| 1 | [SID26666751] | Active | Potency | 0.13 | 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. | 1 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.13 [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 |  |
|
| 2 | [SID26666751] | Active | Potency | 0.13 | 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. | 2 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.13 [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 |  |
|
| 3 | [SID26666751] | Active | Potency | 0.13 | 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 | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.13 [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 | [SID26666751] | Active | Potency | 0.158 | HTS assay for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1: Hit Confirmation [AID624248, Type: confirmatory] | ATAD5 protein [Homo sapiens] [gi:116283940] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.158 [uM] | | BioAssay | HTS assay for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1: Hit Confirmation | | AID | 624248 | | BioAssay type | confirmatory | | Target | ATAD5 protein [Homo sapiens] [gi:116283940] | | PubMed | | | Data Table |  |
|
| 5 | [SID26666751] | Active | AC50 | 0.158 | MLPCN Dyrk1A Kinase Measured in Biochemical System Using Plate Reader - 2124-01_Inhibitor_Dose_CherryPick_Activity [AID588345, Type: confirmatory] | dual specificity tyrosine-phosphorylation-regulated kinase 1A [Rattus norvegicus] [gi:6978787] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | AC50 | 0.158 [uM] | | BioAssay | MLPCN Dyrk1A Kinase Measured in Biochemical System Using Plate Reader - 2124-01_Inhibitor_Dose_CherryPick_Activity | | AID | 588345 | | BioAssay type | confirmatory | | Target | dual specificity tyrosine-phosphorylation-regulated kinase 1A [Rattus norvegicus] [gi:6978787] | | PubMed | | | Data Table |  |
|
| 6 | [SID26666751] | Active | AC50 | 0.158 | MLPCN Dyrk1A Kinase Measured in Biochemical System Using Plate Reader - 2124-01_Inhibitor_Dose_CherryPick_Activity [AID588345, Type: confirmatory] | dual specificity tyrosine-phosphorylation-regulated kinase 1A [Rattus norvegicus] [gi:6978787] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | AC50 | 0.158 [uM] | | BioAssay | MLPCN Dyrk1A Kinase Measured in Biochemical System Using Plate Reader - 2124-01_Inhibitor_Dose_CherryPick_Activity | | AID | 588345 | | BioAssay type | confirmatory | | Target | dual specificity tyrosine-phosphorylation-regulated kinase 1A [Rattus norvegicus] [gi:6978787] | | PubMed | | | Data Table |  |
|
| 7 | [SID26666751] | Active | Potency | 0.1636 | 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. | 7 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.1636 [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 |  |
|
| 8 | [SID26666751] | Active | Potency | 0.1636 | 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. | 8 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.1636 [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 |  |
|
| 9 | [SID26666751] | Active | Potency | 0.1636 | 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 | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.1636 [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 | [SID26666751] | Active | AC50 | 0.26 | HIV entry: Env-mediated Cell Fusion Measured in Cell-Based System Using Plate Reader - 7013-01_Inhibitor_Dose_CherryPick_Activity [AID652057, Type: confirmatory] | |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | AC50 | 0.26 [uM] | | BioAssay | HIV entry: Env-mediated Cell Fusion Measured in Cell-Based System Using Plate Reader - 7013-01_Inhibitor_Dose_CherryPick_Activity | | AID | 652057 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 11 | [SID26666751] | Active | AC50 | 0.26 | Cell fusion assay for clade C HIV-1ZM109 Env Measured in Cell-Based System Using Plate Reader - 7013-05_Inhibitor_Dose_CherryPick_Activity [AID652058, Type: confirmatory] | |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | AC50 | 0.26 [uM] | | BioAssay | Cell fusion assay for clade C HIV-1ZM109 Env Measured in Cell-Based System Using Plate Reader - 7013-05_Inhibitor_Dose_CherryPick_Activity | | AID | 652058 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 12 | [SID26666751] | Active | AC50 | 0.26 | HIV-1 Cell Fusion assay for clade B Env AD8 Measured in Cell-Based System Using Plate Reader - 7013-04_Inhibitor_Dose_CherryPick_Activity [AID652062, Type: confirmatory] | |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | AC50 | 0.26 [uM] | | BioAssay | HIV-1 Cell Fusion assay for clade B Env AD8 Measured in Cell-Based System Using Plate Reader - 7013-04_Inhibitor_Dose_CherryPick_Activity | | AID | 652062 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 13 | [SID26666751] | Active | AC50 | 0.26 | Control Cell Fusion Counterscreen Assay Measured in Cell-Based System Using Plate Reader - 7013-02_Inhibitor_Dose_CherryPick_Activity [AID652040, Type: confirmatory] | |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | AC50 | 0.26 [uM] | | BioAssay | Control Cell Fusion Counterscreen Assay Measured in Cell-Based System Using Plate Reader - 7013-02_Inhibitor_Dose_CherryPick_Activity | | AID | 652040 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 14 | [SID26666751] | Active | Potency | 0.2818 | qHTS Assay for Inhibitors of Hepatitis C Virus (HCV) [AID651820, Type: confirmatory] | |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.2818 [uM] | | BioAssay | qHTS Assay for Inhibitors of Hepatitis C Virus (HCV) | | AID | 651820 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 15 | [SID26666751] | Active | Potency | 0.3153 | qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1: Hit Confirmation using MMS Stimulated ELG1 [AID624249, Type: confirmatory] | ATAD5 protein [Homo sapiens] [gi:116283940] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.3153 [uM] | | BioAssay | qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1: Hit Confirmation using MMS Stimulated ELG1 | | AID | 624249 | | BioAssay type | confirmatory | | Target | ATAD5 protein [Homo sapiens] [gi:116283940] | | PubMed | | | Data Table |  |
|
| 16 | [SID26666751] | Active | Potency | 0.3162 | qHTS for Inhibitors of TGF-b [AID588855, Type: confirmatory] | Smad3 [Homo sapiens] [gi:18418623] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.3162 [uM] | | BioAssay | qHTS for Inhibitors of TGF-b | | AID | 588855 | | BioAssay type | confirmatory | | Target | Smad3 [Homo sapiens] [gi:18418623] | | PubMed | | | Data Table |  |
|
| 17 | [SID26666751] | Active | Potency | 0.3162 | qHTS for Inhibitors of TGF-b [AID588855, Type: confirmatory] | Smad3 [Homo sapiens] [gi:18418623] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.3162 [uM] | | BioAssay | qHTS for Inhibitors of TGF-b | | AID | 588855 | | BioAssay type | confirmatory | | Target | Smad3 [Homo sapiens] [gi:18418623] | | PubMed | | | Data Table |  |
|
| 18 | [SID26666751] | Active | AC50 | 0.344 | CEM21 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7013-03_Inhibitor_Dose_CherryPick_Activity [AID652042, Type: confirmatory] | |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | AC50 | 0.344 [uM] | | BioAssay | CEM21 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7013-03_Inhibitor_Dose_CherryPick_Activity | | AID | 652042 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 19 | [SID26666751] | Active | Potency | 0.4108 | qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 [AID504467, Type: confirmatory] | ATAD5 protein [Homo sapiens] [gi:116283940] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 0.4108 [uM] | | BioAssay | qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 | | AID | 504467 | | BioAssay type | confirmatory | | Target | ATAD5 protein [Homo sapiens] [gi:116283940] | | PubMed | | | Data Table |  |
|
| 20 | [SID26666751] | Active | IC50 | 0.42 | 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. | 20 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | IC50 | 0.42 [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 |  |
|
| 21 | [SID26666751] | Active | IC50 | 0.42 | 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. | 21 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | IC50 | 0.42 [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 |  |
|
| 22 | [SID26666751] | Active | Potency | 1.2995 | 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. | 22 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 1.2995 [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 |  |
|
| 23 | [SID26666751] | Active | Potency | 1.3115 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 1.3115 [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 |  |
|
| 24 | [SID26666751] | Active | IC50 | 1.96 | 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. | 24 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | IC50 | 1.96 [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 |  |
|
| 25 | [SID26666751] | Active | IC50 | 1.96 | 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. | 25 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | IC50 | 1.96 [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 |  |
|
| 26 | [SID26666751] | Active | Potency | 1.9893 | qHTS screen for small molecules that inhibit ELG1-dependent DNA repair: Hit Confirmation with MMS Viability [AID624251, Type: confirmatory] | ATAD5 protein [Homo sapiens] [gi:116283940] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 1.9893 [uM] | | BioAssay | qHTS screen for small molecules that inhibit ELG1-dependent DNA repair: Hit Confirmation with MMS Viability | | AID | 624251 | | BioAssay type | confirmatory | | Target | ATAD5 protein [Homo sapiens] [gi:116283940] | | PubMed | | | Data Table |  |
|
| 27 | [SID26666751] | Active | Potency | 2.5119 | 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. | 27 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 2.5119 [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 |  |
|
| 28 | [SID26666751] | Active | Potency | 2.8184 | qHTS Multiplex Assay to Identify Dual Action Probes in a Cell Model of Huntington: Aggregate Formation (GFP) [AID1688, Type: confirmatory] | huntingtin [Homo sapiens] [gi:90903231] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 2.8184 [uM] | | BioAssay | qHTS Multiplex Assay to Identify Dual Action Probes in a Cell Model of Huntington: Aggregate Formation (GFP) | | AID | 1688 | | BioAssay type | confirmatory | | Target | huntingtin [Homo sapiens] [gi:90903231] | | PubMed | | | Data Table |  |
|
| 29 | [SID26666751] | Active | Potency | 2.8184 | qHTS Multiplex Assay to Identify Dual Action Probes in a Cell Model of Huntington: Aggregate Formation (GFP) [AID1688, Type: confirmatory] | huntingtin [Homo sapiens] [gi:90903231] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 2.8184 [uM] | | BioAssay | qHTS Multiplex Assay to Identify Dual Action Probes in a Cell Model of Huntington: Aggregate Formation (GFP) | | AID | 1688 | | BioAssay type | confirmatory | | Target | huntingtin [Homo sapiens] [gi:90903231] | | PubMed | | | Data Table |  |
|
| 30 | [SID26666751] | Active | EC50 | 3.477 | Luminescence Cell-Free Homogenous Dose Retest to Identify Inhibitors of Serine/Threonine Kinase 33 Activity [AID2821, Type: confirmatory] | serine/threonine-protein kinase 33 [Homo sapiens] [gi:23943882] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | EC50 | 3.477 [uM] | | BioAssay | Luminescence Cell-Free Homogenous Dose Retest to Identify Inhibitors of Serine/Threonine Kinase 33 Activity | | AID | 2821 | | BioAssay type | confirmatory | | Target | serine/threonine-protein kinase 33 [Homo sapiens] [gi:23943882] | | PubMed | | | Data Table |  |
|
| 31 | [SID26666751] | Active | EC50 | 3.477 | Luminescence Cell-Free Homogenous Dose Retest to Identify Inhibitors of Serine/Threonine Kinase 33 Activity [AID2821, Type: confirmatory] | serine/threonine-protein kinase 33 [Homo sapiens] [gi:23943882] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | EC50 | 3.477 [uM] | | BioAssay | Luminescence Cell-Free Homogenous Dose Retest to Identify Inhibitors of Serine/Threonine Kinase 33 Activity | | AID | 2821 | | BioAssay type | confirmatory | | Target | serine/threonine-protein kinase 33 [Homo sapiens] [gi:23943882] | | PubMed | | | Data Table |  |
|
| 32 | [SID26666751] | Active | EC50 | 3.477 | Luminescence Cell-Free Homogenous Dose Retest to Identify Inhibitors of Serine/Threonine Kinase 33 Activity [AID2821, Type: confirmatory] | serine/threonine-protein kinase 33 [Homo sapiens] [gi:23943882] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | EC50 | 3.477 [uM] | | BioAssay | Luminescence Cell-Free Homogenous Dose Retest to Identify Inhibitors of Serine/Threonine Kinase 33 Activity | | AID | 2821 | | BioAssay type | confirmatory | | Target | serine/threonine-protein kinase 33 [Homo sapiens] [gi:23943882] | | PubMed | | | Data Table |  |
|
| 33 | [SID26666751] | Active | Potency | 4.1475 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 4.1475 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation | | AID | 504834 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 34 | [SID26666751] | Active | Potency | 7.0795 | qHTS for inhibitors of ROR gamma transcriptional activity [AID2551, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 7.0795 [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 |  |
|
| 35 | [SID26666751] | Active | Potency | 7.9433 | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 7.9433 [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 |  |
|
| 36 | [SID26666751] | Active | Potency | 7.9433 | 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. | 36 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 7.9433 [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 |  |
|
| 37 | [SID26666751] | Active | Potency | 7.9433 | 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. | 37 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 7.9433 [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 |  |
|
| 38 | [SID26666751] | Active | Potency | 10 | 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. | 38 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 10 [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 |  |
|
| 39 | [SID26666751] | Active | EC50 | 11.99 | Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Synthase Kinase-3 beta Activity [AID434954, Type: confirmatory] | GSK3B gene product [Homo sapiens] [gi:21361340] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | EC50 | 11.99 [uM] | | BioAssay | Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Synthase Kinase-3 beta Activity | | AID | 434954 | | BioAssay type | confirmatory | | Target | GSK3B gene product [Homo sapiens] [gi:21361340] | | PubMed | | | Data Table |  |
|
| 40 | [SID26666751] | Active | EC50 | 11.99 | Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Synthase Kinase-3 beta Activity [AID434954, Type: confirmatory] | GSK3B gene product [Homo sapiens] [gi:21361340] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | EC50 | 11.99 [uM] | | BioAssay | Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Synthase Kinase-3 beta Activity | | AID | 434954 | | BioAssay type | confirmatory | | Target | GSK3B gene product [Homo sapiens] [gi:21361340] | | PubMed | | | Data Table |  |
|
| 41 | [SID26666751] | Active | EC50 | 11.99 | Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Synthase Kinase-3 beta Activity [AID434954, Type: confirmatory] | GSK3B gene product [Homo sapiens] [gi:21361340] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | EC50 | 11.99 [uM] | | BioAssay | Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Synthase Kinase-3 beta Activity | | AID | 434954 | | BioAssay type | confirmatory | | Target | GSK3B gene product [Homo sapiens] [gi:21361340] | | PubMed | | | Data Table |  |
|
| 42 | [SID26666751] | Active | Potency | 14.0919 | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia [AID2451, Type: confirmatory] | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | Potency | 14.0919 [uM] | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia | | AID | 2451 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] | | PubMed | | | Data Table |  |
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| 43 | [SID26666751] | Active | EC50 | 145.9 | 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. | 43 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | EC50 | 145.9 [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 |  |
|
| 44 | [SID26666751] | Active | EC50 | 145.9 | 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. | 44 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | EC50 | 145.9 [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 |  |
|
| 45 | [SID26666751] | Active | EC50 | 145.9 | 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. | 45 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | EC50 | 145.9 [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 |  |
|
| 46 | [SID26666751] | Active | EC50 | 145.9 | 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. | 46 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | EC50 | 145.9 [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 |  |
|
| 47 | [SID26666751] | Active | AC50 | 287.1 | 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. | 47 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | AC50 | 287.1 [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 |  |
|
| 48 | [SID26666751] | Active | AC50 | 287.1 | 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. | 48 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | AC50 | 287.1 [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 |  |
|
| 49 | [SID26666751] | Active | AC50 | 287.1 | 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. | 49 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | AC50 | 287.1 [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 |  |
|
| 50 | [SID26666751] | Active | AC50 | 287.1 | 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. | 50 | | Structure |
| | Substance | | | SID | 26666751 | | CID | 3580213 | | Outcome | Active | | AC50 | 287.1 [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 |  |
|