| 1 | [SID17433966] | Active | AbsAC40_uM | 3.28 | In vivo-based yeast HTS counterscreen to detect compounds rescuing yeast growth/survival of Saccharomyces cerevisiae SKN7-mediated toxicity Measured in Whole Organism System Using Plate Reader - 2120-02_Inhibitor_Dose_CherryPick_Activity [AID624258, Type: confirmatory] | Skn7p [Saccharomyces cerevisiae] [gi:458922] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | AbsAC40_uM | 3.28 [uM] | | BioAssay | In vivo-based yeast HTS counterscreen to detect compounds rescuing yeast growth/survival of Saccharomyces cerevisiae SKN7-mediated toxicity Measured in Whole Organism System Using Plate Reader - 2120-02_Inhibitor_Dose_CherryPick_Activity | | AID | 624258 | | BioAssay type | confirmatory | | Target | Skn7p [Saccharomyces cerevisiae] [gi:458922] | | PubMed | | | Data Table |  |
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| 2 | [SID17433966] | Active | IC50 | 3.37 | Elucidation of physiology of non-replicating, drug-tolerant Mycobacterium tuberculosis [AID488890, Type: confirmatory] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | IC50 | 3.37 [uM] | | BioAssay | Elucidation of physiology of non-replicating, drug-tolerant Mycobacterium tuberculosis | | AID | 488890 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 3 | [SID17433966] | Active | EC50 | 4.81 | Fluorescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of RecA-Intein Splicing Activity [AID435010, Type: confirmatory] | DNA recombination protein RecA [Mycobacterium tuberculosis H37Rv] [gi:15609874] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | EC50 | 4.81 [uM] | | BioAssay | Fluorescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of RecA-Intein Splicing Activity | | AID | 435010 | | BioAssay type | confirmatory | | Target | DNA recombination protein RecA [Mycobacterium tuberculosis H37Rv] [gi:15609874] | | PubMed | | | Data Table |  |
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| 4 | [SID17433966] | Active | IC50 | 5.42 | A Cell Based Secondary Assay to Explore Compounds that Modulate Non-Replicating, Drug-tolerant Compounds in Replicating H37Rv TB of Mycobacterium tuberculosis [AID492952, Type: confirmatory] | |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | IC50 | 5.42 [uM] | | BioAssay | A Cell Based Secondary Assay to Explore Compounds that Modulate Non-Replicating, Drug-tolerant Compounds in Replicating H37Rv TB of Mycobacterium tuberculosis | | AID | 492952 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 5 | [SID17433966] | Active | Potency | 6.3096 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 6.3096 [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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| 6 | [SID17433966] | Active | Potency | 6.3096 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 6.3096 [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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| 7 | [SID17433966] | Active | AC50 | 8.86 | Fluorescence Cell-Free Homogeneous Secondary Screen to Identify Inhibitors of DnaB-Intein Splicing Activity [AID449749, Type: confirmatory] | replicative DNA helicase [Mycobacterium tuberculosis H37Rv] [gi:15607200] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | AC50 | 8.86 [uM] | | BioAssay | Fluorescence Cell-Free Homogeneous Secondary Screen to Identify Inhibitors of DnaB-Intein Splicing Activity | | AID | 449749 | | BioAssay type | confirmatory | | Target | replicative DNA helicase [Mycobacterium tuberculosis H37Rv] [gi:15607200] | | PubMed | | | Data Table |  |
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| 8 | [SID17433966] | Active | Potency | 10 | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a [AID504332, Type: confirmatory] | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a | | AID | 504332 | | BioAssay type | confirmatory | | Target | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] | | PubMed | | | Data Table |  |
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| 9 | [SID17433966] | Active | Potency | 12.5893 | 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. | 9 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 12.5893 [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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| 10 | [SID17433966] | Active | Potency | 12.5893 | 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 | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 12.5893 [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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| 11 | [SID17433966] | Active | Potency | 13.1154 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 13.1154 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation | | AID | 504832 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 12 | [SID17433966] | Active | Potency | 16.9441 | qHTS profiling assay for firefly luciferase inhibitor/activator using purifed enzyme and Km concentrations of substrates (counterscreen for miR-21 project) [AID588342, Type: confirmatory] | Luciferase [Photinus pyralis] [gi:160794] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 16.9441 [uM] | | BioAssay | qHTS profiling assay for firefly luciferase inhibitor/activator using purifed enzyme and Km concentrations of substrates (counterscreen for miR-21 project) | | AID | 588342 | | BioAssay type | confirmatory | | Target | Luciferase [Photinus pyralis] [gi:160794] | | PubMed | | | Data Table |  |
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| 13 | [SID17433966] | Active | Potency | 17.7407 | 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. | 13 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 17.7407 [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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| 14 | [SID17433966] | Active | Potency | 22.3872 | qHTS for Inhibitors of TGF-b [AID588855, Type: confirmatory] | Smad3 [Homo sapiens] [gi:18418623] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 22.3872 [uM] | | BioAssay | qHTS for Inhibitors of TGF-b | | AID | 588855 | | BioAssay type | confirmatory | | Target | Smad3 [Homo sapiens] [gi:18418623] | | PubMed | | | Data Table |  |
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| 15 | [SID17433966] | Active | Potency | 22.3872 | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (with detergent) [AID1478, Type: confirmatory] | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 22.3872 [uM] | | BioAssay | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (with detergent) | | AID | 1478 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] | | PubMed | | | Data Table |  |
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| 16 | [SID17433966] | Active | Potency | 22.3872 | qHTS for Inhibitors of TGF-b [AID588855, Type: confirmatory] | Smad3 [Homo sapiens] [gi:18418623] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 22.3872 [uM] | | BioAssay | qHTS for Inhibitors of TGF-b | | AID | 588855 | | BioAssay type | confirmatory | | Target | Smad3 [Homo sapiens] [gi:18418623] | | PubMed | | | Data Table |  |
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| 17 | [SID17433966] | Active | AC50 | 23.44 | Fluorescence Cell-Free Homogeneous Secondary Screen to Identify Non-Covalent Inhibitors of RecA-Intein Splicing Activity [AID449750, Type: confirmatory] | replicative DNA helicase [Mycobacterium tuberculosis H37Rv] [gi:15607200] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | AC50 | 23.44 [uM] | | BioAssay | Fluorescence Cell-Free Homogeneous Secondary Screen to Identify Non-Covalent Inhibitors of RecA-Intein Splicing Activity | | AID | 449750 | | BioAssay type | confirmatory | | Target | replicative DNA helicase [Mycobacterium tuberculosis H37Rv] [gi:15607200] | | PubMed | | | Data Table |  |
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| 18 | [SID17433966] | Active | Potency | 25.1189 | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1463, Type: confirmatory] | |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 25.1189 [uM] | | BioAssay | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1463 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 19 | [SID17433966] | Active | Potency | 70.7946 | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | Potency | 70.7946 [uM] | | BioAssay | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | | AID | 1490 | | BioAssay type | confirmatory | | Target | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] | | PubMed | | | Data Table |  |
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| 20 | [SID17433966] | Active | EC50 | 161.3 | Fluorescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of GFP Chromophore Formation [AID434968, Type: confirmatory] | DNA recombination protein RecA [Mycobacterium tuberculosis H37Rv] [gi:15609874] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | EC50 | 161.3 [uM] | | BioAssay | Fluorescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of GFP Chromophore Formation | | AID | 434968 | | BioAssay type | confirmatory | | Target | DNA recombination protein RecA [Mycobacterium tuberculosis H37Rv] [gi:15609874] | | PubMed | | | Data Table |  |
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| 21 | [SID17433966] | Active | | | Cycloheximide Counterscreen for Small Molecule Inhibitors of Shiga Toxin [AID2314, Type: screening] | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Cycloheximide Counterscreen for Small Molecule Inhibitors of Shiga Toxin | | AID | 2314 | | BioAssay type | screening | | Target | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | | PubMed | | | Data Table |  |
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| 22 | [SID17433966] | Active | | | A qHTS for Small Molecule Inhibitors of Shiga Toxin [AID2315, Type: screening] | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | A qHTS for Small Molecule Inhibitors of Shiga Toxin | | AID | 2315 | | BioAssay type | screening | | Target | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | | PubMed | | | Data Table |  |
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| 23 | [SID17433966] | Active | | | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - activators [AID1814, Type: screening] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - activators | | AID | 1814 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 24 | [SID17433966] | 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. | 24 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | 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 |  |
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| 25 | [SID17433966] | Active | | | 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. | 25 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | 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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| 26 | [SID17433966] | Active | | | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID1822, Type: screening] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 1822 | | BioAssay type | screening | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
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| 27 | [SID17433966] | Active | | | Fluorescence-based biochemical high throughput screening primary assay to identify inhibitors of Crimean-Congo Hemorrhagic Fever (CCHF) viral ovarian tumor domain protease (vOTU): Pep-AMC substrate [AID651958, Type: screening] | putative polyprotein [Crimean-Congo hemorrhagic fever virus] [gi:76364066] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical high throughput screening primary assay to identify inhibitors of Crimean-Congo Hemorrhagic Fever (CCHF) viral ovarian tumor domain protease (vOTU): Pep-AMC substrate | | AID | 651958 | | BioAssay type | screening | | Target | putative polyprotein [Crimean-Congo hemorrhagic fever virus] [gi:76364066] | | PubMed | | | Data Table |  |
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| 28 | [SID17433966] | Active | | | Leishmania major promastigote HTS [AID1063, Type: screening] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Leishmania major promastigote HTS | | AID | 1063 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 29 | [SID17433966] | Active | | | 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. | 29 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | 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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| 30 | [SID17433966] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists [AID624463, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | | AID | 624463 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 31 | [SID17433966] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators [AID624464, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | | AID | 624464 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 32 | [SID17433966] | Active | | | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID485270, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 485270 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
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| 33 | [SID17433966] | Active | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of Protein Arginine Deiminase 4 (PAD4) (1536 HTS) [AID485272, Type: screening] | protein-arginine deiminase type-4 [Homo sapiens] [gi:216548487] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of Protein Arginine Deiminase 4 (PAD4) (1536 HTS) | | AID | 485272 | | BioAssay type | screening | | Target | protein-arginine deiminase type-4 [Homo sapiens] [gi:216548487] | | PubMed | | | Data Table |  |
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| 34 | [SID17433966] | Active | | | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) [AID485270, Type: screening] | orexin receptor type 1 [Homo sapiens] [gi:222080095] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | FRET-based cell-based primary high throughput screening assay to identify antagonists of the orexin 1 receptor (OX1R; HCRTR1) | | AID | 485270 | | BioAssay type | screening | | Target | orexin receptor type 1 [Homo sapiens] [gi:222080095] | | PubMed | | | Data Table |  |
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| 35 | [SID17433966] | Active | | | uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent assay [AID463190, Type: screening] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent assay | | AID | 463190 | | BioAssay type | screening | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
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| 36 | [SID17433966] | Active | | | Single concentration confirmation of small molecule inhibitors of tim10-1 yeast via a luminescent assay [AID463213, Type: screening] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Single concentration confirmation of small molecule inhibitors of tim10-1 yeast via a luminescent assay | | AID | 463213 | | BioAssay type | screening | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
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| 37 | [SID17433966] | Active | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of Protein Arginine Deiminase 4 (PAD4) (1536 HTS) [AID485272, Type: screening] | protein-arginine deiminase type-4 [Homo sapiens] [gi:216548487] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of Protein Arginine Deiminase 4 (PAD4) (1536 HTS) | | AID | 485272 | | BioAssay type | screening | | Target | protein-arginine deiminase type-4 [Homo sapiens] [gi:216548487] | | PubMed | | | Data Table |  |
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| 38 | [SID17433966] | Active | | | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of RecA Intein Splicing Activity [AID2221, Type: screening] | DNA recombination protein RecA [Mycobacterium tuberculosis H37Rv] [gi:15609874] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of RecA Intein Splicing Activity | | AID | 2221 | | BioAssay type | screening | | Target | DNA recombination protein RecA [Mycobacterium tuberculosis H37Rv] [gi:15609874] | | PubMed | | | Data Table |  |
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| 39 | [SID17433966] | Active | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). [AID1974, Type: screening] | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). | | AID | 1974 | | BioAssay type | screening | | Target | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] | | PubMed | | | Data Table |  |
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| 40 | [SID17433966] | Active | | | Primary cell-based high throughput screening assay to measure STAT1 activation [AID932, Type: screening] | signal transducer and activator of transcription 1-alpha/beta isoform alpha [Homo sapiens] [gi:6274552] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Primary cell-based high throughput screening assay to measure STAT1 activation | | AID | 932 | | BioAssay type | screening | | Target | signal transducer and activator of transcription 1-alpha/beta isoform alpha [Homo sapiens] [gi:6274552] | | PubMed | | | Data Table |  |
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| 41 | [SID17433966] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists [AID624463, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | | AID | 624463 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 42 | [SID17433966] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators [AID624464, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | | AID | 624464 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 43 | [SID17433966] | Active | | | Primary cell-based high throughput screening assay to measure STAT1 activation [AID932, Type: screening] | signal transducer and activator of transcription 1-alpha/beta isoform alpha [Homo sapiens] [gi:6274552] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Primary cell-based high throughput screening assay to measure STAT1 activation | | AID | 932 | | BioAssay type | screening | | Target | signal transducer and activator of transcription 1-alpha/beta isoform alpha [Homo sapiens] [gi:6274552] | | PubMed | | | Data Table |  |
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| 44 | [SID17433966] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists [AID624463, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Antagonists | | AID | 624463 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 45 | [SID17433966] | Active | | | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators [AID624464, Type: other] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Beta-Arrestin HTS for Positive Allosteric Modulators of the Human D2 Dopamine Receptor: Potentiators | | AID | 624464 | | BioAssay type | other | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 46 | [SID17433966] | Active | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). [AID1974, Type: screening] | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). | | AID | 1974 | | BioAssay type | screening | | Target | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] | | PubMed | | | Data Table |  |
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| 47 | [SID17433966] | Active | | | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID1822, Type: screening] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 1822 | | BioAssay type | screening | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
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| 48 | [SID17433966] | Active | | | In vivo-based yeast HTS to detect compounds rescuing yeast growth/survival of Plasmodium Falciparum HSP40-mediated toxicity Measured in Whole Organism System Using Plate Reader - 2120-01_Inhibitor_SinglePoint_HTS_Activity [AID504582, Type: screening] | HSP40, subfamily A, putative [Plasmodium falciparum 3D7] [gi:124809271] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | In vivo-based yeast HTS to detect compounds rescuing yeast growth/survival of Plasmodium Falciparum HSP40-mediated toxicity Measured in Whole Organism System Using Plate Reader - 2120-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 504582 | | BioAssay type | screening | | Target | HSP40, subfamily A, putative [Plasmodium falciparum 3D7] [gi:124809271] | | PubMed | | | Data Table |  |
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| 49 | [SID17433966] | Active | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the prolyl oligopeptidase-like enzyme (PREPL) [AID2751, Type: screening] | Prolyl endopeptidase-like [Homo sapiens] [gi:153217451] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the prolyl oligopeptidase-like enzyme (PREPL) | | AID | 2751 | | BioAssay type | screening | | Target | Prolyl endopeptidase-like [Homo sapiens] [gi:153217451] | | PubMed | | | Data Table |  |
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| 50 | [SID17433966] | Active | | | Fluorescence polarization-based biochemical high throughput confirmation assay to identify inhibitors of the prolyl oligopeptidase-like enzyme (PREPL) [AID2803, Type: screening] | Prolyl endopeptidase-like [Homo sapiens] [gi:153217451] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 17433966 | | CID | 56642923 | | Outcome | Active | | BioAssay | Fluorescence polarization-based biochemical high throughput confirmation assay to identify inhibitors of the prolyl oligopeptidase-like enzyme (PREPL) | | AID | 2803 | | BioAssay type | screening | | Target | Prolyl endopeptidase-like [Homo sapiens] [gi:153217451] | | PubMed | | | Data Table |  |
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