BDBM50226767 CHEMBL160553
SMILES [Br-].C[N+]1(CC#CCN2CCCC2=O)CC1
InChI Key InChIKey=UDOCPFRWZFCDBG-UHFFFAOYSA-N
Data 1 EC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 6 hits for monomerid = 50226767
Affinity DataIC50: 6.95E+3nMAssay Description:Inhibition of dihydrofolate reductase enzyme purified from Escherichia coli at 1x10E6 MMore data for this Ligand-Target Pair
Affinity DataIC50: 6.85E+3nMAssay Description:Inhibition of dihydrofolate reductase enzyme purified from Escherichia coli at 1x10E6 MMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Kansas State University
Curated by ChEMBL
Kansas State University
Curated by ChEMBL
Affinity DataIC50: 2.76E+4nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: 7.41E+3nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of dihydrofolate reductase enzyme purified from Escherichia coli at 1x10E6 MMore data for this Ligand-Target Pair