescence Cell-Based Dose Retest to Identify Inhibitors of A1 Apoptosis | | AID | 2765 | | BioAssay type | confirmatory | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
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| 25 | [SID51086417] | Active | EC50 | 75.25 | Luminescence Cell-Based Dose Retest to Identify Inhibitors of A1 Apoptosis [AID2765, Type: confirmatory] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 75.25 [uM] | | BioAssay | Luminescence Cell-Based Dose Retest to Identify Inhibitors of A1 Apoptosis | | AID | 2765 | | BioAssay type | confirmatory | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
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| 26 | [SID51086417] | Active | EC50 | 75.25 | Luminescence Cell-Based Dose Retest to Identify Inhibitors of A1 Apoptosis [AID2765, Type: confirmatory] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 75.25 [uM] | | BioAssay | Luminescence Cell-Based Dose Retest to Identify Inhibitors of A1 Apoptosis | | AID | 2765 | | BioAssay type | confirmatory | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
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| 27 | [SID51086417] | Active | EC50 | 75.25 | Luminescence Cell-Based Dose Retest to Identify Inhibitors of A1 Apoptosis [AID2765, Type: confirmatory] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | EC50 | 75.25 [uM] | | BioAssay | Luminescence Cell-Based Dose Retest to Identify Inhibitors of A1 Apoptosis | | AID | 2765 | | BioAssay type | confirmatory | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
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| 28 | [SID51086417] | Active | AC50 | 155.4 | Luminescence Cell-Based Counterscreen to Identify Inhibitors of A1 Apoptosis (non-primed) [AID449761, Type: confirmatory] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | AC50 | 155.4 [uM] | | BioAssay | Luminescence Cell-Based Counterscreen to Identify Inhibitors of A1 Apoptosis (non-primed) | | AID | 449761 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 29 | [SID51086417] | Active | AC50 | 195.5 | Luminescence Cell-Based Secondary Screen to Identify Inhibitors of A1(alternate construct) [AID449757, Type: confirmatory] | Bcl-2-like protein 11 [gi:18202042] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | AC50 | 195.5 [uM] | | BioAssay | Luminescence Cell-Based Secondary Screen to Identify Inhibitors of A1(alternate construct) | | AID | 449757 | | BioAssay type | confirmatory | | Target | Bcl-2-like protein 11 [gi:18202042] | | PubMed | | | Data Table |  |
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| 30 | [SID51086417] | Active | AC50 | 195.5 | Luminescence Cell-Based Secondary Screen to Identify Inhibitors of A1(alternate construct) [AID449757, Type: confirmatory] | Bcl-2-like protein 11 [gi:18202042] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | AC50 | 195.5 [uM] | | BioAssay | Luminescence Cell-Based Secondary Screen to Identify Inhibitors of A1(alternate construct) | | AID | 449757 | | BioAssay type | confirmatory | | Target | Bcl-2-like protein 11 [gi:18202042] | | PubMed | | | Data Table |  |
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| 31 | [SID51086417] | Active | AC50 | 195.5 | Luminescence Cell-Based Secondary Screen to Identify Inhibitors of A1(alternate construct) [AID449757, Type: confirmatory] | Bcl-2-like protein 11 [gi:18202042] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | AC50 | 195.5 [uM] | | BioAssay | Luminescence Cell-Based Secondary Screen to Identify Inhibitors of A1(alternate construct) | | AID | 449757 | | BioAssay type | confirmatory | | Target | Bcl-2-like protein 11 [gi:18202042] | | PubMed | | | Data Table |  |
|
| 32 | [SID51086417] | Active | AC50 | 195.5 | Luminescence Cell-Based Secondary Screen to Identify Inhibitors of A1(alternate construct) [AID449757, Type: confirmatory] | Bcl-2-like protein 11 [gi:18202042] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | AC50 | 195.5 [uM] | | BioAssay | Luminescence Cell-Based Secondary Screen to Identify Inhibitors of A1(alternate construct) | | AID | 449757 | | BioAssay type | confirmatory | | Target | Bcl-2-like protein 11 [gi:18202042] | | PubMed | | | Data Table |  |
|
| 33 | [SID51086417] | Active | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. [AID2462, Type: screening] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. | | AID | 2462 | | BioAssay type | screening | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
|
| 34 | [SID51086417] | Active | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. [AID2462, Type: screening] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. | | AID | 2462 | | BioAssay type | screening | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
|
| 35 | [SID51086417] | Active | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. [AID2462, Type: screening] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. | | AID | 2462 | | BioAssay type | screening | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
|
| 36 | [SID51086417] | Active | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. [AID2462, Type: screening] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. | | AID | 2462 | | BioAssay type | screening | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
|
| 37 | [SID51086417] | Active | | | uHTS identification of Caspase-8 TRAIL sensitizers in a luminesence assay [AID624354, Type: screening] | TNFRSF10B gene product [Homo sapiens] [gi:224494019] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | uHTS identification of Caspase-8 TRAIL sensitizers in a luminesence assay | | AID | 624354 | | BioAssay type | screening | | Target | TNFRSF10B gene product [Homo sapiens] [gi:224494019] | | PubMed | | | Data Table |  |
|
| 38 | [SID51086417] | Active | | | uHTS identification of Caspase-8 TRAIL sensitizers in a luminesence assay [AID624354, Type: screening] | TNFRSF10B gene product [Homo sapiens] [gi:224494019] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | uHTS identification of Caspase-8 TRAIL sensitizers in a luminesence assay | | AID | 624354 | | BioAssay type | screening | | Target | TNFRSF10B gene product [Homo sapiens] [gi:224494019] | | PubMed | | | Data Table |  |
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| 39 | [SID51086417] | Active | | | Activator for delta FosB/delta FosB homodimer Measured in Biochemical System Using Plate Reader - 2072-01_Activator_SinglePoint_HTS_Activity [AID493131, Type: screening] | protein fosB [Mus musculus] [gi:6679827] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Activator for delta FosB/delta FosB homodimer Measured in Biochemical System Using Plate Reader - 2072-01_Activator_SinglePoint_HTS_Activity | | AID | 493131 | | BioAssay type | screening | | Target | protein fosB [Mus musculus] [gi:6679827] | | PubMed | | | Data Table |  |
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| 40 | [SID51086417] | Active | | | Single concentration confirmation of Caspase-8 TRAIL sensitizer hits in a luminesence panel assay [AID651596_6, Type: screening] | TNFRSF10B gene product [Homo sapiens] [gi:224494019] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Single concentration confirmation of Caspase-8 TRAIL sensitizer hits in a luminesence panel assay | | AID | 651596 | | BioAssay type | screening | | Target | TNFRSF10B gene product [Homo sapiens] [gi:224494019] | | PubMed | | | Data Table |  |
|
| 41 | [SID51086417] | Active | | | Single concentration confirmation of Caspase-8 TRAIL sensitizer hits in a luminesence panel assay [AID651596_6, Type: screening] | TNFRSF10B gene product [Homo sapiens] [gi:224494019] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Single concentration confirmation of Caspase-8 TRAIL sensitizer hits in a luminesence panel assay | | AID | 651596 | | BioAssay type | screening | | Target | TNFRSF10B gene product [Homo sapiens] [gi:224494019] | | PubMed | | | Data Table |  |
|
| 42 | [SID51086417] | Active | | | uHTS identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay [AID485273, Type: screening] | UBE2N gene product [Homo sapiens] [gi:4507793] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | uHTS identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay | | AID | 485273 | | BioAssay type | screening | | Target | UBE2N gene product [Homo sapiens] [gi:4507793] | | PubMed | | | Data Table |  |
|
| 43 | [SID51086417] | Active | | | uHTS identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay [AID485273, Type: screening] | UBE2N gene product [Homo sapiens] [gi:4507793] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | uHTS identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay | | AID | 485273 | | BioAssay type | screening | | Target | UBE2N gene product [Homo sapiens] [gi:4507793] | | PubMed | | | Data Table |  |
|
| 44 | [SID51086417] | Active | | | Single concentration confirmation of uHTS for the identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay [AID488859, Type: screening] | UBE2N gene product [Homo sapiens] [gi:4507793] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Single concentration confirmation of uHTS for the identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay | | AID | 488859 | | BioAssay type | screening | | Target | UBE2N gene product [Homo sapiens] [gi:4507793] | | PubMed | | | Data Table |  |
|
| 45 | [SID51086417] | Active | | | Single concentration confirmation of uHTS for the identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay [AID488859, Type: screening] | UBE2N gene product [Homo sapiens] [gi:4507793] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Single concentration confirmation of uHTS for the identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay | | AID | 488859 | | BioAssay type | screening | | Target | UBE2N gene product [Homo sapiens] [gi:4507793] | | PubMed | | | Data Table |  |
|
| 46 | [SID51086417] | Active | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase 2 mutant [AID1530, Type: screening] | mitogen-activated protein kinase kinase kinase kinase 2 [Homo sapiens] [gi:22035600] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase 2 mutant | | AID | 1530 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase kinase 2 [Homo sapiens] [gi:22035600] | | PubMed | | | Data Table |  |
|
| 47 | [SID51086417] | Active | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase 2 mutant [AID1530, Type: screening] | mitogen-activated protein kinase kinase kinase kinase 2 [Homo sapiens] [gi:22035600] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase 2 mutant | | AID | 1530 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase kinase 2 [Homo sapiens] [gi:22035600] | | PubMed | | | Data Table |  |
|
| 48 | [SID51086417] | Active | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Wildtype [AID1531, Type: screening] | mitogen-activated protein kinase kinase kinase kinase 2 [Homo sapiens] [gi:22035600] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Wildtype | | AID | 1531 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase kinase 2 [Homo sapiens] [gi:22035600] | | PubMed | | | Data Table |  |
|
| 49 | [SID51086417] | Active | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Wildtype [AID1531, Type: screening] | mitogen-activated protein kinase kinase kinase kinase 2 [Homo sapiens] [gi:22035600] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Wildtype | | AID | 1531 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase kinase 2 [Homo sapiens] [gi:22035600] | | PubMed | | | Data Table |  |
|
| 50 | [SID51086417] | Active | | | Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors [AID504326, Type: screening] | OPRD1 gene product [Homo sapiens] [gi:63477962] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 51086417 | | CID | 24892079 | | Outcome | Active | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | | AID | 504326 | | BioAssay type | screening | | Target | OPRD1 gene product [Homo sapiens] [gi:63477962] | | PubMed | | | Data Table |  |
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