| 1 | [SID87225745] | Active | IC50 | 0.965 | SAR Analysis of Selective Antagonists of GPR55 using an Image-Based Assay - Set 2 [AID2820, Type: confirmatory] | G-protein coupled receptor 55 [Homo sapiens] [gi:33695107] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 87225745 | | CID | 653589 | | Outcome | Active | | IC50 | 0.965 [uM] | | BioAssay | SAR Analysis of Selective Antagonists of GPR55 using an Image-Based Assay - Set 2 | | AID | 2820 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 55 [Homo sapiens] [gi:33695107] | | PubMed | | | Data Table |  |
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| 2 | [SID851037] | Active | Potency | 1 | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-1: Spectroscopic Profiling in AFC Spectral Region [AID923, Type: confirmatory] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | Potency | 1 [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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| 3 | [SID851037] | Active | IC50 | 1.23598 | Image-Based HTS for Selective Antagonists for GPR55 [AID2013, Type: confirmatory] | G-protein coupled receptor 55 [Homo sapiens] [gi:33695107] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | IC50 | 1.23598 [uM] | | BioAssay | Image-Based HTS for Selective Antagonists for GPR55 | | AID | 2013 | | BioAssay type | confirmatory | | Target | G-protein coupled receptor 55 [Homo sapiens] [gi:33695107] | | PubMed | | | Data Table |  |
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| 4 | [SID26668122] | Active | Potency | 3.5481 | 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. | 4 | | Structure |
| | Substance | | | SID | 26668122 | | CID | 653589 | | Outcome | Active | | Potency | 3.5481 [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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| 5 | [SID26668122] | Active | Potency | 7.0795 | A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. [AID624297, Type: confirmatory] | GMNN gene product [Homo sapiens] [gi:7705682] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 26668122 | | CID | 653589 | | Outcome | Active | | Potency | 7.0795 [uM] | | BioAssay | A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. | | AID | 624297 | | BioAssay type | confirmatory | | Target | GMNN gene product [Homo sapiens] [gi:7705682] | | PubMed | | | Data Table |  |
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| 6 | [SID851037] | Active | IC50 | 11.9 | Dose Response confirmation of small molecule Triacylglycerol inhbitors in a panel assay [AID651630, Type: confirmatory] | |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | IC50 | 11.9 [uM] | | BioAssay | Dose Response confirmation of small molecule Triacylglycerol inhbitors in a panel assay | | AID | 651630 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 7 | [SID851037] | Active | IC50 | 11.9 | Dose Response confirmation of small molecule Triacylglycerol inhbitors in a panel assay [AID651630_1, Type: confirmatory] | |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | IC50 | 11.9 [uM] | | BioAssay | Dose Response confirmation of small molecule Triacylglycerol inhbitors in a panel assay | | AID | 651630 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 8 | [SID26668122] | Active | Potency | 16.3601 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 26668122 | | CID | 653589 | | Outcome | Active | | Potency | 16.3601 [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 | | | PubMed | | | Data Table |  |
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| 9 | [SID851037] | Active | Potency | 25.1189 | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 [AID893, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | Potency | 25.1189 [uM] | | BioAssay | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 | | AID | 893 | | BioAssay type | confirmatory | | Target | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] | | PubMed | | | Data Table |  |
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| 10 | [SID851037] | Active | | | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) [AID2796, Type: screening] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 2796 | | BioAssay type | screening | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
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| 11 | [SID851037] | Active | | | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) [AID2796, Type: screening] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 2796 | | BioAssay type | screening | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
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| 12 | [SID851037] | Active | | | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) [AID2796, Type: screening] | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Luminescence-based primary cell-based high throughput screening assay to identify activators of the Aryl Hydrocarbon Receptor (AHR) | | AID | 2796 | | BioAssay type | screening | | Target | aryl hydrocarbon receptor precursor [Homo sapiens] [gi:4502003] | | PubMed | | | Data Table |  |
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| 13 | [SID851037] | Active | | | High throughput discovery of novel modulators of ROMK K+ channel activity: Primary Screen [AID1918, Type: screening] | Potassium inwardly-rectifying channel, subfamily J, member 1 [Homo sapiens] [gi:223460826] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | High throughput discovery of novel modulators of ROMK K+ channel activity: Primary Screen | | AID | 1918 | | BioAssay type | screening | | Target | Potassium inwardly-rectifying channel, subfamily J, member 1 [Homo sapiens] [gi:223460826] | | PubMed | | | Data Table |  |
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| 14 | [SID851037] | Active | | | Confirmatory screen for identification of compounds that inhibit transient receptor potential cation channel C6 (TRPC6) [AID488960, Type: screening] | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Confirmatory screen for identification of compounds that inhibit transient receptor potential cation channel C6 (TRPC6) | | AID | 488960 | | BioAssay type | screening | | Target | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] | | PubMed | | | Data Table |  |
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| 15 | [SID851037] | Active | | | uHTS identification of inhibitors of Rpn11 in a Fluorescent Polarization assay [AID588493, Type: screening] | PSMD14 protein [Homo sapiens] [gi:16306916] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | 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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| 16 | [SID851037] | Active | | | qHTS Assay for Tau Filament Binding [AID596, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | qHTS Assay for Tau Filament Binding | | AID | 596 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
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| 17 | [SID851037] | Active | | | qHTS Assay for Tau Filament Binding [AID596, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | qHTS Assay for Tau Filament Binding | | AID | 596 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 18 | [SID851037] | Active | | | Primary cell-based high-throughput screening assay to identify agonists of Galanin Receptor 2 (GALR2) [AID803, Type: screening] | Galanin receptor type 2 [gi:6016094] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Primary cell-based high-throughput screening assay to identify agonists of Galanin Receptor 2 (GALR2) | | AID | 803 | | BioAssay type | screening | | Target | Galanin receptor type 2 [gi:6016094] | | PubMed | | | Data Table |  |
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| 19 | [SID851037] | Active | | | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen [AID628, Type: screening] | Muscarinic acetylcholine receptor M [gi:113121] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | | AID | 628 | | BioAssay type | screening | | Target | Muscarinic acetylcholine receptor M [gi:113121] | | PubMed | | | Data Table |  |
|
| 20 | [SID851037] | Active | | | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen [AID628, Type: screening] | Muscarinic acetylcholine receptor M [gi:113121] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | | AID | 628 | | BioAssay type | screening | | Target | Muscarinic acetylcholine receptor M [gi:113121] | | PubMed | | | Data Table |  |
|
| 21 | [SID851037] | Active | | | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen [AID628, Type: screening] | Muscarinic acetylcholine receptor M [gi:113121] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen | | AID | 628 | | BioAssay type | screening | | Target | Muscarinic acetylcholine receptor M [gi:113121] | | PubMed | | | Data Table |  |
|
| 22 | [SID851037] | Active | | | Counter screen assay of the parental HEK293 cells for compounds that activate the Choline Transporter (CHT) [AID623908, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Counter screen assay of the parental HEK293 cells for compounds that activate the Choline Transporter (CHT) | | AID | 623908 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
|
| 23 | [SID851037] | Active | | | Counter screen assay of the parental HEK293 cells for compounds that activate the Choline Transporter (CHT) [AID623908, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Counter screen assay of the parental HEK293 cells for compounds that activate the Choline Transporter (CHT) | | AID | 623908 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
|
| 24 | [SID851037] | Active | | | Confirmatory screen for compounds that activate the Choline Transporter (CHT) [AID504833, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Confirmatory screen for compounds that activate the Choline Transporter (CHT) | | AID | 504833 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
|
| 25 | [SID851037] | Active | | | Confirmatory screen for compounds that activate the Choline Transporter (CHT) [AID504833, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Confirmatory screen for compounds that activate the Choline Transporter (CHT) | | AID | 504833 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
|
| 26 | [SID851037] | Active | | | Specificity screen against TRPC4 for compounds that modulate transient receptor potential cation channel C6 (TRPC6) [AID488927, Type: screening] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Specificity screen against TRPC4 for compounds that modulate transient receptor potential cation channel C6 (TRPC6) | | AID | 488927 | | BioAssay type | screening | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
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| 27 | [SID851037] | Active | | | Second specificity screen against TRPC4 for compounds that modulate transient receptor potential cation channel C6 (TRPC6) [AID488928, Type: screening] | alternatively spliced Trp4 [Mus musculus] [gi:2935630] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Second specificity screen against TRPC4 for compounds that modulate transient receptor potential cation channel C6 (TRPC6) | | AID | 488928 | | BioAssay type | screening | | Target | alternatively spliced Trp4 [Mus musculus] [gi:2935630] | | PubMed | | | Data Table |  |
|
| 28 | [SID851037] | Active | | | High throughput screening of inhibitors of transient receptor potential cation channel C6 (TRPC6) [AID2553, Type: screening] | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | High throughput screening of inhibitors of transient receptor potential cation channel C6 (TRPC6) | | AID | 2553 | | BioAssay type | screening | | Target | short transient receptor potential channel 6 [Mus musculus] [gi:160333370] | | PubMed | | | Data Table |  |
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| 29 | [SID851037] | Active | | | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Confirmation Screen [AID677, Type: other] | muscarinic acetylcholine receptor M1 [Rattus norvegicus] [gi:18249941] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Confirmation Screen | | AID | 677 | | BioAssay type | other | | Target | muscarinic acetylcholine receptor M1 [Rattus norvegicus] [gi:18249941] | | PubMed | | | Data Table |  |
|
| 30 | [SID851037] | Active | | | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Confirmation Screen [AID677, Type: other] | muscarinic acetylcholine receptor M1 [Rattus norvegicus] [gi:18249941] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Confirmation Screen | | AID | 677 | | BioAssay type | other | | Target | muscarinic acetylcholine receptor M1 [Rattus norvegicus] [gi:18249941] | | PubMed | | | Data Table |  |
|
| 31 | [SID851037] | Active | | | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Confirmation Screen [AID677, Type: other] | muscarinic acetylcholine receptor M1 [Rattus norvegicus] [gi:18249941] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Confirmation Screen | | AID | 677 | | BioAssay type | other | | Target | muscarinic acetylcholine receptor M1 [Rattus norvegicus] [gi:18249941] | | PubMed | | | Data Table |  |
|
| 32 | [SID26668122] | Active | | | Rml C and D fluorescent artifact dose-response confirmation [AID1696, Type: confirmatory] | dTDP-6-deoxy-L-lyxo-4-hexulose reductase RmlD [Mycobacterium tuberculosis H37Rv] [gi:15610402] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 26668122 | | CID | 653589 | | Outcome | Active | | BioAssay | Rml C and D fluorescent artifact dose-response confirmation | | AID | 1696 | | BioAssay type | confirmatory | | Target | dTDP-6-deoxy-L-lyxo-4-hexulose reductase RmlD [Mycobacterium tuberculosis H37Rv] [gi:15610402] | | PubMed | | | Data Table |  |
|
| 33 | [SID851037] | Active | | | Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis [AID588726, Type: screening] | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis | | AID | 588726 | | BioAssay type | screening | | Target | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] | | PubMed | | | Data Table |  |
|
| 34 | [SID851037] | Active | | | Single concentration confirmation of small molecule Triacylglycerol inhbitors in a fluoresence assay [AID651629, Type: screening] | |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Single concentration confirmation of small molecule Triacylglycerol inhbitors in a fluoresence assay | | AID | 651629 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 35 | [SID851037] | Active | | | uHTS identification of small molecule Triacylglycerol inhbitors in a fluoresence assay [AID651582, Type: screening] | |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | uHTS identification of small molecule Triacylglycerol inhbitors in a fluoresence assay | | AID | 651582 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 36 | [SID851037] | Active | | | Counter screen for compounds that modulate transient receptor potential cation channel C6 (TRPC6) [AID488924, Type: screening] | |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Counter screen for compounds that modulate transient receptor potential cation channel C6 (TRPC6) | | AID | 488924 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 37 | [SID26668122] | Active | | | Rml C and D inhibition 384-well mixture HTS [AID1532, Type: screening] | |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 26668122 | | CID | 653589 | | Outcome | Active | | BioAssay | Rml C and D inhibition 384-well mixture HTS | | AID | 1532 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 38 | [SID851037] | Active | | | 384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC [AID463187, Type: screening] | |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | 384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC | | AID | 463187 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 39 | [SID851037] | Active | EC50 | | Fluorescent HTS Cytotoxicity/Cell viability assay (HT1080 cells) [AID620, Type: confirmatory] | |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | EC50 | [uM] | | BioAssay | Fluorescent HTS Cytotoxicity/Cell viability assay (HT1080 cells) | | AID | 620 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 40 | [SID851037] | Active | | | Human H69AR Lung Tumor Cell Growth Inhibition Assay [AID580, Type: screening] | |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Human H69AR Lung Tumor Cell Growth Inhibition Assay | | AID | 580 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 41 | [SID851037] | Active | | | Fluorescence Cell-Free Homogeneous Primary HTS to Identify Inhibitors of the RanGTP-Importin-beta complex [AID2216, Type: screening] | |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Fluorescence Cell-Free Homogeneous Primary HTS to Identify Inhibitors of the RanGTP-Importin-beta complex | | AID | 2216 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 42 | [SID851037] | Active | | | qHTS Assay for Spectroscopic Profiling in 4-MU Spectral Region [AID589, Type: other] | |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in 4-MU Spectral Region | | AID | 589 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 43 | [SID851037] | Active | | | qHTS Assay for Spectroscopic Profiling in A350 Spectral Region [AID590, Type: other] | |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in A350 Spectral Region | | AID | 590 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 44 | [SID851037] | Active | | | Profiling the NIH Molecular Libraries Small Molecule Repository: Autofluorescence at 339/460 nm [AID709, Type: screening] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | BioAssay | Profiling the NIH Molecular Libraries Small Molecule Repository: Autofluorescence at 339/460 nm | | AID | 709 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 45 | [SID26668122] | Active | | | uHTS identification of small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay [AID504690, Type: screening] | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 26668122 | | CID | 653589 | | Outcome | Active | | BioAssay | uHTS identification of small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay | | AID | 504690 | | BioAssay type | screening | | Target | glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase [Plasmodium berghei] [gi:12381848] | | PubMed | | | Data Table |  |
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| 46 | [SID851037] | Active | IC50 | | uHTS identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb-SMMHC via a fluorescence resonance energy transfer (FRET) assay. [AID1434, Type: confirmatory] | core-binding factor subunit beta isoform 1 [Homo sapiens] [gi:13124881] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | IC50 | [uM] | | BioAssay | uHTS identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb-SMMHC via a fluorescence resonance energy transfer (FRET) assay. | | AID | 1434 | | BioAssay type | confirmatory | | Target | core-binding factor subunit beta isoform 1 [Homo sapiens] [gi:13124881] | | PubMed | | | Data Table |  |
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| 47 | [SID851037] | Active | IC50 | | uHTS identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb-SMMHC via a fluorescence resonance energy transfer (FRET) assay. [AID1434, Type: confirmatory] | core-binding factor subunit beta isoform 1 [Homo sapiens] [gi:13124881] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Active | | IC50 | [uM] | | BioAssay | uHTS identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb-SMMHC via a fluorescence resonance energy transfer (FRET) assay. | | AID | 1434 | | BioAssay type | confirmatory | | Target | core-binding factor subunit beta isoform 1 [Homo sapiens] [gi:13124881] | | PubMed | | | Data Table |  |
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| 48 | [SID851037] | Unspecified | IC50 | 8.067 | Dose Response confirmation of small molecule Triacylglycerol inhbitors in a panel assay [AID651630_2, Type: confirmatory] | |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Unspecified | | IC50 | 8.067 [uM] | | BioAssay | Dose Response confirmation of small molecule Triacylglycerol inhbitors in a panel assay | | AID | 651630 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 49 | [SID851037] | Unspecified | IC50 | 15.762 | Dose Response confirmation of small molecule Triacylglycerol inhbitors in a panel assay [AID651630_3, Type: confirmatory] | |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Unspecified | | IC50 | 15.762 [uM] | | BioAssay | Dose Response confirmation of small molecule Triacylglycerol inhbitors in a panel assay | | AID | 651630 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 50 | [SID851037] | Unspecified | IC50 | 25 | Dose Response confirmation of small molecule Triacylglycerol inhbitors in a panel assay [AID651630_5, Type: confirmatory] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 851037 | | CID | 653589 | | Outcome | Unspecified | | IC50 | 25 [uM] | | BioAssay | Dose Response confirmation of small molecule Triacylglycerol inhbitors in a panel assay | | AID | 651630 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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