| 1 | [SID14723648] | Active | Potency | 50.1187 | 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. | 1 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Active | | Potency | 50.1187 [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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| 2 | [SID14723648] | Active | | | Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis: Fluroescence-based biochemical high throughput Glycerophosphate Dehydrogenase-Triosephosphate Isomerase (GDH-TPI) assay to identify assay artifacts [AID652141, Type: screening] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis: Fluroescence-based biochemical high throughput Glycerophosphate Dehydrogenase-Triosephosphate Isomerase (GDH-TPI) assay to identify assay artifacts | | AID | 652141 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 3 | [SID14723648] | Active | | | Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis [AID588726, Type: screening] | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis | | AID | 588726 | | BioAssay type | screening | | Target | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] | | PubMed | | | Data Table |  |
|
| 4 | [SID14723648] | Active | | | Fluorescence-based biochemical high throughput confirmation assay for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis [AID651616, Type: screening] | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical high throughput confirmation assay for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis | | AID | 651616 | | BioAssay type | screening | | Target | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] | | PubMed | | | Data Table |  |
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| 5 | [SID14723648] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
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| 6 | [SID14723648] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
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| 7 | [SID14723648] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
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| 8 | [SID14723648] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
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| 9 | [SID14723648] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
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| 10 | [SID14723648] | Inactive | Potency | 39.8107 | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588456, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588456 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 11 | [SID14723648] | Inactive | Potency | 39.8107 | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588456, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588456 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
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| 12 | [SID14723648] | Inactive | IC50 | 999 | Luminescent assay for HTS discovery of chemical activators of placental alkaline phosphatase [AID696, Type: confirmatory] | alkaline phosphatase, placental-like preproprotein [Homo sapiens] [gi:157266296] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | IC50 | 999 [uM] | | BioAssay | Luminescent assay for HTS discovery of chemical activators of placental alkaline phosphatase | | AID | 696 | | BioAssay type | confirmatory | | Target | alkaline phosphatase, placental-like preproprotein [Homo sapiens] [gi:157266296] | | PubMed | | | Data Table |  |
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| 13 | [SID14723648] | Inactive | IC50 | 999 | Luminescent assay for HTS discovery of chemical activators of placental alkaline phosphatase [AID696, Type: confirmatory] | alkaline phosphatase, placental-like preproprotein [Homo sapiens] [gi:157266296] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | IC50 | 999 [uM] | | BioAssay | Luminescent assay for HTS discovery of chemical activators of placental alkaline phosphatase | | AID | 696 | | BioAssay type | confirmatory | | Target | alkaline phosphatase, placental-like preproprotein [Homo sapiens] [gi:157266296] | | PubMed | | | Data Table |  |
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| 14 | [SID14723648] | Inactive | IC50 | 999 | Luminescent assay for HTS discovery of chemical inhibitors of placental alkaline phosphatase [AID690, Type: confirmatory] | alkaline phosphatase, placental-like preproprotein [Homo sapiens] [gi:157266296] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | IC50 | 999 [uM] | | BioAssay | Luminescent assay for HTS discovery of chemical inhibitors of placental alkaline phosphatase | | AID | 690 | | BioAssay type | confirmatory | | Target | alkaline phosphatase, placental-like preproprotein [Homo sapiens] [gi:157266296] | | PubMed | | | Data Table |  |
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| 15 | [SID14723648] | Inactive | IC50 | 999 | Luminescent assay for HTS discovery of chemical inhibitors of placental alkaline phosphatase [AID690, Type: confirmatory] | alkaline phosphatase, placental-like preproprotein [Homo sapiens] [gi:157266296] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | IC50 | 999 [uM] | | BioAssay | Luminescent assay for HTS discovery of chemical inhibitors of placental alkaline phosphatase | | AID | 690 | | BioAssay type | confirmatory | | Target | alkaline phosphatase, placental-like preproprotein [Homo sapiens] [gi:157266296] | | PubMed | | | Data Table |  |
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| 16 | [SID14723648] | Inactive | | | uHTS Fluorescent assay for identification of inhibitors of Apaf-1 [AID489030, Type: screening] | Apoptotic peptidase activating factor 1 [Homo sapiens] [gi:187952397] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | uHTS Fluorescent assay for identification of inhibitors of Apaf-1 | | AID | 489030 | | BioAssay type | screening | | Target | Apoptotic peptidase activating factor 1 [Homo sapiens] [gi:187952397] | | PubMed | | | Data Table |  |
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| 17 | [SID14723648] | Inactive | | | uHTS Fluorescent assay for identification of activators of Apaf-1 [AID489031, Type: screening] | Apoptotic peptidase activating factor 1 [Homo sapiens] [gi:187952397] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | uHTS Fluorescent assay for identification of activators of Apaf-1 | | AID | 489031 | | BioAssay type | screening | | Target | Apoptotic peptidase activating factor 1 [Homo sapiens] [gi:187952397] | | PubMed | | | Data Table |  |
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| 18 | [SID14723648] | Inactive | | | Primary screen for compounds that activate Alzheimer's amyloid precursor [AID1276, Type: screening] | amyloid precursor protein; APP [Homo sapiens] [gi:257380] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Primary screen for compounds that activate Alzheimer's amyloid precursor | | AID | 1276 | | BioAssay type | screening | | Target | amyloid precursor protein; APP [Homo sapiens] [gi:257380] | | PubMed | | | Data Table |  |
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| 19 | [SID14723648] | Inactive | | | Primary screen for compounds that activate Alzheimer's amyloid precursor [AID1276, Type: screening] | amyloid precursor protein; APP [Homo sapiens] [gi:257380] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Primary screen for compounds that activate Alzheimer's amyloid precursor | | AID | 1276 | | BioAssay type | screening | | Target | amyloid precursor protein; APP [Homo sapiens] [gi:257380] | | PubMed | | | Data Table |  |
|
| 20 | [SID14723648] | Inactive | | | Primary screen for compounds that activate Alzheimer's amyloid precursor [AID1276, Type: screening] | amyloid precursor protein; APP [Homo sapiens] [gi:257380] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Primary screen for compounds that activate Alzheimer's amyloid precursor | | AID | 1276 | | BioAssay type | screening | | Target | amyloid precursor protein; APP [Homo sapiens] [gi:257380] | | PubMed | | | Data Table |  |
|
| 21 | [SID14723648] | Inactive | | | 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 | 14723648 | | CID | 54689176 | | Outcome | Inactive | | 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 |  |
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| 22 | [SID14723648] | Inactive | | | 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 | 14723648 | | CID | 54689176 | | Outcome | Inactive | | 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 | [SID14723648] | Inactive | | | 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. | 23 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | 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 |  |
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| 24 | [SID14723648] | Inactive | | | ARNT-TAC3: AlphaScreen HTS to detect disruption of ARNT/TAC3 interactions Measured in Biochemical System Using Plate Reader - 2158-01_Inhibitor_SinglePoint_HTS_Activity [AID623870, Type: screening] | aryl hydrocarbon receptor nuclear translocator [Homo sapiens] [gi:2702319] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | ARNT-TAC3: AlphaScreen HTS to detect disruption of ARNT/TAC3 interactions Measured in Biochemical System Using Plate Reader - 2158-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 623870 | | BioAssay type | screening | | Target | aryl hydrocarbon receptor nuclear translocator [Homo sapiens] [gi:2702319] | | PubMed | | | Data Table |  |
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| 25 | [SID14723648] | Inactive | | | ARNT-TAC3: AlphaScreen HTS to detect disruption of ARNT/TAC3 interactions Measured in Biochemical System Using Plate Reader - 2158-01_Inhibitor_SinglePoint_HTS_Activity [AID623870, Type: screening] | aryl hydrocarbon receptor nuclear translocator [Homo sapiens] [gi:2702319] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | ARNT-TAC3: AlphaScreen HTS to detect disruption of ARNT/TAC3 interactions Measured in Biochemical System Using Plate Reader - 2158-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 623870 | | BioAssay type | screening | | Target | aryl hydrocarbon receptor nuclear translocator [Homo sapiens] [gi:2702319] | | PubMed | | | Data Table |  |
|
| 26 | [SID14723648] | Inactive | | | Assay for Inhibitors of the beta-Arrestin-Adaptor Protein 2 Interaction That Mediate GPCR Degradation and Recycling [AID504490, Type: screening] | Arrestin, beta 1 [Homo sapiens] [gi:13177715] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Assay for Inhibitors of the beta-Arrestin-Adaptor Protein 2 Interaction That Mediate GPCR Degradation and Recycling | | AID | 504490 | | BioAssay type | screening | | Target | Arrestin, beta 1 [Homo sapiens] [gi:13177715] | | PubMed | | | Data Table |  |
|
| 27 | [SID14723648] | Inactive | | | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) [AID2797, Type: screening] | vasopressin V1a receptor [Homo sapiens] [gi:4502331] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | | AID | 2797 | | BioAssay type | screening | | Target | vasopressin V1a receptor [Homo sapiens] [gi:4502331] | | PubMed | | | Data Table |  |
|
| 28 | [SID14723648] | Inactive | | | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) [AID2797, Type: screening] | vasopressin V1a receptor [Homo sapiens] [gi:4502331] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | | AID | 2797 | | BioAssay type | screening | | Target | vasopressin V1a receptor [Homo sapiens] [gi:4502331] | | PubMed | | | Data Table |  |
|
| 29 | [SID14723648] | Inactive | | | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) [AID2797, Type: screening] | vasopressin V1a receptor [Homo sapiens] [gi:4502331] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | | AID | 2797 | | BioAssay type | screening | | Target | vasopressin V1a receptor [Homo sapiens] [gi:4502331] | | PubMed | | | Data Table |  |
|
| 30 | [SID14723648] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-2. [AID950, Type: screening] | Apoptosis regulator Bcl- [gi:231632] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-2. | | AID | 950 | | BioAssay type | screening | | Target | Apoptosis regulator Bcl- [gi:231632] | | PubMed | | | Data Table |  |
|
| 31 | [SID14723648] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-2. [AID950, Type: screening] | Apoptosis regulator Bcl- [gi:231632] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-2. | | AID | 950 | | BioAssay type | screening | | Target | Apoptosis regulator Bcl- [gi:231632] | | PubMed | | | Data Table |  |
|
| 32 | [SID14723648] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bfl-1 [AID1008, Type: screening] | bcl-2-related protein A1 isoform 1 [Homo sapiens] [gi:4757840] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bfl-1 | | AID | 1008 | | BioAssay type | screening | | Target | bcl-2-related protein A1 isoform 1 [Homo sapiens] [gi:4757840] | | PubMed | | | Data Table |  |
|
| 33 | [SID14723648] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bfl-1 [AID1008, Type: screening] | bcl-2-related protein A1 isoform 1 [Homo sapiens] [gi:4757840] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bfl-1 | | AID | 1008 | | BioAssay type | screening | | Target | bcl-2-related protein A1 isoform 1 [Homo sapiens] [gi:4757840] | | PubMed | | | Data Table |  |
|
| 34 | [SID14723648] | Inactive | | | Primary biochemical high throughput screening assay to identify inhibitors of BCL2-related protein, long isoform (BCLXL). [AID2129, Type: screening] | bcl-xL [Homo sapiens] [gi:510901] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Primary biochemical high throughput screening assay to identify inhibitors of BCL2-related protein, long isoform (BCLXL). | | AID | 2129 | | BioAssay type | screening | | Target | bcl-xL [Homo sapiens] [gi:510901] | | PubMed | | | Data Table |  |
|
| 35 | [SID14723648] | Inactive | | | Primary biochemical high throughput screening assay to identify inhibitors of BCL2-related protein, long isoform (BCLXL). [AID2129, Type: screening] | bcl-xL [Homo sapiens] [gi:510901] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Primary biochemical high throughput screening assay to identify inhibitors of BCL2-related protein, long isoform (BCLXL). | | AID | 2129 | | BioAssay type | screening | | Target | bcl-xL [Homo sapiens] [gi:510901] | | PubMed | | | Data Table |  |
|
| 36 | [SID14723648] | Inactive | | | Primary biochemical high throughput screening assay to identify inhibitors of BCL2-related protein, long isoform (BCLXL). [AID2129, Type: screening] | bcl-xL [Homo sapiens] [gi:510901] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Primary biochemical high throughput screening assay to identify inhibitors of BCL2-related protein, long isoform (BCLXL). | | AID | 2129 | | BioAssay type | screening | | Target | bcl-xL [Homo sapiens] [gi:510901] | | PubMed | | | Data Table |  |
|
| 37 | [SID14723648] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-XL. [AID1007, Type: screening] | bcl-xL [Homo sapiens] [gi:510901] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-XL. | | AID | 1007 | | BioAssay type | screening | | Target | bcl-xL [Homo sapiens] [gi:510901] | | PubMed | | | Data Table |  |
|
| 38 | [SID14723648] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-XL. [AID1007, Type: screening] | bcl-xL [Homo sapiens] [gi:510901] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-XL. | | AID | 1007 | | BioAssay type | screening | | Target | bcl-xL [Homo sapiens] [gi:510901] | | PubMed | | | Data Table |  |
|
| 39 | [SID14723648] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-XL. [AID1007, Type: screening] | bcl-xL [Homo sapiens] [gi:510901] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-XL. | | AID | 1007 | | BioAssay type | screening | | Target | bcl-xL [Homo sapiens] [gi:510901] | | PubMed | | | Data Table |  |
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| 40 | [SID14723648] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-W. [AID952, Type: screening] | Bcl-w [Homo sapiens] [gi:1572493] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-W. | | AID | 952 | | BioAssay type | screening | | Target | Bcl-w [Homo sapiens] [gi:1572493] | | PubMed | | | Data Table |  |
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| 41 | [SID14723648] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-W. [AID952, Type: screening] | Bcl-w [Homo sapiens] [gi:1572493] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-W. | | AID | 952 | | BioAssay type | screening | | Target | Bcl-w [Homo sapiens] [gi:1572493] | | PubMed | | | Data Table |  |
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| 42 | [SID14723648] | Inactive | Potency | | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) [AID2528, Type: confirmatory] | Bloom syndrome protein [Homo sapiens] [gi:4557365] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) | | AID | 2528 | | BioAssay type | confirmatory | | Target | Bloom syndrome protein [Homo sapiens] [gi:4557365] | | PubMed | | | Data Table |  |
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| 43 | [SID14723648] | Inactive | Potency | | qHTS Assay to Identify Small Molecule Activators of BRCA1 Expression [AID624202, Type: confirmatory] | BRCA1 [Homo sapiens] [gi:1698399] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay to Identify Small Molecule Activators of BRCA1 Expression | | AID | 624202 | | BioAssay type | confirmatory | | Target | BRCA1 [Homo sapiens] [gi:1698399] | | PubMed | | | Data Table |  |
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| 44 | [SID14723648] | Inactive | Potency | | qHTS Assay to Identify Small Molecule Activators of BRCA1 Expression [AID624202, Type: confirmatory] | BRCA1 [Homo sapiens] [gi:1698399] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay to Identify Small Molecule Activators of BRCA1 Expression | | AID | 624202 | | BioAssay type | confirmatory | | Target | BRCA1 [Homo sapiens] [gi:1698399] | | PubMed | | | Data Table |  |
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| 45 | [SID14723648] | Inactive | | | Primary cell-based high throughput screening assay to identify inhibitors of kruppel-like factor 5 (KLF5) [AID1700, Type: screening] | Kruppel-like factor 5 [Homo sapiens] [gi:124263658] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Primary cell-based high throughput screening assay to identify inhibitors of kruppel-like factor 5 (KLF5) | | AID | 1700 | | BioAssay type | screening | | Target | Kruppel-like factor 5 [Homo sapiens] [gi:124263658] | | PubMed | | | Data Table |  |
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| 46 | [SID14723648] | Inactive | | | Absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-3 [AID463141, Type: screening] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-3 | | AID | 463141 | | BioAssay type | screening | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
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| 47 | [SID14723648] | Inactive | | | Absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-3 [AID463141, Type: screening] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-3 | | AID | 463141 | | BioAssay type | screening | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
|
| 48 | [SID14723648] | Inactive | | | Absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-3 [AID463141, Type: screening] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-3 | | AID | 463141 | | BioAssay type | screening | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
|
| 49 | [SID14723648] | Inactive | | | Absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-3 [AID463141, Type: screening] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | BioAssay | Absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-3 | | AID | 463141 | | BioAssay type | screening | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
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| 50 | [SID14723648] | Inactive | IC50 | | uHTS identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb-SMMHC via a fluorescence resonance energy transfer (FRET) assay. [AID1434, Type: confirmatory] | core-binding factor subunit beta isoform 1 [Homo sapiens] [gi:13124881] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 14723648 | | CID | 54689176 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | uHTS identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb-SMMHC via a fluorescence resonance energy transfer (FRET) assay. | | AID | 1434 | | BioAssay type | confirmatory | | Target | core-binding factor subunit beta isoform 1 [Homo sapiens] [gi:13124881] | | PubMed | | | Data Table |  |
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