null

SMILES CC(C)n1nc(-c2nnc(o2)C2CCN(CC2)C2CCC2)c2ccccc12

InChI Key InChIKey=SVIPNSAZTOJNPK-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 325596   

TargetCytochrome P450 2D6(Homo sapiens (Human))TBA
LigandPNGBDBM325596(3-[5-(1-Cyclobutyl-piperidin-4-yl)-[1,3,4]oxadiazo...)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+4nMAssay Description:The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atriaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetCytochrome P450 3A4(Homo sapiens (Human))TBA
LigandPNGBDBM325596(3-[5-(1-Cyclobutyl-piperidin-4-yl)-[1,3,4]oxadiazo...)copy SMILEScopy InChI
Affinity DataIC50: 4.50E+4nMAssay Description:Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
LigandPNGBDBM325596(3-[5-(1-Cyclobutyl-piperidin-4-yl)-[1,3,4]oxadiazo...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails