| 1 | [SID7965986] | Active | Potency | 11.6891 | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation [AID504834, Type: confirmatory] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Active | | Potency | 11.6891 [uM] | | BioAssay | Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation | | AID | 504834 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 2 | [SID7965986] | Active | Potency | 17.7828 | qHTS Assay for Activators of ClpP [AID651965, Type: confirmatory] | ClpP [Bacillus subtilis] [gi:2668494] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Active | | Potency | 17.7828 [uM] | | BioAssay | qHTS Assay for Activators of ClpP | | AID | 651965 | | BioAssay type | confirmatory | | Target | ClpP [Bacillus subtilis] [gi:2668494] | | PubMed | | | Data Table |  |
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| 3 | [SID4264467] | Active | Potency | 19.9526 | 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. | 3 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Active | | Potency | 19.9526 [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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| 4 | [SID7965986] | 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. | 4 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | 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 |  |
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| 5 | [SID7965986] | Active | | | Fluorescence-based biochemical high throughput confirmation assay for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis [AID651616, Type: screening] | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Active | | BioAssay | Fluorescence-based biochemical high throughput confirmation assay for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis | | AID | 651616 | | BioAssay type | screening | | Target | Probable fructose-bisphosphate aldolase Fba [Mycobacterium tuberculosis H37Rv] [gi:15607504] | | PubMed | | | Data Table |  |
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| 6 | [SID7965986] | Active | | | Counterscreen of compound fluorescence effects on High-throughput multiplex microsphere screening for inhibitors of toxin protease [AID624483, Type: screening] | |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Active | | BioAssay | Counterscreen of compound fluorescence effects on High-throughput multiplex microsphere screening for inhibitors of toxin protease | | AID | 624483 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 7 | [SID7965986] | Active | | | Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis: Fluroescence-based biochemical high throughput Glycerophosphate Dehydrogenase-Triosephosphate Isomerase (GDH-TPI) assay to identify assay artifacts [AID652141, Type: screening] | |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Active | | BioAssay | Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis: Fluroescence-based biochemical high throughput Glycerophosphate Dehydrogenase-Triosephosphate Isomerase (GDH-TPI) assay to identify assay artifacts | | AID | 652141 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 8 | [SID4264467] | Active | | | qHTS Assay for Spectroscopic Profiling in 4-MU Spectral Region [AID589, Type: other] | |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in 4-MU Spectral Region | | AID | 589 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 9 | [SID4264467] | Active | | | qHTS Assay for Spectroscopic Profiling in A350 Spectral Region [AID590, Type: other] | |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in A350 Spectral Region | | AID | 590 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 10 | [SID4264467] | Active | | | Profiling the NIH Molecular Libraries Small Molecule Repository: Autofluorescence at 339/460 nm [AID709, Type: screening] | |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | 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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| 11 | [SID7965986] | Active | | | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists [AID485344, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | | AID | 485344 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 12 | [SID7965986] | Active | | | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists [AID485344, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | | AID | 485344 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 13 | [SID7965986] | Active | | | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists [AID485344, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | | AID | 485344 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 14 | [SID7965986] | Active | | | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists [AID485344, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | | AID | 485344 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
|
| 15 | [SID7965986] | Active | | | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists [AID485344, Type: screening] | DRD2 gene product [Homo sapiens] [gi:4503385] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Active | | BioAssay | HTS Assay for Allosteric Antagonists of the Human D2 Dopamine Receptor: Primary Screen for Antagonists | | AID | 485344 | | BioAssay type | screening | | Target | DRD2 gene product [Homo sapiens] [gi:4503385] | | PubMed | | | Data Table |  |
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| 16 | [SID7965986] | 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. | 16 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | 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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| 17 | [SID7965986] | 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. | 17 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | 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 |  |
|
| 18 | [SID4264467] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
|
| 19 | [SID4264467] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
|
| 20 | [SID4264467] | Unspecified | | | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening [AID488969, Type: screening] | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Unspecified | | BioAssay | Assay for HTS of Gi/Go-linked GPCRs using mGluR8: Primary Screening | | AID | 488969 | | BioAssay type | screening | | Target | metabotropic glutamate receptor 8 [Rattus norvegicus] [gi:1575471] | | PubMed | | | Data Table |  |
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| 21 | [SID4264467] | Inactive | Potency | 12.5893 | qHTS Assay for Inhibitors of Influenza NS1 Protein Function [AID2326, Type: confirmatory] | nonstructural protein 1 [Influenza A virus (A/WSN/1933(H1N1))] [gi:194352380] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Inactive | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Inhibitors of Influenza NS1 Protein Function | | AID | 2326 | | BioAssay type | confirmatory | | Target | nonstructural protein 1 [Influenza A virus (A/WSN/1933(H1N1))] [gi:194352380] | | PubMed | | | Data Table |  |
|
| 22 | [SID7965986] | Inactive | Potency | 25.1189 | Inhibitors of Secretory Acid Sphingomyelinase (S-ASM): qHTS [AID504937, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | Potency | 25.1189 [uM] | | BioAssay | Inhibitors of Secretory Acid Sphingomyelinase (S-ASM): qHTS | | AID | 504937 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
|
| 23 | [SID7965986] | Inactive | Potency | 25.1189 | Inhibitors of Secretory Acid Sphingomyelinase (S-ASM): qHTS [AID504937, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | Potency | 25.1189 [uM] | | BioAssay | Inhibitors of Secretory Acid Sphingomyelinase (S-ASM): qHTS | | AID | 504937 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
|
| 24 | [SID7965986] | Inactive | Potency | 39.8107 | qHTS Assay for Inhibitors Targeting the Menin-MLL Interaction in MLL Related Leukemias: Competition With Texas Red Labeled MLL-derived Mutant Peptide [AID1768, Type: confirmatory] | MEN1 gene product [Homo sapiens] [gi:18860839] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors Targeting the Menin-MLL Interaction in MLL Related Leukemias: Competition With Texas Red Labeled MLL-derived Mutant Peptide | | AID | 1768 | | BioAssay type | confirmatory | | Target | MEN1 gene product [Homo sapiens] [gi:18860839] | | PubMed | | | Data Table |  |
|
| 25 | [SID7965986] | Inactive | Potency | 50.1187 | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588456, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | Potency | 50.1187 [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588456 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 26 | [SID7965986] | Inactive | Potency | 50.1187 | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588456, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | Potency | 50.1187 [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588456 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
|
| 27 | [SID7965986] | Inactive | Potency | | qHTS Assay for Agonists of the Relaxin Receptor RXFP1 [AID2676, Type: confirmatory] | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Agonists of the Relaxin Receptor RXFP1 | | AID | 2676 | | BioAssay type | confirmatory | | Target | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] | | PubMed | | | Data Table |  |
|
| 28 | [SID7965986] | Inactive | Potency | | qHTS Assay for Agonists of the Relaxin Receptor RXFP1 [AID2676, Type: confirmatory] | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Agonists of the Relaxin Receptor RXFP1 | | AID | 2676 | | BioAssay type | confirmatory | | Target | relaxin receptor 1 isoform 1 [Homo sapiens] [gi:85986601] | | PubMed | | | Data Table |  |
|
| 29 | [SID7965986] | Inactive | | | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) [AID488975, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) | | AID | 488975 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
|
| 30 | [SID7965986] | Inactive | | | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) [AID488975, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) | | AID | 488975 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
|
| 31 | [SID7965986] | Inactive | | | Primary cell-based screen for identification of compounds that allosterically activate the Choline Transporter (CHT) [AID488977, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Primary cell-based screen for identification of compounds that allosterically activate the Choline Transporter (CHT) | | AID | 488977 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
|
| 32 | [SID7965986] | Inactive | | | Primary cell-based screen for identification of compounds that allosterically activate the Choline Transporter (CHT) [AID488977, Type: screening] | SLC5A7 gene product [Homo sapiens] [gi:11141885] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Primary cell-based screen for identification of compounds that allosterically activate the Choline Transporter (CHT) | | AID | 488977 | | BioAssay type | screening | | Target | SLC5A7 gene product [Homo sapiens] [gi:11141885] | | PubMed | | | Data Table |  |
|
| 33 | [SID7965986] | Inactive | | | uHTS identification of APOBEC3G DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay [AID493012, Type: screening] | APOBEC3G gene product [Homo sapiens] [gi:13399304] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | uHTS identification of APOBEC3G DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay | | AID | 493012 | | BioAssay type | screening | | Target | APOBEC3G gene product [Homo sapiens] [gi:13399304] | | PubMed | | | Data Table |  |
|
| 34 | [SID7965986] | Inactive | Potency | | qHTS for Inhibitors of Vif-A3G Interactions: qHTS [AID602310, Type: confirmatory] | APOBEC3G gene product [Homo sapiens] [gi:13399304] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Vif-A3G Interactions: qHTS | | AID | 602310 | | BioAssay type | confirmatory | | Target | APOBEC3G gene product [Homo sapiens] [gi:13399304] | | PubMed | | | Data Table |  |
|
| 35 | [SID4264467] | Inactive | | | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - DPM-DC [AID556, Type: screening] | diphosphomevalonate decarboxylase [Streptococcus pneumoniae D39] [gi:116076351] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - DPM-DC | | AID | 556 | | BioAssay type | screening | | Target | diphosphomevalonate decarboxylase [Streptococcus pneumoniae D39] [gi:116076351] | | PubMed | | | Data Table |  |
|
| 36 | [SID4264467] | Inactive | | | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - DPM-DC [AID556, Type: screening] | diphosphomevalonate decarboxylase [Streptococcus pneumoniae D39] [gi:116076351] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - DPM-DC | | AID | 556 | | BioAssay type | screening | | Target | diphosphomevalonate decarboxylase [Streptococcus pneumoniae D39] [gi:116076351] | | PubMed | | | Data Table |  |
|
| 37 | [SID4264467] | Inactive | | | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - PMK [AID539, Type: screening] | phosphomevalonate kinase [Streptococcus pneumoniae D39] [gi:116077694] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - PMK | | AID | 539 | | BioAssay type | screening | | Target | phosphomevalonate kinase [Streptococcus pneumoniae D39] [gi:116077694] | | PubMed | | | Data Table |  |
|
| 38 | [SID4264467] | Inactive | | | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - MK [AID555, Type: screening] | mevalonate kinase [Streptococcus pneumoniae D39] [gi:116516899] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - MK | | AID | 555 | | BioAssay type | screening | | Target | mevalonate kinase [Streptococcus pneumoniae D39] [gi:116516899] | | PubMed | | | Data Table |  |
|
| 39 | [SID7965986] | Inactive | | | Fluorescence Polarization Cell-Free Homogeneous Primary HTS to Identify Inhibitors of the LANA Histone H2A/H2B Interaction [AID2629, Type: screening] | LANA [Human herpesvirus 8] [gi:139472804] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Fluorescence Polarization Cell-Free Homogeneous Primary HTS to Identify Inhibitors of the LANA Histone H2A/H2B Interaction | | AID | 2629 | | BioAssay type | screening | | Target | LANA [Human herpesvirus 8] [gi:139472804] | | PubMed | | | Data Table |  |
|
| 40 | [SID7965986] | Inactive | | | uHTS for Small Molecule Inhibitiors of Epstein-Barr Virus Inhibitors [AID1085, Type: screening] | BZLF2 [Human herpesvirus 4 type 2] [gi:139424501] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | uHTS for Small Molecule Inhibitiors of Epstein-Barr Virus Inhibitors | | AID | 1085 | | BioAssay type | screening | | Target | BZLF2 [Human herpesvirus 4 type 2] [gi:139424501] | | PubMed | | | Data Table |  |
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| 41 | [SID7965986] | Inactive | | | Fluorescent Biochemical Primary HTS to Identify Inhibitors of P. aeruginosa PvdQ acylase Measured in Biochemical System Using Plate Reader and Imaging Combination - 2091-01_Inhibitor_SinglePoint_HTS_Activity [AID488965, Type: screening] | pvdQ gene product [Pseudomonas aeruginosa LESB58] [gi:218891639] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Fluorescent Biochemical Primary HTS to Identify Inhibitors of P. aeruginosa PvdQ acylase Measured in Biochemical System Using Plate Reader and Imaging Combination - 2091-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 488965 | | BioAssay type | screening | | Target | pvdQ gene product [Pseudomonas aeruginosa LESB58] [gi:218891639] | | PubMed | | | Data Table |  |
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| 42 | [SID7965986] | Inactive | | | Fluorescence polarization to screen for inhibitor that competite the binding of FadD28 to bisubstrate Measured in Biochemical System Using Plate Reader - 2147-01_Inhibitor_SinglePoint_HTS_Activity [AID588549, Type: screening] | FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE) (FATTY-ACID-CoA SYNTHASE) [Mycobacterium tu [gi:1781172] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Fluorescence polarization to screen for inhibitor that competite the binding of FadD28 to bisubstrate Measured in Biochemical System Using Plate Reader - 2147-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 588549 | | BioAssay type | screening | | Target | FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE) (FATTY-ACID-CoA SYNTHASE) [Mycobacterium tu [gi:1781172] | | PubMed | | | Data Table |  |
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| 43 | [SID7965986] | Inactive | | | Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) [AID493244, Type: screening] | cardiac alpha tropomyosin [Sus scrofa] [gi:1927] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | | AID | 493244 | | BioAssay type | screening | | Target | cardiac alpha tropomyosin [Sus scrofa] [gi:1927] | | PubMed | | | Data Table |  |
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| 44 | [SID7965986] | Inactive | | | Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) [AID493008, Type: screening] | cardiac alpha tropomyosin [Sus scrofa] [gi:1927] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Fluorescence-based biochemical primary high throughput screening assay to identify activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | | AID | 493008 | | BioAssay type | screening | | Target | cardiac alpha tropomyosin [Sus scrofa] [gi:1927] | | PubMed | | | Data Table |  |
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| 45 | [SID7965986] | Inactive | IC50 | | Primary and Confirmatory Screening for Flavivirus Genomic Capping Enzyme Inhibition [AID588689, Type: confirmatory] | Chain A, Crystal Structure Of Dengue-2 Virus Methyltransferase Complexed With S-Adenosyl-L-Homocyste [gi:219689243] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 7965986 | | CID | 56642854 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | Primary and Confirmatory Screening for Flavivirus Genomic Capping Enzyme Inhibition | | AID | 588689 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Dengue-2 Virus Methyltransferase Complexed With S-Adenosyl-L-Homocyste [gi:219689243] | | PubMed | | | Data Table |  |
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| 46 | [SID4264467] | Inactive | | | Cell Proliferation & Viability (Cytotoxicity) Primary Assay 60K MLSMR [AID463, Type: screening] | |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Cell Proliferation & Viability (Cytotoxicity) Primary Assay 60K MLSMR | | AID | 463 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 47 | [SID4264467] | Inactive | | | Primary HTS assay for chemical inhibitors of antigen receptor-induced NF-kappaB activation [AID465, Type: screening] | |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Primary HTS assay for chemical inhibitors of antigen receptor-induced NF-kappaB activation | | AID | 465 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 48 | [SID4264467] | Inactive | | | Ubiquitin-GFP Assay [AID526, Type: confirmatory] | |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Ubiquitin-GFP Assay | | AID | 526 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 49 | [SID4264467] | Inactive | | | Antimicrobial HTS Assay for E. coli BW25113 (wild type) [AID552, Type: screening] | |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Antimicrobial HTS Assay for E. coli BW25113 (wild type) | | AID | 552 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 50 | [SID4264467] | Inactive | | | Primary Antimicrobial Assay for E. coli BW25113 ∆tolC::kan Protocol for 384-well HTS [AID573, Type: screening] | |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 4264467 | | CID | 56642854 | | Outcome | Inactive | | BioAssay | Primary Antimicrobial Assay for E. coli BW25113 ∆tolC::kan Protocol for 384-well HTS | | AID | 573 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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