| 1 | [SID49726858] | Active | IC50 | 0.804539 | Image-Based HTS for Selective Antagonists of GPR35 [AID2058, Type: confirmatory] | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Active | | IC50 | 0.804539 [uM] | | BioAssay | Image-Based HTS for Selective Antagonists of GPR35 | | AID | 2058 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] | | PubMed | | | Data Table |  |
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| 2 | [SID49726858] | Active | IC50 | 0.804539 | Image-Based HTS for Selective Antagonists of GPR35 [AID2058, Type: confirmatory] | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Active | | IC50 | 0.804539 [uM] | | BioAssay | Image-Based HTS for Selective Antagonists of GPR35 | | AID | 2058 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] | | PubMed | | | Data Table |  |
|
| 3 | [SID49726858] | Active | IC50 | 0.804539 | Image-Based HTS for Selective Antagonists of GPR35 [AID2058, Type: confirmatory] | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Active | | IC50 | 0.804539 [uM] | | BioAssay | Image-Based HTS for Selective Antagonists of GPR35 | | AID | 2058 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] | | PubMed | | | Data Table |  |
|
| 4 | [SID87544493] | Active | IC50 | 1.6 | SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 2 [AID2480, Type: confirmatory] | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 1.6 [uM] | | BioAssay | SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 2 | | AID | 2480 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] | | PubMed | | | Data Table |  |
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| 5 | [SID87544493] | Active | IC50 | 1.6 | SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 2 [AID2480, Type: confirmatory] | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 1.6 [uM] | | BioAssay | SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 2 | | AID | 2480 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] | | PubMed | | | Data Table |  |
|
| 6 | [SID87544493] | Active | IC50 | 1.6 | SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 2 [AID2480, Type: confirmatory] | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 1.6 [uM] | | BioAssay | SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 2 | | AID | 2480 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] | | PubMed | | | Data Table |  |
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| 7 | [SID87544493] | Active | IC50 | 1.636 | SAR Analysis for the identification of Selective Antagonists of ERK1/2 Activity in GPR35-Overexpressing U2OS Cells [AID463217, Type: confirmatory] | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 1.636 [uM] | | BioAssay | SAR Analysis for the identification of Selective Antagonists of ERK1/2 Activity in GPR35-Overexpressing U2OS Cells | | AID | 463217 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] | | PubMed | | | Data Table |  |
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| 8 | [SID87544493] | Active | IC50 | 1.636 | SAR Analysis for the identification of Selective Antagonists of ERK1/2 Activity in GPR35-Overexpressing U2OS Cells [AID463217, Type: confirmatory] | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 1.636 [uM] | | BioAssay | SAR Analysis for the identification of Selective Antagonists of ERK1/2 Activity in GPR35-Overexpressing U2OS Cells | | AID | 463217 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] | | PubMed | | | Data Table |  |
|
| 9 | [SID87544493] | Active | IC50 | 1.636 | SAR Analysis for the identification of Selective Antagonists of ERK1/2 Activity in GPR35-Overexpressing U2OS Cells [AID463217, Type: confirmatory] | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 1.636 [uM] | | BioAssay | SAR Analysis for the identification of Selective Antagonists of ERK1/2 Activity in GPR35-Overexpressing U2OS Cells | | AID | 463217 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 35 isoform a [Homo sapiens] [gi:33695097] | | PubMed | | | Data Table |  |
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| 10 | [SID87544493] | Active | IC50 | 2.02 | SAR analysis of compounds that inhibit HePTP - Set 2 [AID449736, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 2.02 [uM] | | BioAssay | SAR analysis of compounds that inhibit HePTP - Set 2 | | AID | 449736 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
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| 11 | [SID87544493] | Active | IC50 | 2.02 | SAR analysis of compounds that inhibit HePTP - Set 2 [AID449736, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 2.02 [uM] | | BioAssay | SAR analysis of compounds that inhibit HePTP - Set 2 | | AID | 449736 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
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| 12 | [SID87544493] | Active | IC50 | 2.02 | SAR analysis of compounds that inhibit HePTP - Set 2 [AID449736, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 2.02 [uM] | | BioAssay | SAR analysis of compounds that inhibit HePTP - Set 2 | | AID | 449736 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 7 isoform 2 [Homo sapiens] [gi:18375660] | | PubMed | | | Data Table |  |
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| 13 | [SID87544493] | Active | IC50 | 23.7 | SAR Selectivity Analysis of small molecule inhibitors of PEST using pCAP in a fluorescence assay [AID488884, Type: confirmatory] | tyrosine-protein phosphatase non-receptor type 12 isoform 2 [Homo sapiens] [gi:196114967] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 23.7 [uM] | | BioAssay | SAR Selectivity Analysis of small molecule inhibitors of PEST using pCAP in a fluorescence assay | | AID | 488884 | | BioAssay type | confirmatory | | Target | tyrosine-protein phosphatase non-receptor type 12 isoform 2 [Homo sapiens] [gi:196114967] | | PubMed | | | Data Table |  |
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| 14 | [SID87544493] | Active | IC50 | 61 | SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 3 [AID449726, Type: confirmatory] | PTPN22 gene product [Homo sapiens] [gi:224586929] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 61 [uM] | | BioAssay | SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 3 | | AID | 449726 | | BioAssay type | confirmatory | | Target | PTPN22 gene product [Homo sapiens] [gi:224586929] | | PubMed | | | Data Table |  |
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| 15 | [SID87544493] | Active | IC50 | 61 | SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 3 [AID449726, Type: confirmatory] | PTPN22 gene product [Homo sapiens] [gi:224586929] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 61 [uM] | | BioAssay | SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 3 | | AID | 449726 | | BioAssay type | confirmatory | | Target | PTPN22 gene product [Homo sapiens] [gi:224586929] | | PubMed | | | Data Table |  |
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| 16 | [SID87544493] | Active | IC50 | 61 | SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 3 [AID449726, Type: confirmatory] | PTPN22 gene product [Homo sapiens] [gi:224586929] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 61 [uM] | | BioAssay | SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 3 | | AID | 449726 | | BioAssay type | confirmatory | | Target | PTPN22 gene product [Homo sapiens] [gi:224586929] | | PubMed | | | Data Table |  |
|
| 17 | [SID87544493] | Active | IC50 | 72.6 | SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 3 [AID449727, Type: confirmatory] | PTPN22 gene product [Homo sapiens] [gi:224586929] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 72.6 [uM] | | BioAssay | SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 3 | | AID | 449727 | | BioAssay type | confirmatory | | Target | PTPN22 gene product [Homo sapiens] [gi:224586929] | | PubMed | | | Data Table |  |
|
| 18 | [SID87544493] | Active | IC50 | 72.6 | SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 3 [AID449727, Type: confirmatory] | PTPN22 gene product [Homo sapiens] [gi:224586929] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 72.6 [uM] | | BioAssay | SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 3 | | AID | 449727 | | BioAssay type | confirmatory | | Target | PTPN22 gene product [Homo sapiens] [gi:224586929] | | PubMed | | | Data Table |  |
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| 19 | [SID87544493] | Active | IC50 | 72.6 | SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 3 [AID449727, Type: confirmatory] | PTPN22 gene product [Homo sapiens] [gi:224586929] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Active | | IC50 | 72.6 [uM] | | BioAssay | SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 3 | | AID | 449727 | | BioAssay type | confirmatory | | Target | PTPN22 gene product [Homo sapiens] [gi:224586929] | | PubMed | | | Data Table |  |
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| 20 | [SID49726858] | Active | | | Fluorescence-based biochemical primary high throughput screening assay to identify molecules that bind r(CAG) RNA repeats [AID651821, Type: screening] | |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical primary high throughput screening assay to identify molecules that bind r(CAG) RNA repeats | | AID | 651821 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 21 | [SID49726858] | Active | | | uHTS Luminescent assay for identification of inhibitors of Sentrin-specific protease 6 (SENP6) [AID2599, Type: screening] | SUMO-1-specific protease [Homo sapiens] [gi:6166485] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Active | | BioAssay | uHTS Luminescent assay for identification of inhibitors of Sentrin-specific protease 6 (SENP6) | | AID | 2599 | | BioAssay type | screening | | Target | SUMO-1-specific protease [Homo sapiens] [gi:6166485] | | PubMed | | | Data Table |  |
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| 22 | [SID49726858] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
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| 23 | [SID49726858] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
|
| 24 | [SID49726858] | Inactive | Potency | 6.5131 | A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. [AID624296, Type: confirmatory] | GMNN gene product [Homo sapiens] [gi:7705682] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | Potency | 6.5131 [uM] | | BioAssay | A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. | | AID | 624296 | | BioAssay type | confirmatory | | Target | GMNN gene product [Homo sapiens] [gi:7705682] | | PubMed | | | Data Table |  |
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| 25 | [SID87544493] | Inactive | IC50 | 27.1 | SAR Analysis of Selective Antagonists of GPR55 using an Image-Based Assay [AID2397, Type: confirmatory] | G-protein coupled receptor 55 [Homo sapiens] [gi:33695107] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 87544493 | | CID | 1205881 | | Outcome | Inactive | | IC50 | 27.1 [uM] | | BioAssay | SAR Analysis of Selective Antagonists of GPR55 using an Image-Based Assay | | AID | 2397 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 55 [Homo sapiens] [gi:33695107] | | PubMed | | | Data Table |  |
|
| 26 | [SID49726858] | Inactive | Potency | | qHTS Assay for Rab9 Promoter Activators [AID485297, Type: confirmatory] | RAB9A gene product [Homo sapiens] [gi:4759012] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Rab9 Promoter Activators | | AID | 485297 | | BioAssay type | confirmatory | | Target | RAB9A gene product [Homo sapiens] [gi:4759012] | | PubMed | | | Data Table |  |
|
| 27 | [SID49726858] | Inactive | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). [AID1974, Type: screening] | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). | | AID | 1974 | | BioAssay type | screening | | Target | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] | | PubMed | | | Data Table |  |
|
| 28 | [SID49726858] | Inactive | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). [AID1974, Type: screening] | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the oxidoreductase glutathione S-transferase omega 1(GSTO1). | | AID | 1974 | | BioAssay type | screening | | Target | glutathione S-transferase omega-1 isoform 1 [Homo sapiens] [gi:4758484] | | PubMed | | | Data Table |  |
|
| 29 | [SID49726858] | Inactive | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the prolyl oligopeptidase-like enzyme (PREPL) [AID2751, Type: screening] | Prolyl endopeptidase-like [Homo sapiens] [gi:153217451] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the prolyl oligopeptidase-like enzyme (PREPL) | | AID | 2751 | | BioAssay type | screening | | Target | Prolyl endopeptidase-like [Homo sapiens] [gi:153217451] | | PubMed | | | Data Table |  |
|
| 30 | [SID49726858] | Inactive | | | Fluorescence polarization to screen for inhibitors that disrupt the protein-protein interaction between Keap1 and Nrf2 Measured in Biochemical System Using Plate Reader - 2119-01_Inhibitor_SinglePoint_HTS_Activity [AID504523, Type: screening] | KEAP1 gene product [Homo sapiens] [gi:45269145] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Fluorescence polarization to screen for inhibitors that disrupt the protein-protein interaction between Keap1 and Nrf2 Measured in Biochemical System Using Plate Reader - 2119-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 504523 | | BioAssay type | screening | | Target | KEAP1 gene product [Homo sapiens] [gi:45269145] | | PubMed | | | Data Table |  |
|
| 31 | [SID49726858] | Inactive | | | Fluorescence polarization to screen for inhibitors that disrupt the protein-protein interaction between Keap1 and Nrf2 Measured in Biochemical System Using Plate Reader - 2119-01_Inhibitor_SinglePoint_HTS_Activity [AID504523, Type: screening] | KEAP1 gene product [Homo sapiens] [gi:45269145] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Fluorescence polarization to screen for inhibitors that disrupt the protein-protein interaction between Keap1 and Nrf2 Measured in Biochemical System Using Plate Reader - 2119-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 504523 | | BioAssay type | screening | | Target | KEAP1 gene product [Homo sapiens] [gi:45269145] | | PubMed | | | Data Table |  |
|
| 32 | [SID49726858] | Inactive | | | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) [AID602229, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) | | AID | 602229 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
|
| 33 | [SID49726858] | Inactive | | | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) [AID602229, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) | | AID | 602229 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
|
| 34 | [SID49726858] | Inactive | | | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) [AID602229, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based high throughput primary screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) | | AID | 602229 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
|
| 35 | [SID49726858] | Inactive | | | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). [AID2300, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). | | AID | 2300 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
|
| 36 | [SID49726858] | Inactive | | | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). [AID2300, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). | | AID | 2300 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
|
| 37 | [SID49726858] | Inactive | | | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). [AID2300, Type: screening] | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | TR-FRET-based primary biochemical high throughput screening assay to identify agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). | | AID | 2300 | | BioAssay type | screening | | Target | photoreceptor-specific nuclear receptor [Homo sapiens] [gi:216409728] | | PubMed | | | Data Table |  |
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| 38 | [SID49726858] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. [AID2462, Type: screening] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. | | AID | 2462 | | BioAssay type | screening | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
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| 39 | [SID49726858] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. [AID2462, Type: screening] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. | | AID | 2462 | | BioAssay type | screening | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
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| 40 | [SID49726858] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. [AID2462, Type: screening] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. | | AID | 2462 | | BioAssay type | screening | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
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| 41 | [SID49726858] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. [AID2462, Type: screening] | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of A1 Apoptosis. | | AID | 2462 | | BioAssay type | screening | | Target | bcl-2-like protein 11 isoform 1 [Homo sapiens] [gi:20336315] | | PubMed | | | Data Table |  |
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| 42 | [SID49726858] | Inactive | | | Flow Cytometric HTS Screen for inhibitors of the ABC transporter ABCB6 for MLPCN Compound Set [AID602162, Type: screening] | ABCB6 gene product [Homo sapiens] [gi:9955963] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Flow Cytometric HTS Screen for inhibitors of the ABC transporter ABCB6 for MLPCN Compound Set | | AID | 602162 | | BioAssay type | screening | | Target | ABCB6 gene product [Homo sapiens] [gi:9955963] | | PubMed | | | Data Table |  |
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| 43 | [SID49726858] | Inactive | Potency | | qHTS Assay for Inhibitors of RanGTP induced Rango (Ran-regulated importin-beta cargo) - Importin beta complex dissociation [AID540253, Type: confirmatory] | snurportin-1 [Homo sapiens] [gi:5031833] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of RanGTP induced Rango (Ran-regulated importin-beta cargo) - Importin beta complex dissociation | | AID | 540253 | | BioAssay type | confirmatory | | Target | snurportin-1 [Homo sapiens] [gi:5031833] | | PubMed | | | Data Table |  |
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| 44 | [SID49726858] | Inactive | Potency | | qHTS Assay for Inhibitors of Rango (Ran-regulated importin-beta cargo) - Importin beta complex formation [AID540263, Type: confirmatory] | snurportin-1 [Homo sapiens] [gi:5031833] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Rango (Ran-regulated importin-beta cargo) - Importin beta complex formation | | AID | 540263 | | BioAssay type | confirmatory | | Target | snurportin-1 [Homo sapiens] [gi:5031833] | | PubMed | | | Data Table |  |
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| 45 | [SID49726858] | 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. | 45 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | 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 |  |
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| 46 | [SID49726858] | Inactive | | | uHTS identification of inhibitors of Rpn11 in a Fluorescent Polarization assay [AID588493, Type: screening] | PSMD14 protein [Homo sapiens] [gi:16306916] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | uHTS identification of inhibitors of Rpn11 in a Fluorescent Polarization assay | | AID | 588493 | | BioAssay type | screening | | Target | PSMD14 protein [Homo sapiens] [gi:16306916] | | PubMed | | | Data Table |  |
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| 47 | [SID49726858] | Inactive | EC50 | | uHTS luminescence assay for the identification of compounds that inhibit NOD1 [AID1578, Type: confirmatory] | nucleotide-binding oligomerization domain-containing protein 1 [Homo sapiens] [gi:5174617] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | EC50 | [uM] | | BioAssay | uHTS luminescence assay for the identification of compounds that inhibit NOD1 | | AID | 1578 | | BioAssay type | confirmatory | | Target | nucleotide-binding oligomerization domain-containing protein 1 [Homo sapiens] [gi:5174617] | | PubMed | | | Data Table |  |
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| 48 | [SID49726858] | Inactive | EC50 | | uHTS luminescence assay for the identification of compounds that inhibit NOD1 [AID1578, Type: confirmatory] | nucleotide-binding oligomerization domain-containing protein 1 [Homo sapiens] [gi:5174617] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | EC50 | [uM] | | BioAssay | uHTS luminescence assay for the identification of compounds that inhibit NOD1 | | AID | 1578 | | BioAssay type | confirmatory | | Target | nucleotide-binding oligomerization domain-containing protein 1 [Homo sapiens] [gi:5174617] | | PubMed | | | Data Table |  |
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| 49 | [SID49726858] | Inactive | | | Counterscreen for PME1 inhibitors: fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of lysophospholipase 1 (LYPLA1). [AID2174, Type: screening] | acyl-protein thioesterase 1 [Homo sapiens] [gi:5453722] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Counterscreen for PME1 inhibitors: fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of lysophospholipase 1 (LYPLA1). | | AID | 2174 | | BioAssay type | screening | | Target | acyl-protein thioesterase 1 [Homo sapiens] [gi:5453722] | | PubMed | | | Data Table |  |
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| 50 | [SID49726858] | Inactive | | | Counterscreen for PME1 inhibitors: fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of lysophospholipase 1 (LYPLA1). [AID2174, Type: screening] | acyl-protein thioesterase 1 [Homo sapiens] [gi:5453722] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 49726858 | | CID | 1205881 | | Outcome | Inactive | | BioAssay | Counterscreen for PME1 inhibitors: fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of lysophospholipase 1 (LYPLA1). | | AID | 2174 | | BioAssay type | screening | | Target | acyl-protein thioesterase 1 [Homo sapiens] [gi:5453722] | | PubMed | | | Data Table |  |
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