| 1 | [SID848038] | Active | Potency | 0.5645 | qHTS Fluorescence Polarization (FP) Assay for Inhibitors of MLL CXXC domain - DNA interaction: Fluorescein FP [AID624160, Type: confirmatory] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 0.5645 [uM] | | BioAssay | qHTS Fluorescence Polarization (FP) Assay for Inhibitors of MLL CXXC domain - DNA interaction: Fluorescein FP | | AID | 624160 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 2 | [SID848038] | Active | IC50 | 0.61948 | Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput counterscreen to identify inhibitors of TEM-1 metallo-beta-lactamase [AID2755, Type: confirmatory] | Beta lactamase [Pseudomonas aeruginosa] [gi:114881106] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | IC50 | 0.61948 [uM] | | BioAssay | Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput counterscreen to identify inhibitors of TEM-1 metallo-beta-lactamase | | AID | 2755 | | BioAssay type | confirmatory | | Target | Beta lactamase [Pseudomonas aeruginosa] [gi:114881106] | | PubMed | | | Data Table |  |
|
| 3 | [SID85303865] | Active | AC50 | 0.786 | C-LANA Counter Screen: DNA intercalators Measured in Biochemical System Using Plate Reader - 2117-02_Inhibitor_Dose_CherryPick_Activity_Set2 [AID504727, Type: confirmatory] | LANA [Human herpesvirus 8] [gi:312275222] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 85303865 | | CID | 650462 | | Outcome | Active | | AC50 | 0.786 [uM] | | BioAssay | C-LANA Counter Screen: DNA intercalators Measured in Biochemical System Using Plate Reader - 2117-02_Inhibitor_Dose_CherryPick_Activity_Set2 | | AID | 504727 | | BioAssay type | confirmatory | | Target | LANA [Human herpesvirus 8] [gi:312275222] | | PubMed | | | Data Table |  |
|
| 4 | [SID85303865] | Active | AC50 | 1.109 | C-LANA FP assay Measured in Biochemical System Using Plate Reader - 2117-01_Inhibitor_Dose_CherryPick_Activity [AID504725, Type: confirmatory] | LANA [Human herpesvirus 8] [gi:312275222] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 85303865 | | CID | 650462 | | Outcome | Active | | AC50 | 1.109 [uM] | | BioAssay | C-LANA FP assay Measured in Biochemical System Using Plate Reader - 2117-01_Inhibitor_Dose_CherryPick_Activity | | AID | 504725 | | BioAssay type | confirmatory | | Target | LANA [Human herpesvirus 8] [gi:312275222] | | PubMed | | | Data Table |  |
|
| 5 | [SID848038] | Active | IC50 | 1.392 | Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase [AID2754, Type: confirmatory] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | IC50 | 1.392 [uM] | | BioAssay | Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase | | AID | 2754 | | BioAssay type | confirmatory | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
|
| 6 | [SID848038] | Active | IC50 | 1.392 | Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase [AID2754, Type: confirmatory] | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | IC50 | 1.392 [uM] | | BioAssay | Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase | | AID | 2754 | | BioAssay type | confirmatory | | Target | metallo beta-lactamase [Pseudomonas aeruginosa] [gi:7381449] | | PubMed | | | Data Table |  |
|
| 7 | [SID848038] | Active | Potency | 1.5849 | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Green Fluorophore) [AID875, Type: confirmatory] | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 1.5849 [uM] | | BioAssay | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Green Fluorophore) | | AID | 875 | | BioAssay type | confirmatory | | Target | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] | | PubMed | | | Data Table |  |
|
| 8 | [SID848038] | Active | IC50 | 1.622 | Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of IMP-1metallo-beta-lactamase [AID2756, Type: confirmatory] | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | IC50 | 1.622 [uM] | | BioAssay | Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of IMP-1metallo-beta-lactamase | | AID | 2756 | | BioAssay type | confirmatory | | Target | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] | | PubMed | | | Data Table |  |
|
| 9 | [SID848038] | Active | IC50 | 4.455 | Tumor Hsp90 Inhibitors Dose Response Confirmation [AID712, Type: confirmatory] | 90-kda heat shock protein beta HSP90 beta [Homo sapiens] [gi:4261762] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | IC50 | 4.455 [uM] | | BioAssay | Tumor Hsp90 Inhibitors Dose Response Confirmation | | AID | 712 | | BioAssay type | confirmatory | | Target | 90-kda heat shock protein beta HSP90 beta [Homo sapiens] [gi:4261762] | | PubMed | | | Data Table |  |
|
| 10 | [SID848038] | Active | EC50 | 4.58 | HCS for Compounds that Up-Regulate Insulin Promoter Activity in MIN6 Cells [AID1625, Type: confirmatory] | |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | EC50 | 4.58 [uM] | | BioAssay | HCS for Compounds that Up-Regulate Insulin Promoter Activity in MIN6 Cells | | AID | 1625 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 11 | [SID848038] | Active | Potency | 11.2202 | qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 [AID504467, Type: confirmatory] | ATAD5 protein [Homo sapiens] [gi:116283940] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 11.2202 [uM] | | BioAssay | qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1 | | AID | 504467 | | BioAssay type | confirmatory | | Target | ATAD5 protein [Homo sapiens] [gi:116283940] | | PubMed | | | Data Table |  |
|
| 12 | [SID848038] | Active | Potency | 12.5893 | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-1: Spectroscopic Profiling in AFC Spectral Region [AID923, Type: confirmatory] | |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-1: Spectroscopic Profiling in AFC Spectral Region | | AID | 923 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 13 | [SID848038] | Active | Potency | 19.9526 | qHTS for Inhibitors of WRN Helicase [AID651768, Type: confirmatory] | WRN [Homo sapiens] [gi:3719421] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | qHTS for Inhibitors of WRN Helicase | | AID | 651768 | | BioAssay type | confirmatory | | Target | WRN [Homo sapiens] [gi:3719421] | | PubMed | | | Data Table |  |
|
| 14 | [SID848038] | Active | Potency | 22.3872 | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) [AID2549, Type: confirmatory] | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 22.3872 [uM] | | BioAssay | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) | | AID | 2549 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] | | PubMed | | | Data Table |  |
|
| 15 | [SID131280334] | Active | IC50 | 25 | Competitive inhibition of human ASK1 [AID593712, Type: Literature] | Mitogen-activated protein kinase kinase kinase 5 [gi:6685617] |   View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 131280334 | | CID | 650462 | | Outcome | Active | | IC50 | 25 [uM] | | BioAssay | Competitive inhibition of human ASK1 | | AID | 593712 | | BioAssay type | Literature | | Target | Mitogen-activated protein kinase kinase kinase 5 [gi:6685617] | | PubMed | 21449566 | | Data Table |  |
|
| 16 | [SID131280334] | Active | IC50 | 25 | Competitive inhibition of human ASK1 [AID593712, Type: Literature] | Mitogen-activated protein kinase kinase kinase 5 [gi:6685617] |   View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 131280334 | | CID | 650462 | | Outcome | Active | | IC50 | 25 [uM] | | BioAssay | Competitive inhibition of human ASK1 | | AID | 593712 | | BioAssay type | Literature | | Target | Mitogen-activated protein kinase kinase kinase 5 [gi:6685617] | | PubMed | 21449566 | | Data Table |  |
|
| 17 | [SID848038] | Active | Potency | 25.1189 | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Red Fluorophore) [AID892, Type: confirmatory] | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 25.1189 [uM] | | BioAssay | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Red Fluorophore) | | AID | 892 | | BioAssay type | confirmatory | | Target | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] | | PubMed | | | Data Table |  |
|
| 18 | [SID848038] | Active | Potency | 31.6228 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 19 | [SID848038] | Active | Potency | 31.6228 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
|
| 20 | [SID848038] | Active | Potency | 39.8107 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
|
| 21 | [SID848038] | Active | Potency | 39.8107 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
|
| 22 | [SID848038] | Active | Potency | 44.6684 | qHTS Assay for the Inhibitors of Human Flap endonuclease 1 (FEN1). [AID588795, Type: confirmatory] | flap endonuclease 1 [Homo sapiens] [gi:4758356] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | qHTS Assay for the Inhibitors of Human Flap endonuclease 1 (FEN1). | | AID | 588795 | | BioAssay type | confirmatory | | Target | flap endonuclease 1 [Homo sapiens] [gi:4758356] | | PubMed | | | Data Table |  |
|
| 23 | [SID848038] | Active | Potency | 141.807 | qHTS Fluorescence Polarization (FP) Assay for Inhibitors of MLL CXXC domain - DNA interaction: Texas Red FP [AID624161, Type: confirmatory] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | Potency | 141.807 [uM] | | BioAssay | qHTS Fluorescence Polarization (FP) Assay for Inhibitors of MLL CXXC domain - DNA interaction: Texas Red FP | | AID | 624161 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 24 | [SID848038] | Active | | | HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules: Confirmation Assay [AID463116, Type: screening] | |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules: Confirmation Assay | | AID | 463116 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 25 | [SID85303865] | Active | | | Full deck counterscreen for agonists of the human M1 muscarinic receptor (CHRM1): Fluorescence-based cell-based high throughput screening assay to identify nonselective activators and assay artifacts using the parental CHOK1 cell line [AID602248, Type: screening] | |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 85303865 | | CID | 650462 | | Outcome | Active | | BioAssay | Full deck counterscreen for agonists of the human M1 muscarinic receptor (CHRM1): Fluorescence-based cell-based high throughput screening assay to identify nonselective activators and assay artifacts using the parental CHOK1 cell line | | AID | 602248 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 26 | [SID848038] | Active | | | Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen [AID626, Type: screening] | |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: Agonist Primary Screen | | AID | 626 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 27 | [SID848038] | Active | | | qHTS Assay for Spectroscopic Profiling in A488 Spectral Region [AID591, Type: other] | |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in A488 Spectral Region | | AID | 591 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 28 | [SID848038] | Active | | | HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules. [AID1381, Type: screening] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules. | | AID | 1381 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 29 | [SID848038] | Active | EC50 | | Counterscreen for Fluorescence in GFP-Spectra Wavelengths Caused By Cell-Permeable Autofluorescent Compounds [AID2124, Type: confirmatory] | |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | EC50 | [uM] | | BioAssay | Counterscreen for Fluorescence in GFP-Spectra Wavelengths Caused By Cell-Permeable Autofluorescent Compounds | | AID | 2124 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 30 | [SID848038] | Active | | | Fluorescence-based counterscreen for orexin 1 receptor (OX1R) antagonists: cell-based assay to identify antagonists of the parental CHO cell line [AID463079, Type: screening] | |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Fluorescence-based counterscreen for orexin 1 receptor (OX1R) antagonists: cell-based assay to identify antagonists of the parental CHO cell line | | AID | 463079 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 31 | [SID848038] | Active | | | qHTS Assay for Spectroscopic Profiling in Resorufin Spectral Region [AID588, Type: other] | |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in Resorufin Spectral Region | | AID | 588 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 32 | [SID848038] | Active | | | qHTS Assay for Spectroscopic Profiling in Fluorescein Spectral Region [AID593, Type: other] | |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in Fluorescein Spectral Region | | AID | 593 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 33 | [SID848038] | Active | | | qHTS Assay for Spectroscopic Profiling in Rhodamine Spectral Region [AID594, Type: confirmatory] | |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in Rhodamine Spectral Region | | AID | 594 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 34 | [SID848038] | Active | | | Counterscreen for PME1 inhibitors: fluorescence polarization-based biochemical high throughput confirmation assay to identify inhibitors of lysophospholipase 2 (LYPLA2). [AID2232, Type: screening] | lysophospholipase II [Homo sapiens] [gi:4581413] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Counterscreen for PME1 inhibitors: fluorescence polarization-based biochemical high throughput confirmation assay to identify inhibitors of lysophospholipase 2 (LYPLA2). | | AID | 2232 | | BioAssay type | screening | | Target | lysophospholipase II [Homo sapiens] [gi:4581413] | | PubMed | | | Data Table |  |
|
| 35 | [SID848038] | Active | | | Counterscreen for PME1 inhibitors: fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of lysophospholipase 2 (LYPLA2). [AID2177, Type: screening] | lysophospholipase II [Homo sapiens] [gi:4581413] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Counterscreen for PME1 inhibitors: fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of lysophospholipase 2 (LYPLA2). | | AID | 2177 | | BioAssay type | screening | | Target | lysophospholipase II [Homo sapiens] [gi:4581413] | | PubMed | | | Data Table |  |
|
| 36 | [SID848038] | Active | | | qHTS Assay for Inhibitors of YjeE [AID605, Type: confirmatory] | UPF0079 ATP-binding protein yjeE [gi:84028058] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | qHTS Assay for Inhibitors of YjeE | | AID | 605 | | BioAssay type | confirmatory | | Target | UPF0079 ATP-binding protein yjeE [gi:84028058] | | PubMed | | | Data Table |  |
|
| 37 | [SID848038] | Active | | | Primary biochemical high-throughput screening assay for inhibitors of the HIV Rev RRE RNA interaction (disruption of protein-RNA interaction) [AID704, Type: screening] | Chain B, Rna Aptamer Complexed With Hiv-1 Rev Peptide, Nmr, 7 Structures [gi:253722402] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Primary biochemical high-throughput screening assay for inhibitors of the HIV Rev RRE RNA interaction (disruption of protein-RNA interaction) | | AID | 704 | | BioAssay type | screening | | Target | Chain B, Rna Aptamer Complexed With Hiv-1 Rev Peptide, Nmr, 7 Structures [gi:253722402] | | PubMed | | | Data Table |  |
|
| 38 | [SID848038] | Active | | | HTS for Tumor Hsp90 Inhibitors [AID429, Type: screening] | 90-kda heat shock protein beta HSP90 beta [Homo sapiens] [gi:4261762] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | HTS for Tumor Hsp90 Inhibitors | | AID | 429 | | BioAssay type | screening | | Target | 90-kda heat shock protein beta HSP90 beta [Homo sapiens] [gi:4261762] | | PubMed | | | Data Table |  |
|
| 39 | [SID85303865] | Active | | | Fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of the HTRA serine peptidase 1 (HTRA1) [AID540248, Type: other] | HTRA1 protein [gi:121945198] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 85303865 | | CID | 650462 | | Outcome | Active | | BioAssay | Fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of the HTRA serine peptidase 1 (HTRA1) | | AID | 540248 | | BioAssay type | other | | Target | HTRA1 protein [gi:121945198] | | PubMed | | | Data Table |  |
|
| 40 | [SID85303865] | Active | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the HTRA serine peptidase 1 (HTRA1) [AID504803, Type: screening] | HTRA1 protein [gi:121945198] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 85303865 | | CID | 650462 | | Outcome | Active | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the HTRA serine peptidase 1 (HTRA1) | | AID | 504803 | | BioAssay type | screening | | Target | HTRA1 protein [gi:121945198] | | PubMed | | | Data Table |  |
|
| 41 | [SID848038] | Active | | | Epi-absorbance-based confirmation assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase. [AID2189, Type: screening] | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Epi-absorbance-based confirmation assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase. | | AID | 2189 | | BioAssay type | screening | | Target | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] | | PubMed | | | Data Table |  |
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| 42 | [SID848038] | Active | | | Epi-absorbance primary biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase [AID1556, Type: screening] | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Epi-absorbance primary biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase | | AID | 1556 | | BioAssay type | screening | | Target | metallo-beta-lactamase IMP-1 [Pseudomonas aeruginosa] [gi:27368096] | | PubMed | | | Data Table |  |
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| 43 | [SID85303865] | Active | | | C-LANA FP assay Measured in Biochemical System Using Plate Reader - 2117-01_Inhibitor_SinglePoint_HTS_Activity [AID504423, Type: screening] | LANA [Human herpesvirus 8] [gi:312275222] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 85303865 | | CID | 650462 | | Outcome | Active | | BioAssay | C-LANA FP assay Measured in Biochemical System Using Plate Reader - 2117-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 504423 | | BioAssay type | screening | | Target | LANA [Human herpesvirus 8] [gi:312275222] | | PubMed | | | Data Table |  |
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| 44 | [SID848038] | Active | | | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) [AID2797, Type: screening] | vasopressin V1a receptor [Homo sapiens] [gi:4502331] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | | AID | 2797 | | BioAssay type | screening | | Target | vasopressin V1a receptor [Homo sapiens] [gi:4502331] | | PubMed | | | Data Table |  |
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| 45 | [SID848038] | Active | | | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) [AID2797, Type: screening] | vasopressin V1a receptor [Homo sapiens] [gi:4502331] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | | AID | 2797 | | BioAssay type | screening | | Target | vasopressin V1a receptor [Homo sapiens] [gi:4502331] | | PubMed | | | Data Table |  |
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| 46 | [SID848038] | Active | | | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) [AID2797, Type: screening] | vasopressin V1a receptor [Homo sapiens] [gi:4502331] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based primary cell-based high throughput assay to identify agonists of the vasopressin 1 receptor (V1R) | | AID | 2797 | | BioAssay type | screening | | Target | vasopressin V1a receptor [Homo sapiens] [gi:4502331] | | PubMed | | | Data Table |  |
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| 47 | [SID848038] | Active | | | Counterscreen for MCL1 inhibitors: fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of BCL2-related protein, long isoform (BCLXL). [AID2166, Type: screening] | bcl-2-like protein 1 isoform 1 [Homo sapiens] [gi:20336335] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Counterscreen for MCL1 inhibitors: fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of BCL2-related protein, long isoform (BCLXL). | | AID | 2166 | | BioAssay type | screening | | Target | bcl-2-like protein 1 isoform 1 [Homo sapiens] [gi:20336335] | | PubMed | | | Data Table |  |
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| 48 | [SID848038] | Active | | | Counterscreen for MCL1 inhibitors: fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of BCL2-related protein, long isoform (BCLXL). [AID2166, Type: screening] | bcl-2-like protein 1 isoform 1 [Homo sapiens] [gi:20336335] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Counterscreen for MCL1 inhibitors: fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of BCL2-related protein, long isoform (BCLXL). | | AID | 2166 | | BioAssay type | screening | | Target | bcl-2-like protein 1 isoform 1 [Homo sapiens] [gi:20336335] | | PubMed | | | Data Table |  |
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| 49 | [SID848038] | Active | | | Counterscreen for MCL1 inhibitors: fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of BCL2-related protein, long isoform (BCLXL). [AID2166, Type: screening] | bcl-2-like protein 1 isoform 1 [Homo sapiens] [gi:20336335] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Counterscreen for MCL1 inhibitors: fluorescence polarization-based biochemical high throughput confirmation assay for inhibitors of BCL2-related protein, long isoform (BCLXL). | | AID | 2166 | | BioAssay type | screening | | Target | bcl-2-like protein 1 isoform 1 [Homo sapiens] [gi:20336335] | | PubMed | | | Data Table |  |
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| 50 | [SID848038] | Active | | | Primary biochemical high throughput screening assay to identify inhibitors of BCL2-related protein, long isoform (BCLXL). [AID2129, Type: screening] | bcl-xL [Homo sapiens] [gi:510901] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 848038 | | CID | 650462 | | Outcome | Active | | BioAssay | Primary biochemical high throughput screening assay to identify inhibitors of BCL2-related protein, long isoform (BCLXL). | | AID | 2129 | | BioAssay type | screening | | Target | bcl-xL [Homo sapiens] [gi:510901] | | PubMed | | | Data Table |  |
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