| 1 | [SID24787120] | Active | IC50 | 3.1 | AlphaScreen confirmatory assay for validation of inhibitors of SUMOylation [AID2018, Type: confirmatory] | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | IC50 | 3.1 [uM] | | BioAssay | AlphaScreen confirmatory assay for validation of inhibitors of SUMOylation | | AID | 2018 | | BioAssay type | confirmatory | | Target | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] | | PubMed | | | Data Table |  |
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| 2 | [SID24787120] | Active | Potency | 3.5481 | 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. | 2 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | Potency | 3.5481 [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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| 3 | [SID24787120] | Active | Potency | 4.4668 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | Potency | 4.4668 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
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| 4 | [SID24787120] | Active | Potency | 4.4668 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | Potency | 4.4668 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Iota | | AID | 588590 | | BioAssay type | confirmatory | | Target | DNA polymerase iota [Homo sapiens] [gi:154350220] | | PubMed | | | Data Table |  |
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| 5 | [SID24787120] | Active | Potency | 5.6101 | 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. | 5 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | Potency | 5.6101 [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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| 6 | [SID24787120] | Active | Potency | 11.2202 | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) [AID2549, Type: confirmatory] | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) | | AID | 2549 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] | | PubMed | | | Data Table |  |
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| 7 | [SID24787120] | Active | Potency | 11.2202 | 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. | 7 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | Potency | 11.2202 [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 |  |
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| 8 | [SID24787120] | Active | Potency | 11.2202 | 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. | 8 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | Potency | 11.2202 [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 |  |
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| 9 | [SID24787120] | Active | IC50 | 13.13 | uHTS HTRF assay for identification of inhibitors of SUMOylation [AID2006, Type: confirmatory] | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | IC50 | 13.13 [uM] | | BioAssay | uHTS HTRF assay for identification of inhibitors of SUMOylation | | AID | 2006 | | BioAssay type | confirmatory | | Target | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] | | PubMed | | | Data Table |  |
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| 10 | [SID24787120] | Active | Potency | 15.8489 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | Potency | 15.8489 [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 |  |
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| 11 | [SID24787120] | Active | Potency | 25.1189 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | Potency | 25.1189 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
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| 12 | [SID24787120] | Active | Potency | 25.1189 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | Potency | 25.1189 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
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| 13 | [SID24787120] | Active | Potency | 56.2341 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | Potency | 56.2341 [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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| 14 | [SID87544552] | Active | IC50 | 56.8 | SAR analysis of the MOA of E2 SUMOylation inhibitors in an HTRF format [AID485393, Type: confirmatory] | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 87544552 | | CID | 3152411 | | Outcome | Active | | IC50 | 56.8 [uM] | | BioAssay | SAR analysis of the MOA of E2 SUMOylation inhibitors in an HTRF format | | AID | 485393 | | BioAssay type | confirmatory | | Target | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] | | PubMed | | | Data Table |  |
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| 15 | [SID24787120] | Active | AC50 | 64.09 | ARNT-TAC3: AlphaScreen HTS to detect disruption of ARNT/TAC3 interactions Measured in Biochemical System Using Plate Reader - 2158-01_Inhibitor_Dose_CherryPick_Activity [AID651703, Type: confirmatory] | aryl hydrocarbon receptor nuclear translocator [Homo sapiens] [gi:2702319] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | AC50 | 64.09 [uM] | | BioAssay | ARNT-TAC3: AlphaScreen HTS to detect disruption of ARNT/TAC3 interactions Measured in Biochemical System Using Plate Reader - 2158-01_Inhibitor_Dose_CherryPick_Activity | | AID | 651703 | | BioAssay type | confirmatory | | Target | aryl hydrocarbon receptor nuclear translocator [Homo sapiens] [gi:2702319] | | PubMed | | | Data Table |  |
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| 16 | [SID24787120] | Active | AC50 | 64.09 | ARNT-TAC3: AlphaScreen HTS to detect disruption of ARNT/TAC3 interactions Measured in Biochemical System Using Plate Reader - 2158-01_Inhibitor_Dose_CherryPick_Activity [AID651703, Type: confirmatory] | aryl hydrocarbon receptor nuclear translocator [Homo sapiens] [gi:2702319] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | AC50 | 64.09 [uM] | | BioAssay | ARNT-TAC3: AlphaScreen HTS to detect disruption of ARNT/TAC3 interactions Measured in Biochemical System Using Plate Reader - 2158-01_Inhibitor_Dose_CherryPick_Activity | | AID | 651703 | | BioAssay type | confirmatory | | Target | aryl hydrocarbon receptor nuclear translocator [Homo sapiens] [gi:2702319] | | PubMed | | | Data Table |  |
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| 17 | [SID24787120] | Active | IC50 | 91.84 | Primary and Confirmatory Screening for Flavivirus Genomic Capping Enzyme Inhibition [AID588689, Type: confirmatory] | Chain A, Crystal Structure Of Dengue-2 Virus Methyltransferase Complexed With S-Adenosyl-L-Homocyste [gi:219689243] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | IC50 | 91.84 [uM] | | BioAssay | Primary and Confirmatory Screening for Flavivirus Genomic Capping Enzyme Inhibition | | AID | 588689 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Dengue-2 Virus Methyltransferase Complexed With S-Adenosyl-L-Homocyste [gi:219689243] | | PubMed | | | Data Table |  |
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| 18 | [SID24787120] | Active | | | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen [AID2472, Type: screening] | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen | | AID | 2472 | | BioAssay type | screening | | Target | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] | | PubMed | | | Data Table |  |
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| 19 | [SID24787120] | Active | | | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen [AID2472, Type: screening] | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen | | AID | 2472 | | BioAssay type | screening | | Target | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] | | PubMed | | | Data Table |  |
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| 20 | [SID24787120] | Active | | | 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. | 20 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | 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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| 21 | [SID24787120] | Active | | | 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. | 21 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | 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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| 22 | [SID24787120] | Active | | | Primary biochemical high-throughput screening assay to measure P97 ATPase inhibition [AID1481, Type: screening] | Valosin-containing protein [Homo sapiens] [gi:111305821] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | BioAssay | Primary biochemical high-throughput screening assay to measure P97 ATPase inhibition | | AID | 1481 | | BioAssay type | screening | | Target | Valosin-containing protein [Homo sapiens] [gi:111305821] | | PubMed | | | Data Table |  |
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| 23 | [SID24787120] | Active | | | Primary biochemical high-throughput screening assay to measure P97 ATPase inhibition [AID1481, Type: screening] | Valosin-containing protein [Homo sapiens] [gi:111305821] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | BioAssay | Primary biochemical high-throughput screening assay to measure P97 ATPase inhibition | | AID | 1481 | | BioAssay type | screening | | Target | Valosin-containing protein [Homo sapiens] [gi:111305821] | | PubMed | | | Data Table |  |
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| 24 | [SID125077303] | Active | | | A screen for small molecule inhibitors of the human deubiquitinating enzyme, UCH37 [AID588478, Type: other] | ubiquitin C-terminal hydrolase UCH37 [Homo sapiens] [gi:4877999] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 125077303 | | CID | 3152411 | | Outcome | Active | | BioAssay | A screen for small molecule inhibitors of the human deubiquitinating enzyme, UCH37 | | AID | 588478 | | BioAssay type | other | | Target | ubiquitin C-terminal hydrolase UCH37 [Homo sapiens] [gi:4877999] | | PubMed | | | Data Table |  |
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| 25 | [SID24787120] | Active | | | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors of ADP-ribosylation factor GTPase activating protein 1 (ARFGAP1) [AID651572, Type: screening] | Arfgap1 gene product [Rattus norvegicus] [gi:21489979] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Active | | BioAssay | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors of ADP-ribosylation factor GTPase activating protein 1 (ARFGAP1) | | AID | 651572 | | BioAssay type | screening | | Target | Arfgap1 gene product [Rattus norvegicus] [gi:21489979] | | PubMed | | | Data Table |  |
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| 26 | [SID24787120] | 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. | 26 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | 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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| 27 | [SID24787120] | 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. | 27 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | 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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| 28 | [SID24787120] | Inactive | Potency | 0.8947 | qHTS Fluorescence Polarization (FP) Assay for Inhibitors of MLL CXXC domain - DNA interaction: Fluorescein FP [AID624160, Type: confirmatory] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | 0.8947 [uM] | | BioAssay | qHTS Fluorescence Polarization (FP) Assay for Inhibitors of MLL CXXC domain - DNA interaction: Fluorescein FP | | AID | 624160 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 29 | [SID24787120] | Inactive | Potency | 1.1264 | qHTS Fluorescence Polarization (FP) Assay for Inhibitors of MLL CXXC domain - DNA interaction: Texas Red FP [AID624161, Type: confirmatory] | |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | 1.1264 [uM] | | BioAssay | qHTS Fluorescence Polarization (FP) Assay for Inhibitors of MLL CXXC domain - DNA interaction: Texas Red FP | | AID | 624161 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 30 | [SID24787120] | Inactive | Potency | 15.8489 | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium [AID1457, Type: confirmatory] | Inositol monophosphatase [gi:44888968] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | 15.8489 [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 |  |
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| 31 | [SID24787120] | Inactive | Potency | 15.8489 | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium [AID1457, Type: confirmatory] | Inositol monophosphatase [gi:44888968] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | 15.8489 [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 |  |
|
| 32 | [SID24787120] | Inactive | Potency | 19.9526 | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase [AID1631, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1631 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
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| 33 | [SID24787120] | Inactive | Potency | 19.9526 | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase [AID1631, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1631 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
|
| 34 | [SID24787120] | Inactive | Potency | 19.9526 | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase [AID1631, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Activators of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1631 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
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| 35 | [SID24787120] | Inactive | Potency | 35.4813 | qHTS of TDP-43 Inhibitors [AID652104, Type: confirmatory] | TAR DNA-binding protein 43 [gi:20140568] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | 35.4813 [uM] | | BioAssay | qHTS of TDP-43 Inhibitors | | AID | 652104 | | BioAssay type | confirmatory | | Target | TAR DNA-binding protein 43 [gi:20140568] | | PubMed | | | Data Table |  |
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| 36 | [SID87544552] | Inactive | IC50 | 100 | SAR analysis of Ubc13-Ubiquitination selectivity in a TR-FRET assay for In Vitro dose response studies [AID2658, Type: confirmatory] | UBE2N gene product [Homo sapiens] [gi:4507793] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 87544552 | | CID | 3152411 | | Outcome | Inactive | | IC50 | 100 [uM] | | BioAssay | SAR analysis of Ubc13-Ubiquitination selectivity in a TR-FRET assay for In Vitro dose response studies | | AID | 2658 | | BioAssay type | confirmatory | | Target | UBE2N gene product [Homo sapiens] [gi:4507793] | | PubMed | | | Data Table |  |
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| 37 | [SID87544552] | Inactive | IC50 | 100 | SAR analysis of Ubc13-Ubiquitination selectivity in a TR-FRET assay for In Vitro dose response studies [AID2658, Type: confirmatory] | UBE2N gene product [Homo sapiens] [gi:4507793] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 87544552 | | CID | 3152411 | | Outcome | Inactive | | IC50 | 100 [uM] | | BioAssay | SAR analysis of Ubc13-Ubiquitination selectivity in a TR-FRET assay for In Vitro dose response studies | | AID | 2658 | | BioAssay type | confirmatory | | Target | UBE2N gene product [Homo sapiens] [gi:4507793] | | PubMed | | | Data Table |  |
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| 38 | [SID87544552] | Inactive | IC50 | 100 | SAR analysis of SUMOylation using HTRF in an in-Vitro dose response assay [AID2614, Type: confirmatory] | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 87544552 | | CID | 3152411 | | Outcome | Inactive | | IC50 | 100 [uM] | | BioAssay | SAR analysis of SUMOylation using HTRF in an in-Vitro dose response assay | | AID | 2614 | | BioAssay type | confirmatory | | Target | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] | | PubMed | | | Data Table |  |
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| 39 | [SID24787120] | Inactive | IC50 | | uHTS identification of small molecule antagonists of the binding of Siah-1 and a peptide ligand via a fluorescence polarization assay. [AID1817, Type: confirmatory] | plectin 1 [Homo sapiens] [gi:40849930] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | uHTS identification of small molecule antagonists of the binding of Siah-1 and a peptide ligand via a fluorescence polarization assay. | | AID | 1817 | | BioAssay type | confirmatory | | Target | plectin 1 [Homo sapiens] [gi:40849930] | | PubMed | | | Data Table |  |
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| 40 | [SID24787120] | Inactive | | | qHTS Assay for Inhibitors of the Six1/Eya2 Interaction [AID651725, Type: screening] | six1 [Homo sapiens] [gi:1246761] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | BioAssay | qHTS Assay for Inhibitors of the Six1/Eya2 Interaction | | AID | 651725 | | BioAssay type | screening | | Target | six1 [Homo sapiens] [gi:1246761] | | PubMed | | | Data Table |  |
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| 41 | [SID24787120] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify activators of the function of SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 (SMARCA2, BRM) [AID652017, Type: screening] | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2, i [gi:119579215] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify activators of the function of SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 (SMARCA2, BRM) | | AID | 652017 | | BioAssay type | screening | | Target | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2, i [gi:119579215] | | PubMed | | | Data Table |  |
|
| 42 | [SID24787120] | Inactive | Potency | | 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. | 42 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | [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 |  |
|
| 43 | [SID24787120] | Inactive | Potency | | 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. | 43 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | [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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| 44 | [SID24787120] | Inactive | Potency | | Inhibitors of Secretory Acid Sphingomyelinase (S-ASM): qHTS [AID504937, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Inhibitors of Secretory Acid Sphingomyelinase (S-ASM): qHTS | | AID | 504937 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
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| 45 | [SID24787120] | Inactive | Potency | | Inhibitors of Secretory Acid Sphingomyelinase (S-ASM): qHTS [AID504937, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Inhibitors of Secretory Acid Sphingomyelinase (S-ASM): qHTS | | AID | 504937 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
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| 46 | [SID24787120] | Inactive | | | uHTS identification of SUMO1-mediated protein-protein interactions [AID602429, Type: screening] | SUMO-1 [Homo sapiens] [gi:1762973] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | BioAssay | uHTS identification of SUMO1-mediated protein-protein interactions | | AID | 602429 | | BioAssay type | screening | | Target | SUMO-1 [Homo sapiens] [gi:1762973] | | PubMed | | | Data Table |  |
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| 47 | [SID24787120] | Inactive | | | Confirmation biochemical high-throughput screening assay for inhibitors of the p97 ATPase [AID1517, Type: screening] | Valosin-containing protein [Homo sapiens] [gi:111305821] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | BioAssay | Confirmation biochemical high-throughput screening assay for inhibitors of the p97 ATPase | | AID | 1517 | | BioAssay type | screening | | Target | Valosin-containing protein [Homo sapiens] [gi:111305821] | | PubMed | | | Data Table |  |
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| 48 | [SID24787120] | Inactive | | | Confirmation biochemical high-throughput screening assay for inhibitors of the p97 ATPase [AID1517, Type: screening] | Valosin-containing protein [Homo sapiens] [gi:111305821] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | BioAssay | Confirmation biochemical high-throughput screening assay for inhibitors of the p97 ATPase | | AID | 1517 | | BioAssay type | screening | | Target | Valosin-containing protein [Homo sapiens] [gi:111305821] | | PubMed | | | Data Table |  |
|
| 49 | [SID24787120] | Inactive | | | 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. | 49 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | 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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| 50 | [SID24787120] | Inactive | | | uHTS for Small Molecule Inhibitors of Eukaryotic Translation Initiation [AID782, Type: screening] | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 24787120 | | CID | 3152411 | | Outcome | Inactive | | BioAssay | uHTS for Small Molecule Inhibitors of Eukaryotic Translation Initiation | | AID | 782 | | BioAssay type | screening | | Target | eukaryotic translation initiation factor 4E [Mus musculus] [gi:83627717] | | PubMed | | | Data Table |  |
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