| 1 | [SID85147391] | Active | IC50 | 1.24 | Dose Response confirmation of uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay [AID504765, Type: confirmatory] | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | IC50 | 1.24 [uM] | | BioAssay | Dose Response confirmation of uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay | | AID | 504765 | | BioAssay type | confirmatory | | Target | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] | | PubMed | | | Data Table |  |
|
| 2 | [SID85147391] | Active | Potency | 1.4716 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 1.4716 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation | | AID | 504834 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 3 | [SID57287555] | Active | IC50 | 1.88 | Confirmation of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. [AID1535, Type: confirmatory] | MPI protein [Homo sapiens] [gi:16878311] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 57287555 | | CID | 25181201 | | Outcome | Active | | IC50 | 1.88 [uM] | | BioAssay | Confirmation of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. | | AID | 1535 | | BioAssay type | confirmatory | | Target | MPI protein [Homo sapiens] [gi:16878311] | | PubMed | | | Data Table |  |
|
| 4 | [SID57287555] | Active | IC50 | 1.88 | Confirmation of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. [AID1535, Type: confirmatory] | MPI protein [Homo sapiens] [gi:16878311] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 57287555 | | CID | 25181201 | | Outcome | Active | | IC50 | 1.88 [uM] | | BioAssay | Confirmation of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. | | AID | 1535 | | BioAssay type | confirmatory | | Target | MPI protein [Homo sapiens] [gi:16878311] | | PubMed | | | Data Table |  |
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| 5 | [SID131273767] | Active | IC50 | 1.9 | Inhibition of human purified phosphomannose isomerase [AID597374, Type: Literature] | Mannose-6-phosphate isomerase [gi:462567] |   View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 131273767 | | CID | 25181201 | | Outcome | Active | | IC50 | 1.9 [uM] | | BioAssay | Inhibition of human purified phosphomannose isomerase | | AID | 597374 | | BioAssay type | Literature | | Target | Mannose-6-phosphate isomerase [gi:462567] | | PubMed | 21539312 | | Data Table |  |
|
| 6 | [SID131273767] | Active | IC50 | 1.9 | Inhibition of human purified phosphomannose isomerase [AID597374, Type: Literature] | Mannose-6-phosphate isomerase [gi:462567] |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 131273767 | | CID | 25181201 | | Outcome | Active | | IC50 | 1.9 [uM] | | BioAssay | Inhibition of human purified phosphomannose isomerase | | AID | 597374 | | BioAssay type | Literature | | Target | Mannose-6-phosphate isomerase [gi:462567] | | PubMed | 21539312 | | Data Table |  |
|
| 7 | [SID85147391] | Active | Potency | 2.0787 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 2.0787 [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 |  |
|
| 8 | [SID85147391] | Active | Potency | 3.0131 | qHTS Assay to Find Inhibitors of T. brucei phosphofructokinase [AID485367, Type: confirmatory] | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 3.0131 [uM] | | BioAssay | qHTS Assay to Find Inhibitors of T. brucei phosphofructokinase | | AID | 485367 | | BioAssay type | confirmatory | | Target | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] | | PubMed | | | Data Table |  |
|
| 9 | [SID85147391] | Active | Potency | 3.2643 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 3.2643 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 10 | [SID85147391] | Active | Potency | 3.5481 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 3.5481 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 11 | [SID85147391] | Active | Potency | 3.5481 | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 3.5481 [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 12 | [SID85147391] | Active | EC50 | 3.624 | HTS for developing T Cell Immune Modulators: Dose-Response Assay [AID485284, Type: confirmatory] | |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | EC50 | 3.624 [uM] | | BioAssay | HTS for developing T Cell Immune Modulators: Dose-Response Assay | | AID | 485284 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 13 | [SID85147391] | Active | Potency | 3.6626 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 3.6626 [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT | | AID | 686978 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 14 | [SID85147391] | Active | Potency | 10 | qHTS for Inhibitors of TGF-b [AID588855, Type: confirmatory] | Smad3 [Homo sapiens] [gi:18418623] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS for Inhibitors of TGF-b | | AID | 588855 | | BioAssay type | confirmatory | | Target | Smad3 [Homo sapiens] [gi:18418623] | | PubMed | | | Data Table |  |
|
| 15 | [SID85147391] | Active | Potency | 10 | qHTS for Inhibitors of TGF-b [AID588855, Type: confirmatory] | Smad3 [Homo sapiens] [gi:18418623] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS for Inhibitors of TGF-b | | AID | 588855 | | BioAssay type | confirmatory | | Target | Smad3 [Homo sapiens] [gi:18418623] | | PubMed | | | Data Table |  |
|
| 16 | [SID85147391] | Active | IC50 | 10.5 | Dose Response orthogonal assay utilizing the direct end-point detection of NADPH for uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase [AID540252, Type: confirmatory] | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | IC50 | 10.5 [uM] | | BioAssay | Dose Response orthogonal assay utilizing the direct end-point detection of NADPH for uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase | | AID | 540252 | | BioAssay type | confirmatory | | Target | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] | | PubMed | | | Data Table |  |
|
| 17 | [SID85147391] | Active | IC50 | 11.3 | Human Glucose-6-Phosphate Dehydrogenase Dose Response Selectivity Assay for Inhibitors of Plasmodium falciparum Glucose-6-Phosphate Dehydrogenase [AID504792, Type: confirmatory] | G6PD gene product [Homo sapiens] [gi:108773793] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | IC50 | 11.3 [uM] | | BioAssay | Human Glucose-6-Phosphate Dehydrogenase Dose Response Selectivity Assay for Inhibitors of Plasmodium falciparum Glucose-6-Phosphate Dehydrogenase | | AID | 504792 | | BioAssay type | confirmatory | | Target | G6PD gene product [Homo sapiens] [gi:108773793] | | PubMed | | | Data Table |  |
|
| 18 | [SID85147391] | Active | IC50 | 11.3 | Human Glucose-6-Phosphate Dehydrogenase Dose Response Selectivity Assay for Inhibitors of Plasmodium falciparum Glucose-6-Phosphate Dehydrogenase [AID504792, Type: confirmatory] | G6PD gene product [Homo sapiens] [gi:108773793] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | IC50 | 11.3 [uM] | | BioAssay | Human Glucose-6-Phosphate Dehydrogenase Dose Response Selectivity Assay for Inhibitors of Plasmodium falciparum Glucose-6-Phosphate Dehydrogenase | | AID | 504792 | | BioAssay type | confirmatory | | Target | G6PD gene product [Homo sapiens] [gi:108773793] | | PubMed | | | Data Table |  |
|
| 19 | [SID85147391] | Active | IC50 | 11.4 | Dose Response orthogonal kinetic assay utilizing the direct detection of NADPH for uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase [AID540269, Type: confirmatory] | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | IC50 | 11.4 [uM] | | BioAssay | Dose Response orthogonal kinetic assay utilizing the direct detection of NADPH for uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase | | AID | 540269 | | BioAssay type | confirmatory | | Target | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] | | PubMed | | | Data Table |  |
|
| 20 | [SID85147391] | Active | IC50 | 13.5 | Dose Response confirmation of small molecule APOBEC3G DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay [AID504719, Type: confirmatory] | APOBEC3G gene product [Homo sapiens] [gi:13399304] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | IC50 | 13.5 [uM] | | BioAssay | Dose Response confirmation of small molecule APOBEC3G DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay | | AID | 504719 | | BioAssay type | confirmatory | | Target | APOBEC3G gene product [Homo sapiens] [gi:13399304] | | PubMed | | | Data Table |  |
|
| 21 | [SID85147391] | Active | Potency | 14.1254 | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain [AID504339, Type: confirmatory] | Chain A, Jmjd2a Tandem Tudor Domains In Complex With A Trimethylated Histone H4-K20 Peptide [gi:162330054] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 14.1254 [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 |  |
|
| 22 | [SID85147391] | Active | Potency | 16.9441 | Inhibitors of T. brucei phosphofructokinase: Hit Validation [AID504637, Type: confirmatory] | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 16.9441 [uM] | | BioAssay | Inhibitors of T. brucei phosphofructokinase: Hit Validation | | AID | 504637 | | BioAssay type | confirmatory | | Target | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] | | PubMed | | | Data Table |  |
|
| 23 | [SID85147391] | Active | Potency | 17.7828 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 17.7828 [uM] | | BioAssay | qHTS Assay for Inhibitors of BAZ2B | | AID | 504333 | | BioAssay type | confirmatory | | Target | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] | | PubMed | | | Data Table |  |
|
| 24 | [SID85147391] | Active | Potency | 18.3564 | A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. [AID624297, Type: confirmatory] | GMNN gene product [Homo sapiens] [gi:7705682] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 18.3564 [uM] | | BioAssay | A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. | | AID | 624297 | | BioAssay type | confirmatory | | Target | GMNN gene product [Homo sapiens] [gi:7705682] | | PubMed | | | Data Table |  |
|
| 25 | [SID85147391] | Active | Potency | 19.0115 | Tb PFK orthogonal confirmatory assay using ATP depletion (Kinase-Glo Plus) as an alternative measure of Tb PFK activity: Hit Validation [AID504636, Type: confirmatory] | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 19.0115 [uM] | | BioAssay | Tb PFK orthogonal confirmatory assay using ATP depletion (Kinase-Glo Plus) as an alternative measure of Tb PFK activity: Hit Validation | | AID | 504636 | | BioAssay type | confirmatory | | Target | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] | | PubMed | | | Data Table |  |
|
| 26 | [SID85147391] | Active | Potency | 19.9526 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 27 | [SID85147391] | Active | Potency | 19.9526 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 28 | [SID85147391] | Active | Potency | 19.9526 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 29 | [SID85147391] | Active | Potency | 19.9526 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 30 | [SID85147391] | Active | Potency | 20.5962 | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line [AID686970, Type: confirmatory] | IDH1 [Homo sapiens] [gi:49168486] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | 20.5962 [uM] | | BioAssay | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line | | AID | 686970 | | BioAssay type | confirmatory | | Target | IDH1 [Homo sapiens] [gi:49168486] | | PubMed | | | Data Table |  |
|
| 31 | [SID57287555] | Active | IC50 | 31.3 | Counter screen SAR assay for PMM2 inhibitors via a fluorescence intensity assay [AID1655, Type: confirmatory] | phosphomannomutase 2 [Homo sapiens] [gi:4557839] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 57287555 | | CID | 25181201 | | Outcome | Active | | IC50 | 31.3 [uM] | | BioAssay | Counter screen SAR assay for PMM2 inhibitors via a fluorescence intensity assay | | AID | 1655 | | BioAssay type | confirmatory | | Target | phosphomannomutase 2 [Homo sapiens] [gi:4557839] | | PubMed | | | Data Table |  |
|
| 32 | [SID57287555] | Active | IC50 | 31.3 | Counter screen SAR assay for PMM2 inhibitors via a fluorescence intensity assay [AID1655, Type: confirmatory] | phosphomannomutase 2 [Homo sapiens] [gi:4557839] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 57287555 | | CID | 25181201 | | Outcome | Active | | IC50 | 31.3 [uM] | | BioAssay | Counter screen SAR assay for PMM2 inhibitors via a fluorescence intensity assay | | AID | 1655 | | BioAssay type | confirmatory | | Target | phosphomannomutase 2 [Homo sapiens] [gi:4557839] | | PubMed | | | Data Table |  |
|
| 33 | [SID131273767] | Active | IC50 | 31.3 | Inhibition of human purified PMM2 [AID597375, Type: Literature] | Phosphomannomutase 2 [gi:3024413] |   View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 131273767 | | CID | 25181201 | | Outcome | Active | | IC50 | 31.3 [uM] | | BioAssay | Inhibition of human purified PMM2 | | AID | 597375 | | BioAssay type | Literature | | Target | Phosphomannomutase 2 [gi:3024413] | | PubMed | 21539312 | | Data Table |  |
|
| 34 | [SID131273767] | Active | IC50 | 31.3 | Inhibition of human purified PMM2 [AID597375, Type: Literature] | Phosphomannomutase 2 [gi:3024413] |   View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 131273767 | | CID | 25181201 | | Outcome | Active | | IC50 | 31.3 [uM] | | BioAssay | Inhibition of human purified PMM2 | | AID | 597375 | | BioAssay type | Literature | | Target | Phosphomannomutase 2 [gi:3024413] | | PubMed | 21539312 | | Data Table |  |
|
| 35 | [SID85147391] | Active | IC50 | 34.04 | 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. | 35 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | IC50 | 34.04 [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 |  |
|
| 36 | [SID85147391] | Active | CC50 | 67.524 | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - HeLa Cytotoxicity [AID624300, Type: confirmatory] | |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | CC50 | 67.524 [uM] | | BioAssay | Discovery of small molecule inhibitors of the oncogenic and cytokinetic protein MgcRacGAP - HeLa Cytotoxicity | | AID | 624300 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 37 | [SID85147391] | Active | Potency | | qHTS for Inhibitors of phosphatidylinositol 5-phosphate 4-kinase (PI5P4K) [AID652105, Type: confirmatory] | |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of phosphatidylinositol 5-phosphate 4-kinase (PI5P4K) | | AID | 652105 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 38 | [SID85147391] | Active | | | Fluorescence-based counterscreen for orexin 1 receptor (OX1R) antagonists: cell-based assay to identify antagonists of the parental CHO cell line [AID463079, Type: screening] | |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | Fluorescence-based counterscreen for orexin 1 receptor (OX1R) antagonists: cell-based assay to identify antagonists of the parental CHO cell line | | AID | 463079 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 39 | [SID85147391] | Active | | | Counterscreen for inhibitors of TLR9-MyD88 binding: luminescence-based cell-based high throughput assay to identify compounds that are cytotoxic to TLR9-MyD88 CHO cells [AID588336, Type: screening] | |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of TLR9-MyD88 binding: luminescence-based cell-based high throughput assay to identify compounds that are cytotoxic to TLR9-MyD88 CHO cells | | AID | 588336 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 40 | [SID85147391] | Active | | | HTS to Find Inhibitors of Pathogenic Pemphigus Antibodies [AID588358, Type: screening] | |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | HTS to Find Inhibitors of Pathogenic Pemphigus Antibodies | | AID | 588358 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 41 | [SID85147391] | Active | | | Counterscreen for IDE inhibitors: Luminescence-based cell-based high throughput assay to identify cytotoxic compounds using HEK cells [AID449730, Type: screening] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | Counterscreen for IDE inhibitors: Luminescence-based cell-based high throughput assay to identify cytotoxic compounds using HEK cells | | AID | 449730 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 42 | [SID85147391] | Active | | | uHTS identification of small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay [AID504690, Type: screening] | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | uHTS identification of small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay | | AID | 504690 | | BioAssay type | screening | | Target | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] | | PubMed | | | Data Table |  |
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| 43 | [SID85147391] | Active | | | Single concentration confirmation of uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay [AID504753, Type: screening] | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | Single concentration confirmation of uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay | | AID | 504753 | | BioAssay type | screening | | Target | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] | | PubMed | | | Data Table |  |
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| 44 | [SID85147391] | Active | | | qHTS of D3 Dopamine Receptor Antagonist: qHTS [AID652054, Type: screening] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | qHTS of D3 Dopamine Receptor Antagonist: qHTS | | AID | 652054 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 45 | [SID85147391] | Active | | | Counterscreen for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5): Luminescence-based biochemical high throughput assay to identify inhibitors of Hepatocyte nuclear factor 4 (HNF4) dimerization [AID651674, Type: screening] | HNF4A gene product [Homo sapiens] [gi:31077205] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5): Luminescence-based biochemical high throughput assay to identify inhibitors of Hepatocyte nuclear factor 4 (HNF4) dimerization | | AID | 651674 | | BioAssay type | screening | | Target | HNF4A gene product [Homo sapiens] [gi:31077205] | | PubMed | | | Data Table |  |
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| 46 | [SID85147391] | Active | | | Counterscreen for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5): Luminescence-based biochemical high throughput assay to identify inhibitors of Hepatocyte nuclear factor 4 (HNF4) dimerization [AID651674, Type: screening] | HNF4A gene product [Homo sapiens] [gi:31077205] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5): Luminescence-based biochemical high throughput assay to identify inhibitors of Hepatocyte nuclear factor 4 (HNF4) dimerization | | AID | 651674 | | BioAssay type | screening | | Target | HNF4A gene product [Homo sapiens] [gi:31077205] | | PubMed | | | Data Table |  |
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| 47 | [SID85147391] | Active | | | Counterscreen for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5): Luminescence-based biochemical high throughput assay to identify inhibitors of Hepatocyte nuclear factor 4 (HNF4) dimerization [AID651674, Type: screening] | HNF4A gene product [Homo sapiens] [gi:31077205] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5): Luminescence-based biochemical high throughput assay to identify inhibitors of Hepatocyte nuclear factor 4 (HNF4) dimerization | | AID | 651674 | | BioAssay type | screening | | Target | HNF4A gene product [Homo sapiens] [gi:31077205] | | PubMed | | | Data Table |  |
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| 48 | [SID85147391] | Active | | | Fluorescence polarization-based cell-based primary high throughput screening assay to identify inhibitors of insulin-degrading enzyme (IDE) [AID434962, Type: screening] | IDE gene product [Homo sapiens] [gi:155969707] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | Fluorescence polarization-based cell-based primary high throughput screening assay to identify inhibitors of insulin-degrading enzyme (IDE) | | AID | 434962 | | BioAssay type | screening | | Target | IDE gene product [Homo sapiens] [gi:155969707] | | PubMed | | | Data Table |  |
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| 49 | [SID85147391] | Active | | | Fluorescence polarization-based cell-based high throughput confirmation assay for inhibitors of insulin-degrading enzyme (IDE) [AID435028, Type: screening] | IDE gene product [Homo sapiens] [gi:155969707] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | Fluorescence polarization-based cell-based high throughput confirmation assay for inhibitors of insulin-degrading enzyme (IDE) | | AID | 435028 | | BioAssay type | screening | | Target | IDE gene product [Homo sapiens] [gi:155969707] | | PubMed | | | Data Table |  |
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| 50 | [SID85147391] | Active | | | Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 4 (CHRM4) [AID624127, Type: screening] | CHRM4 gene product [Homo sapiens] [gi:52426748] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 85147391 | | CID | 25181201 | | Outcome | Active | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify agonists of the human cholinergic receptor, muscarinic 4 (CHRM4) | | AID | 624127 | | BioAssay type | screening | | Target | CHRM4 gene product [Homo sapiens] [gi:52426748] | | PubMed | | | Data Table |  |
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