| 1 | [SID24823265] | Active | IC50 | 1.161 | FRET-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify epi-absorbance assay artifacts. [AID1926, Type: confirmatory] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 1.161 [uM] | | BioAssay | FRET-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify epi-absorbance assay artifacts. | | AID | 1926 | | BioAssay type | confirmatory | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
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| 2 | [SID24823265] | Active | IC50 | 1.161 | FRET-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify epi-absorbance assay artifacts. [AID1926, Type: confirmatory] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 1.161 [uM] | | BioAssay | FRET-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify epi-absorbance assay artifacts. | | AID | 1926 | | BioAssay type | confirmatory | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
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| 3 | [SID24823265] | Active | IC50 | 5.97 | Dose response confirmation of uHTS inhibitor hits from NadD in a Colorimetric assay [AID624317, Type: confirmatory] | hypothetical protein SA1422 [Staphylococcus aureus subsp. aureus N315] [gi:15927174] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 5.97 [uM] | | BioAssay | Dose response confirmation of uHTS inhibitor hits from NadD in a Colorimetric assay | | AID | 624317 | | BioAssay type | confirmatory | | Target | hypothetical protein SA1422 [Staphylococcus aureus subsp. aureus N315] [gi:15927174] | | PubMed | | | Data Table |  |
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| 4 | [SID24823265] | Active | IC50 | 9.147 | Epi-absorbance-based dose response biochemical high throughput screening assay for selective inhibitors of VIM-2 metallo-beta-lactamase [AID1919, Type: confirmatory] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 9.147 [uM] | | BioAssay | Epi-absorbance-based dose response biochemical high throughput screening assay for selective inhibitors of VIM-2 metallo-beta-lactamase | | AID | 1919 | | BioAssay type | confirmatory | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
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| 5 | [SID24823265] | Active | IC50 | 9.147 | Epi-absorbance-based dose response biochemical high throughput screening assay for selective inhibitors of VIM-2 metallo-beta-lactamase [AID1919, Type: confirmatory] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 9.147 [uM] | | BioAssay | Epi-absorbance-based dose response biochemical high throughput screening assay for selective inhibitors of VIM-2 metallo-beta-lactamase | | AID | 1919 | | BioAssay type | confirmatory | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
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| 6 | [SID24823265] | Active | Potency | 11.2202 | qHTS for inhibitors of ROR gamma transcriptional activity [AID2551, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | qHTS for inhibitors of ROR gamma transcriptional activity | | AID | 2551 | | BioAssay type | confirmatory | | Target | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] | | PubMed | | | Data Table |  |
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| 7 | [SID24823265] | Active | IC50 | 13.2 | 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. | 7 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 13.2 [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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| 8 | [SID24823265] | Active | IC50 | 15.78 | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) [AID1619, Type: confirmatory] | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 15.78 [uM] | | BioAssay | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) | | AID | 1619 | | BioAssay type | confirmatory | | Target | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] | | PubMed | | | Data Table |  |
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| 9 | [SID24823265] | Active | IC50 | 15.78 | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) [AID1619, Type: confirmatory] | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 15.78 [uM] | | BioAssay | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) | | AID | 1619 | | BioAssay type | confirmatory | | Target | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] | | PubMed | | | Data Table |  |
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| 10 | [SID24823265] | Active | IC50 | 15.78 | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) [AID1619, Type: confirmatory] | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 15.78 [uM] | | BioAssay | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) | | AID | 1619 | | BioAssay type | confirmatory | | Target | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] | | PubMed | | | Data Table |  |
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| 11 | [SID24823265] | Active | IC50 | 15.8 | Dose response confirmation of uHTS inhibitor hits from NadD in a Colorimetric assay - Set 2 [AID651709, Type: confirmatory] | hypothetical protein SA1422 [Staphylococcus aureus subsp. aureus N315] [gi:15927174] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 15.8 [uM] | | BioAssay | Dose response confirmation of uHTS inhibitor hits from NadD in a Colorimetric assay - Set 2 | | AID | 651709 | | BioAssay type | confirmatory | | Target | hypothetical protein SA1422 [Staphylococcus aureus subsp. aureus N315] [gi:15927174] | | PubMed | | | Data Table |  |
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| 12 | [SID24823265] | Active | Potency | 19.9526 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | Potency | 19.9526 [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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| 13 | [SID24823265] | Active | Potency | 19.9526 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | Potency | 19.9526 [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 | [SID24823265] | Active | EC50 | 22.32 | A Cell Based Assay for the Identification of Lead Compounds with Inhibitory Activity against HIV-1 Fusion (CCR5 Tropic HIV-1 Fusion Inhibition Assay) - Cytotoxicity Counter Screen - Dose Response [AID2286, Type: confirmatory] | |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | EC50 | 22.32 [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) - Cytotoxicity Counter Screen - Dose Response | | AID | 2286 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 15 | [SID24823265] | Active | Potency | 23.1093 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | Potency | 23.1093 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 16 | [SID24823265] | Active | Potency | 23.1093 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | Potency | 23.1093 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 17 | [SID24823265] | Active | Potency | 23.1093 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | Potency | 23.1093 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 18 | [SID24823265] | Active | IC50 | 44.41 | 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. | 18 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 44.41 [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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| 19 | [SID24823265] | 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. | 19 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | 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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| 20 | [SID24823265] | Active | Potency | 44.6684 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | Potency | 44.6684 [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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| 21 | [SID24823265] | Active | Potency | 50.1187 | 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. | 21 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | Potency | 50.1187 [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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| 22 | [SID24823265] | Active | IC50 | 109.18 | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) [AID1445, Type: confirmatory] | m1-family aminopeptidase [Plasmodium falciparum 3D7] [gi:124512980] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 109.18 [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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| 23 | [SID24823265] | Active | IC50 | 109.18 | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) [AID1445, Type: confirmatory] | m1-family aminopeptidase [Plasmodium falciparum 3D7] [gi:124512980] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | IC50 | 109.18 [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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| 24 | [SID24823265] | Active | | | uHTS for Calpain Inhibitors [AID1236, Type: screening] | calpain II [Sus scrofa] [gi:1628587] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | BioAssay | uHTS for Calpain Inhibitors | | AID | 1236 | | BioAssay type | screening | | Target | calpain II [Sus scrofa] [gi:1628587] | | PubMed | | | Data Table |  |
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| 25 | [SID24823265] | Active | | | uHTS for Calpain Inhibitors [AID1236, Type: screening] | calpain II [Sus scrofa] [gi:1628587] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | BioAssay | uHTS for Calpain Inhibitors | | AID | 1236 | | BioAssay type | screening | | Target | calpain II [Sus scrofa] [gi:1628587] | | PubMed | | | Data Table |  |
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| 26 | [SID24823265] | Active | | | Epi-absorbance-based confirmation assay for common VIM-2 and IMP-1 inhibitors: biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase. [AID2187, Type: screening] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | BioAssay | Epi-absorbance-based confirmation assay for common VIM-2 and IMP-1 inhibitors: biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase. | | AID | 2187 | | BioAssay type | screening | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
|
| 27 | [SID24823265] | Active | | | Epi-absorbance-based confirmation assay for common VIM-2 and IMP-1 inhibitors: biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase. [AID2187, Type: screening] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | BioAssay | Epi-absorbance-based confirmation assay for common VIM-2 and IMP-1 inhibitors: biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase. | | AID | 2187 | | BioAssay type | screening | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
|
| 28 | [SID24823265] | Active | | | 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. | 28 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | 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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| 29 | [SID24823265] | Active | | | 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. | 29 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | 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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| 30 | [SID24823265] | 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 | 24823265 | | CID | 44601849 | | 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 | [SID24823265] | Active | | | Single concentration confirmation of uHTS inhibitor hits from NadD in a Colorimetric assay [AID624309, Type: screening] | hypothetical protein SA1422 [Staphylococcus aureus subsp. aureus N315] [gi:15927174] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | BioAssay | Single concentration confirmation of uHTS inhibitor hits from NadD in a Colorimetric assay | | AID | 624309 | | BioAssay type | screening | | Target | hypothetical protein SA1422 [Staphylococcus aureus subsp. aureus N315] [gi:15927174] | | PubMed | | | Data Table |  |
|
| 32 | [SID24823265] | Active | | | FRET-based counterscreen assay for selective VIM-2 inhibitors: biochemical high throughput screening assay to identify epi-absorbance assay artifacts [AID1857, Type: screening] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | BioAssay | FRET-based counterscreen assay for selective VIM-2 inhibitors: biochemical high throughput screening assay to identify epi-absorbance assay artifacts | | AID | 1857 | | BioAssay type | screening | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
|
| 33 | [SID24823265] | Active | | | FRET-based counterscreen assay for selective VIM-2 inhibitors: biochemical high throughput screening assay to identify epi-absorbance assay artifacts [AID1857, Type: screening] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | BioAssay | FRET-based counterscreen assay for selective VIM-2 inhibitors: biochemical high throughput screening assay to identify epi-absorbance assay artifacts | | AID | 1857 | | BioAssay type | screening | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
|
| 34 | [SID24823265] | 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. | 34 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | 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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| 35 | [SID24823265] | 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. | 35 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | 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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| 36 | [SID24823265] | 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. | 36 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | 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 |  |
|
| 37 | [SID24823265] | Active | | | Fluorescence-based biochemical high throughput confirmation assay to identify molecules that bind r(CAG) RNA repeats [AID652065, Type: screening] | |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | 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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| 38 | [SID24823265] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | 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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| 39 | [SID24823265] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | 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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| 40 | [SID24823265] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | 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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| 41 | [SID24823265] | Active | | | uHTS fluorescent assay for identification of inhibitors of ATG4B [AID504462, Type: screening] | cysteine protease ATG4B isoform a [Homo sapiens] [gi:47132611] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | BioAssay | uHTS fluorescent assay for identification of inhibitors of ATG4B | | AID | 504462 | | BioAssay type | screening | | Target | cysteine protease ATG4B isoform a [Homo sapiens] [gi:47132611] | | PubMed | | | Data Table |  |
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| 42 | [SID24823265] | Active | | | Single concentration counterscreen of uHTS hits for ATG4B inhibitors in a Phospholipase A2 assay [AID588402, Type: other] | phospholipase A2 precursor [Homo sapiens] [gi:4505847] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | BioAssay | Single concentration counterscreen of uHTS hits for ATG4B inhibitors in a Phospholipase A2 assay | | AID | 588402 | | BioAssay type | other | | Target | phospholipase A2 precursor [Homo sapiens] [gi:4505847] | | PubMed | | | Data Table |  |
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| 43 | [SID24823265] | Active | | | Single concentration counterscreen of uHTS hits for ATG4B inhibitors in a Phospholipase A2 assay [AID588402, Type: other] | phospholipase A2 precursor [Homo sapiens] [gi:4505847] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Active | | BioAssay | Single concentration counterscreen of uHTS hits for ATG4B inhibitors in a Phospholipase A2 assay | | AID | 588402 | | BioAssay type | other | | Target | phospholipase A2 precursor [Homo sapiens] [gi:4505847] | | PubMed | | | Data Table |  |
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| 44 | [SID24823265] | 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. | 44 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | 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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| 45 | [SID24823265] | 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. | 45 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | 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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| 46 | [SID24823265] | 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. | 46 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | 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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| 47 | [SID24823265] | Inactive | IC50 | 50 | Dose Response Confirmation for Calpain Inhibitors [AID1420, Type: confirmatory] | calpain II [Sus scrofa] [gi:1628587] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Inactive | | IC50 | 50 [uM] | | BioAssay | Dose Response Confirmation for Calpain Inhibitors | | AID | 1420 | | BioAssay type | confirmatory | | Target | calpain II [Sus scrofa] [gi:1628587] | | PubMed | | | Data Table |  |
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| 48 | [SID24823265] | Inactive | IC50 | 50 | Dose Response Confirmation for Calpain Inhibitors [AID1420, Type: confirmatory] | calpain II [Sus scrofa] [gi:1628587] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Inactive | | IC50 | 50 [uM] | | BioAssay | Dose Response Confirmation for Calpain Inhibitors | | AID | 1420 | | BioAssay type | confirmatory | | Target | calpain II [Sus scrofa] [gi:1628587] | | PubMed | | | Data Table |  |
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| 49 | [SID24823265] | Inactive | IC50 | 59.64 | Epi-absorbance-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of TEM-1 serine-beta-lactamase. [AID1925, Type: confirmatory] | Beta lactamase [Pseudomonas aeruginosa] [gi:114881106] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Inactive | | IC50 | 59.64 [uM] | | BioAssay | Epi-absorbance-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of TEM-1 serine-beta-lactamase. | | AID | 1925 | | BioAssay type | confirmatory | | Target | Beta lactamase [Pseudomonas aeruginosa] [gi:114881106] | | PubMed | | | Data Table |  |
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| 50 | [SID24823265] | Inactive | IC50 | 59.64 | Epi-absorbance-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase. [AID1920, Type: confirmatory] | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 24823265 | | CID | 44601849 | | Outcome | Inactive | | IC50 | 59.64 [uM] | | BioAssay | Epi-absorbance-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase. | | AID | 1920 | | BioAssay type | confirmatory | | Target | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] | | PubMed | | | Data Table |  |
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