| 1 | [SID49726196] | Active | Potency | 44.6684 | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a [AID504332, Type: confirmatory] | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a | | AID | 504332 | | BioAssay type | confirmatory | | Target | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] | | PubMed | | | Data Table |  |
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| 2 | [SID49726196] | Active | AC50 | 99.3 | Fluorescent Polarization Homogeneous Dose Retest to Confirm Inhibitors of Mex-5 Binding to TCR-2 [AID449745, Type: confirmatory] | Zinc finger protein mex- [gi:55976631] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Active | | AC50 | 99.3 [uM] | | BioAssay | Fluorescent Polarization Homogeneous Dose Retest to Confirm Inhibitors of Mex-5 Binding to TCR-2 | | AID | 449745 | | BioAssay type | confirmatory | | Target | Zinc finger protein mex- [gi:55976631] | | PubMed | | | Data Table |  |
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| 3 | [SID49726196] | Active | AC50 | 99.3 | Fluorescent Polarization Homogeneous Dose Retest to Confirm Inhibitors of Mex-5 Binding to TCR-2 [AID449745, Type: confirmatory] | Zinc finger protein mex- [gi:55976631] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Active | | AC50 | 99.3 [uM] | | BioAssay | Fluorescent Polarization Homogeneous Dose Retest to Confirm Inhibitors of Mex-5 Binding to TCR-2 | | AID | 449745 | | BioAssay type | confirmatory | | Target | Zinc finger protein mex- [gi:55976631] | | PubMed | | | Data Table |  |
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| 4 | [SID49726196] | Inactive | AC50 | | POS-1 FP counterscreen Measured in Biochemical System Using Plate Reader - 2024-02_Inhibitor_Dose_CherryPick_Activity_Set2 [AID493130, Type: confirmatory] | POsterior Segregation family member (pos-1) [Caenorhabditis elegans] [gi:17562800] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | AC50 | [uM] | | BioAssay | POS-1 FP counterscreen Measured in Biochemical System Using Plate Reader - 2024-02_Inhibitor_Dose_CherryPick_Activity_Set2 | | AID | 493130 | | BioAssay type | confirmatory | | Target | POsterior Segregation family member (pos-1) [Caenorhabditis elegans] [gi:17562800] | | PubMed | | | Data Table |  |
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| 5 | [SID49726196] | Inactive | | | uHTS identification of APOBEC3A DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay [AID493011, Type: screening] | APOBEC3A gene product [Homo sapiens] [gi:21955158] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | uHTS identification of APOBEC3A DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay | | AID | 493011 | | BioAssay type | screening | | Target | APOBEC3A gene product [Homo sapiens] [gi:21955158] | | PubMed | | | Data Table |  |
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| 6 | [SID49726196] | Inactive | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. [AID1947, Type: screening] | Fam108b protein [Mus musculus] [gi:21595511] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. | | AID | 1947 | | BioAssay type | screening | | Target | Fam108b protein [Mus musculus] [gi:21595511] | | PubMed | | | Data Table |  |
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| 7 | [SID49726196] | Inactive | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. [AID1947, Type: screening] | Fam108b protein [Mus musculus] [gi:21595511] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. | | AID | 1947 | | BioAssay type | screening | | Target | Fam108b protein [Mus musculus] [gi:21595511] | | PubMed | | | Data Table |  |
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| 8 | [SID49726196] | Inactive | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. [AID1947, Type: screening] | Fam108b protein [Mus musculus] [gi:21595511] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. | | AID | 1947 | | BioAssay type | screening | | Target | Fam108b protein [Mus musculus] [gi:21595511] | | PubMed | | | Data Table |  |
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| 9 | [SID49726196] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that activate MrgX1 receptor signaling [AID588627, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that activate MrgX1 receptor signaling | | AID | 588627 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
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| 10 | [SID49726196] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that activate MrgX1 receptor signaling [AID588627, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that activate MrgX1 receptor signaling | | AID | 588627 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
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| 11 | [SID49726196] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that allosterically activate MrgX1 receptor signaling [AID588675, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that allosterically activate MrgX1 receptor signaling | | AID | 588675 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
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| 12 | [SID49726196] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that allosterically activate MrgX1 receptor signaling [AID588675, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that allosterically activate MrgX1 receptor signaling | | AID | 588675 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
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| 13 | [SID49726196] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling [AID588676, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling | | AID | 588676 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
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| 14 | [SID49726196] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling [AID588676, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling | | AID | 588676 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
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| 15 | [SID49726196] | Inactive | | | 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. | 15 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | 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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| 16 | [SID49726196] | Inactive | | | 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. | 16 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | 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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| 17 | [SID49726196] | Inactive | | | Multiplex HTS Screen of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae_specifically_ AGP1_MLPCN. [AID2066, Type: screening] | Agp1p [Saccharomyces cerevisiae S288c] [gi:85666113] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Multiplex HTS Screen of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae_specifically_ AGP1_MLPCN. | | AID | 2066 | | BioAssay type | screening | | Target | Agp1p [Saccharomyces cerevisiae S288c] [gi:85666113] | | PubMed | | | Data Table |  |
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| 18 | [SID49726196] | Inactive | | | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of the Ras-converting Enzyme [AID2563, Type: screening] | Rce1p [Saccharomyces cerevisiae S288c] [gi:6323930] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of the Ras-converting Enzyme | | AID | 2563 | | BioAssay type | screening | | Target | Rce1p [Saccharomyces cerevisiae S288c] [gi:6323930] | | PubMed | | | Data Table |  |
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| 19 | [SID49726196] | Inactive | | | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of the Ras-converting Enzyme [AID2563, Type: screening] | Rce1p [Saccharomyces cerevisiae S288c] [gi:6323930] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of the Ras-converting Enzyme | | AID | 2563 | | BioAssay type | screening | | Target | Rce1p [Saccharomyces cerevisiae S288c] [gi:6323930] | | PubMed | | | Data Table |  |
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| 20 | [SID49726196] | Inactive | | | uHTS identification of small molecule inhibitors of tim23-1 yeast via a luminescent assay [AID463212, Type: screening] | TPA: Tim23p [Saccharomyces cerevisiae S288c] [gi:285814664] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of tim23-1 yeast via a luminescent assay | | AID | 463212 | | BioAssay type | screening | | Target | TPA: Tim23p [Saccharomyces cerevisiae S288c] [gi:285814664] | | PubMed | | | Data Table |  |
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| 21 | [SID49726196] | Inactive | | | 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. | 21 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | 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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| 22 | [SID49726196] | Inactive | | | uHTS identification of small molecule inhibitors of tim10 yeast via a luminescent assay [AID463195, Type: screening] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of tim10 yeast via a luminescent assay | | AID | 463195 | | BioAssay type | screening | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
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| 23 | [SID49726196] | Inactive | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the membrane-associated serine protease Rv3671c in M.tuberculosis [AID2606, Type: screening] | membrane-associated serine protease [Mycobacterium tuberculosis H37Rv] [gi:15610807] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the membrane-associated serine protease Rv3671c in M.tuberculosis | | AID | 2606 | | BioAssay type | screening | | Target | membrane-associated serine protease [Mycobacterium tuberculosis H37Rv] [gi:15610807] | | PubMed | | | Data Table |  |
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| 24 | [SID49726196] | Inactive | | | Inhibitors of Mycobacterium tuberculosis UDP-galactopyranose mutase (UGM) enzyme - High throughput screening using Fluorescent polarization assay Measured in Biochemical System Using Plate Reader - 2105-01_Inhibitor_SinglePoint_HTS_Activity_Set6 [AID504406, Type: screening] | glf gene product [Mycobacterium tuberculosis H37Rv] [gi:15610945] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Inhibitors of Mycobacterium tuberculosis UDP-galactopyranose mutase (UGM) enzyme - High throughput screening using Fluorescent polarization assay Measured in Biochemical System Using Plate Reader - 2105-01_Inhibitor_SinglePoint_HTS_Activity_Set6 | | AID | 504406 | | BioAssay type | screening | | Target | glf gene product [Mycobacterium tuberculosis H37Rv] [gi:15610945] | | PubMed | | | Data Table |  |
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| 25 | [SID49726196] | Inactive | | | 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. | 25 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | 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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| 26 | [SID49726196] | Inactive | | | Absorbance-based primary bacterial cell-based high throughput screening assay to identify inhibitors of AddAB recombination protein complex [AID435030, Type: screening] | hypothetical protein HP1089 [Helicobacter pylori 26695] [gi:15645703] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Absorbance-based primary bacterial cell-based high throughput screening assay to identify inhibitors of AddAB recombination protein complex | | AID | 435030 | | BioAssay type | screening | | Target | hypothetical protein HP1089 [Helicobacter pylori 26695] [gi:15645703] | | PubMed | | | Data Table |  |
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| 27 | [SID49726196] | Inactive | | | MLPCN Streptokinase Expression Inhibition [AID1662, Type: screening] | streptokinase A precursor [Streptococcus pyogenes M1 GAS] [gi:15675770] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | 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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| 28 | [SID49726196] | Inactive | IC50 | | Identification of SV40 T antigen inhibitors: A route to novel anti-viral reagents [AID1903, Type: confirmatory] | large T antigen [Simian virus 40] [gi:297591903] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | Identification of SV40 T antigen inhibitors: A route to novel anti-viral reagents | | AID | 1903 | | BioAssay type | confirmatory | | Target | large T antigen [Simian virus 40] [gi:297591903] | | PubMed | | | Data Table |  |
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| 29 | [SID49726196] | Inactive | | | qHTS of Yeast-based Assay for SARS-CoV PLP [AID485353, Type: confirmatory] | orf1ab polyprotein (pp1ab) [SARS coronavirus] [gi:30124074] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | qHTS of Yeast-based Assay for SARS-CoV PLP | | AID | 485353 | | BioAssay type | confirmatory | | Target | orf1ab polyprotein (pp1ab) [SARS coronavirus] [gi:30124074] | | PubMed | | | Data Table |  |
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| 30 | [SID49726196] | Inactive | | | qHTS of Yeast-based Assay for SARS-CoV PLP [AID485353, Type: confirmatory] | orf1ab polyprotein (pp1ab) [SARS coronavirus] [gi:30124074] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | qHTS of Yeast-based Assay for SARS-CoV PLP | | AID | 485353 | | BioAssay type | confirmatory | | Target | orf1ab polyprotein (pp1ab) [SARS coronavirus] [gi:30124074] | | PubMed | | | Data Table |  |
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| 31 | [SID49726196] | Inactive | | | qHTS of Yeast-based Assay for SARS-CoV PLP [AID485353, Type: confirmatory] | orf1ab polyprotein (pp1ab) [SARS coronavirus] [gi:30124074] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | qHTS of Yeast-based Assay for SARS-CoV PLP | | AID | 485353 | | BioAssay type | confirmatory | | Target | orf1ab polyprotein (pp1ab) [SARS coronavirus] [gi:30124074] | | PubMed | | | Data Table |  |
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| 32 | [SID49726196] | Inactive | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of tRNA 2'-phosphotransferase (TPT1). [AID1962, Type: screening] | likely tRNA 2'-phosphotransferase [Candida albicans SC5314] [gi:68476498] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of tRNA 2'-phosphotransferase (TPT1). | | AID | 1962 | | BioAssay type | screening | | Target | likely tRNA 2'-phosphotransferase [Candida albicans SC5314] [gi:68476498] | | PubMed | | | Data Table |  |
|
| 33 | [SID49726196] | Inactive | Potency | | qHTS Assay to Find Inhibitors of T. brucei phosphofructokinase [AID485367, Type: confirmatory] | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay to Find Inhibitors of T. brucei phosphofructokinase | | AID | 485367 | | BioAssay type | confirmatory | | Target | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] | | PubMed | | | Data Table |  |
|
| 34 | [SID49726196] | Inactive | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the Epstein-Barr virus nuclear antigen 1 (EBNA-1). [AID1950, Type: screening] | EBNA-1 protein [Human herpesvirus 4] [gi:23893623] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the Epstein-Barr virus nuclear antigen 1 (EBNA-1). | | AID | 1950 | | BioAssay type | screening | | Target | EBNA-1 protein [Human herpesvirus 4] [gi:23893623] | | PubMed | | | Data Table |  |
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| 35 | [SID49726196] | Inactive | | | Counterscreen for inhibitors of EBNA-1: fluorescence polarization-based biochemical high throughput primary assay to identify inhibitors of the Epstein-Barr virus-encoded protein, ZTA. [AID2234, Type: screening] | BZLF1 [Human herpesvirus 4] [gi:82503229] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Counterscreen for inhibitors of EBNA-1: fluorescence polarization-based biochemical high throughput primary assay to identify inhibitors of the Epstein-Barr virus-encoded protein, ZTA. | | AID | 2234 | | BioAssay type | screening | | Target | BZLF1 [Human herpesvirus 4] [gi:82503229] | | PubMed | | | Data Table |  |
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| 36 | [SID49726196] | Inactive | | | Fluorescence Polarization Cell-Free Homogeneous Primary HTS to Identify Inhibitors of the LANA Histone H2A/H2B Interaction [AID2629, Type: screening] | LANA [Human herpesvirus 8] [gi:139472804] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Fluorescence Polarization Cell-Free Homogeneous Primary HTS to Identify Inhibitors of the LANA Histone H2A/H2B Interaction | | AID | 2629 | | BioAssay type | screening | | Target | LANA [Human herpesvirus 8] [gi:139472804] | | PubMed | | | Data Table |  |
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| 37 | [SID49726196] | Inactive | | | Primary biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase [AID1527, Type: screening] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Primary biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase | | AID | 1527 | | BioAssay type | screening | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
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| 38 | [SID49726196] | Inactive | | | Primary biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase [AID1527, Type: screening] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Primary biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase | | AID | 1527 | | BioAssay type | screening | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
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| 39 | [SID49726196] | Inactive | | | MLPCN Ras selective lethality-BJeLR viability [AID1554, Type: screening] | |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | MLPCN Ras selective lethality-BJeLR viability | | AID | 1554 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 40 | [SID49726196] | Inactive | IC50 | | A Cell Based Assay for the Identification of Lead Compounds with Anti-Viral Activity Against West Nile Virus [AID1621, Type: confirmatory] | |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | A Cell Based Assay for the Identification of Lead Compounds with Anti-Viral Activity Against West Nile Virus | | AID | 1621 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 41 | [SID49726196] | Inactive | | | High Throughput Imaging Assay for Hepatic Lipid Droplet Formation [AID1656, Type: screening] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | High Throughput Imaging Assay for Hepatic Lipid Droplet Formation | | AID | 1656 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 42 | [SID49726196] | Inactive | | | MLPCN Platelet Activation -Dense Granule Release [AID1663, Type: screening] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | MLPCN Platelet Activation -Dense Granule Release | | AID | 1663 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 43 | [SID49726196] | Inactive | | | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - inhibitors [AID1813, Type: screening] | |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - inhibitors | | AID | 1813 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 44 | [SID49726196] | Inactive | | | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - activators [AID1814, Type: screening] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - activators | | AID | 1814 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 45 | [SID49726196] | Inactive | | | 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. | 45 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | 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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| 46 | [SID49726196] | Inactive | IC50 | | A small molecule screen for inhibitors of the PhoP regulon in Salmonella typhi [AID1850, Type: confirmatory] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | A small molecule screen for inhibitors of the PhoP regulon in Salmonella typhi | | AID | 1850 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 47 | [SID49726196] | Inactive | IC50 | | A small molecule screen for inhibitors of the PhoP regulon in Salmonella Typhimurium [AID1863, Type: confirmatory] | |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | A small molecule screen for inhibitors of the PhoP regulon in Salmonella Typhimurium | | AID | 1863 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 48 | [SID49726196] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Polyadenylation [AID1875, Type: screening] | |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Polyadenylation | | AID | 1875 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 49 | [SID49726196] | Inactive | | | Luminescence Cell-Based/Microorganism Primary HTS to Identify Inhibitors of T.Cruzi Replication [AID1885, Type: screening] | |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based/Microorganism Primary HTS to Identify Inhibitors of T.Cruzi Replication | | AID | 1885 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 50 | [SID49726196] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Transcriptional Activators of Hypoxia-Inducible Factor Pathway [AID1910, Type: screening] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 49726196 | | CID | 56642904 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Transcriptional Activators of Hypoxia-Inducible Factor Pathway | | AID | 1910 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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