| 1 | [SID4242219] | Active | Potency | 5.6234 | 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. | 1 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | Potency | 5.6234 [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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| 2 | [SID4242219] | Active | Potency | 11.6891 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | Potency | 11.6891 [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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| 3 | [SID4242219] | Active | Potency | 12.5893 | 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. | 3 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | Potency | 12.5893 [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 |  |
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| 4 | [SID4242219] | Active | Potency | 12.5893 | 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. | 4 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | Potency | 12.5893 [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 |  |
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| 5 | [SID4242219] | Active | Potency | 14.581 | 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. | 5 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | Potency | 14.581 [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 |  |
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| 6 | [SID4242219] | Active | Potency | 25.1189 | 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. | 6 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | Potency | 25.1189 [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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| 7 | [SID4242219] | Active | Potency | 50.1187 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | Potency | 50.1187 [uM] | | BioAssay | qHTS Assay for Inhibitors of BAZ2B | | AID | 504333 | | BioAssay type | confirmatory | | Target | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] | | PubMed | | | Data Table |  |
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| 8 | [SID4242219] | Active | | | Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators [AID449, Type: screening] | S1PR1 gene product [Homo sapiens] [gi:13027636] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators | | AID | 449 | | BioAssay type | screening | | Target | S1PR1 gene product [Homo sapiens] [gi:13027636] | | PubMed | | | Data Table |  |
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| 9 | [SID4242219] | Active | | | Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators [AID449, Type: screening] | S1PR1 gene product [Homo sapiens] [gi:13027636] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | Primary HTS and Confirmation Assays for S1P1 Agonists and Agonism Potentiators | | AID | 449 | | BioAssay type | screening | | Target | S1PR1 gene product [Homo sapiens] [gi:13027636] | | PubMed | | | Data Table |  |
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| 10 | [SID4242219] | Active | | | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) [AID525, Type: screening] | NR5A1 gene product [Homo sapiens] [gi:20070193] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | | AID | 525 | | BioAssay type | screening | | Target | NR5A1 gene product [Homo sapiens] [gi:20070193] | | PubMed | | | Data Table |  |
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| 11 | [SID4242219] | Active | | | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) [AID525, Type: screening] | NR5A1 gene product [Homo sapiens] [gi:20070193] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | | AID | 525 | | BioAssay type | screening | | Target | NR5A1 gene product [Homo sapiens] [gi:20070193] | | PubMed | | | Data Table |  |
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| 12 | [SID4242219] | Active | | | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) [AID525, Type: screening] | NR5A1 gene product [Homo sapiens] [gi:20070193] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | Primary Cell-based High Throughput Screening assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | | AID | 525 | | BioAssay type | screening | | Target | NR5A1 gene product [Homo sapiens] [gi:20070193] | | PubMed | | | Data Table |  |
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| 13 | [SID4242219] | 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. | 13 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | 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 |  |
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| 14 | [SID4242219] | 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. | 14 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | 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 |  |
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| 15 | [SID4242219] | Active | | | Primary cell-based high throughput screening assay to measure STAT3 inhibition [AID862, Type: screening] | STAT3 [Homo sapiens] [gi:13272532] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | Primary cell-based high throughput screening assay to measure STAT3 inhibition | | AID | 862 | | BioAssay type | screening | | Target | STAT3 [Homo sapiens] [gi:13272532] | | PubMed | | | Data Table |  |
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| 16 | [SID4242219] | Active | | | Primary cell-based high throughput screening assay to measure STAT3 inhibition [AID862, Type: screening] | STAT3 [Homo sapiens] [gi:13272532] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | Primary cell-based high throughput screening assay to measure STAT3 inhibition | | AID | 862 | | BioAssay type | screening | | Target | STAT3 [Homo sapiens] [gi:13272532] | | PubMed | | | Data Table |  |
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| 17 | [SID4242219] | Active | | | Primary cell-based high throughput screening assay to measure STAT3 inhibition [AID862, Type: screening] | STAT3 [Homo sapiens] [gi:13272532] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | Primary cell-based high throughput screening assay to measure STAT3 inhibition | | AID | 862 | | BioAssay type | screening | | Target | STAT3 [Homo sapiens] [gi:13272532] | | PubMed | | | Data Table |  |
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| 18 | [SID4242219] | Active | | | High Content Assay for Compounds that inhibit the Assembly of the Perinucleolar Compartment [AID2417, Type: screening] | polypyrimidine tract-binding protein 1 isoform a [Homo sapiens] [gi:4506243] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | High Content Assay for Compounds that inhibit the Assembly of the Perinucleolar Compartment | | AID | 2417 | | BioAssay type | screening | | Target | polypyrimidine tract-binding protein 1 isoform a [Homo sapiens] [gi:4506243] | | PubMed | | | Data Table |  |
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| 19 | [SID4242219] | Active | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype [AID1529, Type: screening] | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype | | AID | 1529 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] | | PubMed | | | Data Table |  |
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| 20 | [SID4242219] | Active | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype [AID1529, Type: screening] | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype | | AID | 1529 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] | | PubMed | | | Data Table |  |
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| 21 | [SID4242219] | Active | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype [AID1529, Type: screening] | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Active | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype | | AID | 1529 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] | | PubMed | | | Data Table |  |
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| 22 | [SID4242219] | Inactive | Potency | 5.6234 | qHTS Assay for Enhancers of SMN2 Splice Variant Expression [AID1458, Type: confirmatory] | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | 5.6234 [uM] | | BioAssay | qHTS Assay for Enhancers of SMN2 Splice Variant Expression | | AID | 1458 | | BioAssay type | confirmatory | | Target | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] | | PubMed | | | Data Table |  |
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| 23 | [SID4242219] | Inactive | Potency | 5.6234 | qHTS Assay for Enhancers of SMN2 Splice Variant Expression [AID1458, Type: confirmatory] | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | 5.6234 [uM] | | BioAssay | qHTS Assay for Enhancers of SMN2 Splice Variant Expression | | AID | 1458 | | BioAssay type | confirmatory | | Target | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] | | PubMed | | | Data Table |  |
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| 24 | [SID4242219] | Inactive | Potency | 10 | qHTS Assay for Inhibitors of Influenza NS1 Protein Function [AID2326, Type: confirmatory] | nonstructural protein 1 [Influenza A virus (A/WSN/1933(H1N1))] [gi:194352380] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Inhibitors of Influenza NS1 Protein Function | | AID | 2326 | | BioAssay type | confirmatory | | Target | nonstructural protein 1 [Influenza A virus (A/WSN/1933(H1N1))] [gi:194352380] | | PubMed | | | Data Table |  |
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| 25 | [SID4242219] | Inactive | Potency | 28.1838 | qHTS Inhibitors of AmpC Beta-Lactamase (assay without detergent) [AID485341, Type: confirmatory] | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | 28.1838 [uM] | | BioAssay | qHTS Inhibitors of AmpC Beta-Lactamase (assay without detergent) | | AID | 485341 | | BioAssay type | confirmatory | | Target | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] | | PubMed | | | Data Table |  |
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| 26 | [SID4242219] | Inactive | Potency | | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [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 |  |
|
| 27 | [SID4242219] | Inactive | | | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the SARS coronavirus 3C-like Protease (3CLPro) [AID1706, Type: screening] | 3C-like protease [Infectious bronchitis virus] [gi:73745819] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the SARS coronavirus 3C-like Protease (3CLPro) | | AID | 1706 | | BioAssay type | screening | | Target | 3C-like protease [Infectious bronchitis virus] [gi:73745819] | | PubMed | | | Data Table |  |
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| 28 | [SID4242219] | Inactive | | | Mycobacterium tuberculosis Pantothenate Synthetase Assay [AID375, Type: confirmatory] | Chain A, Crystal Structure Of A Pantothenate Synthetase, Apo Enzyme In C2 Space Group [gi:90108679] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | Mycobacterium tuberculosis Pantothenate Synthetase Assay | | AID | 375 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of A Pantothenate Synthetase, Apo Enzyme In C2 Space Group [gi:90108679] | | PubMed | | | Data Table |  |
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| 29 | [SID4242219] | Inactive | | | qHTS Assay for Inhibitors of YjeE [AID605, Type: confirmatory] | UPF0079 ATP-binding protein yjeE [gi:84028058] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | qHTS Assay for Inhibitors of YjeE | | AID | 605 | | BioAssay type | confirmatory | | Target | UPF0079 ATP-binding protein yjeE [gi:84028058] | | PubMed | | | Data Table |  |
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| 30 | [SID4242219] | Inactive | | | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay with detergent) [AID584, Type: confirmatory] | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay with detergent) | | AID | 584 | | BioAssay type | confirmatory | | Target | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] | | PubMed | | | Data Table |  |
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| 31 | [SID4242219] | Inactive | | | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay without detergent) [AID585, Type: confirmatory] | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay without detergent) | | AID | 585 | | BioAssay type | confirmatory | | Target | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] | | PubMed | | | Data Table |  |
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| 32 | [SID4242219] | Inactive | | | 384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC [AID463187, Type: screening] | |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | 384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC | | AID | 463187 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 33 | [SID4242219] | Inactive | | | HTS to identify inhibitors of TNF-alpha Induced Cell Death in Jurkat FADD-/- Cells. [AID463075, Type: screening] | |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | HTS to identify inhibitors of TNF-alpha Induced Cell Death in Jurkat FADD-/- Cells. | | AID | 463075 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 34 | [SID4242219] | Inactive | Potency | | qHTS Assay for Small Molecule Inhibitors of Mitochondrial Division or Activators of Mitochondrial Fusion [AID485298, Type: confirmatory] | |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of Mitochondrial Division or Activators of Mitochondrial Fusion | | AID | 485298 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 35 | [SID4242219] | Inactive | Potency | | qHTS Assay to Find Inhibitors of Chronic Active B-Cell Receptor Signaling [AID493014, Type: confirmatory] | |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay to Find Inhibitors of Chronic Active B-Cell Receptor Signaling | | AID | 493014 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 36 | [SID4242219] | Inactive | | | RNA polymerase [AID559, Type: screening] | RNA polymerase beta subunit (EC 2.7.7.6) [gi:147728] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | RNA polymerase | | AID | 559 | | BioAssay type | screening | | Target | RNA polymerase beta subunit (EC 2.7.7.6) [gi:147728] | | PubMed | | | Data Table |  |
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| 37 | [SID4242219] | Inactive | | | Counter Screen for Glucose-6-Phosphate Dehydrogenase-based Primary Assay [AID1020, Type: screening] | glucose-6-phosphate dehydrogenase [Leuconostoc mesenteroides] [gi:149631] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | Counter Screen for Glucose-6-Phosphate Dehydrogenase-based Primary Assay | | AID | 1020 | | BioAssay type | screening | | Target | glucose-6-phosphate dehydrogenase [Leuconostoc mesenteroides] [gi:149631] | | PubMed | | | Data Table |  |
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| 38 | [SID4242219] | Inactive | Potency | | qHTS Assay for Inhibitors of Firefly Luciferase [AID411, Type: confirmatory] | Luciferase [Photinus pyralis] [gi:160794] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Firefly Luciferase | | AID | 411 | | BioAssay type | confirmatory | | Target | Luciferase [Photinus pyralis] [gi:160794] | | PubMed | | | Data Table |  |
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| 39 | [SID4242219] | Inactive | Potency | | qHTS profiling assay for firefly luciferase inhibitor/activator using purifed enzyme and Km concentrations of substrates (counterscreen for miR-21 project) [AID588342, Type: confirmatory] | Luciferase [Photinus pyralis] [gi:160794] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS profiling assay for firefly luciferase inhibitor/activator using purifed enzyme and Km concentrations of substrates (counterscreen for miR-21 project) | | AID | 588342 | | BioAssay type | confirmatory | | Target | Luciferase [Photinus pyralis] [gi:160794] | | PubMed | | | Data Table |  |
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| 40 | [SID4242219] | Inactive | | | Pyruvate Kinase [AID361, Type: confirmatory] | pyruvate kinase [Geobacillus stearothermophilus] [gi:285623] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | Pyruvate Kinase | | AID | 361 | | BioAssay type | confirmatory | | Target | pyruvate kinase [Geobacillus stearothermophilus] [gi:285623] | | PubMed | | | Data Table |  |
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| 41 | [SID4242219] | Inactive | Potency | | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Red Fluorophore) [AID892, Type: confirmatory] | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Red Fluorophore) | | AID | 892 | | BioAssay type | confirmatory | | Target | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] | | PubMed | | | Data Table |  |
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| 42 | [SID4242219] | Inactive | Potency | | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Green Fluorophore) [AID875, Type: confirmatory] | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Green Fluorophore) | | AID | 875 | | BioAssay type | confirmatory | | Target | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] | | PubMed | | | Data Table |  |
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| 43 | [SID4242219] | Inactive | Potency | | qHTS Assay for Inhibitors of Human Jumonji Domain Containing 2E (JMJD2E) [AID2147, Type: confirmatory] | Chain A, Crystal Structure Of The Human 2-Oxoglutarate Oxygenase Loc390245 [gi:221046486] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Jumonji Domain Containing 2E (JMJD2E) | | AID | 2147 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of The Human 2-Oxoglutarate Oxygenase Loc390245 [gi:221046486] | | PubMed | | | Data Table |  |
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| 44 | [SID4242219] | Inactive | Potency | | 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. | 44 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [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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| 45 | [SID4242219] | Inactive | Potency | | qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) [AID886, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) | | AID | 886 | | BioAssay type | confirmatory | | Target | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] | | PubMed | | | Data Table |  |
|
| 46 | [SID4242219] | Inactive | Potency | | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 [AID893, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 | | AID | 893 | | BioAssay type | confirmatory | | Target | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] | | PubMed | | | Data Table |  |
|
| 47 | [SID4242219] | Inactive | IC50 | | High Throughput Screening Assay for Hsp70 Inhibitors [AID583, Type: confirmatory] | heat shock 70kDa protein 1A [Homo sapiens] [gi:123271505] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | High Throughput Screening Assay for Hsp70 Inhibitors | | AID | 583 | | BioAssay type | confirmatory | | Target | heat shock 70kDa protein 1A [Homo sapiens] [gi:123271505] | | PubMed | | | Data Table |  |
|
| 48 | [SID4242219] | Inactive | | | Fluorescence-based counterscreen assay for HCV NS3 helicase inhibitors: biochemical high-throughput screening assay to identify compounds that cause fluorescent intercalator displacement (FID) [AID1845, Type: screening] | NS3 [Hepatitis C virus] [gi:125541954] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | Fluorescence-based counterscreen assay for HCV NS3 helicase inhibitors: biochemical high-throughput screening assay to identify compounds that cause fluorescent intercalator displacement (FID) | | AID | 1845 | | BioAssay type | screening | | Target | NS3 [Hepatitis C virus] [gi:125541954] | | PubMed | | | Data Table |  |
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| 49 | [SID4242219] | Inactive | | | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of the Hepatitis C Virus non-structural protein 3 helicase (NS3) [AID1800, Type: screening] | NS3 [Hepatitis C virus] [gi:125541954] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | BioAssay | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of the Hepatitis C Virus non-structural protein 3 helicase (NS3) | | AID | 1800 | | BioAssay type | screening | | Target | NS3 [Hepatitis C virus] [gi:125541954] | | PubMed | | | Data Table |  |
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| 50 | [SID4242219] | Inactive | Potency | | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (with detergent) [AID1478, Type: confirmatory] | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 4242219 | | CID | 6602843 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (with detergent) | | AID | 1478 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] | | PubMed | | | Data Table |  |
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