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SMILES COCCCN1CCC(CC1)c1nnc(o1)-c1nn(C(C)C)c2ccccc12

InChI Key InChIKey=DWTFBJGTRBMHPG-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 325561   

Target5-hydroxytryptamine receptor 4(Homo sapiens (Human))
SUVEN LIFE SCIENCES LIMITED

US Patent
LigandPNGBDBM325561(1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...)copy SMILEScopy InChI
Affinity DataEC50:  38nMAssay Description:A stable CHO cell line expressing recombinant human 5-HT4 receptor and pCRE-Luc reporter system was used for cell-based assay. The assay offers a non...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PG1TTQUS Patent
Target5-hydroxytryptamine receptor 4(Homo sapiens (Human))
SUVEN LIFE SCIENCES LIMITED

US Patent
LigandPNGBDBM325561(1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...)copy SMILEScopy InChI
Affinity DataEC50:  44nMAssay Description:Antagonist potency against carbachol induced contractions of isolated guinea pig ileum Muscarinic acetylcholine receptorMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM325561(1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails
TargetCytochrome P450 3A4(Homo sapiens (Human))TBA
LigandPNGBDBM325561(1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...)copy SMILEScopy InChI
Affinity DataIC50: 9.10E+3nMAssay Description:Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails
Target5-hydroxytryptamine receptor 4(Homo sapiens (Human))
SUVEN LIFE SCIENCES LIMITED

US Patent
LigandPNGBDBM325561(1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...)copy SMILEScopy InChI
Affinity DataEC50:  32nMAssay Description:Inhibitory activity against Dihydrofolate reductase obtained from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM325561(1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...)copy SMILEScopy InChI
Affinity DataEC50:  185nMAssay Description:Inhibitory activity against Escherichia coli dihydrofolate reductase at 10e8 MMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM325561(1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...)copy SMILEScopy InChI
Affinity DataEC50:  59nMAssay Description:Inhibitory activity against Escherichia coli dihydrofolate reductase at 10e8 MMore data for this Ligand-Target Pair
In DepthDetails
Target5-hydroxytryptamine receptor 4(Homo sapiens (Human))
SUVEN LIFE SCIENCES LIMITED

US Patent
LigandPNGBDBM325561(1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...)copy SMILEScopy InChI
Affinity DataEC50:  32nMAssay Description:Inhibitory activity against Escherichia coli dihydrofolate reductase at 10e8 MMore data for this Ligand-Target Pair
In DepthDetails
Target5-hydroxytryptamine receptor 4(Homo sapiens (Human))
SUVEN LIFE SCIENCES LIMITED

US Patent
LigandPNGBDBM325561(1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...)copy SMILEScopy InChI
Affinity DataEC50:  32nMAssay Description:Inhibitory activity against Dihydrofolate reductase obtained from E. coli; Range 0.005-0.007More data for this Ligand-Target Pair
In DepthDetails
TargetCytochrome P450 2D6(Homo sapiens (Human))TBA
LigandPNGBDBM325561(1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...)copy SMILEScopy InChI
Affinity DataIC50: 4.50E+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
In DepthDetails