| 1 | [SID103256813] | Active | Ki | 0.00012 | Binding affinity towards Leukotriene B4 receptor guinea pig lung membrane using [3H]LTB4 as radioligand [AID102297, Type: Literature] | |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | Ki | 0.00012 [uM] | | BioAssay | Binding affinity towards Leukotriene B4 receptor guinea pig lung membrane using [3H]LTB4 as radioligand | | AID | 102297 | | BioAssay type | Literature | | Target | | | PubMed | 7473568 | | Data Table |  |
|
| 2 | [SID103256813] | Active | Ki | 0.00012 | Tested for inhibition of specific binding of [3H]LTB4 to guinea pig lung membranes expressing LTB4 receptor [AID102301, Type: Literature] | |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | Ki | 0.00012 [uM] | | BioAssay | Tested for inhibition of specific binding of [3H]LTB4 to guinea pig lung membranes expressing LTB4 receptor | | AID | 102301 | | BioAssay type | Literature | | Target | | | PubMed | 8254628 | | Data Table |  |
|
| 3 | [SID103256813] | Active | Ki | 0.00012 | Inhibition of specific binding of [3H]-LTB4 to LTB4 receptor in guinea pig lung membranes [AID101313, Type: other] | |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | Ki | 0.00012 [uM] | | BioAssay | Inhibition of specific binding of [3H]-LTB4 to LTB4 receptor in guinea pig lung membranes | | AID | 101313 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 4 | [SID103256813] | Active | Ki | 0.00012 | LTB4 receptor antagonist activity was determined by inhibition of specific binding of [3H]LTB4 in guinea pig lung membranes [AID101312, Type: other] | |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | Ki | 0.00012 [uM] | | BioAssay | LTB4 receptor antagonist activity was determined by inhibition of specific binding of [3H]LTB4 in guinea pig lung membranes | | AID | 101312 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 5 | [SID103256813] | Active | Ki | 0.00012 | Compound was evaluated for inhibition of binding of [3H]LTB4 to LTB4 receptor in guinea-pig lung membranes [AID101311, Type: other] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | Ki | 0.00012 [uM] | | BioAssay | Compound was evaluated for inhibition of binding of [3H]LTB4 to LTB4 receptor in guinea-pig lung membranes | | AID | 101311 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 6 | [SID103256813] | Active | IC50 | 0.00179 | Compound was tested for inhibitory activity against leukotriene B4 induced neutrophil chemotaxis [AID222481, Type: other] | |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | IC50 | 0.00179 [uM] | | BioAssay | Compound was tested for inhibitory activity against leukotriene B4 induced neutrophil chemotaxis | | AID | 222481 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 7 | [SID103256813] | Active | IC50 | 0.0019 | Inhibition of specific binding of [3H]LTB4 to Leukotriene B4 receptor in human neutrophils [AID102466, Type: Literature] | |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | IC50 | 0.0019 [uM] | | BioAssay | Inhibition of specific binding of [3H]LTB4 to Leukotriene B4 receptor in human neutrophils | | AID | 102466 | | BioAssay type | Literature | | Target | | | PubMed | 2170648 | | Data Table |  |
|
| 8 | [SID103256813] | Active | Ki | 0.0019 | Binding affinity towards human LTB4 receptor measured as inhibition of binding of [3H]LTB4 to isolated human neutrophils [AID102636, Type: Literature] | |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | Ki | 0.0019 [uM] | | BioAssay | Binding affinity towards human LTB4 receptor measured as inhibition of binding of [3H]LTB4 to isolated human neutrophils | | AID | 102636 | | BioAssay type | Literature | | Target | | | PubMed | 7473568 | | Data Table |  |
|
| 9 | [SID103256813] | Active | Ki | 0.0019 | Tested for inhibition of specific binding of [3H]LTB4 to human neutrophil expressing LTB4 receptor [AID102647, Type: Literature] | |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | Ki | 0.0019 [uM] | | BioAssay | Tested for inhibition of specific binding of [3H]LTB4 to human neutrophil expressing LTB4 receptor | | AID | 102647 | | BioAssay type | Literature | | Target | | | PubMed | 8254628 | | Data Table |  |
|
| 10 | [SID103256813] | Active | IC50 | 0.0019 | Inhibition of specific binding of [3H]LTB4 to LTB4 receptor in human neutrophils [AID101322, Type: other] | Leukotriene B4 receptor 1 [gi:3041713] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | IC50 | 0.0019 [uM] | | BioAssay | Inhibition of specific binding of [3H]LTB4 to LTB4 receptor in human neutrophils | | AID | 101322 | | BioAssay type | other | | Target | Leukotriene B4 receptor 1 [gi:3041713] | | PubMed | | | Data Table |  |
|
| 11 | [SID103256813] | Active | IC50 | 0.0019 | In vitro antagonistic activity towards LTB4 receptor was evaluated by inhibition of binding of [3H]LTB4 to human neutrophils [AID101318, Type: other] | |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | IC50 | 0.0019 [uM] | | BioAssay | In vitro antagonistic activity towards LTB4 receptor was evaluated by inhibition of binding of [3H]LTB4 to human neutrophils | | AID | 101318 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 12 | [SID103256813] | Active | Ki | 0.0019 | LTB4 receptor antagonist activity was determined by inhibition of specific binding of [3H]LTB4 in human neutrophil [AID101435, Type: other] | |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | Ki | 0.0019 [uM] | | BioAssay | LTB4 receptor antagonist activity was determined by inhibition of specific binding of [3H]LTB4 in human neutrophil | | AID | 101435 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 13 | [SID103256813] | Active | Ki | 0.0029 | Displacement of [3H]LTB4 from LTB4R [AID338156, Type: other] | |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | Ki | 0.0029 [uM] | | BioAssay | Displacement of [3H]LTB4 from LTB4R | | AID | 338156 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 14 | [SID103256813] | Active | IC50 | 0.032 | Inhibitory activity against leukotriene B4 receptor [AID102454, Type: other] | Leukotriene B4 receptor 1 [gi:3041713] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | IC50 | 0.032 [uM] | | BioAssay | Inhibitory activity against leukotriene B4 receptor | | AID | 102454 | | BioAssay type | other | | Target | Leukotriene B4 receptor 1 [gi:3041713] | | PubMed | | | Data Table |  |
|
| 15 | [SID103256813] | Active | | | Inhibition of tube formation in human EAhy926 cells at 10 uM pre-incubated for 12 hrs measured after 24 hrs by phase-contrast microscopy [AID396465, Type: Literature] | |   View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Active | | BioAssay | Inhibition of tube formation in human EAhy926 cells at 10 uM pre-incubated for 12 hrs measured after 24 hrs by phase-contrast microscopy | | AID | 396465 | | BioAssay type | Literature | | Target | | | PubMed | 19036594 | | Data Table |  |
|
| 16 | [SID103256813] | Unspecified | Kd | 0.0007 | GRAC: human BLT1 probe [AID540703, Type: other] | Leukotriene B4 receptor 1 [gi:3041713] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Unspecified | | Kd | 0.0007 [uM] | | BioAssay | GRAC: human BLT1 probe | | AID | 540703 | | BioAssay type | other | | Target | Leukotriene B4 receptor 1 [gi:3041713] | | PubMed | | | Data Table |  |
|
| 17 | [SID103256813] | Unspecified | Kd | 0.023 | GRAC: human BLT2 probe [AID540564, Type: other] | Leukotriene B4 receptor 2 [gi:23821812] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Unspecified | | Kd | 0.023 [uM] | | BioAssay | GRAC: human BLT2 probe | | AID | 540564 | | BioAssay type | other | | Target | Leukotriene B4 receptor 2 [gi:23821812] | | PubMed | | | Data Table |  |
|
| 18 | [SID103256813] | Unspecified | | | In vitro Ka value against human serum albumin; N=1 [AID238099, Type: Literature] | Serum albumin [gi:113576] |   View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Unspecified | | BioAssay | In vitro Ka value against human serum albumin; N=1 | | AID | 238099 | | BioAssay type | Literature | | Target | Serum albumin [gi:113576] | | PubMed | 15993588 | | Data Table |  |
|
| 19 | [SID103256813] | Unspecified | | | Displacement of [3H]LTB4 from LTB4R assessed as specific binding relative to total binding [AID338193, Type: other] | |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 103256813 | | CID | 5280492 | | Outcome | Unspecified | | BioAssay | Displacement of [3H]LTB4 from LTB4R assessed as specific binding relative to total binding | | AID | 338193 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 20 | [SID26754791] | Inactive | Potency | | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1463, Type: confirmatory] | |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 26754791 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1463 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 21 | [SID26754791] | Inactive | Potency | | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia [AID1477, Type: confirmatory] | |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 26754791 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia | | AID | 1477 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 22 | [SID26754791] | Inactive | Potency | | Quantitative High-Throughput Screen for Regulators of Epigenetic Control [AID1865, Type: confirmatory] | |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 26754791 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Quantitative High-Throughput Screen for Regulators of Epigenetic Control | | AID | 1865 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 23 | [SID26754792] | Inactive | Potency | | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1463, Type: confirmatory] | |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1463 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 24 | [SID26754792] | Inactive | Potency | | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia [AID1477, Type: confirmatory] | |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia | | AID | 1477 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 25 | [SID26754792] | Inactive | Potency | | Quantitative High-Throughput Screen for Regulators of Epigenetic Control [AID1865, Type: confirmatory] | |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Quantitative High-Throughput Screen for Regulators of Epigenetic Control | | AID | 1865 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 26 | [SID26754792] | Inactive | Potency | | qHTS Assay for Compounds that Induce Erasure of Genomic Imprints [AID1948, Type: confirmatory] | |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Compounds that Induce Erasure of Genomic Imprints | | AID | 1948 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 27 | [SID26754793] | Inactive | Potency | | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1463, Type: confirmatory] | |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 26754793 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1463 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 28 | [SID26754793] | Inactive | Potency | | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia [AID1477, Type: confirmatory] | |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 26754793 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Compounds Blocking the Interaction Between CBF-beta and RUNX1 for the Treatment of Acute Myeloid Leukemia | | AID | 1477 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 29 | [SID26754793] | Inactive | Potency | | Quantitative High-Throughput Screen for Regulators of Epigenetic Control [AID1865, Type: confirmatory] | |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 26754793 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Quantitative High-Throughput Screen for Regulators of Epigenetic Control | | AID | 1865 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 30 | [SID104046421] | Inactive | | | Screening small molecules to find regulators of human embryonic stem cell survival. [AID493140, Type: screening] | |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 104046421 | | CID | 5280492 | | Outcome | Inactive | | BioAssay | Screening small molecules to find regulators of human embryonic stem cell survival. | | AID | 493140 | | BioAssay type | screening | | Target | | | PubMed | | | Data Table |  |
|
| 31 | [SID99302212] | Inactive | | | A screen for compounds that inhibit processive DNA synthesis of vaccinia virus [AID493162, Type: other] | DNA polymerase [Vaccinia virus] [gi:335756] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 99302212 | | CID | 5280492 | | Outcome | Inactive | | BioAssay | A screen for compounds that inhibit processive DNA synthesis of vaccinia virus | | AID | 493162 | | BioAssay type | other | | Target | DNA polymerase [Vaccinia virus] [gi:335756] | | PubMed | | | Data Table |  |
|
| 32 | [SID26754792] | Inactive | Potency | | Counterscreen for Luciferase (Kinase-Glo TM) Inhibition [AID1379, Type: confirmatory] | luciferase [Photuris pennsylvanica] [gi:1669525] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen for Luciferase (Kinase-Glo TM) Inhibition | | AID | 1379 | | BioAssay type | confirmatory | | Target | luciferase [Photuris pennsylvanica] [gi:1669525] | | PubMed | | | Data Table |  |
|
| 33 | [SID26754791] | Inactive | Potency | | Counterscreen for Luciferase (Kinase-Glo TM) Inhibition [AID1379, Type: confirmatory] | luciferase [Photuris pennsylvanica] [gi:1669525] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 26754791 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen for Luciferase (Kinase-Glo TM) Inhibition | | AID | 1379 | | BioAssay type | confirmatory | | Target | luciferase [Photuris pennsylvanica] [gi:1669525] | | PubMed | | | Data Table |  |
|
| 34 | [SID26754791] | Inactive | Potency | | 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. | 34 | | Structure |
| | Substance | | | SID | 26754791 | | CID | 5280492 | | Outcome | Inactive | | Potency | [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 |  |
|
| 35 | [SID26754792] | Inactive | Potency | | 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. | 35 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | Outcome | Inactive | | Potency | [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 |  |
|
| 36 | [SID26754793] | Inactive | Potency | | 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. | 36 | | Structure |
| | Substance | | | SID | 26754793 | | CID | 5280492 | | Outcome | Inactive | | Potency | [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 |  |
|
| 37 | [SID26754792] | Inactive | Potency | | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | | AID | 1490 | | BioAssay type | confirmatory | | Target | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] | | PubMed | | | Data Table |  |
|
| 38 | [SID26754791] | Inactive | Potency | | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 26754791 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | | AID | 1490 | | BioAssay type | confirmatory | | Target | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] | | PubMed | | | Data Table |  |
|
| 39 | [SID26754793] | Inactive | Potency | | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 26754793 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | | AID | 1490 | | BioAssay type | confirmatory | | Target | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] | | PubMed | | | Data Table |  |
|
| 40 | [SID26754791] | Inactive | Potency | | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) [AID485290, Type: confirmatory] | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 26754791 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | | AID | 485290 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | | PubMed | | | Data Table |  |
|
| 41 | [SID26754793] | Inactive | Potency | | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) [AID485290, Type: confirmatory] | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 26754793 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | | AID | 485290 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | | PubMed | | | Data Table |  |
|
| 42 | [SID26754792] | Inactive | Potency | | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) [AID485290, Type: confirmatory] | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | | AID | 485290 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | | PubMed | | | Data Table |  |
|
| 43 | [SID26754792] | Inactive | | | Cycloheximide Counterscreen for Small Molecule Inhibitors of Shiga Toxin [AID2314, Type: screening] | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | Outcome | Inactive | | BioAssay | Cycloheximide Counterscreen for Small Molecule Inhibitors of Shiga Toxin | | AID | 2314 | | BioAssay type | screening | | Target | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | | PubMed | | | Data Table |  |
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| 44 | [SID26754792] | Inactive | | | A qHTS for Small Molecule Inhibitors of Shiga Toxin [AID2315, Type: screening] | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | Outcome | Inactive | | BioAssay | A qHTS for Small Molecule Inhibitors of Shiga Toxin | | AID | 2315 | | BioAssay type | screening | | Target | shiga toxin 1 variant A subunit [Escherichia coli O157:H7] [gi:32400299] | | PubMed | | | Data Table |  |
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| 45 | [SID99302212] | Inactive | | | A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities [AID588519, Type: Literature] | Chain A, Poliovirus Polymerase With Gtp [gi:52695378] |   View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 99302212 | | CID | 5280492 | | Outcome | Inactive | | BioAssay | A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities | | AID | 588519 | | BioAssay type | Literature | | Target | Chain A, Poliovirus Polymerase With Gtp [gi:52695378] | | PubMed | 21722674 | | Data Table |  |
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| 46 | [SID99300694] | Inactive | | | A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities [AID588519, Type: Literature] | Chain A, Poliovirus Polymerase With Gtp [gi:52695378] |   View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 99300694 | | CID | 5280492 | | Outcome | Inactive | | BioAssay | A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities | | AID | 588519 | | BioAssay type | Literature | | Target | Chain A, Poliovirus Polymerase With Gtp [gi:52695378] | | PubMed | 21722674 | | Data Table |  |
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| 47 | [SID99300694] | Inactive | | | A screen for compounds that inhibit the bacterial siderophore biosynthetic enzyme MbtI [AID493033, Type: other] | Isochorismate synthase/isochorismate-pyruvate lyase mbtI [gi:81706979] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 99300694 | | CID | 5280492 | | Outcome | Inactive | | BioAssay | A screen for compounds that inhibit the bacterial siderophore biosynthetic enzyme MbtI | | AID | 493033 | | BioAssay type | other | | Target | Isochorismate synthase/isochorismate-pyruvate lyase mbtI [gi:81706979] | | PubMed | | | Data Table |  |
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| 48 | [SID26754792] | Inactive | Potency | | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia [AID2451, Type: confirmatory] | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia | | AID | 2451 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] | | PubMed | | | Data Table |  |
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| 49 | [SID26754791] | Inactive | Potency | | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia [AID2451, Type: confirmatory] | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 26754791 | | CID | 5280492 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia | | AID | 2451 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] | | PubMed | | | Data Table |  |
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| 50 | [SID26754792] | 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. | 50 | | Structure |
| | Substance | | | SID | 26754792 | | CID | 5280492 | | 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 |  |
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