Assay ID | Title | Year | Journal | Article |
AID613176 | Inhibition of IKK-beta expressed in Escherichia coli or baculovirus-infected insect cells by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613148 | Inhibition of AKT2 expressed in Escherichia coli or baculovirus-infected insect cells using gamma-[33P]ATP at 400 uM by scintillation proximity assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID1891831 | Lipid-water distribution ratio of the compound | 2022 | Journal of medicinal chemistry, 05-12, Volume: 65, Issue:9
| Development of Azaindole-Based Frameworks as Potential Antiviral Agents and Their Future Perspectives. |
AID613155 | Inhibition of ErbB2 expressed in Escherichia coli or baculovirus-infected insect cells at 400 uM by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID286921 | Inhibition of PC3M cells by SRB assay after 96 hrs | 2007 | Journal of medicinal chemistry, May-17, Volume: 50, Issue:10
| Rapid evolution of 6-phenylpurine inhibitors of protein kinase B through structure-based design. |
AID613174 | Inhibition of AKT1 expressed in Escherichia coli or baculovirus-infected insect cells by scintillation proximity assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613160 | Inhibition of ITK expressed in Escherichia coli or baculovirus-infected insect cells at 667 uM by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613170 | Inhibition of RIP2 expressed in Escherichia coli or baculovirus-infected insect cells at 400 uM by fluorescence polarization assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID1781832 | Inhibition of Axl (unknown origin) using 5'FAM labeled KKKKEEIYFFF-NH2 peptide as substrate incubated for 1.5 hrs | 2021 | Bioorganic & medicinal chemistry, 11-01, Volume: 49 | Fragment-based lead discovery of indazole-based compounds as AXL kinase inhibitors. |
AID613175 | Inhibition of JNK1 expressed in Escherichia coli or baculovirus-infected insect cells by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613152 | Inhibition of B-Raf expressed in Escherichia coli or baculovirus-infected insect cells using ATP as substrate at 400 uM by fluorescence polarization assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613169 | Inhibition of PIM1 expressed in Escherichia coli or baculovirus-infected insect cells at 400 uM by IMAP assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID1254099 | Binding affinity to rabbit muscle glycogen phosphorylase by STD NMR spectrometric analysis | 2015 | Journal of medicinal chemistry, Nov-12, Volume: 58, Issue:21
| Ligand-Orientation Based Fragment Selection in STD NMR Screening. |
AID613157 | Inhibition of FAK expressed in Escherichia coli or baculovirus-infected insect cells at 400 uM by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613167 | Inhibition of PI3Kalpha expressed in Escherichia coli or baculovirus-infected insect cells using gamma-[33P]ATP at 400 uM by scintillation proximity assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID327087 | Inhibition of PKBbeta recombinant by radiometric filter binding assay | 2008 | Journal of medicinal chemistry, Apr-10, Volume: 51, Issue:7
| Identification of 4-(4-aminopiperidin-1-yl)-7H-pyrrolo[2,3-d]pyrimidines as selective inhibitors of protein kinase B through fragment elaboration. |
AID613159 | Inhibition of IGF1R expressed in Escherichia coli or baculovirus-infected insect cells at 400 uM by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613154 | Inhibition of FES expressed in Escherichia coli or baculovirus-infected insect cells using ATP as substrate at 400 uM by fluorescence polarization assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613143 | Inhibition of IKK-beta expressed in Escherichia coli or baculovirus-infected insect cells at 667 uM by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613163 | Inhibition of p38alpha expressed in Escherichia coli or baculovirus-infected insect cells at 667 uM by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613156 | Inhibition of ErbB4 expressed in Escherichia coli or baculovirus-infected insect cells at 400 to 667 uM by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613161 | Inhibition of JAK3 expressed in Escherichia coli or baculovirus-infected insect cells at 667 uM by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID70363 | The binding affinity towards N-labeled Erythromycin-resistant ErmAM methylase evaluated by NMR | 1999 | Journal of medicinal chemistry, Sep-23, Volume: 42, Issue:19
| Novel inhibitors of Erm methyltransferases from NMR and parallel synthesis. |
AID613151 | Inhibition of AurB expressed in Escherichia coli or baculovirus-infected insect cells at 400 uM by IMAP assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613173 | Inhibition of SYK expressed in Escherichia coli or baculovirus-infected insect cells at 667 uM by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID73213 | Residual porcine GSK-3-alpha/beta kinase activity with L240C/N297Q mutant cytochrome P450 2A6 extract | 2004 | Journal of medicinal chemistry, Jun-03, Volume: 47, Issue:12
| Generation of new protein kinase inhibitors utilizing cytochrome p450 mutant enzymes for indigoid synthesis. |
AID613172 | Inhibition of SGK1 expressed in Escherichia coli or baculovirus-infected insect cells at 400 uM by IMAP assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613145 | Inhibition of JNK1 expressed in Escherichia coli or baculovirus-infected insect cells at 667 uM by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID1254102 | Binding affinity to ERK1 (unknown origin) expressed in Escherichia coli by STD NMR spectrometric analysis | 2015 | Journal of medicinal chemistry, Nov-12, Volume: 58, Issue:21
| Ligand-Orientation Based Fragment Selection in STD NMR Screening. |
AID1596624 | Inhibition of recombinant His-tagged MTH1 (unknown origin) expressed in Escherichia coli BL21(DE3) cells using dGTP as substrate incubated for 15 mins by malachite green dye based pyrophosphatase coupled colorimetric assay | 2019 | European journal of medicinal chemistry, Aug-01, Volume: 175 | Ligand retargeting by binding site analogy. |
AID613165 | Inhibition of PAK2 expressed in Escherichia coli or baculovirus-infected insect cells at 400 uM by IMAP assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613153 | Inhibition of EGFR expressed in Escherichia coli or baculovirus-infected insect cells at 400 uM by TR-FRET assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613158 | Inhibition of GSK3-beta expressed in Escherichia coli or baculovirus-infected insect cells using ATP as substrate at 667 uM by fluorescence polarization assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613162 | Inhibition of MK2 expressed in Escherichia coli or baculovirus-infected insect cells at 667 uM by IMAP assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613168 | Inhibition of PI3Kdelta expressed in Escherichia coli or baculovirus-infected insect cells using gamma-[33P]ATP at 400 uM by scintillation proximity assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613150 | Inhibition of AurA expressed in Escherichia coli or baculovirus-infected insect cells at 400 uM by IMAP assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID613147 | Inhibition of AKT1 expressed in Escherichia coli or baculovirus-infected insect cells using gamma-[33P]ATP at 400 uM by scintillation proximity assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID1891830 | Basic dissociation constant, pKa of the compound | 2022 | Journal of medicinal chemistry, 05-12, Volume: 65, Issue:9
| Development of Azaindole-Based Frameworks as Potential Antiviral Agents and Their Future Perspectives. |
AID613166 | Inhibition of PDK1 expressed in Escherichia coli or baculovirus-infected insect cells using gamma-[33P]ATP at 400 uM by scintillation proximity assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID54188 | Residual Cyclin-dependent kinase 5-p35nck5a activity with L240C/N297Q mutant cytochrome P450 2A6 extract | 2004 | Journal of medicinal chemistry, Jun-03, Volume: 47, Issue:12
| Generation of new protein kinase inhibitors utilizing cytochrome p450 mutant enzymes for indigoid synthesis. |
AID613171 | Inhibition of ROCK1 expressed in Escherichia coli or baculovirus-infected insect cells at 400 uM by IMAP assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID286920 | Inhibition of PKA by radiometric filter binding assay | 2007 | Journal of medicinal chemistry, May-17, Volume: 50, Issue:10
| Rapid evolution of 6-phenylpurine inhibitors of protein kinase B through structure-based design. |
AID1596626 | Binding affinity to recombinant His-tagged MTH1 (unknown origin) expressed in Escherichia coli BL21(DE3) assessed as dissociation constant by isothermal titration calorimetry | 2019 | European journal of medicinal chemistry, Aug-01, Volume: 175 | Ligand retargeting by binding site analogy. |
AID613149 | Inhibition of ASK1 expressed in Escherichia coli or baculovirus-infected insect cells at 667 uM by IMAP assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID1596625 | Binding affinity to recombinant His-tagged MTH1 (unknown origin) expressed in Escherichia coli BL21(DE3) cells by isothermal titration calorimetry | 2019 | European journal of medicinal chemistry, Aug-01, Volume: 175 | Ligand retargeting by binding site analogy. |
AID613144 | Inhibition of PI3Kgamma expressed in Escherichia coli or baculovirus-infected insect cells at 667 uM by fluorescence polarization assay | 2011 | Journal of medicinal chemistry, Jul-28, Volume: 54, Issue:14
| Selectivity of kinase inhibitor fragments. |
AID286919 | Inhibition of PKBbeta by radiometric filter binding assay | 2007 | Journal of medicinal chemistry, May-17, Volume: 50, Issue:10
| Rapid evolution of 6-phenylpurine inhibitors of protein kinase B through structure-based design. |
AID1797482 | PKB In Vitro Enzyme Assay from Article 10.1021/jm0700924: \\Rapid Evolution of 6-Phenylpurine Inhibitors of Protein Kinase B through Structure-Based Design.\\ | 2007 | Journal of medicinal chemistry, May-17, Volume: 50, Issue:10
| Rapid evolution of 6-phenylpurine inhibitors of protein kinase B through structure-based design. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |