| 1 | [SID26749249] | Active | Potency | 0.1032 | 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. | 1 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 0.1032 [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 |  |
|
| 2 | [SID26749249] | Active | Potency | 0.1032 | 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. | 2 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 0.1032 [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 |  |
|
| 3 | [SID26749249] | Active | Potency | 0.1032 | 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. | 3 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 0.1032 [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 |  |
|
| 4 | [SID26749249] | Active | Potency | 0.1458 | 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. | 4 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 0.1458 [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 |  |
|
| 5 | [SID26749249] | Active | Potency | 0.1458 | 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. | 5 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 0.1458 [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 |  |
|
| 6 | [SID26749249] | Active | Potency | 0.1458 | 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. | 6 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 0.1458 [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 |  |
|
| 7 | [SID26749249] | Active | Potency | 0.8913 | 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. | 7 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 0.8913 [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 |  |
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| 8 | [SID26749249] | Active | Potency | 1.122 | qHTS for inhibitors of ROR gamma transcriptional activity [AID2551, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 1.122 [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 |  |
|
| 9 | [SID26749249] | Active | Potency | 1.9953 | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1468, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 1.9953 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1468 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
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| 10 | [SID26749249] | Active | Potency | 1.9953 | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1468, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 1.9953 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1468 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 11 | [SID26749249] | Active | Potency | 2.2387 | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 12 | [SID26749249] | Active | Potency | 2.2387 | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 13 | [SID103248293] | Active | IC50 | 3.8 | Inhibitory concentration against hepatitis C virus NS3 protease [AID241120, Type: Literature] | |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103248293 | | CID | 4696 | | Outcome | Active | | IC50 | 3.8 [uM] | | BioAssay | Inhibitory concentration against hepatitis C virus NS3 protease | | AID | 241120 | | BioAssay type | Literature | | Target | | | PubMed | 15633995 | | Data Table |  |
|
| 14 | [SID26749249] | Active | Potency | 7.9433 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 15 | [SID26749249] | Active | Potency | 7.9433 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 16 | [SID26749249] | Active | Potency | 7.9433 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 17 | [SID26749249] | Active | Potency | 7.9433 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 18 | [SID26749249] | Active | Potency | 12.5893 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature [AID902, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | | AID | 902 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 19 | [SID26749249] | Active | Potency | 12.5893 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature [AID902, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | | AID | 902 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 20 | [SID26749249] | Active | Potency | 12.5893 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature [AID902, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | | AID | 902 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 21 | [SID26749249] | Active | Potency | 12.5893 | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature [AID902, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | | AID | 902 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
|
| 22 | [SID26749249] | Active | Potency | 12.5893 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 12.5893 [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 |  |
|
| 23 | [SID26749249] | Active | Potency | 12.5893 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 12.5893 [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 |  |
|
| 24 | [SID26749249] | Active | Potency | 12.5893 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 12.5893 [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 |  |
|
| 25 | [SID26749249] | Active | Potency | 12.5893 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 12.5893 [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 |  |
|
| 26 | [SID26753752] | Active | Potency | 19.9526 | qHTS assay for small molecule antagonists of peroxisome proliferator-activated receptor gamma signaling [AID588537, Type: confirmatory] | peroxisome proliferator activated receptor gamma [Homo sapiens] [gi:216409692] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | qHTS assay for small molecule antagonists of peroxisome proliferator-activated receptor gamma signaling | | AID | 588537 | | BioAssay type | confirmatory | | Target | peroxisome proliferator activated receptor gamma [Homo sapiens] [gi:216409692] | | PubMed | | | Data Table |  |
|
| 27 | [SID26753752] | Active | Potency | 19.9526 | qHTS assay for small molecule antagonists of peroxisome proliferator-activated receptor gamma signaling [AID588537, Type: confirmatory] | peroxisome proliferator activated receptor gamma [Homo sapiens] [gi:216409692] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | qHTS assay for small molecule antagonists of peroxisome proliferator-activated receptor gamma signaling | | AID | 588537 | | BioAssay type | confirmatory | | Target | peroxisome proliferator activated receptor gamma [Homo sapiens] [gi:216409692] | | PubMed | | | Data Table |  |
|
| 28 | [SID26753752] | Active | Potency | 19.9526 | qHTS assay for small molecule antagonists of peroxisome proliferator-activated receptor gamma signaling [AID588537, Type: confirmatory] | peroxisome proliferator activated receptor gamma [Homo sapiens] [gi:216409692] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | qHTS assay for small molecule antagonists of peroxisome proliferator-activated receptor gamma signaling | | AID | 588537 | | BioAssay type | confirmatory | | Target | peroxisome proliferator activated receptor gamma [Homo sapiens] [gi:216409692] | | PubMed | | | Data Table |  |
|
| 29 | [SID26753752] | Active | Potency | 19.9526 | qHTS assay for small molecule antagonists of peroxisome proliferator-activated receptor gamma signaling [AID588537, Type: confirmatory] | peroxisome proliferator activated receptor gamma [Homo sapiens] [gi:216409692] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | qHTS assay for small molecule antagonists of peroxisome proliferator-activated receptor gamma signaling | | AID | 588537 | | BioAssay type | confirmatory | | Target | peroxisome proliferator activated receptor gamma [Homo sapiens] [gi:216409692] | | PubMed | | | Data Table |  |
|
| 30 | [SID103248293] | Active | IC50 | 24.7 | Inhibition of HCV protease [AID358845, Type: Literature] | |   View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 103248293 | | CID | 4696 | | Outcome | Active | | IC50 | 24.7 [uM] | | BioAssay | Inhibition of HCV protease | | AID | 358845 | | BioAssay type | Literature | | Target | | | PubMed | 11170686 | | Data Table |  |
|
| 31 | [SID26749249] | Active | Potency | 31.6228 | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay [AID995, Type: confirmatory] | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | | AID | 995 | | BioAssay type | confirmatory | | Target | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] | | PubMed | | | Data Table |  |
|
| 32 | [SID26749249] | Active | Potency | 31.6228 | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay [AID995, Type: confirmatory] | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | | AID | 995 | | BioAssay type | confirmatory | | Target | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] | | PubMed | | | Data Table |  |
|
| 33 | [SID26749249] | Active | Potency | 31.6228 | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay [AID995, Type: confirmatory] | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | | AID | 995 | | BioAssay type | confirmatory | | Target | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] | | PubMed | | | Data Table |  |
|
| 34 | [SID26749249] | Active | Potency | 50.1187 | Inhibitors of USP1/UAF1: Pilot qHTS [AID504865, Type: confirmatory] | USP1 protein [Homo sapiens] [gi:118600387] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 26749249 | | CID | 4696 | | Outcome | Active | | Potency | 50.1187 [uM] | | BioAssay | Inhibitors of USP1/UAF1: Pilot qHTS | | AID | 504865 | | BioAssay type | confirmatory | | Target | USP1 protein [Homo sapiens] [gi:118600387] | | PubMed | | | Data Table |  |
|
| 35 | [SID103248293] | Active | | | Effect on Cdc2 expressed in HEK293 cells assessed as effect on Cdc2:Cdc25C interaction complexes in presence of camptothesin by EYFP and/or YFP Venus fragment based reporter gene assay [AID503332, Type: Literature] | |   View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 103248293 | | CID | 4696 | | Outcome | Active | | BioAssay | Effect on Cdc2 expressed in HEK293 cells assessed as effect on Cdc2:Cdc25C interaction complexes in presence of camptothesin by EYFP and/or YFP Venus fragment based reporter gene assay | | AID | 503332 | | BioAssay type | Literature | | Target | | | PubMed | 16680159 | | Data Table |  |
|
| 36 | [SID103248293] | Active | | | Effect on Cdc2 expressed in HEK293 cells assessed as effect on Cdc2:Cdc25A interaction complexes in presence of camptothesin by EYFP and/or YFP Venus fragment based reporter gene assay [AID503333, Type: Literature] | |   View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 103248293 | | CID | 4696 | | Outcome | Active | | BioAssay | Effect on Cdc2 expressed in HEK293 cells assessed as effect on Cdc2:Cdc25A interaction complexes in presence of camptothesin by EYFP and/or YFP Venus fragment based reporter gene assay | | AID | 503333 | | BioAssay type | Literature | | Target | | | PubMed | 16680159 | | Data Table |  |
|
| 37 | [SID103248293] | Active | | | Effect on p53 expressed in HEK293 cells assessed as effect on p53-p53 interaction complexes in presence of camptothesin by EYFP and/or YFP Venus fragment based reporter gene assay [AID503334, Type: Literature] | |   View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 103248293 | | CID | 4696 | | Outcome | Active | | BioAssay | Effect on p53 expressed in HEK293 cells assessed as effect on p53-p53 interaction complexes in presence of camptothesin by EYFP and/or YFP Venus fragment based reporter gene assay | | AID | 503334 | | BioAssay type | Literature | | Target | | | PubMed | 16680159 | | Data Table |  |
|
| 38 | [SID103248293] | Active | | | Inhibition of of c-Jun expressed in HEK293 cells assessed as induction of protein interaction in presence of camptothesin with Pin1 by EYFP based reporter gene assay [AID503335, Type: Literature] | |   View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 103248293 | | CID | 4696 | | Outcome | Active | | BioAssay | Inhibition of of c-Jun expressed in HEK293 cells assessed as induction of protein interaction in presence of camptothesin with Pin1 by EYFP based reporter gene assay | | AID | 503335 | | BioAssay type | Literature | | Target | | | PubMed | 16680159 | | Data Table |  |
|
| 39 | [SID103248293] | Active | | | Effect on cofilin1 expressed in HEK293 cells assessed as effect on cofilin1; Limk2 interaction complexes in presence of camptothesin by EYFP and/or YFP Venus fragment based reporter gene assay [AID503336, Type: Literature] | |   View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 103248293 | | CID | 4696 | | Outcome | Active | | BioAssay | Effect on cofilin1 expressed in HEK293 cells assessed as effect on cofilin1; Limk2 interaction complexes in presence of camptothesin by EYFP and/or YFP Venus fragment based reporter gene assay | | AID | 503336 | | BioAssay type | Literature | | Target | | | PubMed | 16680159 | | Data Table |  |
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| 40 | [SID26753752] | Active | | | 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_1, Type: other] | |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | 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 |  |
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| 41 | [SID26753752] | Active | | | 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_2, Type: other] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | 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 |  |
|
| 42 | [SID26753752] | Active | | | 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_3, Type: other] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | 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 |  |
|
| 43 | [SID26753752] | Active | | | 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_4, Type: other] | |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | 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 |  |
|
| 44 | [SID26753752] | Active | | | 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_5, Type: other] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | 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 |  |
|
| 45 | [SID26753752] | Active | | | 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_6, Type: other] | |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | 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 |  |
|
| 46 | [SID26753752] | Active | | | 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_7, Type: other] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | 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 |  |
|
| 47 | [SID26753752] | Active | | | 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_8, Type: other] | |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 26753752 | | CID | 4696 | | Outcome | Active | | 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 |  |
|
| 48 | [SID91264] | Active | | | NCI In Vivo Anticancer Drug Screen. Data for tumor model P388 Leukemia (intraperitoneal) in B6D2F1 (BDF1) mice [AID328, Type: other] | |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 91264 | | CID | 4696 | | Outcome | Active | | BioAssay | NCI In Vivo Anticancer Drug Screen. Data for tumor model P388 Leukemia (intraperitoneal) in B6D2F1 (BDF1) mice | | AID | 328 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 49 | [SID8150055] | Active | | | Protection from expanded polyglutamine huntingtin toxicity in PC12 cells (LDH100) [AID1596, Type: other] | |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 8150055 | | CID | 4696 | | Outcome | Active | | BioAssay | Protection from expanded polyglutamine huntingtin toxicity in PC12 cells (LDH100) | | AID | 1596 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 50 | [SID8150055] | Active | | | Screen for compounds that selectively increase SMN2 splicing relative to SMN1 splicing (SMNLUC) [AID1598, Type: other] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 8150055 | | CID | 4696 | | Outcome | Active | | BioAssay | Screen for compounds that selectively increase SMN2 splicing relative to SMN1 splicing (SMNLUC) | | AID | 1598 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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