| 1 | [SID24813462] | Active | EC50 | 2.8 | 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. | 1 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | EC50 | 2.8 [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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| 2 | [SID24813462] | Active | Potency | 3.5481 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 3.5481 [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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| 3 | [SID24813462] | Active | Potency | 3.5481 | qHTS for Inhibitors of Polymerase Iota [AID588590, Type: confirmatory] | DNA polymerase iota [Homo sapiens] [gi:154350220] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 3.5481 [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 | [SID24813462] | Active | AC50 | 4.119 | 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. | 4 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | AC50 | 4.119 [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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| 5 | [SID24813462] | Active | EC50 | 5.392 | 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. | 5 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | EC50 | 5.392 [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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| 6 | [SID24813462] | Active | Potency | 6.3096 | qHTS for Inhibitors of Glutaminase (GLS) [AID624170, Type: confirmatory] | GLS protein [Homo sapiens] [gi:71051501] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS for Inhibitors of Glutaminase (GLS) | | AID | 624170 | | BioAssay type | confirmatory | | Target | GLS protein [Homo sapiens] [gi:71051501] | | PubMed | | | Data Table |  |
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| 7 | [SID24813462] | Active | AC50 | 9.176 | 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. | 7 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | AC50 | 9.176 [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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| 8 | [SID24813462] | Active | IC50 | 9.45 | AlphaScreen confirmatory assay for validation of inhibitors of SUMOylation [AID2018, Type: confirmatory] | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | IC50 | 9.45 [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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| 9 | [SID24813462] | Active | IC50 | 11.67 | A Cell Based Assay for the Identification of Lead Compounds with Inhibitory Activity against HIV-1 Fusion (CCR5 Tropic HIV-1 Fusion Inhibition Assay) - Dose Response [AID2279, Type: confirmatory] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | IC50 | 11.67 [uM] | | BioAssay | A Cell Based Assay for the Identification of Lead Compounds with Inhibitory Activity against HIV-1 Fusion (CCR5 Tropic HIV-1 Fusion Inhibition Assay) - Dose Response | | AID | 2279 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 10 | [SID24813462] | Active | IC50 | 12.15 | 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. | 10 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | IC50 | 12.15 [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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| 11 | [SID24813462] | Active | Potency | 12.5893 | qHTS Assay for Inhibitors of Human Jumonji Domain Containing 2E (JMJD2E) [AID2147, Type: confirmatory] | Chain A, Crystal Structure Of The Human 2-Oxoglutarate Oxygenase Loc390245 [gi:221046486] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Jumonji Domain Containing 2E (JMJD2E) | | AID | 2147 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of The Human 2-Oxoglutarate Oxygenase Loc390245 [gi:221046486] | | PubMed | | | Data Table |  |
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| 12 | [SID24813462] | Active | Potency | 12.5893 | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
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| 13 | [SID24813462] | Active | Potency | 12.5893 | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
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| 14 | [SID87544717] | Active | IC50 | 15.1 | SAR analysis of compounds that inhibit Human Immunodeficiency Virus Fusion. [AID434967, Type: confirmatory] | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 87544717 | | CID | 16194028 | | Outcome | Active | | IC50 | 15.1 [uM] | | BioAssay | SAR analysis of compounds that inhibit Human Immunodeficiency Virus Fusion. | | AID | 434967 | | BioAssay type | confirmatory | | Target | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] | | PubMed | | | Data Table |  |
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| 15 | [SID87544717] | Active | IC50 | 20.1 | SAR analysis of compounds that inhibit Human Immunodeficiency Virus Fusion, cell-cell fusion assay [AID435029, Type: confirmatory] | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 87544717 | | CID | 16194028 | | Outcome | Active | | IC50 | 20.1 [uM] | | BioAssay | SAR analysis of compounds that inhibit Human Immunodeficiency Virus Fusion, cell-cell fusion assay | | AID | 435029 | | BioAssay type | confirmatory | | Target | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] | | PubMed | | | Data Table |  |
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| 16 | [SID24813462] | Active | Potency | 22.3872 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 22.3872 [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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| 17 | [SID24813462] | Active | Potency | 22.3872 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 22.3872 [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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| 18 | [SID24813462] | Active | IC50 | 22.8 | uHTS fluorescence assay for the identification of Human Immunodeficiency Virus Fusion Inhibitors. [AID1986, Type: confirmatory] | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | IC50 | 22.8 [uM] | | BioAssay | uHTS fluorescence assay for the identification of Human Immunodeficiency Virus Fusion Inhibitors. | | AID | 1986 | | BioAssay type | confirmatory | | Target | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] | | PubMed | | | Data Table |  |
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| 19 | [SID24813462] | Active | Potency | 23.9341 | 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. | 19 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 23.9341 [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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| 20 | [SID24813462] | Active | Potency | 31.6228 | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a [AID504332, Type: confirmatory] | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a | | AID | 504332 | | BioAssay type | confirmatory | | Target | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] | | PubMed | | | Data Table |  |
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| 21 | [SID24813462] | Active | IC50 | 37.7 | uHTS HTRF assay for identification of inhibitors of SUMOylation [AID2006, Type: confirmatory] | SUMO-conjugating enzyme UBC9 [Homo sapiens] [gi:4507785] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | IC50 | 37.7 [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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| 22 | [SID87544717] | Active | IC50 | 41.9 | A Cell Based Assay for the Characterization of Lead Compounds with Antiviral Activity against HIV-1 (CCR5-Tropic HIV-1 MAGI Antiviral Assay) - Secondary Assay [AID2644, Type: confirmatory] | |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 87544717 | | CID | 16194028 | | Outcome | Active | | IC50 | 41.9 [uM] | | BioAssay | A Cell Based Assay for the Characterization of Lead Compounds with Antiviral Activity against HIV-1 (CCR5-Tropic HIV-1 MAGI Antiviral Assay) - Secondary Assay | | AID | 2644 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 23 | [SID24813462] | Active | Potency | 44.6684 | 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. | 23 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 44.6684 [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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| 24 | [SID24813462] | Active | Potency | 44.6684 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
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| 25 | [SID24813462] | Active | Potency | 44.6684 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
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| 26 | [SID24813462] | Active | Potency | 44.6684 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
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| 27 | [SID24813462] | Active | Potency | 44.6684 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
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| 28 | [SID24813462] | 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. | 28 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | 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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| 29 | [SID24813462] | Active | | | uHTS Fluorescent Assay Using Nedd8 Protein Substrate for Identification of Inhibitors of Sentrin-Specific Protease 8 (SENP8) [AID602440, Type: screening] | SENP8 gene product [Homo sapiens] [gi:262118306] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | BioAssay | uHTS Fluorescent Assay Using Nedd8 Protein Substrate for Identification of Inhibitors of Sentrin-Specific Protease 8 (SENP8) | | AID | 602440 | | BioAssay type | screening | | Target | SENP8 gene product [Homo sapiens] [gi:262118306] | | PubMed | | | Data Table |  |
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| 30 | [SID24813462] | Active | | | uHTS identification of inhibitors of NadD in a Colorimetric assay [AID602399, Type: screening] | hypothetical protein SA1422 [Staphylococcus aureus subsp. aureus N315] [gi:15927174] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | BioAssay | uHTS identification of inhibitors of NadD in a Colorimetric assay | | AID | 602399 | | BioAssay type | screening | | Target | hypothetical protein SA1422 [Staphylococcus aureus subsp. aureus N315] [gi:15927174] | | PubMed | | | Data Table |  |
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| 31 | [SID24813462] | 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. | 31 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | 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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| 32 | [SID24813462] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 33 | [SID24813462] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 34 | [SID24813462] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 35 | [SID24813462] | Active | | | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac activated mutant [AID764, Type: screening] | Rac1 protein [Homo sapiens] [gi:8574038] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | BioAssay | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac activated mutant | | AID | 764 | | BioAssay type | screening | | Target | Rac1 protein [Homo sapiens] [gi:8574038] | | PubMed | | | Data Table |  |
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| 36 | [SID24813462] | Active | | | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac activated mutant [AID764, Type: screening] | Rac1 protein [Homo sapiens] [gi:8574038] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | BioAssay | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac activated mutant | | AID | 764 | | BioAssay type | screening | | Target | Rac1 protein [Homo sapiens] [gi:8574038] | | PubMed | | | Data Table |  |
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| 37 | [SID24813462] | Active | | | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype [AID761, Type: screening] | cell division cycle 42 (GTP binding protein, 25kDa) [Homo sapiens] [gi:56202836] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Active | | BioAssay | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype | | AID | 761 | | BioAssay type | screening | | Target | cell division cycle 42 (GTP binding protein, 25kDa) [Homo sapiens] [gi:56202836] | | PubMed | | | Data Table |  |
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| 38 | [SID24813462] | 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. | 38 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | 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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| 39 | [SID24813462] | 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. | 39 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | 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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| 40 | [SID24813462] | 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. | 40 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | 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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| 41 | [SID24813462] | Inactive | Potency | 0.0738 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Inactive | | Potency | 0.0738 [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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| 42 | [SID24813462] | Inactive | Potency | 1.8526 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Inactive | | Potency | 1.8526 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation | | AID | 504834 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 43 | [SID24813462] | Inactive | Potency | 20.0308 | qHTS Fluorescence Polarization (FP) Assay for Inhibitors of MLL CXXC domain - DNA interaction: Texas Red FP [AID624161, Type: confirmatory] | |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Inactive | | Potency | 20.0308 [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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| 44 | [SID87544717] | Inactive | TC50 | 100 | A Cell Based Assay for the Characterization of Lead Compounds with Antiviral Activity against HIV-1 (CCR5-Tropic HIV-1 MAGI Antiviral Assay) - Secondary Cytotoxicity Screen [AID2649, Type: confirmatory] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 87544717 | | CID | 16194028 | | Outcome | Inactive | | TC50 | 100 [uM] | | BioAssay | A Cell Based Assay for the Characterization of Lead Compounds with Antiviral Activity against HIV-1 (CCR5-Tropic HIV-1 MAGI Antiviral Assay) - Secondary Cytotoxicity Screen | | AID | 2649 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 45 | [SID87544717] | Inactive | CC50 | 220 | SAR analysis of compounds that inhibit Human Immunodeficiency Virus Fusion, cytoxicity assay [AID435031, Type: confirmatory] | |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 87544717 | | CID | 16194028 | | Outcome | Inactive | | CC50 | 220 [uM] | | BioAssay | SAR analysis of compounds that inhibit Human Immunodeficiency Virus Fusion, cytoxicity assay | | AID | 435031 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 46 | [SID24813462] | Inactive | | | uHTS identification of small molecule activators of the adaptive arm of the Unfolded Protein response via a luminescent-based reporter assay [AID463104, Type: screening] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule activators of the adaptive arm of the Unfolded Protein response via a luminescent-based reporter assay | | AID | 463104 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 47 | [SID24813462] | Inactive | | | 384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC [AID463187, Type: screening] | |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Inactive | | BioAssay | 384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC | | AID | 463187 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 48 | [SID24813462] | Inactive | | | Phenotypic HTS multiplex for antifungal efflux pump inhibitors [AID485275, Type: screening] | |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Inactive | | BioAssay | Phenotypic HTS multiplex for antifungal efflux pump inhibitors | | AID | 485275 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 49 | [SID24813462] | Inactive | Potency | | qHTS Assay for Small Molecule Inhibitors of Mitochondrial Division or Activators of Mitochondrial Fusion [AID485298, Type: confirmatory] | |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of Mitochondrial Division or Activators of Mitochondrial Fusion | | AID | 485298 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 50 | [SID24813462] | Inactive | | | Fluorescence-based counterscreen for orexin 1 receptor (OX1R) antagonists: cell-based assay to identify antagonists of the parental CHO cell line [AID463079, Type: screening] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 24813462 | | CID | 16194028 | | Outcome | Inactive | | BioAssay | Fluorescence-based counterscreen for orexin 1 receptor (OX1R) antagonists: cell-based assay to identify antagonists of the parental CHO cell line | | AID | 463079 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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