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Inhibition of FABP5 (unknown origin)
Assay data:11 Active, 8 Activity ≤ 1 µM, 14 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition of human FABP5
Assay data:6 Active, 5 Activity ≤ 1 µM, 6 Tested
Inhibition of FABP5 (unknown origin) by fluorescence polarization assay
Assay data:4 Active, 6 Tested
SummaryCompounds, ActivePubMed CitationRelated BioAssays by Target
Inhibition of FABP5 (unknown origin) assessed as inhibition constant
Assay data:3 Active, 1 Activity ≤ 1 µM, 4 Tested
FABP3, FABP5, and FABP7 Binding Assay from US Patent US20230365488: "TRUXILLIC ACID MONOESTER-DERIVATIVES AS SELECTIVE FABP5 INHIBITORS AND PHARMACEUTICAL COMPOSITIONS AND USES THEREOF"
Assay data:47 Active, 22 Activity ≤ 1 µM, 47 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMRelated BioAssays by Target
Assay data:1 Tested
SummaryPubMed CitationRelated BioAssays by Target
High Throughput Fluorescence Displacement Assay from US Patent US10968163: "Alpha-truxillic acid derivatives and pharmaceutical compositions thereof"
Assay data:34 Active, 33 Activity ≤ 1 µM, 34 Tested
Time Resolved-Fluorescence Energy Transfer (TR-FRET) Assay from US Patent US9353102: "Non-annulated thiophenylamides"
Assay data:42 Active, 40 Activity ≤ 1 µM, 42 Tested
Ligand Binding Assay from Article 10.1074/jbc.M113.514646: "Structural basis for ligand regulation of the fatty acid-binding protein 5, peroxisome proliferator-activated receptor /d (FABP5-PPAR /d) signaling pathway."
Assay data:6 Active, 2 Activity ≤ 1 µM, 6 Tested
Time Resolved-Fluorescence Energy Transfer (TR-FRET) Assay from US Patent US9278918: "Urea derivatives and their use as fatty-acid binding protein (FABP) inhibitors"
Assay data:16 Active, 14 Activity ≤ 1 µM, 16 Tested
Time Resolved-Fluorescence Energy Transfer (TR-FRET) Assay from US Patent US9604977: "Bicyclic thiophenylamide compounds"
Assay data:251 Active, 212 Activity ≤ 1 µM, 251 Tested
Binding affinity to FABP5 (unknown origin) by microscale thermophoresis analysis
Assay data:3 Tested
Displacement of 1,8-ANS from FABP5 (unknown origin) incubated for 3 mins by fluorescence based analysis
Assay data:11 Active, 30 Tested
Displacement of 1,8-ANS from FABP5 (unknown origin) at 25 uM incubated for 3 mins by fluorescence based analysis relative to control
Assay data:30 Tested
Covalent binding affinity to FABP5 at Cys67 residue in human NCI-H358 cells assessed as log2 H/L ratio at 10 uM pretreated for 3 hrs followed by N-(((6S,7R)-7-(4-chloro-3-fluorophenyl)-1,4-oxazepan-6-yl)methyl)-2-hydroxyacetamide treatment for 3 hrs by competitive TMT click chemistry pull-down experiment based LC-MS/MS analysis
Displacement of 1,8-ANS from recombinant human 6His-tagged FABP5 expressed in Escherichia coli BL21 DE3 incubated for 15 mins followed by 1,8-ANS addition and measured after 3 mins by fluorescence based assay
Assay data:10 Active, 6 Activity ≤ 1 µM, 12 Tested
Displacement of NBD-Stearate from recombinant human FABP5 measured after 30 mins by fluorescence polarization assay
Displacement of 1,8-ANS from human recombinant full length N-terminal his-tagged FABP5 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of fluorescence at 100 uM incubated for 3 mins by fluorescence based assay relative to control
Assay data:2 Tested
Displacement of 1,8-ANS from human recombinant full length N-terminal his-tagged FABP5 expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by fluorescence based assay
Assay data:12 Active, 23 Tested
Displacement of 1,8-ANS from human recombinant full length N-terminal his-tagged FABP5 expressed in Escherichia coli BL21 (DE3) at 25 uM incubated for 3 mins by fluorescence based assay relative to control
Assay data:35 Tested
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