| 1 | [SID17512507] | Active | AC50 | 0.009 | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity_Set2 [AID624274, Type: confirmatory] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | AC50 | 0.009 [uM] | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity_Set2 | | AID | 624274 | | BioAssay type | confirmatory | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
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| 2 | [SID17512507] | Active | AC50 | 0.009 | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity_Set2 [AID624274, Type: confirmatory] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | AC50 | 0.009 [uM] | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity_Set2 | | AID | 624274 | | BioAssay type | confirmatory | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
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| 3 | [SID17512507] | Active | AC50 | 0.009 | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity [AID602350, Type: confirmatory] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | AC50 | 0.009 [uM] | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity | | AID | 602350 | | BioAssay type | confirmatory | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
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| 4 | [SID17512507] | Active | AC50 | 0.009 | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity [AID602350, Type: confirmatory] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | AC50 | 0.009 [uM] | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_Dose_CherryPick_Activity | | AID | 602350 | | BioAssay type | confirmatory | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
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| 5 | [SID17512507] | Active | Potency | 2.8184 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 2.8184 [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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| 6 | [SID17512507] | Active | Potency | 2.8184 | qHTS for Inhibitors of Polymerase Eta [AID588591, Type: confirmatory] | DNA polymerase eta [Homo sapiens] [gi:5729982] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 2.8184 [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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| 7 | [SID17512507] | Active | AC50 | 2.89 | C-LANA FP assay Measured in Biochemical System Using Plate Reader - 2117-01_Inhibitor_Dose_CherryPick_Activity [AID504725, Type: confirmatory] | LANA [Human herpesvirus 8] [gi:312275222] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | AC50 | 2.89 [uM] | | BioAssay | C-LANA FP assay Measured in Biochemical System Using Plate Reader - 2117-01_Inhibitor_Dose_CherryPick_Activity | | AID | 504725 | | BioAssay type | confirmatory | | Target | LANA [Human herpesvirus 8] [gi:312275222] | | PubMed | | | Data Table |  |
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| 8 | [SID17512507] | Active | Potency | 2.9935 | qHTS Assay for the Inhibitors of L3MBTL1: Hit Validation [AID540279, Type: confirmatory] | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 2.9935 [uM] | | BioAssay | qHTS Assay for the Inhibitors of L3MBTL1: Hit Validation | | AID | 540279 | | BioAssay type | confirmatory | | Target | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] | | PubMed | | | Data Table |  |
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| 9 | [SID17512507] | Active | Potency | 2.9935 | qHTS Assay for the Inhibitors of L3MBTL1: Hit Validation [AID540279, Type: confirmatory] | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 2.9935 [uM] | | BioAssay | qHTS Assay for the Inhibitors of L3MBTL1: Hit Validation | | AID | 540279 | | BioAssay type | confirmatory | | Target | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] | | PubMed | | | Data Table |  |
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| 10 | [SID17512507] | Active | Potency | 3.9716 | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia [AID2451, Type: confirmatory] | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 3.9716 [uM] | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia | | AID | 2451 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] | | PubMed | | | Data Table |  |
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| 11 | [SID17512507] | Active | Potency | 3.9811 | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) [AID2517, Type: confirmatory] | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 3.9811 [uM] | | BioAssay | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | | AID | 2517 | | BioAssay type | confirmatory | | Target | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] | | PubMed | | | Data Table |  |
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| 12 | [SID17512507] | Active | Potency | 7.9433 | qHTS Assay for Activators of ClpP [AID651965, Type: confirmatory] | ClpP [Bacillus subtilis] [gi:2668494] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Assay for Activators of ClpP | | AID | 651965 | | BioAssay type | confirmatory | | Target | ClpP [Bacillus subtilis] [gi:2668494] | | PubMed | | | Data Table |  |
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| 13 | [SID17512507] | Active | Potency | 10 | 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. | 13 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 10 [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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| 14 | [SID17512507] | Active | IC50 | 12.83 | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) [AID1619, Type: confirmatory] | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | IC50 | 12.83 [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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| 15 | [SID17512507] | Active | IC50 | 12.83 | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) [AID1619, Type: confirmatory] | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | IC50 | 12.83 [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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| 16 | [SID17512507] | Active | IC50 | 12.83 | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) [AID1619, Type: confirmatory] | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | IC50 | 12.83 [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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| 17 | [SID17512507] | Active | AC50 | 23.837 | C-LANA Counter Screen: DNA intercalators Measured in Biochemical System Using Plate Reader - 2117-02_Inhibitor_Dose_CherryPick_Activity_Set2 [AID504727, Type: confirmatory] | LANA [Human herpesvirus 8] [gi:312275222] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | AC50 | 23.837 [uM] | | BioAssay | C-LANA Counter Screen: DNA intercalators Measured in Biochemical System Using Plate Reader - 2117-02_Inhibitor_Dose_CherryPick_Activity_Set2 | | AID | 504727 | | BioAssay type | confirmatory | | Target | LANA [Human herpesvirus 8] [gi:312275222] | | PubMed | | | Data Table |  |
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| 18 | [SID17512507] | Active | Potency | 31.6228 | qHTS Assay for the Inhibitors of L3MBTL1 [AID485360, Type: confirmatory] | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS Assay for the Inhibitors of L3MBTL1 | | AID | 485360 | | BioAssay type | confirmatory | | Target | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] | | PubMed | | | Data Table |  |
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| 19 | [SID17512507] | Active | Potency | 31.6228 | qHTS Assay for the Inhibitors of L3MBTL1 [AID485360, Type: confirmatory] | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS Assay for the Inhibitors of L3MBTL1 | | AID | 485360 | | BioAssay type | confirmatory | | Target | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] | | PubMed | | | Data Table |  |
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| 20 | [SID17512507] | Active | Potency | 39.8107 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
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| 21 | [SID17512507] | Active | Potency | 39.8107 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
|
| 22 | [SID124360090] | Active | AC50 | 55.79 | C-LANA FP assay Measured in Biochemical System Using Plate Reader - 2117-01_Inhibitor_Dose_DryPowder_Activity [AID588363, Type: confirmatory] | LANA [Human herpesvirus 8] [gi:312275222] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 124360090 | | CID | 4230279 | | Outcome | Active | | AC50 | 55.79 [uM] | | BioAssay | C-LANA FP assay Measured in Biochemical System Using Plate Reader - 2117-01_Inhibitor_Dose_DryPowder_Activity | | AID | 588363 | | BioAssay type | confirmatory | | Target | LANA [Human herpesvirus 8] [gi:312275222] | | PubMed | | | Data Table |  |
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| 23 | [SID17512507] | Active | EC50 | 61.638 | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 [AID1960, Type: confirmatory] | Zinc finger protein mex- [gi:55976631] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | EC50 | 61.638 [uM] | | BioAssay | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 | | AID | 1960 | | BioAssay type | confirmatory | | Target | Zinc finger protein mex- [gi:55976631] | | PubMed | | | Data Table |  |
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| 24 | [SID17512507] | Active | EC50 | 61.638 | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 [AID1960, Type: confirmatory] | Zinc finger protein mex- [gi:55976631] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | EC50 | 61.638 [uM] | | BioAssay | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 | | AID | 1960 | | BioAssay type | confirmatory | | Target | Zinc finger protein mex- [gi:55976631] | | PubMed | | | Data Table |  |
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| 25 | [SID17512507] | Active | Potency | 79.4328 | 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. | 25 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | Potency | 79.4328 [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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| 26 | [SID17512507] | Active | EC50 | 270.475 | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of POS-1 Binding to mex-3-RNA [AID1964, Type: confirmatory] | POsterior Segregation family member (pos-1) [Caenorhabditis elegans] [gi:17562800] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | EC50 | 270.475 [uM] | | BioAssay | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of POS-1 Binding to mex-3-RNA | | AID | 1964 | | BioAssay type | confirmatory | | Target | POsterior Segregation family member (pos-1) [Caenorhabditis elegans] [gi:17562800] | | PubMed | | | Data Table |  |
|
| 27 | [SID17512507] | Active | | | MLPCN maternal gene expression-MEX-5 TCR-2 binding assay-Primary Screen [AID1832, Type: screening] | Zinc finger protein mex- [gi:55976631] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | MLPCN maternal gene expression-MEX-5 TCR-2 binding assay-Primary Screen | | AID | 1832 | | BioAssay type | screening | | Target | Zinc finger protein mex- [gi:55976631] | | PubMed | | | Data Table |  |
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| 28 | [SID17512507] | Active | | | MLPCN maternal gene expression-MEX-5 TCR-2 binding assay-Primary Screen [AID1832, Type: screening] | Zinc finger protein mex- [gi:55976631] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | MLPCN maternal gene expression-MEX-5 TCR-2 binding assay-Primary Screen | | AID | 1832 | | BioAssay type | screening | | Target | Zinc finger protein mex- [gi:55976631] | | PubMed | | | Data Table |  |
|
| 29 | [SID17512507] | Active | | | Fluorescence-based biochemical primary high throughput confirmation assay to identify inhibitors of T-cell receptor (TCR)-CD3 interaction using a TAMRA-labeled TCR probe [AID652036, Type: screening] | TCRAV4S1 [Homo sapiens] [gi:2358024] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical primary high throughput confirmation assay to identify inhibitors of T-cell receptor (TCR)-CD3 interaction using a TAMRA-labeled TCR probe | | AID | 652036 | | BioAssay type | screening | | Target | TCRAV4S1 [Homo sapiens] [gi:2358024] | | PubMed | | | Data Table |  |
|
| 30 | [SID17512507] | Active | | | Fluorescence-based biochemical primary high throughput assay to identify inhibitors of T-cell receptor (TCR)-CD3 interaction using a TAMRA-labeled TCR probe [AID651800, Type: screening] | TCRAV4S1 [Homo sapiens] [gi:2358024] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical primary high throughput assay to identify inhibitors of T-cell receptor (TCR)-CD3 interaction using a TAMRA-labeled TCR probe | | AID | 651800 | | BioAssay type | screening | | Target | TCRAV4S1 [Homo sapiens] [gi:2358024] | | PubMed | | | Data Table |  |
|
| 31 | [SID17512507] | 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. | 31 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | 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 |  |
|
| 32 | [SID17512507] | 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. | 32 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | 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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| 33 | [SID17512507] | Active | | | Luminescence-based biochemical primary high throughput screening assay to identify inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) [AID624268, Type: screening] | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | Luminescence-based biochemical primary high throughput screening assay to identify inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) | | AID | 624268 | | BioAssay type | screening | | Target | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] | | PubMed | | | Data Table |  |
|
| 34 | [SID17512507] | Active | | | Luminescence-based biochemical high throughput confirmation assay for inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) [AID624412, Type: screening] | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | Luminescence-based biochemical high throughput confirmation assay for inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) | | AID | 624412 | | BioAssay type | screening | | Target | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] | | PubMed | | | Data Table |  |
|
| 35 | [SID17512507] | Active | | | Fluorescent Polarization-based biochemical high throughput orthogonal assay for inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) [AID651607, Type: screening] | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | Fluorescent Polarization-based biochemical high throughput orthogonal assay for inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) | | AID | 651607 | | BioAssay type | screening | | Target | methionyl-tRNA synthetase [Trypanosoma brucei brucei strain 927/4 GUTat10.1] [gi:71746704] | | PubMed | | | Data Table |  |
|
| 36 | [SID17512507] | Active | | | High Throughput Screen to Identify Compounds that Inhibit Class II HMG-CoA Reductases - Primary Screen [AID1066, Type: screening] | acetyl-CoA acetyltransferase/HMG-CoA reductase [Enterococcus faecalis] [gi:9937384] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | High Throughput Screen to Identify Compounds that Inhibit Class II HMG-CoA Reductases - Primary Screen | | AID | 1066 | | BioAssay type | screening | | Target | acetyl-CoA acetyltransferase/HMG-CoA reductase [Enterococcus faecalis] [gi:9937384] | | PubMed | | | Data Table |  |
|
| 37 | [SID17512507] | Active | | | uHTS identification of TNAP inhibitors in the absence of phosphate acceptor performed in luminescent assay [AID1012, Type: screening] | alkaline phosphatase, tissue-nonspecific isozyme isoform 1 precursor [Homo sapiens] [gi:116734717] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | uHTS identification of TNAP inhibitors in the absence of phosphate acceptor performed in luminescent assay | | AID | 1012 | | BioAssay type | screening | | Target | alkaline phosphatase, tissue-nonspecific isozyme isoform 1 precursor [Homo sapiens] [gi:116734717] | | PubMed | | | Data Table |  |
|
| 38 | [SID17512507] | Active | | | uHTS identification of TNAP inhibitors in the absence of phosphate acceptor performed in luminescent assay [AID1012, Type: screening] | alkaline phosphatase, tissue-nonspecific isozyme isoform 1 precursor [Homo sapiens] [gi:116734717] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | uHTS identification of TNAP inhibitors in the absence of phosphate acceptor performed in luminescent assay | | AID | 1012 | | BioAssay type | screening | | Target | alkaline phosphatase, tissue-nonspecific isozyme isoform 1 precursor [Homo sapiens] [gi:116734717] | | PubMed | | | Data Table |  |
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| 39 | [SID17512507] | 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. | 39 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | 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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| 40 | [SID17512507] | Active | | | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_SinglePoint_HTS_Activity [AID588391, Type: screening] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 588391 | | BioAssay type | screening | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
|
| 41 | [SID17512507] | Active | | | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_SinglePoint_HTS_Activity [AID588391, Type: screening] | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of Protein Disulfide Isomerase Measured in Biochemical System Using Plate Reader - 2137-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 588391 | | BioAssay type | screening | | Target | Prolyl 4-hydroxylase, beta polypeptide [Homo sapiens] [gi:14790033] | | PubMed | | | Data Table |  |
|
| 42 | [SID17512507] | Active | | | Primary biochemical fluorescence polarization-based high throughput screening assay to identify inhibitors of protein arginine methyltransferase 1 (PRMT1) [AID652257, Type: screening] | PRMT1 protein [Homo sapiens] [gi:32425330] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | Primary biochemical fluorescence polarization-based high throughput screening assay to identify inhibitors of protein arginine methyltransferase 1 (PRMT1) | | AID | 652257 | | BioAssay type | screening | | Target | PRMT1 protein [Homo sapiens] [gi:32425330] | | PubMed | | | Data Table |  |
|
| 43 | [SID17512507] | Active | | | Primary biochemical fluorescence polarization-based high throughput screening assay to identify inhibitors of protein arginine methyltransferase 1 (PRMT1) [AID652257, Type: screening] | PRMT1 protein [Homo sapiens] [gi:32425330] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Active | | BioAssay | Primary biochemical fluorescence polarization-based high throughput screening assay to identify inhibitors of protein arginine methyltransferase 1 (PRMT1) | | AID | 652257 | | BioAssay type | screening | | Target | PRMT1 protein [Homo sapiens] [gi:32425330] | | PubMed | | | Data Table |  |
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| 44 | [SID17512507] | 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. | 44 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | 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 |  |
|
| 45 | [SID17512507] | 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 | 17512507 | | CID | 4230279 | | 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 | [SID17512507] | Inactive | Potency | 4.6535 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Inactive | | Potency | 4.6535 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation | | AID | 504832 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 47 | [SID17512507] | Inactive | Potency | 11.2202 | qHTS for Agonist of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS [AID624287, Type: confirmatory] | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short [gi:52000961] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Inactive | | Potency | 11.2202 [uM] | | BioAssay | qHTS for Agonist of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS | | AID | 624287 | | BioAssay type | confirmatory | | Target | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short [gi:52000961] | | PubMed | | | Data Table |  |
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| 48 | [SID17512507] | Inactive | Potency | 20.5962 | A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. [AID624296, Type: confirmatory] | GMNN gene product [Homo sapiens] [gi:7705682] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Inactive | | Potency | 20.5962 [uM] | | BioAssay | A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. | | AID | 624296 | | BioAssay type | confirmatory | | Target | GMNN gene product [Homo sapiens] [gi:7705682] | | PubMed | | | Data Table |  |
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| 49 | [SID17512507] | Inactive | Potency | 35.4813 | qHTS for Inhibitors of Glutaminase (GLS) [AID624170, Type: confirmatory] | GLS protein [Homo sapiens] [gi:71051501] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Inactive | | Potency | 35.4813 [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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| 50 | [SID17512507] | Inactive | EC50 | 110 | Luminescence-based Microorganism Dose Response HTS to Identify Inhibitors of E. Coli Growth [AID1959, Type: confirmatory] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 17512507 | | CID | 4230279 | | Outcome | Inactive | | EC50 | 110 [uM] | | BioAssay | Luminescence-based Microorganism Dose Response HTS to Identify Inhibitors of E. Coli Growth | | AID | 1959 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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