| 1 | [SID22400692] | Active | EC50 | 0.796 | Fluorescence Cell-Based Secondary Assay to Identify Inhibitors of Resistant C. albicans Growth in the Presence of Fluconazole [AID2423, Type: confirmatory] | heat shock protein 90 [Candida albicans] [gi:994798] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | EC50 | 0.796 [uM] | | BioAssay | Fluorescence Cell-Based Secondary Assay to Identify Inhibitors of Resistant C. albicans Growth in the Presence of Fluconazole | | AID | 2423 | | BioAssay type | confirmatory | | Target | heat shock protein 90 [Candida albicans] [gi:994798] | | PubMed | | | Data Table |  |
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| 2 | [SID22400692] | Active | EC50 | 2.154 | Fluorescence Cell-Based Retest of C. albicans Growth in the Presence of Fluconazole [AID2467, Type: confirmatory] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | EC50 | 2.154 [uM] | | BioAssay | Fluorescence Cell-Based Retest of C. albicans Growth in the Presence of Fluconazole | | AID | 2467 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 3 | [SID22400692] | Active | Potency | 5.0119 | 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 | 22400692 | | CID | 1725587 | | Outcome | Active | | Potency | 5.0119 [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 |  |
|
| 4 | [SID22400692] | Active | Potency | 5.0119 | 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 | 22400692 | | CID | 1725587 | | Outcome | Active | | Potency | 5.0119 [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 |  |
|
| 5 | [SID22400692] | Active | Potency | 5.0119 | 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. | 5 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | Potency | 5.0119 [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 |  |
|
| 6 | [SID22400692] | Active | Potency | 5.8048 | 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. | 6 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | Potency | 5.8048 [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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| 7 | [SID22400692] | Active | Potency | 5.8048 | A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. [AID624297, Type: confirmatory] | GMNN gene product [Homo sapiens] [gi:7705682] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | Potency | 5.8048 [uM] | | BioAssay | A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. | | AID | 624297 | | BioAssay type | confirmatory | | Target | GMNN gene product [Homo sapiens] [gi:7705682] | | PubMed | | | Data Table |  |
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| 8 | [SID22400692] | Active | Potency | 7.0795 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | Potency | 7.0795 [uM] | | BioAssay | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins | | AID | 485364 | | BioAssay type | confirmatory | | Target | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] | | PubMed | | | Data Table |  |
|
| 9 | [SID22400692] | 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. | 9 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | 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 |  |
|
| 10 | [SID22400692] | Active | Potency | 7.9433 | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 11 | [SID22400692] | Active | Potency | 7.9433 | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 12 | [SID22400692] | Active | EC50 | 20.015 | Fluorescence Cell-Based Secondary Assay for toxicity in mammalian fibroblasts [AID2327, Type: confirmatory] | |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | EC50 | 20.015 [uM] | | BioAssay | Fluorescence Cell-Based Secondary Assay for toxicity in mammalian fibroblasts | | AID | 2327 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 13 | [SID22400692] | Active | Potency | 31.6228 | 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. | 13 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | Potency | 31.6228 [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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| 14 | [SID22400692] | Active | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Beta Cell Apoptosis. [AID435005, Type: screening] | |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Beta Cell Apoptosis. | | AID | 435005 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 15 | [SID22400692] | Active | | | Counterscreen for inhibitors of Janus kinase 2 mutant JAK2V617F: Cell-based high throughput assay to identify inhibitors of parental Ba/F3 cell viability. [AID1486, Type: screening] | |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of Janus kinase 2 mutant JAK2V617F: Cell-based high throughput assay to identify inhibitors of parental Ba/F3 cell viability. | | AID | 1486 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 16 | [SID22400692] | Active | | | Luminescence-based counterscreen assay for KLF5 inhibitors: cell-based high throughput screening assay to identify cytotoxic compounds using the IEC-6 intestinal epithelial cell line. [AID1825, Type: screening] | |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Luminescence-based counterscreen assay for KLF5 inhibitors: cell-based high throughput screening assay to identify cytotoxic compounds using the IEC-6 intestinal epithelial cell line. | | AID | 1825 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 17 | [SID22400692] | Active | | | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F [AID1446, Type: screening] | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | | AID | 1446 | | BioAssay type | screening | | Target | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] | | PubMed | | | Data Table |  |
|
| 18 | [SID22400692] | Active | | | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F [AID1446, Type: screening] | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | | AID | 1446 | | BioAssay type | screening | | Target | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] | | PubMed | | | Data Table |  |
|
| 19 | [SID22400692] | Active | | | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F [AID1446, Type: screening] | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Primary cell-based high throughput assay for inhibitors of the Janus kinase 2 mutant JAK2V617F | | AID | 1446 | | BioAssay type | screening | | Target | Janus kinase 2 (a protein tyrosine kinase) [Homo sapiens] [gi:119579178] | | PubMed | | | Data Table |  |
|
| 20 | [SID22400692] | Active | | | Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation [AID1285, Type: screening] | amyloid precursor protein; APP [Homo sapiens] [gi:257380] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | | AID | 1285 | | BioAssay type | screening | | Target | amyloid precursor protein; APP [Homo sapiens] [gi:257380] | | PubMed | | | Data Table |  |
|
| 21 | [SID22400692] | Active | | | Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation [AID1285, Type: screening] | amyloid precursor protein; APP [Homo sapiens] [gi:257380] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | | AID | 1285 | | BioAssay type | screening | | Target | amyloid precursor protein; APP [Homo sapiens] [gi:257380] | | PubMed | | | Data Table |  |
|
| 22 | [SID22400692] | Active | | | Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation [AID1285, Type: screening] | amyloid precursor protein; APP [Homo sapiens] [gi:257380] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Primary screen for compounds that inhibit Alzheimer's amyloid precursor protein (APP) translation | | AID | 1285 | | BioAssay type | screening | | Target | amyloid precursor protein; APP [Homo sapiens] [gi:257380] | | PubMed | | | Data Table |  |
|
| 23 | [SID22400692] | Active | | | High throughput discovery of novel modulators of ROMK K+ channel activity: Primary Screen [AID1918, Type: screening] | Potassium inwardly-rectifying channel, subfamily J, member 1 [Homo sapiens] [gi:223460826] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | High throughput discovery of novel modulators of ROMK K+ channel activity: Primary Screen | | AID | 1918 | | BioAssay type | screening | | Target | Potassium inwardly-rectifying channel, subfamily J, member 1 [Homo sapiens] [gi:223460826] | | PubMed | | | Data Table |  |
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| 24 | [SID22400692] | Active | | | HTS for small molecule inhibitors of CHOP to regulate the unfolded protein response to ER stress [AID2732, Type: screening] | Ddit3 gene product [Mus musculus] [gi:160707929] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | HTS for small molecule inhibitors of CHOP to regulate the unfolded protein response to ER stress | | AID | 2732 | | BioAssay type | screening | | Target | Ddit3 gene product [Mus musculus] [gi:160707929] | | PubMed | | | Data Table |  |
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| 25 | [SID22400692] | Active | | | Primary cell-based high-throughput screening assay to identify antagonists of Galanin Receptor 2 (GALR2) [AID828, Type: screening] | Galanin receptor type 2 [gi:6016094] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening assay to identify antagonists of Galanin Receptor 2 (GALR2) | | AID | 828 | | BioAssay type | screening | | Target | Galanin receptor type 2 [gi:6016094] | | PubMed | | | Data Table |  |
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| 26 | [SID22400692] | Active | | | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling [AID588676, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling | | AID | 588676 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
|
| 27 | [SID22400692] | Active | | | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling [AID588676, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling | | AID | 588676 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
|
| 28 | [SID22400692] | Active | | | Fluorescence polarization-based counterscreen assay for inhibitors of tRNA 2'-phosphotransferase (TPT1): biochemical high throughput screening assay to identify inhibitors of RNAse T1. [AID2153, Type: screening] | unnamed protein product [Aspergillus oryzae] [gi:83774548] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Fluorescence polarization-based counterscreen assay for inhibitors of tRNA 2'-phosphotransferase (TPT1): biochemical high throughput screening assay to identify inhibitors of RNAse T1. | | AID | 2153 | | BioAssay type | screening | | Target | unnamed protein product [Aspergillus oryzae] [gi:83774548] | | PubMed | | | Data Table |  |
|
| 29 | [SID22400692] | Active | | | Fluorescence polarization-based counterscreen assay for inhibitors of tRNA 2'-phosphotransferase (TPT1): biochemical high throughput screening assay to identify inhibitors of RNAse T1. [AID2153, Type: screening] | unnamed protein product [Aspergillus oryzae] [gi:83774548] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Fluorescence polarization-based counterscreen assay for inhibitors of tRNA 2'-phosphotransferase (TPT1): biochemical high throughput screening assay to identify inhibitors of RNAse T1. | | AID | 2153 | | BioAssay type | screening | | Target | unnamed protein product [Aspergillus oryzae] [gi:83774548] | | PubMed | | | Data Table |  |
|
| 30 | [SID22400692] | Active | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of tRNA 2'-phosphotransferase (TPT1). [AID1962, Type: screening] | likely tRNA 2'-phosphotransferase [Candida albicans SC5314] [gi:68476498] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of tRNA 2'-phosphotransferase (TPT1). | | AID | 1962 | | BioAssay type | screening | | Target | likely tRNA 2'-phosphotransferase [Candida albicans SC5314] [gi:68476498] | | PubMed | | | Data Table |  |
|
| 31 | [SID22400692] | Active | | | Fluorescence polarization-based biochemical high throughput confirmation assay to identify inhibitors of tRNA 2'-phosphotransferase (TPT1). [AID2149, Type: screening] | likely tRNA 2'-phosphotransferase [Candida albicans SC5314] [gi:68476498] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Active | | BioAssay | Fluorescence polarization-based biochemical high throughput confirmation assay to identify inhibitors of tRNA 2'-phosphotransferase (TPT1). | | AID | 2149 | | BioAssay type | screening | | Target | likely tRNA 2'-phosphotransferase [Candida albicans SC5314] [gi:68476498] | | PubMed | | | Data Table |  |
|
| 32 | [SID22400692] | Inactive | Potency | 7.0795 | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase [AID1634, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | Potency | 7.0795 [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1634 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
|
| 33 | [SID22400692] | Inactive | Potency | 7.0795 | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase [AID1634, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | Potency | 7.0795 [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1634 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
|
| 34 | [SID22400692] | Inactive | Potency | 7.0795 | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase [AID1634, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | Potency | 7.0795 [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1634 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
|
| 35 | [SID22400692] | Inactive | Potency | 7.9433 | qHTS Fluorescence Polarization Assay for Inhibitors of MLL CXXC domain - DNA interaction [AID2662, Type: confirmatory] | MLL gene product [Homo sapiens] [gi:56550039] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | Potency | 7.9433 [uM] | | BioAssay | qHTS Fluorescence Polarization Assay for Inhibitors of MLL CXXC domain - DNA interaction | | AID | 2662 | | BioAssay type | confirmatory | | Target | MLL gene product [Homo sapiens] [gi:56550039] | | PubMed | | | Data Table |  |
|
| 36 | [SID22400692] | Inactive | Potency | 19.9526 | qHTS Assay for Inhibitors of MBNL1-poly(CUG) RNA binding [AID2675, Type: confirmatory] | muscleblind-like protein 1 isoform a [Homo sapiens] [gi:41281591] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Inhibitors of MBNL1-poly(CUG) RNA binding | | AID | 2675 | | BioAssay type | confirmatory | | Target | muscleblind-like protein 1 isoform a [Homo sapiens] [gi:41281591] | | PubMed | | | Data Table |  |
|
| 37 | [SID22400692] | Inactive | Potency | 28.1838 | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium [AID1457, Type: confirmatory] | Inositol monophosphatase [gi:44888968] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | Potency | 28.1838 [uM] | | BioAssay | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | | AID | 1457 | | BioAssay type | confirmatory | | Target | Inositol monophosphatase [gi:44888968] | | PubMed | | | Data Table |  |
|
| 38 | [SID22400692] | Inactive | Potency | 28.1838 | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium [AID1457, Type: confirmatory] | Inositol monophosphatase [gi:44888968] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | Potency | 28.1838 [uM] | | BioAssay | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | | AID | 1457 | | BioAssay type | confirmatory | | Target | Inositol monophosphatase [gi:44888968] | | PubMed | | | Data Table |  |
|
| 39 | [SID22400692] | Inactive | AC50 | 120 | Luminescence Cell-Based Counter Screen to Identify Inhibitors of Cytokine Induced Apoptosis [AID463206, Type: confirmatory] | |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | AC50 | 120 [uM] | | BioAssay | Luminescence Cell-Based Counter Screen to Identify Inhibitors of Cytokine Induced Apoptosis | | AID | 463206 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 40 | [SID22400692] | Inactive | AC50 | 260 | Luminescence Cell-Based Dose Retest to Confirm Inhibitors of Beta Cell Apoptosis [AID449756, Type: confirmatory] | |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | AC50 | 260 [uM] | | BioAssay | Luminescence Cell-Based Dose Retest to Confirm Inhibitors of Beta Cell Apoptosis | | AID | 449756 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 41 | [SID22400692] | Inactive | IC50 | | High Throughput Screening Assay used to Identify Novel Compounds that Inhibit Mycobacterium Tuberculosis in 7H9 Media [AID449762, Type: confirmatory] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | High Throughput Screening Assay used to Identify Novel Compounds that Inhibit Mycobacterium Tuberculosis in 7H9 Media | | AID | 449762 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 42 | [SID22400692] | Inactive | | | uHTS identification of small molecule activators of the apoptotic arm of the Unfolded Protein response via a luminescent-based reporter assay [AID449763, Type: screening] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule activators of the apoptotic arm of the Unfolded Protein response via a luminescent-based reporter assay | | AID | 449763 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 43 | [SID22400692] | Inactive | | | uHTS identification of small molecule activators of the adaptive arm of the Unfolded Protein response via a luminescent-based reporter assay [AID463104, Type: screening] | |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule activators of the adaptive arm of the Unfolded Protein response via a luminescent-based reporter assay | | AID | 463104 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 44 | [SID22400692] | Inactive | | | 384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC [AID463187, Type: screening] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | 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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| 45 | [SID22400692] | Inactive | | | uHTS luminescence assay for the identification of chemical inhibitors of B-cell specific antigen receptor-induced NF-kB activation [AID435022, Type: screening] | |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | BioAssay | uHTS luminescence assay for the identification of chemical inhibitors of B-cell specific antigen receptor-induced NF-kB activation | | AID | 435022 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 46 | [SID22400692] | Inactive | | | Counterscreen for inhibitors of AddAB: absorbance-based bacterial cell-based high throughput screening assay to identify inhibitors of bacterial viability [AID449728, Type: screening] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | BioAssay | Counterscreen for inhibitors of AddAB: absorbance-based bacterial cell-based high throughput screening assay to identify inhibitors of bacterial viability | | AID | 449728 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 47 | [SID22400692] | Inactive | | | Heat Shock Factor-1 (HSF-1) Measured in Cell-Based System Using Plate Reader - 2038-01_Activator_SinglePoint_HTS_Activity [AID504408, Type: screening] | |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | BioAssay | Heat Shock Factor-1 (HSF-1) Measured in Cell-Based System Using Plate Reader - 2038-01_Activator_SinglePoint_HTS_Activity | | AID | 504408 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 48 | [SID22400692] | Inactive | | | Fluorescence Cell-Based Primary HTS of C.albicans growth in the presence of Fluconazole and compound [AID1979, Type: screening] | heat shock protein 90 [Candida albicans] [gi:994798] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | BioAssay | Fluorescence Cell-Based Primary HTS of C.albicans growth in the presence of Fluconazole and compound | | AID | 1979 | | BioAssay type | screening | | Target | heat shock protein 90 [Candida albicans] [gi:994798] | | PubMed | | | Data Table |  |
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| 49 | [SID22400692] | Inactive | | | Counterscreen for PME1 inhibitors: fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of lysophospholipase 2 (LYPLA2). [AID2177, Type: screening] | lysophospholipase II [Homo sapiens] [gi:4581413] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | BioAssay | Counterscreen for PME1 inhibitors: fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of lysophospholipase 2 (LYPLA2). | | AID | 2177 | | BioAssay type | screening | | Target | lysophospholipase II [Homo sapiens] [gi:4581413] | | PubMed | | | Data Table |  |
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| 50 | [SID22400692] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 2 (SRC2; NCOA2) [AID651957, Type: screening] | NCOA2 gene product [Homo sapiens] [gi:5729858] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 22400692 | | CID | 1725587 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 2 (SRC2; NCOA2) | | AID | 651957 | | BioAssay type | screening | | Target | NCOA2 gene product [Homo sapiens] [gi:5729858] | | PubMed | | | Data Table |  |
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