| 1 | [SID22413272] | Active | Potency | 2.5119 | qHTS for Inhibitors of Glutaminase (GLS) [AID624170, Type: confirmatory] | GLS protein [Homo sapiens] [gi:71051501] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | Potency | 2.5119 [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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| 2 | [SID22413272] | Active | Potency | 8.9125 | 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. | 2 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | Potency | 8.9125 [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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| 3 | [SID22413272] | Active | Potency | 11.2202 | 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. | 3 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | Potency | 11.2202 [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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| 4 | [SID22413272] | Active | Potency | 15.8489 | 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. | 4 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | Potency | 15.8489 [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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| 5 | [SID22413272] | Active | AC50 | 18.93 | Luminescence assay for the detection of hydrogen peroxide activity in the abscence of ALR and DTT, at dose Measured in Biochemical System Using Plate Reader - 2036-03_Inhibitor_Dose_CherryPick_Activity [AID540356, Type: confirmatory] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | AC50 | 18.93 [uM] | | BioAssay | Luminescence assay for the detection of hydrogen peroxide activity in the abscence of ALR and DTT, at dose Measured in Biochemical System Using Plate Reader - 2036-03_Inhibitor_Dose_CherryPick_Activity | | AID | 540356 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 6 | [SID22413272] | Active | IC50 | 30.41 | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) [AID1619, Type: confirmatory] | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | IC50 | 30.41 [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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| 7 | [SID22413272] | Active | IC50 | 30.41 | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) [AID1619, Type: confirmatory] | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | IC50 | 30.41 [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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| 8 | [SID22413272] | Active | IC50 | 30.41 | 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 | 22413272 | | CID | 5332280 | | Outcome | Active | | IC50 | 30.41 [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 | [SID22413272] | Active | IC50 | 33.24 | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - Counter Screen Coupled Enzyme [AID624351, Type: confirmatory] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | IC50 | 33.24 [uM] | | BioAssay | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - Counter Screen Coupled Enzyme | | AID | 624351 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 10 | [SID22413272] | Active | IC50 | 44.54 | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - Primary and Confirmatory Screens [AID624330, Type: confirmatory] | RACGAP1 gene product [Homo sapiens] [gi:21361397] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | IC50 | 44.54 [uM] | | BioAssay | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - Primary and Confirmatory Screens | | AID | 624330 | | BioAssay type | confirmatory | | Target | RACGAP1 gene product [Homo sapiens] [gi:21361397] | | PubMed | | | Data Table |  |
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| 11 | [SID22413272] | Active | | | uHTS Luminescent assay for identification of inhibitors of Sentrin-specific protease 6 (SENP6) [AID2599, Type: screening] | SUMO-1-specific protease [Homo sapiens] [gi:6166485] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | uHTS Luminescent assay for identification of inhibitors of Sentrin-specific protease 6 (SENP6) | | AID | 2599 | | BioAssay type | screening | | Target | SUMO-1-specific protease [Homo sapiens] [gi:6166485] | | PubMed | | | Data Table |  |
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| 12 | [SID22413272] | Active | | | HTS Luminescent assay for identification of inhibitors of Sentrin-specific protease 8 (SENP8) [AID2540, Type: screening] | SENP8 gene product [Homo sapiens] [gi:262118306] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | HTS Luminescent assay for identification of inhibitors of Sentrin-specific protease 8 (SENP8) | | AID | 2540 | | BioAssay type | screening | | Target | SENP8 gene product [Homo sapiens] [gi:262118306] | | PubMed | | | Data Table |  |
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| 13 | [SID22413272] | Active | | | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID1822, Type: screening] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 1822 | | BioAssay type | screening | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
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| 14 | [SID22413272] | Active | | | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID1822, Type: screening] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 1822 | | BioAssay type | screening | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
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| 15 | [SID22413272] | Active | | | QFRET-based biochemical high throughput confirmation assay for inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID2170, Type: screening] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | QFRET-based biochemical high throughput confirmation assay for inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 2170 | | BioAssay type | screening | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
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| 16 | [SID22413272] | Active | | | QFRET-based biochemical high throughput confirmation assay for inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID2170, Type: screening] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | QFRET-based biochemical high throughput confirmation assay for inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 2170 | | BioAssay type | screening | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
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| 17 | [SID22413272] | Active | | | HTS-Luminescent assay for inhibitors of ALR by detection of hydrogen peroxide production Measured in Biochemical System Using Plate Reader - 2036-02_Inhibitor_SinglePoint_HTS [AID485317, Type: screening] | FAD-linked sulfhydryl oxidase ALR [Homo sapiens] [gi:54112432] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | HTS-Luminescent assay for inhibitors of ALR by detection of hydrogen peroxide production Measured in Biochemical System Using Plate Reader - 2036-02_Inhibitor_SinglePoint_HTS | | AID | 485317 | | BioAssay type | screening | | Target | FAD-linked sulfhydryl oxidase ALR [Homo sapiens] [gi:54112432] | | PubMed | | | Data Table |  |
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| 18 | [SID22413272] | Active | | | HTS for small molecule inhibitors of CHOP to regulate the unfolded protein response to ER stress [AID2732, Type: screening] | Ddit3 gene product [Mus musculus] [gi:160707929] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | HTS for small molecule inhibitors of CHOP to regulate the unfolded protein response to ER stress | | AID | 2732 | | BioAssay type | screening | | Target | Ddit3 gene product [Mus musculus] [gi:160707929] | | PubMed | | | Data Table |  |
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| 19 | [SID22413272] | Active | | | Single concentration confirmation of uHTS for inhibitors of Sentrin-specific protease 7 (SENP7) using a Luminescent assay [AID488917, Type: screening] | SUMO1/sentrin specific peptidase 7 [Homo sapiens] [gi:120538355] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | Single concentration confirmation of uHTS for inhibitors of Sentrin-specific protease 7 (SENP7) using a Luminescent assay | | AID | 488917 | | BioAssay type | screening | | Target | SUMO1/sentrin specific peptidase 7 [Homo sapiens] [gi:120538355] | | PubMed | | | Data Table |  |
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| 20 | [SID22413272] | Active | | | Single concentration confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Luminescent Interference Counterscreen assay [AID488919, Type: screening] | SENP8 gene product [Homo sapiens] [gi:262118306] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | Single concentration confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Luminescent Interference Counterscreen assay | | AID | 488919 | | BioAssay type | screening | | Target | SENP8 gene product [Homo sapiens] [gi:262118306] | | PubMed | | | Data Table |  |
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| 21 | [SID22413272] | Active | | | A qHTS for Small Molecule Inhibitors of Shiga Toxin [AID2315, Type: screening] | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | A qHTS for Small Molecule Inhibitors of Shiga Toxin | | AID | 2315 | | BioAssay type | screening | | Target | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | | PubMed | | | Data Table |  |
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| 22 | [SID22413272] | Active | | | Single concentration confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Caspase-3 Selectivity assay [AID488918, Type: screening] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | Single concentration confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Caspase-3 Selectivity assay | | AID | 488918 | | BioAssay type | screening | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
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| 23 | [SID22413272] | Active | | | Single concentration confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Caspase-3 Selectivity assay [AID488918, Type: screening] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | Single concentration confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Caspase-3 Selectivity assay | | AID | 488918 | | BioAssay type | screening | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
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| 24 | [SID22413272] | Active | | | Single concentration confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Caspase-3 Selectivity assay [AID488918, Type: screening] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | Single concentration confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Caspase-3 Selectivity assay | | AID | 488918 | | BioAssay type | screening | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
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| 25 | [SID22413272] | Active | | | Single concentration confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Caspase-3 Selectivity assay [AID488918, Type: screening] | CASP3 gene product [Homo sapiens] [gi:14790119] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | Single concentration confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Caspase-3 Selectivity assay | | AID | 488918 | | BioAssay type | screening | | Target | CASP3 gene product [Homo sapiens] [gi:14790119] | | PubMed | | | Data Table |  |
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| 26 | [SID22413272] | 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. | 26 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | 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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| 27 | [SID22413272] | Active | | | Counter Screen for Luciferase-based Primary Inhibition Assays [AID1006, Type: screening] | |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | Counter Screen for Luciferase-based Primary Inhibition Assays | | AID | 1006 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 28 | [SID22413272] | Active | | | uHTS identification of small molecule activators of the apoptotic arm of the Unfolded Protein response via a luminescent-based reporter assay [AID449763, Type: screening] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | uHTS identification of small molecule activators of the apoptotic arm of the Unfolded Protein response via a luminescent-based reporter assay | | AID | 449763 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 29 | [SID22413272] | Active | | | 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. | 29 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | 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 |  |
|
| 30 | [SID22413272] | Active | | | Single concentration confirmation of small molecule activators of the adaptive arm of the Unfolded Protein response via a luminescent-based reporter assay [AID485299, Type: screening] | |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | Single concentration confirmation of small molecule activators of the adaptive arm of the Unfolded Protein response via a luminescent-based reporter assay | | AID | 485299 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 31 | [SID22413272] | Active | | | uHTS identification of small molecule modulators of myocardial damage [AID588492, Type: screening] | |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | uHTS identification of small molecule modulators of myocardial damage | | AID | 588492 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 32 | [SID22413272] | Active | | | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) [AID588664, Type: screening] | ABL1 gene product [Homo sapiens] [gi:62362414] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) | | AID | 588664 | | BioAssay type | screening | | Target | ABL1 gene product [Homo sapiens] [gi:62362414] | | PubMed | | | Data Table |  |
|
| 33 | [SID22413272] | Active | | | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) [AID588664, Type: screening] | ABL1 gene product [Homo sapiens] [gi:62362414] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Active | | BioAssay | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) | | AID | 588664 | | BioAssay type | screening | | Target | ABL1 gene product [Homo sapiens] [gi:62362414] | | PubMed | | | Data Table |  |
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| 34 | [SID22413272] | 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 | 22413272 | | CID | 5332280 | | 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 |  |
|
| 35 | [SID22413272] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | 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 |  |
|
| 36 | [SID22413272] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | 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 |  |
|
| 37 | [SID22413272] | 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. | 37 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | 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 |  |
|
| 38 | [SID22413272] | 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. | 38 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | 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 |  |
|
| 39 | [SID22413272] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
|
| 40 | [SID22413272] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
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| 41 | [SID22413272] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
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| 42 | [SID22413272] | Inactive | Potency | 10 | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) [AID624417, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Inactive | | Potency | 10 [uM] | | BioAssay | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | | AID | 624417 | | BioAssay type | confirmatory | | Target | glp-1 receptor [Homo sapiens] [gi:1724069] | | PubMed | | | Data Table |  |
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| 43 | [SID22413272] | Inactive | Potency | 10 | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) [AID624417, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Inactive | | Potency | 10 [uM] | | BioAssay | qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode) | | AID | 624417 | | BioAssay type | confirmatory | | Target | glp-1 receptor [Homo sapiens] [gi:1724069] | | PubMed | | | Data Table |  |
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| 44 | [SID22413272] | Inactive | EC50 | 46.7 | Dose response counterscreen for uHTS small molecule activators of the adaptive arm of the Unfolded Protein Response via a luminescent-based reporter assay [AID489027, Type: confirmatory] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Inactive | | EC50 | 46.7 [uM] | | BioAssay | Dose response counterscreen for uHTS small molecule activators of the adaptive arm of the Unfolded Protein Response via a luminescent-based reporter assay | | AID | 489027 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 45 | [SID22413272] | Inactive | EC50 | 80 | Dose response confirmation of small molecule activators of the adaptive arm of the Unfolded Protein response via a luminescent-based reporter assay [AID489032, Type: confirmatory] | |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Inactive | | EC50 | 80 [uM] | | BioAssay | Dose response confirmation of small molecule activators of the adaptive arm of the Unfolded Protein response via a luminescent-based reporter assay | | AID | 489032 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 46 | [SID22413272] | Inactive | | | Fluorescence-based counterscreen assay for HCV NS3 helicase inhibitors: biochemical high-throughput screening assay to identify compounds that cause fluorescent intercalator displacement (FID) [AID1845, Type: screening] | NS3 [Hepatitis C virus] [gi:125541954] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Inactive | | BioAssay | Fluorescence-based counterscreen assay for HCV NS3 helicase inhibitors: biochemical high-throughput screening assay to identify compounds that cause fluorescent intercalator displacement (FID) | | AID | 1845 | | BioAssay type | screening | | Target | NS3 [Hepatitis C virus] [gi:125541954] | | PubMed | | | Data Table |  |
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| 47 | [SID22413272] | Inactive | | | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of the Hepatitis C Virus non-structural protein 3 helicase (NS3) [AID1800, Type: screening] | NS3 [Hepatitis C virus] [gi:125541954] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Inactive | | BioAssay | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of the Hepatitis C Virus non-structural protein 3 helicase (NS3) | | AID | 1800 | | BioAssay type | screening | | Target | NS3 [Hepatitis C virus] [gi:125541954] | | PubMed | | | Data Table |  |
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| 48 | [SID22413272] | Inactive | | | uHTS identification of modulators of interaction between CendR and NRP-1 using Fluorescence Polarization assay [AID602438, Type: screening] | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Inactive | | BioAssay | uHTS identification of modulators of interaction between CendR and NRP-1 using Fluorescence Polarization assay | | AID | 602438 | | BioAssay type | screening | | Target | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] | | PubMed | | | Data Table |  |
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| 49 | [SID22413272] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify activators of the GAA850 frataxin (FXN) promoter [AID540364, Type: screening] | |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify activators of the GAA850 frataxin (FXN) promoter | | AID | 540364 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 50 | [SID22413272] | Inactive | | | MITF Measured in Cell-Based System Using Plate Reader - 2084-01_Activator_SinglePoint_HTS_Activity [AID588334, Type: screening] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 22413272 | | CID | 5332280 | | Outcome | Inactive | | BioAssay | MITF Measured in Cell-Based System Using Plate Reader - 2084-01_Activator_SinglePoint_HTS_Activity | | AID | 588334 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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