| 1 | [SID24822911] | Active | Potency | 1 | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 1 [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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| 2 | [SID24822911] | Active | EC50 | 3.022 | Luminescence Microorganism-Based Dose Confirmation HTS to Identify Inhibitors of Streptokinase Promotor Activity [AID1902, Type: confirmatory] | streptokinase A precursor [Streptococcus pyogenes M1 GAS] [gi:15675770] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | EC50 | 3.022 [uM] | | BioAssay | Luminescence Microorganism-Based Dose Confirmation HTS to Identify Inhibitors of Streptokinase Promotor Activity | | AID | 1902 | | BioAssay type | confirmatory | | Target | streptokinase A precursor [Streptococcus pyogenes M1 GAS] [gi:15675770] | | PubMed | | | Data Table |  |
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| 3 | [SID24822911] | Active | EC50 | 4.281 | Luminescence Microorganism-Based Dose Confirmation HTS to Identify Compounds Cytotoxic to SK(-)GAS Group A Streptococcus [AID1900, Type: confirmatory] | |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | EC50 | 4.281 [uM] | | BioAssay | Luminescence Microorganism-Based Dose Confirmation HTS to Identify Compounds Cytotoxic to SK(-)GAS Group A Streptococcus | | AID | 1900 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 4 | [SID24822911] | Active | EC50 | 4.634 | Luminescence Microorganism-Based Dose Response HTS to Identify Compounds Cytotoxic to Streptococcus [AID1915, Type: confirmatory] | |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | EC50 | 4.634 [uM] | | BioAssay | Luminescence Microorganism-Based Dose Response HTS to Identify Compounds Cytotoxic to Streptococcus | | AID | 1915 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 5 | [SID24822911] | Active | Potency | 7.9433 | 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. | 5 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 7.9433 [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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| 6 | [SID24822911] | Active | IC50 | 12.54 | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) [AID1445, Type: confirmatory] | m1-family aminopeptidase [Plasmodium falciparum 3D7] [gi:124512980] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | IC50 | 12.54 [uM] | | BioAssay | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) | | AID | 1445 | | BioAssay type | confirmatory | | Target | m1-family aminopeptidase [Plasmodium falciparum 3D7] [gi:124512980] | | PubMed | | | Data Table |  |
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| 7 | [SID24822911] | Active | IC50 | 12.54 | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) [AID1445, Type: confirmatory] | m1-family aminopeptidase [Plasmodium falciparum 3D7] [gi:124512980] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | IC50 | 12.54 [uM] | | BioAssay | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) | | AID | 1445 | | BioAssay type | confirmatory | | Target | m1-family aminopeptidase [Plasmodium falciparum 3D7] [gi:124512980] | | PubMed | | | Data Table |  |
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| 8 | [SID24822911] | Active | Potency | 12.5893 | Confirmation qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) [AID2572, Type: confirmatory] | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | | AID | 2572 | | BioAssay type | confirmatory | | Target | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] | | PubMed | | | Data Table |  |
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| 9 | [SID24822911] | Active | Potency | 14.1254 | Confirmation Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) [AID489007, Type: confirmatory] | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 14.1254 [uM] | | BioAssay | Confirmation Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | | AID | 489007 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | | PubMed | | | Data Table |  |
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| 10 | [SID24822911] | Active | Potency | 14.1254 | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) [AID485290, Type: confirmatory] | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 14.1254 [uM] | | BioAssay | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | | AID | 485290 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | | PubMed | | | Data Table |  |
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| 11 | [SID24822911] | Active | Potency | 17.7828 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 17.7828 [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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| 12 | [SID24822911] | Active | Potency | 17.7828 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 17.7828 [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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| 13 | [SID24822911] | Active | Potency | 17.7828 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 17.7828 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
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| 14 | [SID24822911] | Active | Potency | 17.7828 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 17.7828 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Eta | | AID | 588591 | | BioAssay type | confirmatory | | Target | DNA polymerase eta [Homo sapiens] [gi:5729982] | | PubMed | | | Data Table |  |
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| 15 | [SID24822911] | Active | Potency | 19.9526 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 19.9526 [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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| 16 | [SID24822911] | Active | Potency | 19.9526 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 19.9526 [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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| 17 | [SID24822911] | Active | Potency | 19.9526 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 19.9526 [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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| 18 | [SID24822911] | Active | Potency | 26.8545 | 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. | 18 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 26.8545 [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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| 19 | [SID24822911] | Active | Potency | 28.1838 | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) [AID2517, Type: confirmatory] | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 28.1838 [uM] | | BioAssay | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | | AID | 2517 | | BioAssay type | confirmatory | | Target | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] | | PubMed | | | Data Table |  |
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| 20 | [SID24822911] | Active | Potency | 39.8107 | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain [AID504339, Type: confirmatory] | Chain A, Jmjd2a Tandem Tudor Domains In Complex With A Trimethylated Histone H4-K20 Peptide [gi:162330054] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain | | AID | 504339 | | BioAssay type | confirmatory | | Target | Chain A, Jmjd2a Tandem Tudor Domains In Complex With A Trimethylated Histone H4-K20 Peptide [gi:162330054] | | PubMed | | | Data Table |  |
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| 21 | [SID24822911] | Active | Potency | 39.8107 | qHTS for Inhibitors of WRN Helicase [AID651768, Type: confirmatory] | WRN [Homo sapiens] [gi:3719421] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS for Inhibitors of WRN Helicase | | AID | 651768 | | BioAssay type | confirmatory | | Target | WRN [Homo sapiens] [gi:3719421] | | PubMed | | | Data Table |  |
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| 22 | [SID24822911] | Active | Potency | 44.6684 | qHTS Assay for the Inhibitors of Human Flap endonuclease 1 (FEN1). [AID588795, Type: confirmatory] | flap endonuclease 1 [Homo sapiens] [gi:4758356] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | qHTS Assay for the Inhibitors of Human Flap endonuclease 1 (FEN1). | | AID | 588795 | | BioAssay type | confirmatory | | Target | flap endonuclease 1 [Homo sapiens] [gi:4758356] | | PubMed | | | Data Table |  |
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| 23 | [SID24822911] | Active | Potency | 50.1187 | HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails [AID540317, Type: confirmatory] | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 50.1187 [uM] | | BioAssay | HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails | | AID | 540317 | | BioAssay type | confirmatory | | Target | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] | | PubMed | | | Data Table |  |
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| 24 | [SID24822911] | Active | Potency | 50.1187 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | 50.1187 [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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| 25 | [SID24822911] | Active | | | MLPCN Streptokinase Expression Inhibition [AID1662, Type: screening] | streptokinase A precursor [Streptococcus pyogenes M1 GAS] [gi:15675770] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | BioAssay | MLPCN Streptokinase Expression Inhibition | | AID | 1662 | | BioAssay type | screening | | Target | streptokinase A precursor [Streptococcus pyogenes M1 GAS] [gi:15675770] | | PubMed | | | Data Table |  |
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| 26 | [SID24822911] | Active | IC50 | | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (PABP) [AID2014, Type: confirmatory] | polyadenylate-binding protein 1 [Homo sapiens] [gi:46367787] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | IC50 | [uM] | | BioAssay | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (PABP) | | AID | 2014 | | BioAssay type | confirmatory | | Target | polyadenylate-binding protein 1 [Homo sapiens] [gi:46367787] | | PubMed | | | Data Table |  |
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| 27 | [SID24822911] | Active | | | uHTS Colorimetric assay for identification of inhibitors of Scp-1 [AID493091, Type: screening] | carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 1 [Homo sapiens] [gi:10864009] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | BioAssay | uHTS Colorimetric assay for identification of inhibitors of Scp-1 | | AID | 493091 | | BioAssay type | screening | | Target | carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform 1 [Homo sapiens] [gi:10864009] | | PubMed | | | Data Table |  |
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| 28 | [SID24822911] | Active | | | Absorbance-based biochemical primary high throughput screening assay to identify inhibitors of Methionine sulfoxide reductase A (MsrA) [AID651718, Type: screening] | MSRA protein [Bos taurus] [gi:73586699] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | BioAssay | Absorbance-based biochemical primary high throughput screening assay to identify inhibitors of Methionine sulfoxide reductase A (MsrA) | | AID | 651718 | | BioAssay type | screening | | Target | MSRA protein [Bos taurus] [gi:73586699] | | PubMed | | | Data Table |  |
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| 29 | [SID24822911] | Active | | | Absorbance-based biochemical high throughput confirmation assay to identify inhibitors of Methionine sulfoxide reductase A (MsrA) [AID651822, Type: screening] | MSRA protein [Bos taurus] [gi:73586699] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | BioAssay | Absorbance-based biochemical high throughput confirmation assay to identify inhibitors of Methionine sulfoxide reductase A (MsrA) | | AID | 651822 | | BioAssay type | screening | | Target | MSRA protein [Bos taurus] [gi:73586699] | | PubMed | | | Data Table |  |
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| 30 | [SID24822911] | Active | IC50 | | Fluorescent assay for identification of compounds that inhibit VHR1 [AID1878, Type: confirmatory] | dual specificity protein phosphatase 3 [Homo sapiens] [gi:4758208] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | IC50 | [uM] | | BioAssay | Fluorescent assay for identification of compounds that inhibit VHR1 | | AID | 1878 | | BioAssay type | confirmatory | | Target | dual specificity protein phosphatase 3 [Homo sapiens] [gi:4758208] | | PubMed | | | Data Table |  |
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| 31 | [SID24822911] | Active | IC50 | | Fluorescent assay for identification of compounds that inhibit VHR1 [AID1878, Type: confirmatory] | dual specificity protein phosphatase 3 [Homo sapiens] [gi:4758208] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | IC50 | [uM] | | BioAssay | Fluorescent assay for identification of compounds that inhibit VHR1 | | AID | 1878 | | BioAssay type | confirmatory | | Target | dual specificity protein phosphatase 3 [Homo sapiens] [gi:4758208] | | PubMed | | | Data Table |  |
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| 32 | [SID24822911] | Active | | | uHTS Identification of Diaphorase Inhibitors and Chemcical Oxidizers: Counter Screen for Diaphorase-based Primary Assays [AID1217, Type: screening] | Dihydrolipoamide dehydrogenase [Homo sapiens] [gi:17391426] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | BioAssay | uHTS Identification of Diaphorase Inhibitors and Chemcical Oxidizers: Counter Screen for Diaphorase-based Primary Assays | | AID | 1217 | | BioAssay type | screening | | Target | Dihydrolipoamide dehydrogenase [Homo sapiens] [gi:17391426] | | PubMed | | | Data Table |  |
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| 33 | [SID24822911] | 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. | 33 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | 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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| 34 | [SID24822911] | 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. | 34 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | 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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| 35 | [SID24822911] | Active | | | Fluorescence-based biochemical primary high throughput screening assay to identify molecules that bind r(CAG) RNA repeats [AID651821, Type: screening] | |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical primary high throughput screening assay to identify molecules that bind r(CAG) RNA repeats | | AID | 651821 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 36 | [SID24822911] | Active | | | Fluorescence-based biochemical high throughput confirmation assay to identify molecules that bind r(CAG) RNA repeats [AID652065, Type: screening] | |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical high throughput confirmation assay to identify molecules that bind r(CAG) RNA repeats | | AID | 652065 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 37 | [SID24822911] | Active | | | Counterscreen for molecules that bind rCAG RNA repeats: fluorescent based biochemical counterscreen assay for inhibitors of the DNA-based (5'CAG/3'GTC) TO-PRO-1 dye complex [AID652068, Type: screening] | |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | BioAssay | Counterscreen for molecules that bind rCAG RNA repeats: fluorescent based biochemical counterscreen assay for inhibitors of the DNA-based (5'CAG/3'GTC) TO-PRO-1 dye complex | | AID | 652068 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 38 | [SID24822911] | Active | | | 384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC [AID463187, Type: screening] | |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | BioAssay | 384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC | | AID | 463187 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 39 | [SID24822911] | Active | | | 384-well Z-Lyte format Hck-Nef inhibitor HTS: Confirmation Assays [AID463188, Type: other] | |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | BioAssay | 384-well Z-Lyte format Hck-Nef inhibitor HTS: Confirmation Assays | | AID | 463188 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 40 | [SID24822911] | Active | Potency | | qHTS for Inhibitors of phosphatidylinositol 5-phosphate 4-kinase (PI5P4K) [AID652105, Type: confirmatory] | Phosphatidylinositol 5-phosphate 4-kinase type-2 alpha [gi:18266879] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of phosphatidylinositol 5-phosphate 4-kinase (PI5P4K) | | AID | 652105 | | BioAssay type | confirmatory | | Target | Phosphatidylinositol 5-phosphate 4-kinase type-2 alpha [gi:18266879] | | PubMed | | | Data Table |  |
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| 41 | [SID24822911] | Active | IC50 | | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (eIF4H) [AID2012, Type: confirmatory] | Eukaryotic translation initiation factor 4H [Homo sapiens] [gi:45219878] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Active | | IC50 | [uM] | | BioAssay | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (eIF4H) | | AID | 2012 | | BioAssay type | confirmatory | | Target | Eukaryotic translation initiation factor 4H [Homo sapiens] [gi:45219878] | | PubMed | | | Data Table |  |
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| 42 | [SID24822911] | 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. | 42 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | 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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| 43 | [SID24822911] | 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. | 43 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | 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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| 44 | [SID24822911] | Inactive | Potency | 39.8107 | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase [AID1634, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Inactive | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1634 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
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| 45 | [SID24822911] | Inactive | Potency | 39.8107 | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase [AID1634, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Inactive | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1634 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
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| 46 | [SID24822911] | Inactive | Potency | 39.8107 | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase [AID1634, Type: confirmatory] | PKM gene product [Homo sapiens] [gi:33286418] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Inactive | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Muscle isoform 2 Pyruvate Kinase | | AID | 1634 | | BioAssay type | confirmatory | | Target | PKM gene product [Homo sapiens] [gi:33286418] | | PubMed | | | Data Table |  |
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| 47 | [SID24822911] | 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. | 47 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | 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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| 48 | [SID24822911] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao. [AID1439, Type: screening] | RGS7 [Homo sapiens] [gi:1166512] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao. | | AID | 1439 | | BioAssay type | screening | | Target | RGS7 [Homo sapiens] [gi:1166512] | | PubMed | | | Data Table |  |
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| 49 | [SID24822911] | Inactive | | | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Red Fluorophore) [AID880, Type: confirmatory] | RGS12 [Homo sapiens] [gi:3290016] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Inactive | | BioAssay | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Red Fluorophore) | | AID | 880 | | BioAssay type | confirmatory | | Target | RGS12 [Homo sapiens] [gi:3290016] | | PubMed | | | Data Table |  |
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| 50 | [SID24822911] | Inactive | | | S100A4: HTS Measured in Biochemical System Using Plate Reader - 7045-01_Inhibitor_SinglePoint_HTS_Activity [AID652163, Type: screening] | S100A4 [Homo sapiens] [gi:47496637] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 24822911 | | CID | 21234031 | | Outcome | Inactive | | BioAssay | S100A4: HTS Measured in Biochemical System Using Plate Reader - 7045-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 652163 | | BioAssay type | screening | | Target | S100A4 [Homo sapiens] [gi:47496637] | | PubMed | | | Data Table |  |
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