| 1 | [SID11112976] | Active | Potency | 4.7444 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 4.7444 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
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| 2 | [SID11112976] | Active | Potency | 4.7444 | qHTS for Inhibitors of Polymerase Kappa [AID588579, Type: confirmatory] | DNA polymerase kappa [Homo sapiens] [gi:7705344] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 4.7444 [uM] | | BioAssay | qHTS for Inhibitors of Polymerase Kappa | | AID | 588579 | | BioAssay type | confirmatory | | Target | DNA polymerase kappa [Homo sapiens] [gi:7705344] | | PubMed | | | Data Table |  |
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| 3 | [SID11112976] | Active | Potency | 5.0119 | 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. | 3 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 5.0119 [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 |  |
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| 4 | [SID11112976] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) [AID886, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) | | AID | 886 | | 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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| 5 | [SID11112976] | Active | Potency | 7.9433 | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) [AID2517, Type: confirmatory] | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 7.9433 [uM] | | BioAssay | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | | AID | 2517 | | BioAssay type | confirmatory | | Target | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] | | PubMed | | | Data Table |  |
|
| 6 | [SID11112976] | Active | Potency | 11.2202 | 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. | 6 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 11.2202 [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 |  |
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| 7 | [SID11112976] | Active | Potency | 12.5893 | 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 | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 12.5893 [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 | [SID11112976] | Active | Potency | 12.5893 | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) [AID2549, Type: confirmatory] | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) | | AID | 2549 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] | | PubMed | | | Data Table |  |
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| 9 | [SID11112976] | Active | Potency | 31.6228 | Inhibitors of USP1/UAF1: Pilot qHTS [AID504865, Type: confirmatory] | USP1 protein [Homo sapiens] [gi:118600387] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | Inhibitors of USP1/UAF1: Pilot qHTS | | AID | 504865 | | BioAssay type | confirmatory | | Target | USP1 protein [Homo sapiens] [gi:118600387] | | PubMed | | | Data Table |  |
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| 10 | [SID11112976] | Active | Potency | 31.6228 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
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| 11 | [SID11112976] | Active | Potency | 31.6228 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
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| 12 | [SID11112976] | Active | Potency | 31.6228 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
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| 13 | [SID11112976] | Active | Potency | 31.6228 | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 31.6228 [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
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| 14 | [SID11112976] | Active | Potency | 44.6684 | Counterscreen for RECQ1 Inhibitors: ADP Fluorescence Polarization Displacement Assay [AID2711, Type: confirmatory] | |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | Counterscreen for RECQ1 Inhibitors: ADP Fluorescence Polarization Displacement Assay | | AID | 2711 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 15 | [SID11112976] | Active | Potency | 44.6684 | Counterscreen for BLMA Inhibitors: ADP Fluorescence Polarization Displacement Assay [AID2712, Type: confirmatory] | |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | Potency | 44.6684 [uM] | | BioAssay | Counterscreen for BLMA Inhibitors: ADP Fluorescence Polarization Displacement Assay | | AID | 2712 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
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| 16 | [SID11112976] | Active | | | qHTS Assay for Spectroscopic Profiling in 4-MU Spectral Region [AID589, Type: other] | |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | 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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| 17 | [SID11112976] | Active | | | qHTS Assay for Spectroscopic Profiling in A350 Spectral Region [AID590, Type: other] | |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | 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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| 18 | [SID11112976] | Active | | | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Red Fluorophore) [AID880, Type: confirmatory] | RGS12 [Homo sapiens] [gi:3290016] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Active | | BioAssay | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Red Fluorophore) | | AID | 880 | | BioAssay type | confirmatory | | Target | RGS12 [Homo sapiens] [gi:3290016] | | PubMed | | | Data Table |  |
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| 19 | [SID11112976] | Unspecified | | | Cytochrome panel assay with activity outcomes [AID1851, Type: other] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Unspecified | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
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| 20 | [SID11112976] | Unspecified | | | Cytochrome panel assay with activity outcomes [AID1851, Type: other] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Unspecified | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
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| 21 | [SID11112976] | Inactive | Potency | 15.8489 | 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. | 21 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | 15.8489 [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 |  |
|
| 22 | [SID11112976] | Inactive | Potency | 39.8107 | Confirmation qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) [AID2708, Type: confirmatory] | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | 39.8107 [uM] | | BioAssay | Confirmation qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) | | AID | 2708 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] | | PubMed | | | Data Table |  |
|
| 23 | [SID11112976] | Inactive | | | qHTS Assay for Tau Filament Binding [AID596, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | qHTS Assay for Tau Filament Binding | | AID | 596 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
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| 24 | [SID11112976] | Inactive | | | qHTS Assay for Tau Filament Binding [AID596, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | qHTS Assay for Tau Filament Binding | | AID | 596 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
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| 25 | [SID11112976] | Inactive | Potency | | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 [AID899, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 | | AID | 899 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
|
| 26 | [SID11112976] | Inactive | Potency | | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 [AID899, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 | | AID | 899 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
|
| 27 | [SID11112976] | Inactive | Potency | | 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. | 27 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | [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 |  |
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| 28 | [SID11112976] | Inactive | | | IkB Signaling [AID445, Type: confirmatory] | nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha [Homo sapiens] [gi:10092619] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | IkB Signaling | | AID | 445 | | BioAssay type | confirmatory | | Target | nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha [Homo sapiens] [gi:10092619] | | PubMed | | | Data Table |  |
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| 29 | [SID11112976] | Inactive | | | IkB Signaling [AID445, Type: confirmatory] | nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha [Homo sapiens] [gi:10092619] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | IkB Signaling | | AID | 445 | | BioAssay type | confirmatory | | Target | nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha [Homo sapiens] [gi:10092619] | | PubMed | | | Data Table |  |
|
| 30 | [SID11112976] | Inactive | | | qHTS Assay for Inhibitors of PDE-IV [AID607, Type: confirmatory] | phosphodiesterase 4B, cAMP-specific isoform 1 [Homo sapiens] [gi:82799486] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | qHTS Assay for Inhibitors of PDE-IV | | AID | 607 | | BioAssay type | confirmatory | | Target | phosphodiesterase 4B, cAMP-specific isoform 1 [Homo sapiens] [gi:82799486] | | PubMed | | | Data Table |  |
|
| 31 | [SID11112976] | Inactive | | | qHTS Assay for Inhibitors of PDE-IV [AID607, Type: confirmatory] | phosphodiesterase 4B, cAMP-specific isoform 1 [Homo sapiens] [gi:82799486] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | qHTS Assay for Inhibitors of PDE-IV | | AID | 607 | | BioAssay type | confirmatory | | Target | phosphodiesterase 4B, cAMP-specific isoform 1 [Homo sapiens] [gi:82799486] | | PubMed | | | Data Table |  |
|
| 32 | [SID11112976] | Inactive | Potency | | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF [AID1454, Type: confirmatory] | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | | AID | 1454 | | BioAssay type | confirmatory | | Target | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] | | PubMed | | | Data Table |  |
|
| 33 | [SID11112976] | Inactive | Potency | | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF [AID1454, Type: confirmatory] | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | | AID | 1454 | | BioAssay type | confirmatory | | Target | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] | | PubMed | | | Data Table |  |
|
| 34 | [SID11112976] | Inactive | Potency | | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF [AID1454, Type: confirmatory] | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay; Stimulation with EGF | | AID | 1454 | | BioAssay type | confirmatory | | Target | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] | | PubMed | | | Data Table |  |
|
| 35 | [SID11112976] | Inactive | Potency | | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay [AID995, Type: confirmatory] | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | | AID | 995 | | BioAssay type | confirmatory | | Target | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] | | PubMed | | | Data Table |  |
|
| 36 | [SID11112976] | Inactive | Potency | | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay [AID995, Type: confirmatory] | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | | AID | 995 | | BioAssay type | confirmatory | | Target | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] | | PubMed | | | Data Table |  |
|
| 37 | [SID11112976] | Inactive | Potency | | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay [AID995, Type: confirmatory] | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of the ERK Signaling Pathway using a Homogeneous Screening Assay | | AID | 995 | | BioAssay type | confirmatory | | Target | mitogen-activated protein kinase 1 [Homo sapiens] [gi:66932916] | | PubMed | | | Data Table |  |
|
| 38 | [SID11112976] | 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. | 38 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | 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 |  |
|
| 39 | [SID11112976] | 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. | 39 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | 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 |  |
|
| 40 | [SID11112976] | 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. | 40 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | 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 |  |
|
| 41 | [SID11112976] | 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. | 41 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | 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 |  |
|
| 42 | [SID11112976] | Inactive | | | GR-GFP Redistribution [AID450, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | GR-GFP Redistribution | | AID | 450 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
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| 43 | [SID11112976] | Inactive | | | GR-GFP Redistribution [AID450, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | GR-GFP Redistribution | | AID | 450 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
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| 44 | [SID11112976] | Inactive | | | GR-GFP Redistribution [AID450, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | GR-GFP Redistribution | | AID | 450 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
|
| 45 | [SID11112976] | Inactive | | | GR-GFP Redistribution [AID450, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | GR-GFP Redistribution | | AID | 450 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
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| 46 | [SID11112976] | Inactive | | | GR-EFC Redistribution [AID451, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | GR-EFC Redistribution | | AID | 451 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
|
| 47 | [SID11112976] | Inactive | | | GR-EFC Redistribution [AID451, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | GR-EFC Redistribution | | AID | 451 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
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| 48 | [SID11112976] | Inactive | | | GR-EFC Redistribution [AID451, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | GR-EFC Redistribution | | AID | 451 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
|
| 49 | [SID11112976] | Inactive | | | GR-EFC Redistribution [AID451, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | BioAssay | GR-EFC Redistribution | | AID | 451 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
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| 50 | [SID11112976] | Inactive | Potency | | qHTS Assay for Modulators of Hemoglobin Beta Chain Splicing [AID925, Type: confirmatory] | hemoglobin subunit beta [Homo sapiens] [gi:4504349] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 11112976 | | CID | 54705188 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Modulators of Hemoglobin Beta Chain Splicing | | AID | 925 | | BioAssay type | confirmatory | | Target | hemoglobin subunit beta [Homo sapiens] [gi:4504349] | | PubMed | | | Data Table |  |
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