| 1 | [SID103497415] | Active | IC50 | 5 | Compound was tested for the inhibition of Fucosyltransferase 4 alpha 1,3 at 8.5 uM GDP-fucose [AID71972, Type: other] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103497415 | | CID | 8977 | | Outcome | Active | | IC50 | 5 [uM] | | BioAssay | Compound was tested for the inhibition of Fucosyltransferase 4 alpha 1,3 at 8.5 uM GDP-fucose | | AID | 71972 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 2 | [SID103497415] | Active | EC50 | 45 | Agonist activity at human recombinant P2Y6 receptor expressed in 1321N1 cells assessed as PLC-mediated [3H]IP production [AID271163, Type: Literature] | P2Y purinoceptor 6 [gi:2495018] |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103497415 | | CID | 8977 | | Outcome | Active | | EC50 | 45 [uM] | | BioAssay | Agonist activity at human recombinant P2Y6 receptor expressed in 1321N1 cells assessed as PLC-mediated [3H]IP production | | AID | 271163 | | BioAssay type | Literature | | Target | P2Y purinoceptor 6 [gi:2495018] | | PubMed | 16942026 | | Data Table |  |
|
| 3 | [SID46393118] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Alternative Splicing Of Rac1 Generates Rac1b, A Self-Activating Gtpase [gi:42543638] |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 46393118 | | CID | 8977 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Alternative Splicing Of Rac1 Generates Rac1b, A Self-Activating Gtpase [gi:42543638] | | PubMed | 14625275 | | Data Table |  |
|
| 4 | [SID46393419] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | [gi:46016018] |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 46393419 | | CID | 8977 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | [gi:46016018] | | PubMed | 14645372 | | Data Table |  |
|
| 5 | [SID46393054] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Crystal Structure Analysis Of Sup35 Complexed With Gdp [gi:49258657] |   View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 46393054 | | CID | 8977 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Crystal Structure Analysis Of Sup35 Complexed With Gdp [gi:49258657] | | PubMed | 15099522 | | Data Table |  |
|
| 6 | [SID46393258] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Crystal Structure Of Iigp1: A Paradigm For Interferon Inducible P47 Resistance Gtpases [gi:55669981] |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 46393258 | | CID | 8977 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Crystal Structure Of Iigp1: A Paradigm For Interferon Inducible P47 Resistance Gtpases [gi:55669981] | | PubMed | 15350217 | | Data Table |  |
|
| 7 | [SID46393259] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Crystal Structure Of Iigp1: A Paradigm For Interferon Inducible P47 Resistance Gtpases [gi:55669985] |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 46393259 | | CID | 8977 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Crystal Structure Of Iigp1: A Paradigm For Interferon Inducible P47 Resistance Gtpases [gi:55669985] | | PubMed | 15350217 | | Data Table |  |
|
| 8 | [SID46393286] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Crystal Structure Of Adp-ribosylated Ribosomal Translocase From Saccharomyces Cerevisiae [gi:55670150] |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 46393286 | | CID | 8977 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Crystal Structure Of Adp-ribosylated Ribosomal Translocase From Saccharomyces Cerevisiae [gi:55670150] | | PubMed | 15316019 | | Data Table |  |
|
| 9 | [SID46391716] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Elongation Factor G In Complex With Gdp [gi:157830795] |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 46391716 | | CID | 8977 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Elongation Factor G In Complex With Gdp [gi:157830795] | | PubMed | 8736554 | | Data Table |  |
|
| 10 | [SID46391940] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Crystal Structure Of Murine Arl3-Gdp [gi:12084691] |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 46391940 | | CID | 8977 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Crystal Structure Of Murine Arl3-Gdp [gi:12084691] | | PubMed | 11188688 | | Data Table |  |
|
| 11 | [SID46391691] | Active | | | Experimentally measured binding affinity data derived from PDB [AID1811, Type: Literature] | Chain A, Crystal Structure Of Mitochondrial Ef-Tu In Complex With Gdp [gi:6137414] |   View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 46391691 | | CID | 8977 | | Outcome | Active | | BioAssay | Experimentally measured binding affinity data derived from PDB | | AID | 1811 | | BioAssay type | Literature | | Target | Chain A, Crystal Structure Of Mitochondrial Ef-Tu In Complex With Gdp [gi:6137414] | | PubMed | 10715211 | | Data Table |  |
|
| 12 | [SID103497415] | Unspecified | IC50 | 67 | Inhibitory activity against fucosyltransferase (FucT V) in the presence of fucosyl acceptor N-acetyllactosamine [AID72098, Type: Literature] | |   View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103497415 | | CID | 8977 | | Outcome | Unspecified | | IC50 | 67 [uM] | | BioAssay | Inhibitory activity against fucosyltransferase (FucT V) in the presence of fucosyl acceptor N-acetyllactosamine | | AID | 72098 | | BioAssay type | Literature | | Target | | | PubMed | 11459637 | | Data Table |  |
|
| 13 | [SID103497415] | Unspecified | Kd | 373 | Binding affinity to Escherichia coli KPR [AID269136, Type: Literature] | |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103497415 | | CID | 8977 | | Outcome | Unspecified | | Kd | 373 [uM] | | BioAssay | Binding affinity to Escherichia coli KPR | | AID | 269136 | | BioAssay type | Literature | | Target | | | PubMed | 16884311 | | Data Table |  |
|
| 14 | [SID103497415] | Unspecified | | | Induction of phagocytosis in Wistar rat microglia assessed as uptake of microspheres at 100 uM after 20 mins by FACS [AID330929, Type: Literature] | |   View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103497415 | | CID | 8977 | | Outcome | Unspecified | | BioAssay | Induction of phagocytosis in Wistar rat microglia assessed as uptake of microspheres at 100 uM after 20 mins by FACS | | AID | 330929 | | BioAssay type | Literature | | Target | | | PubMed | 17410128 | | Data Table |  |
|
| 15 | [SID103497415] | Unspecified | | | Agonist activity at human recombinant P2Y2 receptor expressed in 1321N1 cells assessed as PLC-mediated [3H]IP production relative to UTP [AID271169, Type: Literature] | P2Y purinoceptor 2 [gi:311033490] |   View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 103497415 | | CID | 8977 | | Outcome | Unspecified | | BioAssay | Agonist activity at human recombinant P2Y2 receptor expressed in 1321N1 cells assessed as PLC-mediated [3H]IP production relative to UTP | | AID | 271169 | | BioAssay type | Literature | | Target | P2Y purinoceptor 2 [gi:311033490] | | PubMed | 16942026 | | Data Table |  |
|
| 16 | [SID103497415] | Unspecified | | | Agonist activity at human recombinant P2Y4 receptor expressed in 1321N1 cells assessed as PLC-mediated [3H]IP production relative to UTP [AID271170, Type: Literature] | P2Y purinoceptor 4 [gi:1709524] |   View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 103497415 | | CID | 8977 | | Outcome | Unspecified | | BioAssay | Agonist activity at human recombinant P2Y4 receptor expressed in 1321N1 cells assessed as PLC-mediated [3H]IP production relative to UTP | | AID | 271170 | | BioAssay type | Literature | | Target | P2Y purinoceptor 4 [gi:1709524] | | PubMed | 16942026 | | Data Table |  |
|
| 17 | [SID103497415] | Unspecified | | | Agonist activity at human recombinant P2Y6 receptor expressed in 1321N1 cells assessed as PLC-mediated [3H]IP production relative to UDP [AID271168, Type: Literature] | P2Y purinoceptor 6 [gi:2495018] |   View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 103497415 | | CID | 8977 | | Outcome | Unspecified | | BioAssay | Agonist activity at human recombinant P2Y6 receptor expressed in 1321N1 cells assessed as PLC-mediated [3H]IP production relative to UDP | | AID | 271168 | | BioAssay type | Literature | | Target | P2Y purinoceptor 6 [gi:2495018] | | PubMed | 16942026 | | Data Table |  |
|
| 18 | [SID26756683] | Inactive | Potency | 2.8184 | 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. | 18 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | 2.8184 [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 |  |
|
| 19 | [SID26756683] | Inactive | Potency | 2.8184 | 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. | 19 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | 2.8184 [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 |  |
|
| 20 | [SID26756683] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate [AID2112, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate | | AID | 2112 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
|
| 21 | [SID26756683] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate [AID2112, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate | | AID | 2112 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
|
| 22 | [SID26756683] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate [AID2112, Type: confirmatory] | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of Human alpha-Glucosidase From Spleen Homogenate | | AID | 2112 | | BioAssay type | confirmatory | | Target | lysosomal alpha-glucosidase preproprotein [Homo sapiens] [gi:119393891] | | PubMed | | | Data Table |  |
|
| 23 | [SID26756683] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease [AID2101, Type: confirmatory] | glucocerebrosidase [Homo sapiens] [gi:496369] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease | | AID | 2101 | | BioAssay type | confirmatory | | Target | glucocerebrosidase [Homo sapiens] [gi:496369] | | PubMed | | | Data Table |  |
|
| 24 | [SID26756683] | Inactive | Potency | | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease [AID2101, Type: confirmatory] | glucocerebrosidase [Homo sapiens] [gi:496369] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors and Activators of N370S glucocerebrosidase as a Potential Chaperone Treatment of Gaucher Disease | | AID | 2101 | | BioAssay type | confirmatory | | Target | glucocerebrosidase [Homo sapiens] [gi:496369] | | PubMed | | | Data Table |  |
|
| 25 | [SID26756683] | Inactive | Potency | | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 26 | [SID26756683] | Inactive | Potency | | qHTS Assay for Inhibitors of GCN5L2 [AID504327, Type: confirmatory] | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of GCN5L2 | | AID | 504327 | | BioAssay type | confirmatory | | Target | histone acetyltransferase KAT2A [Homo sapiens] [gi:153791535] | | PubMed | | | Data Table |  |
|
| 27 | [SID26756683] | 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. | 27 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | 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 |  |
|
| 28 | [SID26756683] | 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. | 28 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | 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 |  |
|
| 29 | [SID26756683] | 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. | 29 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | 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 |  |
|
| 30 | [SID26756683] | 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. | 30 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | 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 |  |
|
| 31 | [SID26756683] | Inactive | Potency | | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 32 | [SID26756683] | Inactive | Potency | | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding [AID1460, Type: confirmatory] | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Tau Fibril Formation, Thioflavin T Binding | | AID | 1460 | | BioAssay type | confirmatory | | Target | Microtubule-associated protein tau [Homo sapiens] [gi:92096784] | | PubMed | | | Data Table |  |
|
| 33 | [SID26756683] | 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. | 33 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | 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 |  |
|
| 34 | [SID26756683] | 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. | 34 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | 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 |  |
|
| 35 | [SID26756683] | Inactive | Potency | | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization [AID1463, Type: confirmatory] | |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Counterscreen qHTS for Inhibitors of Tau Fibril Formation, Fluorescence Polarization | | AID | 1463 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 36 | [SID26756683] | 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. | 36 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | 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 |  |
|
| 37 | [SID26756683] | Inactive | Potency | | Quantitative High-Throughput Screen for Regulators of Epigenetic Control [AID1865, Type: confirmatory] | |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Quantitative High-Throughput Screen for Regulators of Epigenetic Control | | AID | 1865 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 38 | [SID26756683] | Inactive | Potency | | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in absence of CPT [AID686978, Type: confirmatory] | |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [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 | | | PubMed | | | Data Table |  |
|
| 39 | [SID26756683] | Inactive | Potency | | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT [AID686979, Type: confirmatory] | |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in presence of CPT | | AID | 686979 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 40 | [SID26756683] | 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. | 40 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | 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 |  |
|
| 41 | [SID26756683] | 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. | 41 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | 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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| 42 | [SID26756683] | Inactive | Potency | | 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. | 42 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [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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| 43 | [SID26756683] | Inactive | Potency | | qHTS Assay for Identification of Novel General Anesthetics [AID485281, Type: confirmatory] | Chain A, Horse Spleen Apoferritin [gi:254220970] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Identification of Novel General Anesthetics | | AID | 485281 | | BioAssay type | confirmatory | | Target | Chain A, Horse Spleen Apoferritin [gi:254220970] | | PubMed | | | Data Table |  |
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| 44 | [SID26756683] | Inactive | Potency | | 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. | 44 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [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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| 45 | [SID26756683] | Inactive | | | qHTS Assay for Inhibitors of RGS12 GoLoco Motif Activity (Red Fluorophore) [AID880, Type: confirmatory] | RGS12 [Homo sapiens] [gi:3290016] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | 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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| 46 | [SID26756683] | Inactive | Potency | | qHTS for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 [AID1469, Type: confirmatory] | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | | AID | 1469 | | BioAssay type | confirmatory | | Target | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] | | PubMed | | | Data Table |  |
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| 47 | [SID26756683] | Inactive | Potency | | qHTS for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 [AID1469, Type: confirmatory] | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | | AID | 1469 | | BioAssay type | confirmatory | | Target | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] | | PubMed | | | Data Table |  |
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| 48 | [SID26756683] | Inactive | Potency | | qHTS for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 [AID1469, Type: confirmatory] | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | | AID | 1469 | | BioAssay type | confirmatory | | Target | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] | | PubMed | | | Data Table |  |
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| 49 | [SID26756683] | Inactive | Potency | | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 [AID1479, Type: confirmatory] | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | | AID | 1479 | | BioAssay type | confirmatory | | Target | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] | | PubMed | | | Data Table |  |
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| 50 | [SID26756683] | Inactive | Potency | | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 [AID1479, Type: confirmatory] | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 26756683 | | CID | 8977 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Total Fluorescence Counterscreen for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2 | | AID | 1479 | | BioAssay type | confirmatory | | Target | thyroid hormone receptor beta [Homo sapiens] [gi:189491771] | | PubMed | | | Data Table |  |
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