| 1 | [SID855617] | Active | Potency | 3.1623 | qHTS Inhibitors of AmpC Beta-Lactamase (assay without detergent) [AID485341, Type: confirmatory] | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 3.1623 [uM] | | BioAssay | qHTS Inhibitors of AmpC Beta-Lactamase (assay without detergent) | | AID | 485341 | | BioAssay type | confirmatory | | Target | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] | | PubMed | | | Data Table |  |
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| 2 | [SID855617] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
|
| 3 | [SID855617] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
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| 4 | [SID855617] | Active | EC50 | 12.4 | Fluorescent HTS Cytotoxicity/Cell viability assay (HPDE-C7 cells) [AID430, Type: confirmatory] | |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | EC50 | 12.4 [uM] | | BioAssay | Fluorescent HTS Cytotoxicity/Cell viability assay (HPDE-C7 cells) | | AID | 430 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 5 | [SID855617] | Active | Potency | 12.5893 | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (without detergent) [AID1476, Type: confirmatory] | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (without detergent) | | AID | 1476 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] | | PubMed | | | Data Table |  |
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| 6 | [SID855617] | Active | EC50 | 13.7 | Fluorescent HTS Cytotoxicity/Cell viability assay (HPDE-C7K cells) [AID431, Type: confirmatory] | |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | EC50 | 13.7 [uM] | | BioAssay | Fluorescent HTS Cytotoxicity/Cell viability assay (HPDE-C7K cells) | | AID | 431 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 7 | [SID855617] | Active | IC50 | 14.6874 | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors [AID1417, Type: confirmatory] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | IC50 | 14.6874 [uM] | | BioAssay | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors | | AID | 1417 | | BioAssay type | confirmatory | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 8 | [SID855617] | Active | IC50 | 14.6874 | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors [AID1417, Type: confirmatory] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | IC50 | 14.6874 [uM] | | BioAssay | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors | | AID | 1417 | | BioAssay type | confirmatory | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 9 | [SID855617] | Active | IC50 | 14.6874 | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors [AID1417, Type: confirmatory] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | IC50 | 14.6874 [uM] | | BioAssay | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors | | AID | 1417 | | BioAssay type | confirmatory | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 10 | [SID855617] | Active | Potency | 19.9526 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
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| 11 | [SID855617] | Active | Potency | 19.9526 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
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| 12 | [SID855617] | Active | Potency | 20.5962 | 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. | 12 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 20.5962 [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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| 13 | [SID855617] | Active | Potency | 25.1189 | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) [AID2528, Type: confirmatory] | Bloom syndrome protein [Homo sapiens] [gi:4557365] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 25.1189 [uM] | | BioAssay | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) | | AID | 2528 | | BioAssay type | confirmatory | | Target | Bloom syndrome protein [Homo sapiens] [gi:4557365] | | PubMed | | | Data Table |  |
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| 14 | [SID855617] | Active | Potency | 28.1838 | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID894, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 28.1838 [uM] | | BioAssay | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 894 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 15 | [SID855617] | Active | Potency | 28.1838 | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID894, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 28.1838 [uM] | | BioAssay | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 894 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 16 | [SID855617] | Active | Potency | 28.1838 | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) [AID894, Type: confirmatory] | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 28.1838 [uM] | | BioAssay | qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase) | | AID | 894 | | BioAssay type | confirmatory | | Target | 15-hydroxyprostaglandin dehydrogenase [NAD+] isoform 1 [Homo sapiens] [gi:31542939] | | PubMed | | | Data Table |  |
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| 17 | [SID855617] | Active | Potency | 50.1187 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | Potency | 50.1187 [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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| 18 | [SID855617] | Active | | | MLPCN Streptokinase Expression Inhibition [AID1662, Type: screening] | streptokinase A precursor [Streptococcus pyogenes M1 GAS] [gi:15675770] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | BioAssay | MLPCN Streptokinase Expression Inhibition | | AID | 1662 | | BioAssay type | screening | | Target | streptokinase A precursor [Streptococcus pyogenes M1 GAS] [gi:15675770] | | PubMed | | | Data Table |  |
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| 19 | [SID855617] | Active | IC50 | | Image-Based HTS for Selective Antagonists for GPR55 [AID2013, Type: confirmatory] | G-protein coupled receptor 55 [Homo sapiens] [gi:33695107] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | IC50 | [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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| 20 | [SID855617] | Active | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 21 | [SID855617] | Active | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 22 | [SID855617] | Active | | | uHTS of Mcl-1/Bid interaction inhibitors [AID1021, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Bid interaction inhibitors | | AID | 1021 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 23 | [SID855617] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 24 | [SID855617] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 25 | [SID855617] | Active | | | uHTS of Mcl-1/Noxa interaction inhibitors [AID1022, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | BioAssay | uHTS of Mcl-1/Noxa interaction inhibitors | | AID | 1022 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
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| 26 | [SID855617] | Active | | | Anti-Viral Drugs Against Arbovirus Infections, a Primary Screen [AID1251, Type: screening] | |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Active | | BioAssay | Anti-Viral Drugs Against Arbovirus Infections, a Primary Screen | | AID | 1251 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 27 | [SID855617] | Inactive | Potency | 8.9125 | qHTS Assay for Enhancers of SMN2 Splice Variant Expression [AID1458, Type: confirmatory] | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | Potency | 8.9125 [uM] | | BioAssay | qHTS Assay for Enhancers of SMN2 Splice Variant Expression | | AID | 1458 | | BioAssay type | confirmatory | | Target | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] | | PubMed | | | Data Table |  |
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| 28 | [SID855617] | Inactive | Potency | 8.9125 | qHTS Assay for Enhancers of SMN2 Splice Variant Expression [AID1458, Type: confirmatory] | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | Potency | 8.9125 [uM] | | BioAssay | qHTS Assay for Enhancers of SMN2 Splice Variant Expression | | AID | 1458 | | BioAssay type | confirmatory | | Target | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] | | PubMed | | | Data Table |  |
|
| 29 | [SID855617] | Inactive | Potency | 22.3872 | qHTS Assay for Inhibitors of MBNL1-poly(CUG) RNA binding [AID2675, Type: confirmatory] | muscleblind-like protein 1 isoform a [Homo sapiens] [gi:41281591] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | Potency | 22.3872 [uM] | | BioAssay | qHTS Assay for Inhibitors of MBNL1-poly(CUG) RNA binding | | AID | 2675 | | BioAssay type | confirmatory | | Target | muscleblind-like protein 1 isoform a [Homo sapiens] [gi:41281591] | | PubMed | | | Data Table |  |
|
| 30 | [SID855617] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Mcl-1 [AID1009, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Mcl-1 | | AID | 1009 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 31 | [SID855617] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Mcl-1 [AID1009, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Mcl-1 | | AID | 1009 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 32 | [SID855617] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Mcl-1 [AID1009, Type: screening] | Mcl-1 [Homo sapiens] [gi:7582271] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Mcl-1 | | AID | 1009 | | BioAssay type | screening | | Target | Mcl-1 [Homo sapiens] [gi:7582271] | | PubMed | | | Data Table |  |
|
| 33 | [SID855617] | Inactive | Potency | | 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. | 33 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | Potency | [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 |  |
|
| 34 | [SID855617] | Inactive | Potency | | qHTS Assay for Inhibitors of Human Jumonji Domain Containing 2E (JMJD2E) [AID2147, Type: confirmatory] | Chain A, Crystal Structure Of The Human 2-Oxoglutarate Oxygenase Loc390245 [gi:221046486] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Jumonji Domain Containing 2E (JMJD2E) | | AID | 2147 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of The Human 2-Oxoglutarate Oxygenase Loc390245 [gi:221046486] | | PubMed | | | Data Table |  |
|
| 35 | [SID855617] | Inactive | Potency | | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1468, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1468 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 36 | [SID855617] | Inactive | Potency | | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1468, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1468 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 37 | [SID855617] | Inactive | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype [AID1529, Type: screening] | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype | | AID | 1529 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] | | PubMed | | | Data Table |  |
|
| 38 | [SID855617] | Inactive | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype [AID1529, Type: screening] | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype | | AID | 1529 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] | | PubMed | | | Data Table |  |
|
| 39 | [SID855617] | Inactive | | | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype [AID1529, Type: screening] | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 MEK Kinase3 Wildtype | | AID | 1529 | | BioAssay type | screening | | Target | mitogen-activated protein kinase kinase kinase 3 isoform 1 [Homo sapiens] [gi:42794767] | | PubMed | | | Data Table |  |
|
| 40 | [SID855617] | Inactive | | | HTS of Smad transcription factor inhibitors [AID630, Type: screening] | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | HTS of Smad transcription factor inhibitors | | AID | 630 | | BioAssay type | screening | | Target | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] | | PubMed | | | Data Table |  |
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| 41 | [SID855617] | Inactive | | | HTS of Smad transcription factor inhibitors [AID630, Type: screening] | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | HTS of Smad transcription factor inhibitors | | AID | 630 | | BioAssay type | screening | | Target | mothers against decapentaplegic homolog 3 [Homo sapiens] [gi:5174513] | | PubMed | | | Data Table |  |
|
| 42 | [SID855617] | Inactive | Potency | | qHTS Assay for Inhibitors of Human alpha-Galactosidase at pH 4.5. [AID1467, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human alpha-Galactosidase at pH 4.5. | | AID | 1467 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
|
| 43 | [SID855617] | Inactive | Potency | | qHTS Assay for Inhibitors of Human alpha-Galactosidase at pH 4.5. [AID1467, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human alpha-Galactosidase at pH 4.5. | | AID | 1467 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
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| 44 | [SID855617] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate [AID2107, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate | | AID | 2107 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
|
| 45 | [SID855617] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate [AID2107, Type: confirmatory] | alpha-galactosidase [Homo sapiens] [gi:757912] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Galactosidase From Spleen Homogenate | | AID | 2107 | | BioAssay type | confirmatory | | Target | alpha-galactosidase [Homo sapiens] [gi:757912] | | PubMed | | | Data Table |  |
|
| 46 | [SID855617] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1423, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1423 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 47 | [SID855617] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1423, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1423 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 48 | [SID855617] | Inactive | | | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. [AID1423, Type: screening] | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | Multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | | AID | 1423 | | BioAssay type | screening | | Target | guanine nucleotide-binding protein G(o) subunit alpha isoform a [Homo sapiens] [gi:10567816] | | PubMed | | | Data Table |  |
|
| 49 | [SID855617] | Inactive | | | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype [AID759, Type: screening] | ras protein [Homo sapiens] [gi:190938] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | | AID | 759 | | BioAssay type | screening | | Target | ras protein [Homo sapiens] [gi:190938] | | PubMed | | | Data Table |  |
|
| 50 | [SID855617] | Inactive | | | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype [AID759, Type: screening] | ras protein [Homo sapiens] [gi:190938] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 855617 | | CID | 23666110 | | Outcome | Inactive | | BioAssay | HTS to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | | AID | 759 | | BioAssay type | screening | | Target | ras protein [Homo sapiens] [gi:190938] | | PubMed | | | Data Table |  |
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