| 1 | [SID50106016] | Active | Potency | 7.9433 | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line GB4 [AID1816, Type: confirmatory] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line GB4 | | AID | 1816 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 2 | [SID50106016] | Active | Potency | 10 | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line W2 [AID1883, Type: confirmatory] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line W2 | | AID | 1883 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 3 | [SID50106016] | Active | Potency | 10 | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line HB3 [AID1886, Type: confirmatory] | |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS for differential inhibitors of proliferation of Plasmodium falciparum line HB3 | | AID | 1886 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 4 | [SID50106016] | Unspecified | Potency | | qHTS Assay for Inhibitors of MBNL1-poly(CUG) RNA binding [AID2675, Type: confirmatory] | muscleblind-like protein 1 isoform a [Homo sapiens] [gi:41281591] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of MBNL1-poly(CUG) RNA binding | | AID | 2675 | | BioAssay type | confirmatory | | Target | muscleblind-like protein 1 isoform a [Homo sapiens] [gi:41281591] | | PubMed | | | Data Table |  |
|
| 5 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors Targeting the Menin-MLL Interaction in MLL Related Leukemias: Competition With Fluorescein Labeled MLL-derived Peptide [AID1766, Type: confirmatory] | MEN1 gene product [Homo sapiens] [gi:18860839] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors Targeting the Menin-MLL Interaction in MLL Related Leukemias: Competition With Fluorescein Labeled MLL-derived Peptide | | AID | 1766 | | BioAssay type | confirmatory | | Target | MEN1 gene product [Homo sapiens] [gi:18860839] | | PubMed | | | Data Table |  |
|
| 6 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors Targeting the Menin-MLL Interaction in MLL Related Leukemias: Competition With Texas Red Labeled MLL-derived Mutant Peptide [AID1768, Type: confirmatory] | MEN1 gene product [Homo sapiens] [gi:18860839] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors Targeting the Menin-MLL Interaction in MLL Related Leukemias: Competition With Texas Red Labeled MLL-derived Mutant Peptide | | AID | 1768 | | BioAssay type | confirmatory | | Target | MEN1 gene product [Homo sapiens] [gi:18860839] | | PubMed | | | Data Table |  |
|
| 7 | [SID50106016] | Inactive | Potency | | qHTS Fluorescence Polarization Assay for Inhibitors of MLL CXXC domain - DNA interaction [AID2662, Type: confirmatory] | MLL gene product [Homo sapiens] [gi:56550039] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Fluorescence Polarization Assay for Inhibitors of MLL CXXC domain - DNA interaction | | AID | 2662 | | BioAssay type | confirmatory | | Target | MLL gene product [Homo sapiens] [gi:56550039] | | PubMed | | | Data Table |  |
|
| 8 | [SID50106016] | Inactive | Potency | | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium [AID1457, Type: confirmatory] | Inositol monophosphatase [gi:44888968] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | | AID | 1457 | | BioAssay type | confirmatory | | Target | Inositol monophosphatase [gi:44888968] | | PubMed | | | Data Table |  |
|
| 9 | [SID50106016] | Inactive | Potency | | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium [AID1457, Type: confirmatory] | Inositol monophosphatase [gi:44888968] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Identifying the Cell-Membrane Permeable IMPase Inhibitors: Potentiation with Lithium | | AID | 1457 | | BioAssay type | confirmatory | | Target | Inositol monophosphatase [gi:44888968] | | PubMed | | | Data Table |  |
|
| 10 | [SID50106016] | Inactive | Potency | | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction [AID1461, Type: confirmatory] | NPSR1 gene product [Homo sapiens] [gi:46395496] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction | | AID | 1461 | | BioAssay type | confirmatory | | Target | NPSR1 gene product [Homo sapiens] [gi:46395496] | | PubMed | | | Data Table |  |
|
| 11 | [SID50106016] | Inactive | Potency | | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction [AID1461, Type: confirmatory] | NPSR1 gene product [Homo sapiens] [gi:46395496] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction | | AID | 1461 | | BioAssay type | confirmatory | | Target | NPSR1 gene product [Homo sapiens] [gi:46395496] | | PubMed | | | Data Table |  |
|
| 12 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate [AID2112, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate | | AID | 2112 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
|
| 13 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate [AID2112, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate | | AID | 2112 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
|
| 14 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate [AID2112, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate | | AID | 2112 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
|
| 15 | [SID50106016] | Inactive | Potency | | qHTS Validation Assay for Inhibitors of Human Galactokinase (GALK) [AID493189, Type: confirmatory] | galactokinase [Homo sapiens] [gi:4503895] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of Human Galactokinase (GALK) | | AID | 493189 | | BioAssay type | confirmatory | | Target | galactokinase [Homo sapiens] [gi:4503895] | | PubMed | | | Data Table |  |
|
| 16 | [SID50106016] | Inactive | Potency | | qHTS Validation Assay for Inhibitors of Human Galactokinase (GALK) [AID493189, Type: confirmatory] | galactokinase [Homo sapiens] [gi:4503895] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of Human Galactokinase (GALK) | | AID | 493189 | | BioAssay type | confirmatory | | Target | galactokinase [Homo sapiens] [gi:4503895] | | PubMed | | | Data Table |  |
|
| 17 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease [AID2101, Type: confirmatory] | glucocerebrosidase [Homo sapiens] [gi:496369] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease | | AID | 2101 | | BioAssay type | confirmatory | | Target | glucocerebrosidase [Homo sapiens] [gi:496369] | | PubMed | | | Data Table |  |
|
| 18 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease [AID2101, Type: confirmatory] | glucocerebrosidase [Homo sapiens] [gi:496369] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease | | AID | 2101 | | BioAssay type | confirmatory | | Target | glucocerebrosidase [Homo sapiens] [gi:496369] | | PubMed | | | Data Table |  |
|
| 19 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate [AID2107, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate | | AID | 2107 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
|
| 20 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate [AID2107, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate | | AID | 2107 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
|
| 21 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors of Human alpha-Galactosidase at pH 4.5. [AID1467, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human alpha-Galactosidase at pH 4.5. | | AID | 1467 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
|
| 22 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors of Human alpha-Galactosidase at pH 4.5. [AID1467, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human alpha-Galactosidase at pH 4.5. | | AID | 1467 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
|
| 23 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID894, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 894 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
|
| 24 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID894, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 894 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
|
| 25 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID894, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 894 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
|
| 26 | [SID50106016] | Inactive | Potency | | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity [AID588834, Type: Literature] | KCNH2 gene product [Homo sapiens] [gi:325651834] |   View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity | | AID | 588834 | | BioAssay type | Literature | | Target | KCNH2 gene product [Homo sapiens] [gi:325651834] | | PubMed | 19583963 | | Data Table |  |
|
| 27 | [SID50106016] | Inactive | Potency | | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity [AID588834, Type: Literature] | KCNH2 gene product [Homo sapiens] [gi:325651834] |   View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity | | AID | 588834 | | BioAssay type | Literature | | Target | KCNH2 gene product [Homo sapiens] [gi:325651834] | | PubMed | 19583963 | | Data Table |  |
|
| 28 | [SID50106016] | Inactive | Potency | | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity [AID588834, Type: Literature] | KCNH2 gene product [Homo sapiens] [gi:325651834] |   View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity | | AID | 588834 | | BioAssay type | Literature | | Target | KCNH2 gene product [Homo sapiens] [gi:325651834] | | PubMed | 19583963 | | Data Table |  |
|
| 29 | [SID50106016] | Inactive | Potency | | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity [AID588834, Type: Literature] | KCNH2 gene product [Homo sapiens] [gi:325651834] |   View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity | | AID | 588834 | | BioAssay type | Literature | | Target | KCNH2 gene product [Homo sapiens] [gi:325651834] | | PubMed | 19583963 | | Data Table |  |
|
| 30 | [SID50106016] | Inactive | Potency | | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity [AID588834, Type: Literature] | KCNH2 gene product [Homo sapiens] [gi:325651834] |   View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity | | AID | 588834 | | BioAssay type | Literature | | Target | KCNH2 gene product [Homo sapiens] [gi:325651834] | | PubMed | 19583963 | | Data Table |  |
|
| 31 | [SID50106016] | Inactive | Potency | | Validation of Assay for Modulators of Lamin A Splicing [AID1459, Type: confirmatory] | prelamin-A/C isoform 3 [Homo sapiens] [gi:27436948] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Validation of Assay for Modulators of Lamin A Splicing | | AID | 1459 | | BioAssay type | confirmatory | | Target | prelamin-A/C isoform 3 [Homo sapiens] [gi:27436948] | | PubMed | | | Data Table |  |
|
| 32 | [SID50106016] | Inactive | Potency | | qHTS Assay for Modulators of Lamin A Splicing [AID1487, Type: confirmatory] | prelamin-A/C isoform 3 [Homo sapiens] [gi:27436948] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Modulators of Lamin A Splicing | | AID | 1487 | | BioAssay type | confirmatory | | Target | prelamin-A/C isoform 3 [Homo sapiens] [gi:27436948] | | PubMed | | | Data Table |  |
|
| 33 | [SID50106016] | Inactive | Potency | | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 34 | [SID50106016] | Inactive | Potency | | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 35 | [SID50106016] | Inactive | Potency | | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1468, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1468 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 36 | [SID50106016] | Inactive | Potency | | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1468, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1468 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 37 | [SID50106016] | Inactive | Potency | | qHTS Assay for Compounds that Induce Erasure of Genomic Imprints [AID1948, Type: confirmatory] | |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Compounds that Induce Erasure of Genomic Imprints | | AID | 1948 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 38 | [SID50106016] | Inactive | Potency | | Counterscreen for APE1 Inhibitors: Fluorescent Dye Displacement Validation Assay [AID1707, Type: confirmatory] | |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen for APE1 Inhibitors: Fluorescent Dye Displacement Validation Assay | | AID | 1707 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 39 | [SID50106016] | Inactive | Potency | | Quantitative high throughput screen for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID488745, Type: confirmatory] | |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Quantitative high throughput screen for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation | | AID | 488745 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 40 | [SID50106016] | Inactive | Potency | | Quantitative high throughput screen for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID488752, Type: confirmatory] | |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Quantitative high throughput screen for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation | | AID | 488752 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 41 | [SID50106016] | Inactive | Potency | | qHTS for Inhibitors of binding or entry into cells for Lassa Virus [AID540256, Type: confirmatory] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of binding or entry into cells for Lassa Virus | | AID | 540256 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 42 | [SID50106016] | Inactive | Potency | | Validation screen for inhibitors of Lassa infection [AID463096, Type: confirmatory] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Validation screen for inhibitors of Lassa infection | | AID | 463096 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 43 | [SID50106016] | Inactive | Potency | | Counterscreen for APE1 Inhibitors: qHTS Validation Assay for Inhibitors of Endonuclease IV [AID1708, Type: confirmatory] | endonuclease IV [Escherichia coli] [gi:405898] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen for APE1 Inhibitors: qHTS Validation Assay for Inhibitors of Endonuclease IV | | AID | 1708 | | BioAssay type | confirmatory | | Target | endonuclease IV [Escherichia coli] [gi:405898] | | PubMed | | | Data Table |  |
|
| 44 | [SID50106016] | Inactive | Potency | | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1463, Type: confirmatory] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1463 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 45 | [SID50106016] | Inactive | Potency | | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia [AID1477, Type: confirmatory] | |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia | | AID | 1477 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 46 | [SID50106016] | Inactive | Potency | | Quantitative High-Throughput Screen for Regulators of Epigenetic Control [AID1865, Type: confirmatory] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Quantitative High-Throughput Screen for Regulators of Epigenetic Control | | AID | 1865 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 47 | [SID50106016] | Inactive | Potency | | Counterscreen for Luciferase (Kinase-Glo TM) Inhibition [AID1379, Type: confirmatory] | luciferase [Photuris pennsylvanica] [gi:1669525] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen for Luciferase (Kinase-Glo TM) Inhibition | | AID | 1379 | | BioAssay type | confirmatory | | Target | luciferase [Photuris pennsylvanica] [gi:1669525] | | PubMed | | | Data Table |  |
|
| 48 | [SID50106016] | Inactive | Potency | | 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. | 48 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [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 |  |
|
| 49 | [SID50106016] | Inactive | Potency | | qHTS Validation Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) [AID1705, Type: confirmatory] | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | | AID | 1705 | | BioAssay type | confirmatory | | Target | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] | | PubMed | | | Data Table |  |
|
| 50 | [SID50106016] | Inactive | Potency | | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) [AID485290, Type: confirmatory] | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 50106016 | | CID | 24867484 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | | AID | 485290 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | | PubMed | | | Data Table |  |
|