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Inhibition of human liver FBPase expressed in Escherichia coli by spectrophotometry method
Assay data:1 Active, 1 Activity ≤ 1 µM, 3 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Cytochrome P450 Family 2 Subfamily C Member 9 (CYP2C9) small molecule antagonists: luciferase reporter qHTS assay
Assay data:2931 Active, 3 Activity ≤ 1 nM, 133 Activity ≤ 1 µM, 9667 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by DepositorRelated BioAssays by Target
qHTS assay to identify small molecule antagonists of the retinoid-related orphan receptor gamma (ROR-gamma) signaling pathway
Assay data:1034 Active, 2 Activity ≤ 1 nM, 491 Activity ≤ 1 µM, 9667 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMRelated BioAssays by DepositorRelated BioAssays by Same ProjectRelated BioAssays by Target
Inhibition of FBPase (unknown origin)
Assay data:2 Active, 2 Activity ≤ 1 µM, 2 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMRelated BioAssays by Target
qHTS assay for small molecule disruptors of the mitochondrial membrane potential: Summary
Assay data:1260 Active, 187 Activity ≤ 1 µM, 10486 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by DepositorRelated BioAssays by Same Project
qHTS assay for small molecule disruptors of the mitochondrial membrane potential
Assay data:1817 Active, 1 Activity ≤ 1 nM, 393 Activity ≤ 1 µM, 10486 Tested
Agonist activity at human A1AR expressed in HEK293T/17 cells assessed as inhibition of isoproterenol-induced cAMP accumulation incubated for 10 mins by luciferase reporter assay
Assay data:14 Active, 9 Activity ≤ 1 µM, 15 Tested
Inhibition of rat FBPase
Assay data:2 Active, 1 Activity ≤ 1 µM, 2 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed Citation
qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a
Assay data:31109 Active, 1 Activity ≤ 1 nM, 5166 Activity ≤ 1 µM, 353740 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by DepositorRelated BioAssays by Same ProjectRelated BioAssays by Target
Inhibition of FBPase in human liver using fructose-2,6phosphate as a substrate
Assay data:29 Active, 28 Activity ≤ 1 µM, 29 Tested
Inhibition of FBPase in human liver
Assay data:41 Active, 39 Activity ≤ 1 µM, 43 Tested
Inhibition of p60c-src expressed in chick embryo fibroblast
Assay data:2 Active, 1 Activity ≤ 1 µM, 4 Tested
Inhibition of Rous sarcoma virus p60 v-src-induced IgG phosphorylation in tumor bearing rabbits by SDS PAGE
Assay data:3 Active, 2 Activity ≤ 1 µM, 4 Tested
Inhibition of human liver FBPase expressed in Escherichia coli by spectrophotometry
Assay data:16 Active, 4 Activity ≤ 1 µM, 58 Tested
Equilibrium constant for the interaction between inhibitor and HIV-1 Protease
Assay data:37 Active, 4 Activity ≤ 1 nM, 34 Activity ≤ 1 µM, 39 Tested
Inhibition constant against HIV-1 Protease
Assay data:45 Active, 16 Activity ≤ 1 nM, 41 Activity ≤ 1 µM, 52 Tested
Measure of Agonist Potency at human P2Y purinoceptor 2 (hP2Y2) stably expressed in 131N1 astrocytoma cell
Assay data:3 Active, 3 Activity ≤ 1 µM, 3 Tested
Concentration required to inhibit the human liver recombinant fructose-1,6-bisphosphatase.
Assay data:18 Active, 6 Activity ≤ 1 µM, 37 Tested
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