| 1 | [SID49724095] | Active | | | Fluorescence-based biochemical high throughput confirmation assay to identify inhibitors of Protein Phosphatase 1 (PP1) [AID2358, Type: screening] | PPP1CA gene product [Homo sapiens] [gi:56790945] |  View X | Row No. | 1 | | Structure | 
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical high throughput confirmation assay to identify inhibitors of Protein Phosphatase 1 (PP1) | | AID | 2358 | | BioAssay type | screening | | Target | PPP1CA gene product [Homo sapiens] [gi:56790945] | | PubMed | | | Data Table | |
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| 2 | [SID49724095] | Active | | | Counterscreen for inhibitors of PP5: fluorescence-based biochemical high throughput primary assay to identify inhibitors of Protein Phosphatase 1 (PP1). [AID2235, Type: screening] | PPP1CA gene product [Homo sapiens] [gi:56790945] | View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of PP5: fluorescence-based biochemical high throughput primary assay to identify inhibitors of Protein Phosphatase 1 (PP1). | | AID | 2235 | | BioAssay type | screening | | Target | PPP1CA gene product [Homo sapiens] [gi:56790945] | | PubMed | | | Data Table | |
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| 3 | [SID49724095] | Active | | | Fluorescence-based biochemical high throughput confirmation assay for activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) [AID504383, Type: screening] | cardiac alpha tropomyosin [Sus scrofa] [gi:1927] | View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical high throughput confirmation assay for activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | | AID | 504383 | | BioAssay type | screening | | Target | cardiac alpha tropomyosin [Sus scrofa] [gi:1927] | | PubMed | | | Data Table | |
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| 4 | [SID49724095] | Inactive | Potency | 7.3753 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation [AID504832, Type: confirmatory] | | View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | Potency | 7.3753 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation | | AID | 504832 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
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| 5 | [SID49724095] | Inactive | Potency | 89.1251 | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins [AID485364, Type: confirmatory] | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] | View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | Potency | 89.1251 [uM] | | BioAssay | qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins | | AID | 485364 | | BioAssay type | confirmatory | | Target | thioredoxin glutathione reductase [Schistosoma mansoni] [gi:15149312] | | PubMed | | | Data Table | |
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| 6 | [SID49724095] | Inactive | Potency | | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) [AID485290, Type: confirmatory] | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | | AID | 485290 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | | PubMed | | | Data Table | |
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| 7 | [SID49724095] | Inactive | | | 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. | 7 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | 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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| 8 | [SID8053540] | Inactive | | | HIV-1 RNase H Inhibition [AID372, Type: screening] | Chain A, Solution Structure Of The Rnase H Domain Of The Hiv-1 Reverse Transcriptase In The Presence [gi:28949057] | View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 8053540 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | HIV-1 RNase H Inhibition | | AID | 372 | | BioAssay type | screening | | Target | Chain A, Solution Structure Of The Rnase H Domain Of The Hiv-1 Reverse Transcriptase In The Presence [gi:28949057] | | PubMed | | | Data Table | |
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| 9 | [SID49724095] | Inactive | | | Cycloheximide Counterscreen for Small Molecule Inhibitors of Shiga Toxin [AID2314, Type: screening] | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Cycloheximide Counterscreen for Small Molecule Inhibitors of Shiga Toxin | | AID | 2314 | | BioAssay type | screening | | Target | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | | PubMed | | | Data Table | |
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| 10 | [SID49724095] | Inactive | | | A qHTS for Small Molecule Inhibitors of Shiga Toxin [AID2315, Type: screening] | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | A qHTS for Small Molecule Inhibitors of Shiga Toxin | | AID | 2315 | | BioAssay type | screening | | Target | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | | PubMed | | | Data Table | |
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| 11 | [SID49724095] | Inactive | IC50 | | uHTS fluorescence assay for the identification of Human Immunodeficiency Virus Fusion Inhibitors. [AID1986, Type: confirmatory] | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] | View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | uHTS fluorescence assay for the identification of Human Immunodeficiency Virus Fusion Inhibitors. | | AID | 1986 | | BioAssay type | confirmatory | | Target | envelope glycoprotein [Human immunodeficiency virus 1] [gi:45357394] | | PubMed | | | Data Table | |
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| 12 | [SID49724095] | Inactive | | | QFRET-based counterscreen for PFM18AAP inhibitors: biochemical high throughput screening assay to identify inhibitors of the Cathepsin L proteinase (CTSL1). [AID1906, Type: screening] | cathepsin L1 [Homo sapiens] [gi:55958172] | View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | QFRET-based counterscreen for PFM18AAP inhibitors: biochemical high throughput screening assay to identify inhibitors of the Cathepsin L proteinase (CTSL1). | | AID | 1906 | | BioAssay type | screening | | Target | cathepsin L1 [Homo sapiens] [gi:55958172] | | PubMed | | | Data Table | |
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| 13 | [SID49724095] | Inactive | | | Counterscreen for procaspase-3 activators: absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-7 [AID463210, Type: screening] | caspase 7, apoptosis-related cysteine peptidase [Homo sapiens] [gi:55960760] | View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Counterscreen for procaspase-3 activators: absorbance-based primary biochemical high throughput screening assay to identify activators of procaspase-7 | | AID | 463210 | | BioAssay type | screening | | Target | caspase 7, apoptosis-related cysteine peptidase [Homo sapiens] [gi:55960760] | | PubMed | | | Data Table | |
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| 14 | [SID49724095] | Inactive | | | Plate Read Microorganism-Based Primary HTS to Identify Modulators of the AI-2 Quorum Sensing System [AID2094, Type: screening] | Chain A, Crystal Structure Of The Apo Form Of Vibrio Harveyi Luxp Complexed With The Periplasmic Dom [gi:67463988] | View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Plate Read Microorganism-Based Primary HTS to Identify Modulators of the AI-2 Quorum Sensing System | | AID | 2094 | | BioAssay type | screening | | Target | Chain A, Crystal Structure Of The Apo Form Of Vibrio Harveyi Luxp Complexed With The Periplasmic Dom [gi:67463988] | | PubMed | | | Data Table | |
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| 15 | [SID49724095] | Inactive | | | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the SARS coronavirus 3C-like Protease (3CLPro) [AID1706, Type: screening] | 3C-like protease [Infectious bronchitis virus] [gi:73745819] | View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the SARS coronavirus 3C-like Protease (3CLPro) | | AID | 1706 | | BioAssay type | screening | | Target | 3C-like protease [Infectious bronchitis virus] [gi:73745819] | | PubMed | | | Data Table | |
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| 16 | [SID49724095] | Inactive | | | PgID: DNTB colorimetric HTS to detect inhibitor of PgID Measured in Biochemical System Using Plate Reader - 2164-01_Inhibitor_SinglePoint_HTS_Activity [AID602405, Type: screening] | WlaI protein (PglD) [gi:75495260] | View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | PgID: DNTB colorimetric HTS to detect inhibitor of PgID Measured in Biochemical System Using Plate Reader - 2164-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 602405 | | BioAssay type | screening | | Target | WlaI protein (PglD) [gi:75495260] | | PubMed | | | Data Table | |
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| 17 | [SID49724095] | Inactive | | | TR-FRET-based primary biochemical high-throughput screening assay to identify inhibitors of Hepatitis C Virus (HCV) core protein dimerization [AID1899, Type: screening] | core protein [Hepatitis C virus] [gi:83779224] | View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | TR-FRET-based primary biochemical high-throughput screening assay to identify inhibitors of Hepatitis C Virus (HCV) core protein dimerization | | AID | 1899 | | BioAssay type | screening | | Target | core protein [Hepatitis C virus] [gi:83779224] | | PubMed | | | Data Table | |
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| 18 | [SID49724095] | Inactive | | | Counterscreen for inhibitors of 5-meCpG-binding domain protein 2 (MBD2): TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of binding of ubiquitin-like with PHD and ring finger domains 1 (UHRF1) to methylated oligonucleotide [AID687016, Type: screening] | UHRF1 gene product [Homo sapiens] [gi:115430235] | View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Counterscreen for inhibitors of 5-meCpG-binding domain protein 2 (MBD2): TRFRET-based biochemical primary high throughput screening assay to identify inhibitors of binding of ubiquitin-like with PHD and ring finger domains 1 (UHRF1) to methylated oligonucleotide | | AID | 687016 | | BioAssay type | screening | | Target | UHRF1 gene product [Homo sapiens] [gi:115430235] | | PubMed | | | Data Table | |
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| 19 | [SID49724095] | Inactive | | | uHTS luminescence assay for the identification of chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation [AID435003, Type: screening] | | View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | uHTS luminescence assay for the identification of chemical inhibitors of T-cell specific antigen receptor-induced NF-kB activation | | AID | 435003 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 20 | [SID49724095] | Inactive | | | uHTS luminescence assay for the identification of chemical inhibitors of B-cell specific antigen receptor-induced NF-kB activation [AID435022, Type: screening] | | View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | uHTS luminescence assay for the identification of chemical inhibitors of B-cell specific antigen receptor-induced NF-kB activation | | AID | 435022 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 21 | [SID49724095] | Inactive | | | Counterscreen for inhibitors of AddAB: absorbance-based bacterial cell-based high throughput screening assay to identify inhibitors of bacterial viability [AID449728, Type: screening] | | View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Counterscreen for inhibitors of AddAB: absorbance-based bacterial cell-based high throughput screening assay to identify inhibitors of bacterial viability | | AID | 449728 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 22 | [SID49724095] | Inactive | IC50 | | High Throughput Screening Assay used to Identify Novel Compounds that Inhibit Mycobacterium Tuberculosis in 7H9 Media [AID449762, Type: confirmatory] | | View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | High Throughput Screening Assay used to Identify Novel Compounds that Inhibit Mycobacterium Tuberculosis in 7H9 Media | | AID | 449762 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
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| 23 | [SID49724095] | Inactive | | | uHTS identification of small molecule activators of the apoptotic arm of the Unfolded Protein response via a luminescent-based reporter assay [AID449763, Type: screening] | | View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule activators of the apoptotic arm of the Unfolded Protein response via a luminescent-based reporter assay | | AID | 449763 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 24 | [SID49724095] | Inactive | | | uHTS identification of small molecule activators of the adaptive arm of the Unfolded Protein response via a luminescent-based reporter assay [AID463104, Type: screening] | | View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule activators of the adaptive arm of the Unfolded Protein response via a luminescent-based reporter assay | | AID | 463104 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 25 | [SID49724095] | Inactive | | | 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. | 25 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | 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 | |
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| 26 | [SID49724095] | Inactive | | | Phenotypic HTS multiplex for antifungal efflux pump inhibitors [AID485275, Type: screening] | | View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Phenotypic HTS multiplex for antifungal efflux pump inhibitors | | AID | 485275 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 27 | [SID49724095] | Inactive | Potency | | qHTS Assay for Small Molecule Inhibitors of Mitochondrial Division or Activators of Mitochondrial Fusion [AID485298, Type: confirmatory] | | View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Small Molecule Inhibitors of Mitochondrial Division or Activators of Mitochondrial Fusion | | AID | 485298 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
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| 28 | [SID49724095] | Inactive | | | Inhibitors of Prion Protein 5' UTR mRNA Measured in Cell-Based System Using Plate Reader - 2078-01_Inhibitor_SinglePoint_HTS_Activity [AID488862, Type: screening] | | View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Inhibitors of Prion Protein 5' UTR mRNA Measured in Cell-Based System Using Plate Reader - 2078-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 488862 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 29 | [SID49724095] | Inactive | IC50 | | Elucidation of physiology of non-replicating, drug-tolerant Mycobacterium tuberculosis [AID488890, Type: confirmatory] | | View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | Elucidation of physiology of non-replicating, drug-tolerant Mycobacterium tuberculosis | | AID | 488890 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
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| 30 | [SID49724095] | Inactive | IC50 | | Primary and Confirmatory Screening for Inhibitors of Bacterial Capsule Biogenesis [AID488966, Type: confirmatory] | | View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | Primary and Confirmatory Screening for Inhibitors of Bacterial Capsule Biogenesis | | AID | 488966 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
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| 31 | [SID49724095] | Inactive | | | MLPCN Ras selective lethality-BJeLR viability [AID1554, Type: screening] | | View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | MLPCN Ras selective lethality-BJeLR viability | | AID | 1554 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 32 | [SID49724095] | Inactive | IC50 | | A Cell Based Assay for the Identification of Lead Compounds with Anti-Viral Activity Against West Nile Virus [AID1621, Type: confirmatory] | | View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | A Cell Based Assay for the Identification of Lead Compounds with Anti-Viral Activity Against West Nile Virus | | AID | 1621 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
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| 33 | [SID49724095] | Inactive | | | High Throughput Imaging Assay for Hepatic Lipid Droplet Formation [AID1656, Type: screening] | | View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | High Throughput Imaging Assay for Hepatic Lipid Droplet Formation | | AID | 1656 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 34 | [SID49724095] | Inactive | | | MLPCN Platelet Activation -Dense Granule Release [AID1663, Type: screening] | | View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | MLPCN Platelet Activation -Dense Granule Release | | AID | 1663 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 35 | [SID49724095] | Inactive | | | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - inhibitors [AID1813, Type: screening] | | View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - inhibitors | | AID | 1813 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 36 | [SID49724095] | Inactive | | | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - activators [AID1814, Type: screening] | | View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | MLPCN Alpha-Synuclein 5'UTR - 5'-UTR binding - activators | | AID | 1814 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 37 | [SID49724095] | Inactive | | | Luminescence-based counterscreen assay for KLF5 inhibitors: cell-based high throughput screening assay to identify cytotoxic compounds using the IEC-6 intestinal epithelial cell line. [AID1825, Type: screening] | | View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Luminescence-based counterscreen assay for KLF5 inhibitors: cell-based high throughput screening assay to identify cytotoxic compounds using the IEC-6 intestinal epithelial cell line. | | AID | 1825 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 38 | [SID49724095] | Inactive | IC50 | | A small molecule screen for inhibitors of the PhoP regulon in Salmonella typhi [AID1850, Type: confirmatory] | | View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | A small molecule screen for inhibitors of the PhoP regulon in Salmonella typhi | | AID | 1850 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
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| 39 | [SID49724095] | Inactive | IC50 | | A small molecule screen for inhibitors of the PhoP regulon in Salmonella Typhimurium [AID1863, Type: confirmatory] | | View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | A small molecule screen for inhibitors of the PhoP regulon in Salmonella Typhimurium | | AID | 1863 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
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| 40 | [SID49724095] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Polyadenylation [AID1875, Type: screening] | | View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Inhibitors of Polyadenylation | | AID | 1875 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 41 | [SID49724095] | Inactive | | | Luminescence Cell-Based/Microorganism Primary HTS to Identify Inhibitors of T.Cruzi Replication [AID1885, Type: screening] | | View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based/Microorganism Primary HTS to Identify Inhibitors of T.Cruzi Replication | | AID | 1885 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 42 | [SID49724095] | Inactive | | | Luminescence Cell-Based Primary HTS to Identify Transcriptional Activators of Hypoxia-Inducible Factor Pathway [AID1910, Type: screening] | | View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Luminescence Cell-Based Primary HTS to Identify Transcriptional Activators of Hypoxia-Inducible Factor Pathway | | AID | 1910 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 43 | [SID49724095] | Inactive | | | Fluorescence Biochemical Primary HTS to Identify Inhibitors of GASC-1 Activity [AID2099, Type: screening] | | View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | Fluorescence Biochemical Primary HTS to Identify Inhibitors of GASC-1 Activity | | AID | 2099 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
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| 44 | [SID49724095] | Inactive | | | Fluorescence Cell-Free Homogeneous Primary HTS to Identify Inhibitors of the RanGTP-Importin-beta complex [AID2216, Type: screening] | | View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | 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 | |
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| 45 | [SID49724095] | Inactive | Potency | | qHTS Assay for Modulators of miRNAs and/orActivators of miR-21 [AID2288, Type: confirmatory] | | View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Modulators of miRNAs and/orActivators of miR-21 | | AID | 2288 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
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| 46 | [SID49724095] | Inactive | Potency | | qHTS Assay for Modulators of miRNAs and/or Inhibitors of miR-21 [AID2289, Type: confirmatory] | | View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Modulators of miRNAs and/or Inhibitors of miR-21 | | AID | 2289 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
|
| 47 | [SID49724095] | Inactive | | | uHTS identification of small molecules that induce b-cell replication in the MIN-6 cell line [AID2380, Type: screening] | | View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecules that induce b-cell replication in the MIN-6 cell line | | AID | 2380 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
|
| 48 | [SID49724095] | Inactive | IC50 | | A Cell Based HTS Approach for the Discovery of New Inhibitors of Respiratory syncytial virus (RSV) [AID2391, Type: confirmatory] | | View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | A Cell Based HTS Approach for the Discovery of New Inhibitors of Respiratory syncytial virus (RSV) | | AID | 2391 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
|
| 49 | [SID49724095] | Inactive | Potency | | qHTS Assay for Lipid Storage Modulators in Drosophila S3 Cells [AID2685, Type: confirmatory] | | View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Lipid Storage Modulators in Drosophila S3 Cells | | AID | 2685 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table | |
|
| 50 | [SID49724095] | Inactive | | | A yeast HTS for caloric restriction mimetics that inhibit age-related superoxide [AID2690, Type: screening] | | View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 49724095 | | CID | 54686339 | | Outcome | Inactive | | BioAssay | A yeast HTS for caloric restriction mimetics that inhibit age-related superoxide | | AID | 2690 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table | |
|
Chemical Probe 
Active 
Inactive 
Inconclusive 
Unspecified 
