| 1 | [SID48415046] | Active | | | DSSTox (EPAFHM) EPA Fathead Minnow Acute Toxicity [AID1188, Type: other] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 48415046 | | CID | 7681 | | Outcome | Active | | BioAssay | DSSTox (EPAFHM) EPA Fathead Minnow Acute Toxicity | | AID | 1188 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 2 | [SID103229389] | Unspecified | | | Michaelis-Menten constant was determined for Monoamine oxidase-B from Bovine liver; b=not a substrate [AID102886, Type: Literature] | |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103229389 | | CID | 7681 | | Outcome | Unspecified | | BioAssay | Michaelis-Menten constant was determined for Monoamine oxidase-B from Bovine liver; b=not a substrate | | AID | 102886 | | BioAssay type | Literature | | Target | | | PubMed | 8510099 | | Data Table |  |
|
| 3 | [SID103229389] | Unspecified | | | Catalysis activity was calculated for Monoamine oxidase-B from Bovine liver; b=not a substrate [AID102889, Type: Literature] | |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103229389 | | CID | 7681 | | Outcome | Unspecified | | BioAssay | Catalysis activity was calculated for Monoamine oxidase-B from Bovine liver; b=not a substrate | | AID | 102889 | | BioAssay type | Literature | | Target | | | PubMed | 8510099 | | Data Table |  |
|
| 4 | [SID103229389] | Unspecified | | | Dissociation constant, pKa of the compound [AID350216, Type: Literature] | |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103229389 | | CID | 7681 | | Outcome | Unspecified | | BioAssay | Dissociation constant, pKa of the compound | | AID | 350216 | | BioAssay type | Literature | | Target | | | PubMed | 19397318 | | Data Table |  |
|
| 5 | [SID103229389] | Unspecified | | | Octanol-water partition coefficient, log PC of the compound [AID350218, Type: Literature] | |   View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103229389 | | CID | 7681 | | Outcome | Unspecified | | BioAssay | Octanol-water partition coefficient, log PC of the compound | | AID | 350218 | | BioAssay type | Literature | | Target | | | PubMed | 19397318 | | Data Table |  |
|
| 6 | [SID103229389] | Unspecified | | | Lipophilicity, log K at pH 2 by by hydrophilic interaction chromatography using 95% acetonitrile as mobile phase [AID350219, Type: Literature] | |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103229389 | | CID | 7681 | | Outcome | Unspecified | | BioAssay | Lipophilicity, log K at pH 2 by by hydrophilic interaction chromatography using 95% acetonitrile as mobile phase | | AID | 350219 | | BioAssay type | Literature | | Target | | | PubMed | 19397318 | | Data Table |  |
|
| 7 | [SID103229389] | Unspecified | | | Lipophilicity, log K at pH 2 by by hydrophilic interaction chromatography using 100% water as mobile phase [AID350220, Type: Literature] | |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103229389 | | CID | 7681 | | Outcome | Unspecified | | BioAssay | Lipophilicity, log K at pH 2 by by hydrophilic interaction chromatography using 100% water as mobile phase | | AID | 350220 | | BioAssay type | Literature | | Target | | | PubMed | 19397318 | | Data Table |  |
|
| 8 | [SID17389614] | Unspecified | | | qHTS assay for identifying genotoxic compounds that show differential cytotoxicity against a panel of isogenic chicken DT40 cell lines with known DNA damage response pathways [AID651838, Type: other] | |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Unspecified | | BioAssay | qHTS assay for identifying genotoxic compounds that show differential cytotoxicity against a panel of isogenic chicken DT40 cell lines with known DNA damage response pathways | | AID | 651838 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 9 | [SID17389614] | Inactive | Potency | 0.0016 | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 [AID938, Type: confirmatory] | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | 0.0016 [uM] | | BioAssay | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 | | AID | 938 | | BioAssay type | confirmatory | | Target | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] | | PubMed | | | Data Table |  |
|
| 10 | [SID17389614] | Inactive | Potency | 0.0016 | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 [AID938, Type: confirmatory] | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | 0.0016 [uM] | | BioAssay | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 | | AID | 938 | | BioAssay type | confirmatory | | Target | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] | | PubMed | | | Data Table |  |
|
| 11 | [SID17389614] | Inactive | Potency | 0.0016 | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 [AID938, Type: confirmatory] | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | 0.0016 [uM] | | BioAssay | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 | | AID | 938 | | BioAssay type | confirmatory | | Target | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] | | PubMed | | | Data Table |  |
|
| 12 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 13 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 14 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 15 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 16 | [SID17389614] | 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. | 16 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | 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 |  |
|
| 17 | [SID17389614] | Inactive | Potency | | qHTS Assay for Inhibitors of 12-hLO (12-human lipoxygenase) [AID1452, Type: confirmatory] | arachidonate 12-lipoxygenase, 12S-type [Homo sapiens] [gi:154426292] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of 12-hLO (12-human lipoxygenase) | | AID | 1452 | | BioAssay type | confirmatory | | Target | arachidonate 12-lipoxygenase, 12S-type [Homo sapiens] [gi:154426292] | | PubMed | | | Data Table |  |
|
| 18 | [SID17389614] | Inactive | Potency | | qHTS Assay for Inhibitors of 12-hLO (12-human lipoxygenase) [AID1452, Type: confirmatory] | arachidonate 12-lipoxygenase, 12S-type [Homo sapiens] [gi:154426292] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of 12-hLO (12-human lipoxygenase) | | AID | 1452 | | BioAssay type | confirmatory | | Target | arachidonate 12-lipoxygenase, 12S-type [Homo sapiens] [gi:154426292] | | PubMed | | | Data Table |  |
|
| 19 | [SID17389614] | Inactive | Potency | | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID887, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) | | AID | 887 | | BioAssay type | confirmatory | | Target | 15-lipoxygenase [Homo sapiens] [gi:1832253] | | PubMed | | | Data Table |  |
|
| 20 | [SID17389614] | Inactive | Potency | | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) [AID887, Type: confirmatory] | 15-lipoxygenase [Homo sapiens] [gi:1832253] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of 15-hLO (15-human lipoxygenase) | | AID | 887 | | BioAssay type | confirmatory | | Target | 15-lipoxygenase [Homo sapiens] [gi:1832253] | | PubMed | | | Data Table |  |
|
| 21 | [SID17389614] | Inactive | Potency | | qHTS Assay for Inhibitors of 15-hLO-2 (15-human lipoxygenase 2) [AID881, Type: confirmatory] | Arachidonate 15-lipoxygenase B [gi:317373425] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of 15-hLO-2 (15-human lipoxygenase 2) | | AID | 881 | | BioAssay type | confirmatory | | Target | Arachidonate 15-lipoxygenase B [gi:317373425] | | PubMed | | | Data Table |  |
|
| 22 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule agonists of androgen receptor signaling [AID588515, Type: confirmatory] | AR protein [Homo sapiens] [gi:124375976] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of androgen receptor signaling | | AID | 588515 | | BioAssay type | confirmatory | | Target | AR protein [Homo sapiens] [gi:124375976] | | PubMed | | | Data Table |  |
|
| 23 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule agonists of androgen receptor signaling [AID588515, Type: confirmatory] | AR protein [Homo sapiens] [gi:124375976] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of androgen receptor signaling | | AID | 588515 | | BioAssay type | confirmatory | | Target | AR protein [Homo sapiens] [gi:124375976] | | PubMed | | | Data Table |  |
|
| 24 | [SID99355618] | Inactive | | | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the Galanin Receptor 3 (GalR3) [AID651719, Type: screening] | GALR3 gene product [Homo sapiens] [gi:4503907] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 99355618 | | CID | 7681 | | Outcome | Inactive | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the Galanin Receptor 3 (GalR3) | | AID | 651719 | | BioAssay type | screening | | Target | GALR3 gene product [Homo sapiens] [gi:4503907] | | PubMed | | | Data Table |  |
|
| 25 | [SID99355618] | Inactive | | | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the Galanin Receptor 3 (GalR3) [AID651719, Type: screening] | GALR3 gene product [Homo sapiens] [gi:4503907] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 99355618 | | CID | 7681 | | Outcome | Inactive | | BioAssay | Fluorescence-based cell-based primary high throughput screening assay to identify antagonists of the Galanin Receptor 3 (GalR3) | | AID | 651719 | | BioAssay type | screening | | Target | GALR3 gene product [Homo sapiens] [gi:4503907] | | PubMed | | | Data Table |  |
|
| 26 | [SID99355618] | Inactive | | | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of 5-meCpG-binding domain protein 2 (MBD2)-DBD binding to methylated oligonucleotide [AID686964, Type: screening] | Methyl-CpG binding domain protein 2 [Homo sapiens] [gi:21595776] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 99355618 | | CID | 7681 | | Outcome | Inactive | | BioAssay | TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of 5-meCpG-binding domain protein 2 (MBD2)-DBD binding to methylated oligonucleotide | | AID | 686964 | | BioAssay type | screening | | Target | Methyl-CpG binding domain protein 2 [Homo sapiens] [gi:21595776] | | PubMed | | | Data Table |  |
|
| 27 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule antagonists of farnesoid X receptor signaling [AID588526, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of farnesoid X receptor signaling | | AID | 588526 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 28 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule antagonists of farnesoid X receptor signaling [AID588526, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of farnesoid X receptor signaling | | AID | 588526 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 29 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule antagonists of farnesoid X receptor signaling [AID588526, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of farnesoid X receptor signaling | | AID | 588526 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 30 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule antagonists of farnesoid X receptor signaling [AID588526, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of farnesoid X receptor signaling | | AID | 588526 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 31 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule agonists of farnesoid X receptor signaling [AID588527, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of farnesoid X receptor signaling | | AID | 588527 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 32 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule agonists of farnesoid X receptor signaling [AID588527, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of farnesoid X receptor signaling | | AID | 588527 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 33 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule agonists of farnesoid X receptor signaling [AID588527, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of farnesoid X receptor signaling | | AID | 588527 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 34 | [SID17389614] | Inactive | Potency | | qHTS assay for small molecule agonists of farnesoid X receptor signaling [AID588527, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of farnesoid X receptor signaling | | AID | 588527 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 35 | [SID99355618] | Inactive | | | Turbidometric Biochemical Primary HTS to identify inhibitors of ERp5 Measured in Biochemical System Using Plate Reader - 7002-01_Inhibitor_SinglePoint_HTS_Activity [AID651711, Type: screening] | Protein disulfide-isomerase A6 [gi:2501205] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 99355618 | | CID | 7681 | | Outcome | Inactive | | BioAssay | Turbidometric Biochemical Primary HTS to identify inhibitors of ERp5 Measured in Biochemical System Using Plate Reader - 7002-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 651711 | | BioAssay type | screening | | Target | Protein disulfide-isomerase A6 [gi:2501205] | | PubMed | | | Data Table |  |
|
| 36 | [SID99355618] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 2 (SRC2; NCOA2) [AID651957, Type: screening] | NCOA2 gene product [Homo sapiens] [gi:5729858] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 99355618 | | CID | 7681 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 2 (SRC2; NCOA2) | | AID | 651957 | | BioAssay type | screening | | Target | NCOA2 gene product [Homo sapiens] [gi:5729858] | | PubMed | | | Data Table |  |
|
| 37 | [SID99355618] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 2 (SRC2; NCOA2) [AID651957, Type: screening] | NCOA2 gene product [Homo sapiens] [gi:5729858] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 99355618 | | CID | 7681 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify inhibitors of the Steroid Receptor Coactivator 2 (SRC2; NCOA2) | | AID | 651957 | | BioAssay type | screening | | Target | NCOA2 gene product [Homo sapiens] [gi:5729858] | | PubMed | | | Data Table |  |
|
| 38 | [SID17389614] | Inactive | Potency | | qHTS for inhibitors of ROR gamma transcriptional activity [AID2551, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for inhibitors of ROR gamma transcriptional activity | | AID | 2551 | | BioAssay type | confirmatory | | Target | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] | | PubMed | | | Data Table |  |
|
| 39 | [SID17389614] | Inactive | Potency | | VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity [AID2546, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity | | AID | 2546 | | BioAssay type | confirmatory | | Target | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] | | PubMed | | | Data Table |  |
|
| 40 | [SID17389614] | Inactive | | | JNK3 AlphaScreen Assay [AID530, Type: confirmatory] | Mitogen-activated protein kinase 10 (Stress-activated protein kinase JNK3) (c-Jun N-terminal kinase [gi:2499604] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 17389614 | | CID | 7681 | | Outcome | Inactive | | BioAssay | JNK3 AlphaScreen Assay | | AID | 530 | | BioAssay type | confirmatory | | Target | Mitogen-activated protein kinase 10 (Stress-activated protein kinase JNK3) (c-Jun N-terminal kinase [gi:2499604] | | PubMed | | | Data Table |  |
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| 41 | [SID99355618] | Inactive | | | Small Molecule Inhibitors of FGF22-Mediated Excitatory Synaptogenesis & Epilepsy Measured in Biochemical System Using RT-PCR - 7012-01_Inhibitor_SinglePoint_HTS_Activity [AID651658, Type: screening] | FGF22 gene product [Homo sapiens] [gi:10190672] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 99355618 | | CID | 7681 | | Outcome | Inactive | | BioAssay | Small Molecule Inhibitors of FGF22-Mediated Excitatory Synaptogenesis & Epilepsy Measured in Biochemical System Using RT-PCR - 7012-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 651658 | | BioAssay type | screening | | Target | FGF22 gene product [Homo sapiens] [gi:10190672] | | PubMed | | | Data Table |  |
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| 42 | [SID99355618] | Inactive | | | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors of ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 (ASAP1) [AID624377, Type: screening] | ASAP1 gene product [Homo sapiens] [gi:351542238] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 99355618 | | CID | 7681 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors of ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 (ASAP1) | | AID | 624377 | | BioAssay type | screening | | Target | ASAP1 gene product [Homo sapiens] [gi:351542238] | | PubMed | | | Data Table |  |
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| 43 | [SID99355618] | Inactive | | | MLPCN ERAP1 Measured in Biochemical System Using Plate Reader - 7016-01_Inhibitor_SinglePoint_HTS_Activity [AID652197, Type: screening] | ERAP1 protein [Homo sapiens] [gi:21315078] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 99355618 | | CID | 7681 | | Outcome | Inactive | | BioAssay | MLPCN ERAP1 Measured in Biochemical System Using Plate Reader - 7016-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 652197 | | BioAssay type | screening | | Target | ERAP1 protein [Homo sapiens] [gi:21315078] | | PubMed | | | Data Table |  |
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| 44 | [SID99355618] | Inactive | | | MLPCN ERAP1 Measured in Biochemical System Using Plate Reader - 7016-01_Inhibitor_SinglePoint_HTS_Activity [AID652197, Type: screening] | ERAP1 protein [Homo sapiens] [gi:21315078] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 99355618 | | CID | 7681 | | Outcome | Inactive | | BioAssay | MLPCN ERAP1 Measured in Biochemical System Using Plate Reader - 7016-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 652197 | | BioAssay type | screening | | Target | ERAP1 protein [Homo sapiens] [gi:21315078] | | PubMed | | | Data Table |  |
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| 45 | [SID144207006] | Inactive | Potency | | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 144207006 | | CID | 7681 | | Outcome | Inactive | | Potency | [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 46 | [SID144207006] | Inactive | Potency | | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 144207006 | | CID | 7681 | | Outcome | Inactive | | Potency | [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 47 | [SID144207006] | Inactive | Potency | | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 144207006 | | CID | 7681 | | Outcome | Inactive | | Potency | [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 48 | [SID144207006] | Inactive | Potency | | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 144207006 | | CID | 7681 | | Outcome | Inactive | | Potency | [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 49 | [SID144207006] | Inactive | Potency | | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 144207006 | | CID | 7681 | | Outcome | Inactive | | Potency | [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 50 | [SID144207006] | Inactive | Potency | | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 144207006 | | CID | 7681 | | Outcome | Inactive | | Potency | [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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