| 1 | [SID90341258] | Active | Potency | 0.0532 | qHTS Validation Assay for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails [AID488953, Type: confirmatory] | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 0.0532 [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails | | AID | 488953 | | BioAssay type | confirmatory | | Target | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] | | PubMed | | | Data Table |  |
|
| 2 | [SID90341258] | Active | Potency | 8.9125 | 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. | 2 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 8.9125 [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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| 3 | [SID90341258] | Active | Potency | 10 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists [AID488983, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists | | AID | 488983 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 4 | [SID90341258] | Active | Potency | 10 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists [AID488983, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists | | AID | 488983 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 5 | [SID90341258] | Active | Potency | 10 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists [AID488983, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists | | AID | 488983 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 6 | [SID90341258] | Active | Potency | 10 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists [AID488983, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Antagonists | | AID | 488983 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 7 | [SID90341258] | Active | Potency | 18.8876 | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS [AID504845, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 18.8876 [uM] | | BioAssay | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS | | AID | 504845 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] | | PubMed | | | Data Table |  |
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| 8 | [SID90341258] | Active | Potency | 18.8876 | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS [AID504845, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 18.8876 [uM] | | BioAssay | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS | | AID | 504845 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] | | PubMed | | | Data Table |  |
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| 9 | [SID90341258] | Active | Potency | 18.8876 | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS [AID504845, Type: confirmatory] | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 18.8876 [uM] | | BioAssay | Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS | | AID | 504845 | | BioAssay type | confirmatory | | Target | regulator of G-protein signaling 4 [Homo sapiens] [gi:86301163] | | PubMed | | | Data Table |  |
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| 10 | [SID90341258] | Active | Potency | 25.1189 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 25.1189 [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 |  |
|
| 11 | [SID90341258] | Active | Potency | 25.1189 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 25.1189 [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 |  |
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| 12 | [SID90341258] | Active | Potency | 25.1189 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 25.1189 [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 |  |
|
| 13 | [SID90341258] | Active | Potency | 25.1189 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 25.1189 [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 |  |
|
| 14 | [SID90341258] | Active | Potency | 29.9349 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488773, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 29.9349 [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) | | AID | 488773 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 15 | [SID90341258] | Active | Potency | 29.9349 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488773, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 29.9349 [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) | | AID | 488773 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 16 | [SID90341258] | Active | Potency | 29.9349 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588453, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 29.9349 [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588453 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 17 | [SID90341258] | Active | Potency | 29.9349 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588453, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Active | | Potency | 29.9349 [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588453 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 18 | [SID90341258] | Inactive | Potency | 5.1732 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators [AID488982, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 5.1732 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators | | AID | 488982 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 19 | [SID90341258] | Inactive | Potency | 5.1732 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators [AID488982, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 5.1732 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators | | AID | 488982 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 20 | [SID90341258] | Inactive | Potency | 5.1732 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators [AID488982, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 5.1732 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators | | AID | 488982 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 21 | [SID90341258] | Inactive | Potency | 5.1732 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators [AID488982, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 5.1732 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators | | AID | 488982 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 22 | [SID90341258] | Inactive | Potency | 5.8048 | qHTS of alpha-syn Inhibitors [AID652106, Type: confirmatory] | Alpha-synuclein [gi:586067] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 5.8048 [uM] | | BioAssay | qHTS of alpha-syn Inhibitors | | AID | 652106 | | BioAssay type | confirmatory | | Target | Alpha-synuclein [gi:586067] | | PubMed | | | Data Table |  |
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| 23 | [SID90341258] | Inactive | Potency | 5.8048 | qHTS of alpha-syn Inhibitors [AID652106, Type: confirmatory] | Alpha-synuclein [gi:586067] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 5.8048 [uM] | | BioAssay | qHTS of alpha-syn Inhibitors | | AID | 652106 | | BioAssay type | confirmatory | | Target | Alpha-synuclein [gi:586067] | | PubMed | | | Data Table |  |
|
| 24 | [SID90341258] | Inactive | Potency | 7.9433 | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588456, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 7.9433 [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588456 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 25 | [SID90341258] | Inactive | Potency | 7.9433 | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588456, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 7.9433 [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588456 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 26 | [SID90341258] | Inactive | Potency | 14.6892 | qHTS for Inducers of the Endoplasmic Reticulum Stress Response (ERSR) in Human Glioma: qHTS [AID602332, Type: confirmatory] | heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) [Homo sapiens] [gi:168984549] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 14.6892 [uM] | | BioAssay | qHTS for Inducers of the Endoplasmic Reticulum Stress Response (ERSR) in Human Glioma: qHTS | | AID | 602332 | | BioAssay type | confirmatory | | Target | heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) [Homo sapiens] [gi:168984549] | | PubMed | | | Data Table |  |
|
| 27 | [SID90341258] | Inactive | Potency | 29.0929 | qHTS Assay for Small Molecule Inhibitors of Mitochondrial Division or Activators of Mitochondrial Fusion [AID485298, Type: confirmatory] | |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 29.0929 [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of Mitochondrial Division or Activators of Mitochondrial Fusion | | AID | 485298 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 28 | [SID90341258] | Inactive | Potency | 58.0479 | qHTS Assay for NPC1 Promoter Activators [AID485313, Type: confirmatory] | NPC1 gene product [Homo sapiens] [gi:255652944] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 58.0479 [uM] | | BioAssay | qHTS Assay for NPC1 Promoter Activators | | AID | 485313 | | BioAssay type | confirmatory | | Target | NPC1 gene product [Homo sapiens] [gi:255652944] | | PubMed | | | Data Table |  |
|
| 29 | [SID90341258] | Inactive | Potency | 58.0479 | qHTS Assay for Rab9 Promoter Activators [AID485297, Type: confirmatory] | RAB9A gene product [Homo sapiens] [gi:4759012] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | 58.0479 [uM] | | BioAssay | qHTS Assay for Rab9 Promoter Activators | | AID | 485297 | | BioAssay type | confirmatory | | Target | RAB9A gene product [Homo sapiens] [gi:4759012] | | PubMed | | | Data Table |  |
|
| 30 | [SID90341258] | Inactive | Potency | | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488772, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) | | AID | 488772 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 31 | [SID90341258] | Inactive | Potency | | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488772, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) | | AID | 488772 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 32 | [SID90341258] | Inactive | Potency | | Validation screen for small molecules that induce genotoxicity in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 [AID493106, Type: confirmatory] | ATAD5 protein [Homo sapiens] [gi:116283940] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Validation screen for small molecules that induce genotoxicity in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 | | AID | 493106 | | BioAssay type | confirmatory | | Target | ATAD5 protein [Homo sapiens] [gi:116283940] | | PubMed | | | Data Table |  |
|
| 33 | [SID90341258] | Inactive | Potency | | Validation screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 [AID493107, Type: confirmatory] | ATAD5 protein [Homo sapiens] [gi:116283940] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Validation screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 | | AID | 493107 | | BioAssay type | confirmatory | | Target | ATAD5 protein [Homo sapiens] [gi:116283940] | | PubMed | | | Data Table |  |
|
| 34 | [SID90341258] | Inactive | Potency | | High-Throughput Screening for Modulators of Cytosolic Chaperonin Activity: MmCpn Primary Screen [AID488978, Type: confirmatory] | chaperonin GroEL [Methanococcus maripaludis S2] [gi:45359078] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | High-Throughput Screening for Modulators of Cytosolic Chaperonin Activity: MmCpn Primary Screen | | AID | 488978 | | BioAssay type | confirmatory | | Target | chaperonin GroEL [Methanococcus maripaludis S2] [gi:45359078] | | PubMed | | | Data Table |  |
|
| 35 | [SID90341258] | Inactive | Potency | | qHTS Validation Assay to Find Inhibitors of T. brucei phosphofructokinase [AID485368, Type: confirmatory] | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay to Find Inhibitors of T. brucei phosphofructokinase | | AID | 485368 | | BioAssay type | confirmatory | | Target | ATP-dependent phosphofructokinase [Trypanosoma brucei] [gi:72386991] | | PubMed | | | Data Table |  |
|
| 36 | [SID90341258] | Inactive | Potency | | qHTS Validation Assay to Find Inhibitors of Phosphoglycerate Kinase [AID504547, Type: confirmatory] | phosphoglycerate kinase [Trypanosoma brucei] [gi:115503961] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay to Find Inhibitors of Phosphoglycerate Kinase | | AID | 504547 | | BioAssay type | confirmatory | | Target | phosphoglycerate kinase [Trypanosoma brucei] [gi:115503961] | | PubMed | | | Data Table |  |
|
| 37 | [SID90341258] | Inactive | Potency | | qHTS Validation Assay to Find Inhibitors of Phosphoglycerate Mutase [AID504548, Type: confirmatory] | 2,3-bisphosphoglycerate-independent phosphoglycerate mutase; 2,3-bisphosphoglycerate-independentphos [gi:157877932] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay to Find Inhibitors of Phosphoglycerate Mutase | | AID | 504548 | | BioAssay type | confirmatory | | Target | 2,3-bisphosphoglycerate-independent phosphoglycerate mutase; 2,3-bisphosphoglycerate-independentphos [gi:157877932] | | PubMed | | | Data Table |  |
|
| 38 | [SID90341258] | Inactive | Potency | | qHTS Validation Assay to Find Inhibitors of Pin1 [AID504536, Type: confirmatory] | PIN1 gene product [Homo sapiens] [gi:5453898] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay to Find Inhibitors of Pin1 | | AID | 504536 | | BioAssay type | confirmatory | | Target | PIN1 gene product [Homo sapiens] [gi:5453898] | | PubMed | | | Data Table |  |
|
| 39 | [SID90341258] | Inactive | Potency | | qHTS Validation Assay to Find Inhibitors of Pin1 [AID504536, Type: confirmatory] | PIN1 gene product [Homo sapiens] [gi:5453898] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay to Find Inhibitors of Pin1 | | AID | 504536 | | BioAssay type | confirmatory | | Target | PIN1 gene product [Homo sapiens] [gi:5453898] | | PubMed | | | Data Table |  |
|
| 40 | [SID90341258] | Inactive | Potency | | qHTS of GLP-1 Receptor Agonists: LOPAC Validation [AID624148, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS of GLP-1 Receptor Agonists: LOPAC Validation | | AID | 624148 | | BioAssay type | confirmatory | | Target | glp-1 receptor [Homo sapiens] [gi:1724069] | | PubMed | | | Data Table |  |
|
| 41 | [SID90341258] | Inactive | Potency | | qHTS of GLP-1 Receptor Agonists: LOPAC Validation [AID624148, Type: confirmatory] | glp-1 receptor [Homo sapiens] [gi:1724069] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS of GLP-1 Receptor Agonists: LOPAC Validation | | AID | 624148 | | BioAssay type | confirmatory | | Target | glp-1 receptor [Homo sapiens] [gi:1724069] | | PubMed | | | Data Table |  |
|
| 42 | [SID90341258] | Inactive | Potency | | Nrf2 qHTS screen for inhibitors: Validation [AID493153, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors: Validation | | AID | 493153 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 43 | [SID90341258] | Inactive | Potency | | Nrf2 qHTS screen for inhibitors: Validation [AID493153, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors: Validation | | AID | 493153 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 44 | [SID90341258] | Inactive | Potency | | Nrf2 qHTS screen for inhibitors: Validation [AID493153, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors: Validation | | AID | 493153 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 45 | [SID90341258] | Inactive | Potency | | Nrf2 qHTS screen for inhibitors: Validation [AID493153, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors: Validation | | AID | 493153 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 46 | [SID90341258] | Inactive | Potency | | qHTS Validation Assay for Iinhibitors of HIV-1 Budding by Blocking the Interaction of PTAP/TSG101 [AID485342, Type: confirmatory] | TSG101 gene product [Homo sapiens] [gi:5454140] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay for Iinhibitors of HIV-1 Budding by Blocking the Interaction of PTAP/TSG101 | | AID | 485342 | | BioAssay type | confirmatory | | Target | TSG101 gene product [Homo sapiens] [gi:5454140] | | PubMed | | | Data Table |  |
|
| 47 | [SID90341258] | Inactive | Potency | | qHTS Validation Assay for Iinhibitors of HIV-1 Budding by Blocking the Interaction of PTAP/TSG101 [AID485342, Type: confirmatory] | TSG101 gene product [Homo sapiens] [gi:5454140] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay for Iinhibitors of HIV-1 Budding by Blocking the Interaction of PTAP/TSG101 | | AID | 485342 | | BioAssay type | confirmatory | | Target | TSG101 gene product [Homo sapiens] [gi:5454140] | | PubMed | | | Data Table |  |
|
| 48 | [SID90341258] | Inactive | | | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign [AID504810, Type: Literature] | TSHR protein [Homo sapiens] [gi:118341367] |   View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | BioAssay | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | | AID | 504810 | | BioAssay type | Literature | | Target | TSHR protein [Homo sapiens] [gi:118341367] | | PubMed | 20427476 | | Data Table |  |
|
| 49 | [SID90341258] | Inactive | | | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign [AID504810, Type: Literature] | TSHR protein [Homo sapiens] [gi:118341367] |   View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | BioAssay | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | | AID | 504810 | | BioAssay type | Literature | | Target | TSHR protein [Homo sapiens] [gi:118341367] | | PubMed | 20427476 | | Data Table |  |
|
| 50 | [SID90341258] | Inactive | | | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign [AID504810, Type: Literature] | TSHR protein [Homo sapiens] [gi:118341367] |   View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 90341258 | | CID | 12480412 | | Outcome | Inactive | | BioAssay | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | | AID | 504810 | | BioAssay type | Literature | | Target | TSHR protein [Homo sapiens] [gi:118341367] | | PubMed | 20427476 | | Data Table |  |
|