| 1 | [SID4251553] | Active | CC50 | 9.43e-06 | Cytotoxicity counterscreen assay for transcriptional activators of heat shock protein 70 (Hsp70) [AID1259, Type: confirmatory] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | CC50 | 9.43e-06 [uM] | | BioAssay | Cytotoxicity counterscreen assay for transcriptional activators of heat shock protein 70 (Hsp70) | | AID | 1259 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 2 | [SID4251553] | Active | Potency | 0.0184 | 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 | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 0.0184 [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 | [SID4251553] | Active | Potency | 0.0184 | 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 | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 0.0184 [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 | [SID4251553] | Active | Potency | 0.0184 | 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. | 4 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 0.0184 [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 |  |
|
| 5 | [SID4251553] | Active | Potency | 0.0231 | 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 | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 0.0231 [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 | [SID4251553] | Active | Potency | 0.0231 | 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 | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 0.0231 [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 | [SID4251553] | Active | Potency | 0.0231 | 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. | 7 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 0.0231 [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 |  |
|
| 8 | [SID4251553] | Active | Potency | 0.7079 | 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 | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 0.7079 [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 | [SID4251553] | Active | IC50 | 0.72 | Dose response confirmation of uHTS chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation in a Jurkat cell line using a luminescence assay [AID489035, Type: confirmatory] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 0.72 [uM] | | BioAssay | Dose response confirmation of uHTS chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation in a Jurkat cell line using a luminescence assay | | AID | 489035 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 10 | [SID4251553] | 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. | 10 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | 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 |  |
|
| 11 | [SID4251553] | Active | IC50 | 1.276 | Fluorescence dose response cell-based high throughput screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) [AID1692, Type: confirmatory] | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 1.276 [uM] | | BioAssay | Fluorescence dose response cell-based high throughput screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | | AID | 1692 | | BioAssay type | confirmatory | | Target | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] | | PubMed | | | Data Table |  |
|
| 12 | [SID4251553] | Active | IC50 | 1.276 | Fluorescence dose response cell-based high throughput screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) [AID1692, Type: confirmatory] | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 1.276 [uM] | | BioAssay | Fluorescence dose response cell-based high throughput screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | | AID | 1692 | | BioAssay type | confirmatory | | Target | Sphingosine-1-phosphate receptor 4 [Homo sapiens] [gi:15929025] | | PubMed | | | Data Table |  |
|
| 13 | [SID4251553] | Active | IC50 | 1.35 | High Throughput Screening Assay used to Identify Novel Compounds that Inhibit Mycobacterium Tuberculosis in 7H9 Media [AID449762, Type: confirmatory] | |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 1.35 [uM] | | BioAssay | High Throughput Screening Assay used to Identify Novel Compounds that Inhibit Mycobacterium Tuberculosis in 7H9 Media | | AID | 449762 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 14 | [SID4251553] | Active | EC50 | 1.678 | Leishmania major promastigote EC50 determinations [AID2008, Type: confirmatory] | |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | EC50 | 1.678 [uM] | | BioAssay | Leishmania major promastigote EC50 determinations | | AID | 2008 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 15 | [SID4251553] | Active | IC50 | 1.964 | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA [AID856, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 1.964 [uM] | | BioAssay | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA | | AID | 856 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 16 | [SID4251553] | Active | IC50 | 1.964 | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA [AID856, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 1.964 [uM] | | BioAssay | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA | | AID | 856 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 17 | [SID4251553] | Active | IC50 | 1.964 | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA [AID856, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 1.964 [uM] | | BioAssay | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA | | AID | 856 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 18 | [SID4251553] | Active | IC50 | 2.12 | CHOP dose-response primary assay [AID504322, Type: confirmatory] | Ddit3 gene product [Mus musculus] [gi:160707929] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 2.12 [uM] | | BioAssay | CHOP dose-response primary assay | | AID | 504322 | | BioAssay type | confirmatory | | Target | Ddit3 gene product [Mus musculus] [gi:160707929] | | PubMed | | | Data Table |  |
|
| 19 | [SID4251553] | Active | Potency | 2.2387 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 2.2387 [uM] | | BioAssay | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins | | AID | 485364 | | BioAssay type | confirmatory | | Target | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] | | PubMed | | | Data Table |  |
|
| 20 | [SID4251553] | Active | IC50 | 2.24 | A High Throughput Confirmatory Assay used to Identify Novel Compounds that Inhibit Mycobacterium Tuberculosis in the absence of Glycerol [AID449764, Type: confirmatory] | |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 2.24 [uM] | | BioAssay | A High Throughput Confirmatory Assay used to Identify Novel Compounds that Inhibit Mycobacterium Tuberculosis in the absence of Glycerol | | AID | 449764 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 21 | [SID4251553] | Active | Potency | 2.5119 | qHTS Assay for Inhibitors of Hepatitis C Virus (HCV) [AID651820, Type: confirmatory] | |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 2.5119 [uM] | | BioAssay | qHTS Assay for Inhibitors of Hepatitis C Virus (HCV) | | AID | 651820 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 22 | [SID4251553] | Active | EC50 | 2.541 | Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically LAP4 based on MLPCN hits [AID2745, Type: confirmatory] | LAP4 [Saccharomyces cerevisiae] [gi:486173] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | EC50 | 2.541 [uM] | | BioAssay | Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically LAP4 based on MLPCN hits | | AID | 2745 | | BioAssay type | confirmatory | | Target | LAP4 [Saccharomyces cerevisiae] [gi:486173] | | PubMed | | | Data Table |  |
|
| 23 | [SID4251553] | Active | IC50 | 2.68 | XBP1 DR counterscreen for CHOP [AID504313, Type: confirmatory] | XBP1 [Homo sapiens] [gi:47678753] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 2.68 [uM] | | BioAssay | XBP1 DR counterscreen for CHOP | | AID | 504313 | | BioAssay type | confirmatory | | Target | XBP1 [Homo sapiens] [gi:47678753] | | PubMed | | | Data Table |  |
|
| 24 | [SID4251553] | Active | EC50 | 3.038 | Luminescence Cell-Based Dose Confimation HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1) [AID2382, Type: confirmatory] | Hsf1 protein [Mus musculus] [gi:62740231] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | EC50 | 3.038 [uM] | | BioAssay | Luminescence Cell-Based Dose Confimation HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1) | | AID | 2382 | | BioAssay type | confirmatory | | Target | Hsf1 protein [Mus musculus] [gi:62740231] | | PubMed | | | Data Table |  |
|
| 25 | [SID4251553] | Active | EC50 | 3.038 | Luminescence Cell-Based Dose Confimation HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1) [AID2382, Type: confirmatory] | Hsf1 protein [Mus musculus] [gi:62740231] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | EC50 | 3.038 [uM] | | BioAssay | Luminescence Cell-Based Dose Confimation HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1) | | AID | 2382 | | BioAssay type | confirmatory | | Target | Hsf1 protein [Mus musculus] [gi:62740231] | | PubMed | | | Data Table |  |
|
| 26 | [SID4251553] | Active | CC50 | 3.126 | A Cell Based Secondary Assay To Explore Cytotoxicity of Compounds that Inhibit Mycobacterium Tuberculosis [AID435019, Type: confirmatory] | |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | CC50 | 3.126 [uM] | | BioAssay | A Cell Based Secondary Assay To Explore Cytotoxicity of Compounds that Inhibit Mycobacterium Tuberculosis | | AID | 435019 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 27 | [SID4251553] | Active | Potency | 3.1623 | 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. | 27 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 3.1623 [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 |  |
|
| 28 | [SID4251553] | Active | Potency | 3.1623 | 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. | 28 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 3.1623 [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 |  |
|
| 29 | [SID4251553] | Active | Potency | 3.1623 | 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. | 29 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 3.1623 [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 |  |
|
| 30 | [SID4251553] | Active | AC50 | 3.247 | Luminescence Cell-Based Dose Retest to Confirm Inhibitors of Beta Cell Apoptosis [AID449756, Type: confirmatory] | |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | AC50 | 3.247 [uM] | | BioAssay | Luminescence Cell-Based Dose Retest to Confirm Inhibitors of Beta Cell Apoptosis | | AID | 449756 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 31 | [SID4251553] | Active | IC50 | 3.51 | Dose Response selectivity of uHTS chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation in a 697B cell line using a luminescence assay [AID489033, Type: confirmatory] | |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 3.51 [uM] | | BioAssay | Dose Response selectivity of uHTS chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation in a 697B cell line using a luminescence assay | | AID | 489033 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 32 | [SID4251553] | Active | Potency | 3.5481 | 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. | 32 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 3.5481 [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 |  |
|
| 33 | [SID4251553] | Active | Potency | 3.5481 | 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. | 33 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 3.5481 [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 |  |
|
| 34 | [SID4251553] | Active | IC50 | 3.673 | Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor [AID463214, Type: confirmatory] | type-1 angiotensin II receptor [Homo sapiens] [gi:4501997] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 3.673 [uM] | | BioAssay | Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor | | AID | 463214 | | BioAssay type | confirmatory | | Target | type-1 angiotensin II receptor [Homo sapiens] [gi:4501997] | | PubMed | | | Data Table |  |
|
| 35 | [SID4251553] | Active | IC50 | 3.673 | Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor [AID463214, Type: confirmatory] | type-1 angiotensin II receptor [Homo sapiens] [gi:4501997] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 3.673 [uM] | | BioAssay | Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor | | AID | 463214 | | BioAssay type | confirmatory | | Target | type-1 angiotensin II receptor [Homo sapiens] [gi:4501997] | | PubMed | | | Data Table |  |
|
| 36 | [SID4251553] | Active | Potency | 3.9811 | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 3.9811 [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
|
| 37 | [SID4251553] | Active | Potency | 3.9811 | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 3.9811 [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
|
| 38 | [SID4251553] | Active | IC50 | 4.499 | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor [AID851, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 4.499 [uM] | | BioAssay | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor | | AID | 851 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 39 | [SID4251553] | Active | IC50 | 4.499 | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor [AID851, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 4.499 [uM] | | BioAssay | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor | | AID | 851 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 40 | [SID4251553] | Active | IC50 | 4.499 | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor [AID851, Type: confirmatory] | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | IC50 | 4.499 [uM] | | BioAssay | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor | | AID | 851 | | BioAssay type | confirmatory | | Target | sphingosine 1-phosphate receptor 2 [Homo sapiens] [gi:134244587] | | PubMed | | | Data Table |  |
|
| 41 | [SID4251553] | Active | Potency | 5.0119 | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction [AID1461, Type: confirmatory] | NPSR1 gene product [Homo sapiens] [gi:46395496] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 5.0119 [uM] | | BioAssay | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction | | AID | 1461 | | BioAssay type | confirmatory | | Target | NPSR1 gene product [Homo sapiens] [gi:46395496] | | PubMed | | | Data Table |  |
|
| 42 | [SID4251553] | Active | Potency | 5.0119 | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction [AID1461, Type: confirmatory] | NPSR1 gene product [Homo sapiens] [gi:46395496] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 5.0119 [uM] | | BioAssay | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction | | AID | 1461 | | BioAssay type | confirmatory | | Target | NPSR1 gene product [Homo sapiens] [gi:46395496] | | PubMed | | | Data Table |  |
|
| 43 | [SID4251553] | Active | AC50 | 5.464 | HSF-1 induced GFP reporter and Doxycycline induced RFP reporter Measured in Cell-Based System Using Plate Reader - 2038-03_Inhibitor_DoseNoFile_CherryPick_Activity_Set3 [AID493083, Type: confirmatory] | Hsf1 protein [Mus musculus] [gi:62740231] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | AC50 | 5.464 [uM] | | BioAssay | HSF-1 induced GFP reporter and Doxycycline induced RFP reporter Measured in Cell-Based System Using Plate Reader - 2038-03_Inhibitor_DoseNoFile_CherryPick_Activity_Set3 | | AID | 493083 | | BioAssay type | confirmatory | | Target | Hsf1 protein [Mus musculus] [gi:62740231] | | PubMed | | | Data Table |  |
|
| 44 | [SID4251553] | Active | AC50 | 5.464 | HSF-1 induced GFP reporter and Doxycycline induced RFP reporter Measured in Cell-Based System Using Plate Reader - 2038-03_Inhibitor_DoseNoFile_CherryPick_Activity_Set3 [AID493083, Type: confirmatory] | Hsf1 protein [Mus musculus] [gi:62740231] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | AC50 | 5.464 [uM] | | BioAssay | HSF-1 induced GFP reporter and Doxycycline induced RFP reporter Measured in Cell-Based System Using Plate Reader - 2038-03_Inhibitor_DoseNoFile_CherryPick_Activity_Set3 | | AID | 493083 | | BioAssay type | confirmatory | | Target | Hsf1 protein [Mus musculus] [gi:62740231] | | PubMed | | | Data Table |  |
|
| 45 | [SID4251553] | Active | AC50 | 5.475 | ATP-based Luminescence in the Absence of Cytokines Measured in Cell-Based System Using Plate Reader - 2061-06_Inhibitor_Dose_CherryPick [AID463229, Type: confirmatory] | |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | AC50 | 5.475 [uM] | | BioAssay | ATP-based Luminescence in the Absence of Cytokines Measured in Cell-Based System Using Plate Reader - 2061-06_Inhibitor_Dose_CherryPick | | AID | 463229 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 46 | [SID4251553] | Active | EC50 | 5.527 | Counterscreen assay for inhibitors of Wee1 degradation: dose response cell-based assay to identify inhibitors of cyclin B degradation [AID1414, Type: confirmatory] | cyclin B1 [Homo sapiens] [gi:119571691] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | EC50 | 5.527 [uM] | | BioAssay | Counterscreen assay for inhibitors of Wee1 degradation: dose response cell-based assay to identify inhibitors of cyclin B degradation | | AID | 1414 | | BioAssay type | confirmatory | | Target | cyclin B1 [Homo sapiens] [gi:119571691] | | PubMed | | | Data Table |  |
|
| 47 | [SID4251553] | Active | EC50 | 5.527 | Counterscreen assay for inhibitors of Wee1 degradation: dose response cell-based assay to identify inhibitors of cyclin B degradation [AID1414, Type: confirmatory] | cyclin B1 [Homo sapiens] [gi:119571691] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | EC50 | 5.527 [uM] | | BioAssay | Counterscreen assay for inhibitors of Wee1 degradation: dose response cell-based assay to identify inhibitors of cyclin B degradation | | AID | 1414 | | BioAssay type | confirmatory | | Target | cyclin B1 [Homo sapiens] [gi:119571691] | | PubMed | | | Data Table |  |
|
| 48 | [SID4251553] | Active | EC50 | 5.527 | Counterscreen assay for inhibitors of Wee1 degradation: dose response cell-based assay to identify inhibitors of cyclin B degradation [AID1414, Type: confirmatory] | cyclin B1 [Homo sapiens] [gi:119571691] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | EC50 | 5.527 [uM] | | BioAssay | Counterscreen assay for inhibitors of Wee1 degradation: dose response cell-based assay to identify inhibitors of cyclin B degradation | | AID | 1414 | | BioAssay type | confirmatory | | Target | cyclin B1 [Homo sapiens] [gi:119571691] | | PubMed | | | Data Table |  |
|
| 49 | [SID4251553] | Active | Potency | 6.5131 | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line [AID686970, Type: confirmatory] | IDH1 [Homo sapiens] [gi:49168486] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 6.5131 [uM] | | BioAssay | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line | | AID | 686970 | | BioAssay type | confirmatory | | Target | IDH1 [Homo sapiens] [gi:49168486] | | PubMed | | | Data Table |  |
|
| 50 | [SID4251553] | Active | Potency | 6.5131 | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line [AID686970, Type: confirmatory] | IDH1 [Homo sapiens] [gi:49168486] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 4251553 | | CID | 5286934 | | Outcome | Active | | Potency | 6.5131 [uM] | | BioAssay | qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line | | AID | 686970 | | BioAssay type | confirmatory | | Target | IDH1 [Homo sapiens] [gi:49168486] | | PubMed | | | Data Table |  |
|