| 1 | [SID4258750] | Active | Potency | 0.1 | qHTS for Inhibitors of TGF-b: Cytotox Counterscreen [AID588856, Type: confirmatory] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Active | | Potency | 0.1 [uM] | | BioAssay | qHTS for Inhibitors of TGF-b: Cytotox Counterscreen | | AID | 588856 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 2 | [SID4258750] | Active | Potency | 7.9433 | qHTS Assay for Inhibitors of Hepatitis C Virus (HCV) [AID651820, Type: confirmatory] | |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Assay for Inhibitors of Hepatitis C Virus (HCV) | | AID | 651820 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 3 | [SID4258750] | Active | Potency | 9.2 | 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. | 3 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Active | | Potency | 9.2 [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 |  |
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| 4 | [SID4258750] | Active | Potency | 25.929 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Active | | Potency | 25.929 [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 5 | [SID4258750] | Active | Potency | 25.929 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Active | | Potency | 25.929 [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
|
| 6 | [SID4258750] | Active | Potency | 25.929 | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | TDP1 protein [Homo sapiens] [gi:79154014] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Active | | Potency | 25.929 [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 | TDP1 protein [Homo sapiens] [gi:79154014] | | PubMed | | | Data Table |  |
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| 7 | [SID4258750] | Active | Potency | 31.6228 | 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. | 7 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Active | | Potency | 31.6228 [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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| 8 | [SID4258750] | Active | | | Factor XIa Mixture HTS [AID680, Type: screening] | coagulation factor XI [gi:180352] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Active | | BioAssay | Factor XIa Mixture HTS | | AID | 680 | | BioAssay type | screening | | Target | coagulation factor XI [gi:180352] | | PubMed | | | Data Table |  |
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| 9 | [SID4258750] | Active | | | Factor XIa Mixture HTS [AID680, Type: screening] | coagulation factor XI [gi:180352] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Active | | BioAssay | Factor XIa Mixture HTS | | AID | 680 | | BioAssay type | screening | | Target | coagulation factor XI [gi:180352] | | PubMed | | | Data Table |  |
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| 10 | [SID4258750] | Active | | | Flow Cytometric HTS Screening for Inhibitors of Lytic Granule Exocytosis with MLPCN Compound Library [AID651702, Type: screening] | |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Active | | BioAssay | Flow Cytometric HTS Screening for Inhibitors of Lytic Granule Exocytosis with MLPCN Compound Library | | AID | 651702 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
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| 11 | [SID4258750] | Active | | | qHTS Assay for Spectroscopic Profiling in 4-MU Spectral Region [AID589, Type: other] | |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in 4-MU Spectral Region | | AID | 589 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 12 | [SID4258750] | Active | | | qHTS Assay for Spectroscopic Profiling in A350 Spectral Region [AID590, Type: other] | |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | 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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| 13 | [SID4258750] | Active | | | Profiling the NIH Molecular Libraries Small Molecule Repository: Autofluorescence at 339/460 nm [AID709, Type: screening] | |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | 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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| 14 | [SID4258750] | 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. | 14 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | 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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| 15 | [SID4258750] | 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. | 15 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | 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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| 16 | [SID4258750] | Inactive | Potency | 19.9526 | 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. | 16 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | 19.9526 [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 |  |
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| 17 | [SID87225467] | Inactive | IC50 | 20 | SAR analysis of compounds that are cytotoxic to HEK293 revised [AID2335, Type: confirmatory] | |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 87225467 | | CID | 1251136 | | Outcome | Inactive | | IC50 | 20 [uM] | | BioAssay | SAR analysis of compounds that are cytotoxic to HEK293 revised | | AID | 2335 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 18 | [SID87225467] | Inactive | IC50 | 20 | SAR analysis of inhibitors of TNFa specific NF-kB induction revised [AID2337, Type: confirmatory] | TNF gene product [Homo sapiens] [gi:25952111] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 87225467 | | CID | 1251136 | | Outcome | Inactive | | IC50 | 20 [uM] | | BioAssay | SAR analysis of inhibitors of TNFa specific NF-kB induction revised | | AID | 2337 | | BioAssay type | confirmatory | | Target | TNF gene product [Homo sapiens] [gi:25952111] | | PubMed | | | Data Table |  |
|
| 19 | [SID87225467] | Inactive | IC50 | 20 | SAR analysis of inhibitors of TNFa specific NF-kB induction revised [AID2337, Type: confirmatory] | TNF gene product [Homo sapiens] [gi:25952111] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 87225467 | | CID | 1251136 | | Outcome | Inactive | | IC50 | 20 [uM] | | BioAssay | SAR analysis of inhibitors of TNFa specific NF-kB induction revised | | AID | 2337 | | BioAssay type | confirmatory | | Target | TNF gene product [Homo sapiens] [gi:25952111] | | PubMed | | | Data Table |  |
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| 20 | [SID87225467] | Inactive | IC50 | 20 | SAR analysis of compounds that inhibit NOD1 revised [AID2333, Type: confirmatory] | nucleotide-binding oligomerization domain-containing protein 1 [Homo sapiens] [gi:5174617] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 87225467 | | CID | 1251136 | | Outcome | Inactive | | IC50 | 20 [uM] | | BioAssay | SAR analysis of compounds that inhibit NOD1 revised | | AID | 2333 | | BioAssay type | confirmatory | | Target | nucleotide-binding oligomerization domain-containing protein 1 [Homo sapiens] [gi:5174617] | | PubMed | | | Data Table |  |
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| 21 | [SID87225467] | Inactive | IC50 | 20 | SAR analysis of compounds that inhibit NOD1 revised [AID2333, Type: confirmatory] | nucleotide-binding oligomerization domain-containing protein 1 [Homo sapiens] [gi:5174617] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 87225467 | | CID | 1251136 | | Outcome | Inactive | | IC50 | 20 [uM] | | BioAssay | SAR analysis of compounds that inhibit NOD1 revised | | AID | 2333 | | BioAssay type | confirmatory | | Target | nucleotide-binding oligomerization domain-containing protein 1 [Homo sapiens] [gi:5174617] | | PubMed | | | Data Table |  |
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| 22 | [SID87225467] | Inactive | IC50 | 20 | SAR analysis of compounds that inhibit NOD2 revised [AID2334, Type: confirmatory] | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 87225467 | | CID | 1251136 | | Outcome | Inactive | | IC50 | 20 [uM] | | BioAssay | SAR analysis of compounds that inhibit NOD2 revised | | AID | 2334 | | BioAssay type | confirmatory | | Target | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] | | PubMed | | | Data Table |  |
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| 23 | [SID87225467] | Inactive | IC50 | 20 | SAR analysis of compounds that inhibit NOD2 revised [AID2334, Type: confirmatory] | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 87225467 | | CID | 1251136 | | Outcome | Inactive | | IC50 | 20 [uM] | | BioAssay | SAR analysis of compounds that inhibit NOD2 revised | | AID | 2334 | | BioAssay type | confirmatory | | Target | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] | | PubMed | | | Data Table |  |
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| 24 | [SID87225467] | Inactive | IC50 | 20 | SAR analysis of compounds that inhibit NOD2 revised [AID2334, Type: confirmatory] | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 87225467 | | CID | 1251136 | | Outcome | Inactive | | IC50 | 20 [uM] | | BioAssay | SAR analysis of compounds that inhibit NOD2 revised | | AID | 2334 | | BioAssay type | confirmatory | | Target | nucleotide-binding oligomerization domain-containing protein 2 [Homo sapiens] [gi:11545912] | | PubMed | | | Data Table |  |
|
| 25 | [SID4258750] | Inactive | Potency | 25.1189 | qHTS Assay for the Inhibitors of L3MBTL1 [AID485360, Type: confirmatory] | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | 25.1189 [uM] | | BioAssay | qHTS Assay for the Inhibitors of L3MBTL1 | | AID | 485360 | | BioAssay type | confirmatory | | Target | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] | | PubMed | | | Data Table |  |
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| 26 | [SID4258750] | Inactive | Potency | 25.1189 | qHTS Assay for the Inhibitors of L3MBTL1 [AID485360, Type: confirmatory] | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | 25.1189 [uM] | | BioAssay | qHTS Assay for the Inhibitors of L3MBTL1 | | AID | 485360 | | BioAssay type | confirmatory | | Target | lethal(3)malignant brain tumor-like protein 1 isoform I [Homo sapiens] [gi:117938328] | | PubMed | | | Data Table |  |
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| 27 | [SID4258750] | Inactive | Potency | 28.1838 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | 28.1838 [uM] | | BioAssay | qHTS Assay for Inhibitors of BAZ2B | | AID | 504333 | | BioAssay type | confirmatory | | Target | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] | | PubMed | | | Data Table |  |
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| 28 | [SID4258750] | Inactive | Potency | 39.8107 | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a [AID504332, Type: confirmatory] | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a | | AID | 504332 | | BioAssay type | confirmatory | | Target | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] | | PubMed | | | Data Table |  |
|
| 29 | [SID4258750] | Inactive | Potency | 75.6863 | qHTS Assay to Find Inhibitors of Pin1 [AID504891, Type: confirmatory] | PIN1 gene product [Homo sapiens] [gi:5453898] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | 75.6863 [uM] | | BioAssay | qHTS Assay to Find Inhibitors of Pin1 | | AID | 504891 | | BioAssay type | confirmatory | | Target | PIN1 gene product [Homo sapiens] [gi:5453898] | | PubMed | | | Data Table |  |
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| 30 | [SID4258750] | Inactive | Potency | 75.6863 | qHTS Assay to Find Inhibitors of Pin1 [AID504891, Type: confirmatory] | PIN1 gene product [Homo sapiens] [gi:5453898] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | 75.6863 [uM] | | BioAssay | qHTS Assay to Find Inhibitors of Pin1 | | AID | 504891 | | BioAssay type | confirmatory | | Target | PIN1 gene product [Homo sapiens] [gi:5453898] | | PubMed | | | Data Table |  |
|
| 31 | [SID4258750] | Inactive | Potency | 89.1251 | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain [AID504339, Type: confirmatory] | Chain A, Jmjd2a Tandem Tudor Domains In Complex With A Trimethylated Histone H4-K20 Peptide [gi:162330054] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | 89.1251 [uM] | | BioAssay | qHTS Assay for Inhibitors of JMJD2A-Tudor Domain | | AID | 504339 | | BioAssay type | confirmatory | | Target | Chain A, Jmjd2a Tandem Tudor Domains In Complex With A Trimethylated Histone H4-K20 Peptide [gi:162330054] | | PubMed | | | Data Table |  |
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| 32 | [SID4258750] | Inactive | | | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set [AID588497, Type: Literature] | botulinum neurotoxin type F, BoNT/F [Clostridium botulinum Bf] [gi:168184763] |   View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | | AID | 588497 | | BioAssay type | Literature | | Target | botulinum neurotoxin type F, BoNT/F [Clostridium botulinum Bf] [gi:168184763] | | PubMed | 16604538 | | Data Table |  |
|
| 33 | [SID4258750] | Inactive | Potency | | qHTS for Inducers of the Endoplasmic Reticulum Stress Response (ERSR) in Human Glioma: qHTS [AID602332, Type: confirmatory] | heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) [Homo sapiens] [gi:168984549] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inducers of the Endoplasmic Reticulum Stress Response (ERSR) in Human Glioma: qHTS | | AID | 602332 | | BioAssay type | confirmatory | | Target | heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) [Homo sapiens] [gi:168984549] | | PubMed | | | Data Table |  |
|
| 34 | [SID4258750] | 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. | 34 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | 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 |  |
|
| 35 | [SID4258750] | Inactive | IC50 | | High Throughput Screening Assay for Hsp70 Inhibitors [AID583, Type: confirmatory] | heat shock 70kDa protein 1A [Homo sapiens] [gi:123271505] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | High Throughput Screening Assay for Hsp70 Inhibitors | | AID | 583 | | BioAssay type | confirmatory | | Target | heat shock 70kDa protein 1A [Homo sapiens] [gi:123271505] | | PubMed | | | Data Table |  |
|
| 36 | [SID4258750] | Inactive | | | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of the Hepatitis C Virus non-structural protein 3 helicase (NS3) [AID1800, Type: screening] | NS3 [Hepatitis C virus] [gi:125541954] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of the Hepatitis C Virus non-structural protein 3 helicase (NS3) | | AID | 1800 | | BioAssay type | screening | | Target | NS3 [Hepatitis C virus] [gi:125541954] | | PubMed | | | Data Table |  |
|
| 37 | [SID4258750] | Inactive | | | Fluorescence-based counterscreen assay for HCV NS3 helicase inhibitors: biochemical high-throughput screening assay to identify compounds that cause fluorescent intercalator displacement (FID) [AID1845, Type: screening] | NS3 [Hepatitis C virus] [gi:125541954] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | Fluorescence-based counterscreen assay for HCV NS3 helicase inhibitors: biochemical high-throughput screening assay to identify compounds that cause fluorescent intercalator displacement (FID) | | AID | 1845 | | BioAssay type | screening | | Target | NS3 [Hepatitis C virus] [gi:125541954] | | PubMed | | | Data Table |  |
|
| 38 | [SID4258750] | Inactive | Potency | | 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. | 38 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | [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 |  |
|
| 39 | [SID4258750] | Inactive | Potency | | 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. | 39 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | [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 |  |
|
| 40 | [SID4258750] | Inactive | | | uHTS identification of modulators of interaction between CendR and NRP-1 using Fluorescence Polarization assay [AID602438, Type: screening] | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | uHTS identification of modulators of interaction between CendR and NRP-1 using Fluorescence Polarization assay | | AID | 602438 | | BioAssay type | screening | | Target | Chain A, Crystal Structure Of The B1b2 Domains From Human Neuropilin- 1 [gi:160877737] | | PubMed | | | Data Table |  |
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| 41 | [SID4258750] | Inactive | Potency | | qHTS Assay for Inhibitors of Human Galactokinase (GALK) [AID1868, Type: confirmatory] | galactokinase [Homo sapiens] [gi:4503895] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Galactokinase (GALK) | | AID | 1868 | | BioAssay type | confirmatory | | Target | galactokinase [Homo sapiens] [gi:4503895] | | PubMed | | | Data Table |  |
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| 42 | [SID4258750] | Inactive | Potency | | qHTS Assay for Inhibitors of Human Galactokinase (GALK) [AID1868, Type: confirmatory] | galactokinase [Homo sapiens] [gi:4503895] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Galactokinase (GALK) | | AID | 1868 | | BioAssay type | confirmatory | | Target | galactokinase [Homo sapiens] [gi:4503895] | | PubMed | | | Data Table |  |
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| 43 | [SID4258750] | Inactive | | | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen [AID2472, Type: screening] | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen | | AID | 2472 | | BioAssay type | screening | | Target | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] | | PubMed | | | Data Table |  |
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| 44 | [SID4258750] | Inactive | | | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen [AID2472, Type: screening] | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia: Coupling assay counterscreen | | AID | 2472 | | BioAssay type | screening | | Target | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens] [gi:7669492] | | PubMed | | | Data Table |  |
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| 45 | [SID4258750] | Inactive | | | Primary Cell Based High Throughput Screening Assay for Enhancers of Beta-Glucosidase Activity [AID784, Type: screening] | Glucosylceramidase [gi:55584151] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | Primary Cell Based High Throughput Screening Assay for Enhancers of Beta-Glucosidase Activity | | AID | 784 | | BioAssay type | screening | | Target | Glucosylceramidase [gi:55584151] | | PubMed | | | Data Table |  |
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| 46 | [SID4258750] | Inactive | | | Primary Cell Based High Throughput Screening Assay for Enhancers of Beta-Glucosidase Activity [AID784, Type: screening] | Glucosylceramidase [gi:55584151] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | Primary Cell Based High Throughput Screening Assay for Enhancers of Beta-Glucosidase Activity | | AID | 784 | | BioAssay type | screening | | Target | Glucosylceramidase [gi:55584151] | | PubMed | | | Data Table |  |
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| 47 | [SID4258750] | Inactive | | | Factor XIa 1536 HTS [AID798, Type: screening] | coagulation factor XI [gi:180352] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | Factor XIa 1536 HTS | | AID | 798 | | BioAssay type | screening | | Target | coagulation factor XI [gi:180352] | | PubMed | | | Data Table |  |
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| 48 | [SID4258750] | Inactive | | | Factor XIa 1536 HTS [AID798, Type: screening] | coagulation factor XI [gi:180352] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | Factor XIa 1536 HTS | | AID | 798 | | BioAssay type | screening | | Target | coagulation factor XI [gi:180352] | | PubMed | | | Data Table |  |
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| 49 | [SID4258750] | Inactive | | | Factor XIIa 1536 HTS [AID800, Type: screening] | Coagulation factor XII [gi:317373446] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | Factor XIIa 1536 HTS | | AID | 800 | | BioAssay type | screening | | Target | Coagulation factor XII [gi:317373446] | | PubMed | | | Data Table |  |
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| 50 | [SID4258750] | Inactive | | | Factor XIIa Mixture HTS [AID684, Type: screening] | Coagulation factor XII [gi:317373446] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 4258750 | | CID | 1251136 | | Outcome | Inactive | | BioAssay | Factor XIIa Mixture HTS | | AID | 684 | | BioAssay type | screening | | Target | Coagulation factor XII [gi:317373446] | | PubMed | | | Data Table |  |
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