BDBM141816 US8921397, 58

SMILES O=C(N[C@H]1CC[C@H](CCN2CCC(CC2)c2coc3ccccc23)CC1)c1ccc2OCOc2c1

InChI Key InChIKey=MASFGJOTAOERQU-UHFFFAOYSA-N

Data  3 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 141816   

TargetD(3) dopamine receptor(Human)
Hoffmann-La Roche

US Patent
LigandPNGBDBM141816(US8921397, 58)
Affinity DataKi:  2.79nMAssay Description:liquots of membrane preparations were thawed at RT, resuspended in assay buffer (D2, D3: 50 mM Tris-HCl, 120 mM NaCl, 5 mM MgCl2, 1 mM EDTA, 5 mM KC1...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/26/2015
Entry Details
Go to US Patent

Target5-hydroxytryptamine receptor 2A(Human)
Hoffmann-La Roche

US Patent
LigandPNGBDBM141816(US8921397, 58)
Affinity DataKi:  8.78nMAssay Description:liquots of membrane preparations were thawed at RT, resuspended in assay buffer (D2, D3: 50 mM Tris-HCl, 120 mM NaCl, 5 mM MgCl2, 1 mM EDTA, 5 mM KC1...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/26/2015
Entry Details
Go to US Patent

TargetD(2) dopamine receptor(Human)
Hoffmann-La Roche

US Patent
LigandPNGBDBM141816(US8921397, 58)
Affinity DataKi:  28.6nMAssay Description:liquots of membrane preparations were thawed at RT, resuspended in assay buffer (D2, D3: 50 mM Tris-HCl, 120 mM NaCl, 5 mM MgCl2, 1 mM EDTA, 5 mM KC1...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/26/2015
Entry Details
Go to US Patent