BDBM50641711 CHEMBL5594994
SMILES Clc1ccc2c(c1)CC1(Cc3nnc([C@H]4CC[C@H](Oc5ccccn5)CC4)n3-2)OCCO1
InChI Key InChIKey=LFXCGLFTXRJJLT-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 7 hits for monomerid = 50641711
Affinity DataKi: 0.300nMAssay Description:Displacement of [3H]vasopressin from human V1A receptor assessed as inhibition constant by Cheng-Prusoff equation analysisMore data for this Ligand-Target Pair
Affinity DataKi: 0.300nMAssay Description:Positive allosteric modulation of human mGlu1 receptor by cell based calcium mobilizationMore data for this Ligand-Target Pair
Affinity DataIC50: 0.900nMAssay Description:Agonist activity at LXRbeta (unknown origin) expressed in human H4 cells co-expressing ABCA1 promoter measured after 48 hrs by cell-based transactiva...More data for this Ligand-Target Pair
Affinity DataKi: 1.10nMAssay Description:Agonist activity at LXRbeta (unknown origin) expressed in human H4 cells co-expressing ABCA1 promoter measured after 48 hrs by cell-based transactiva...More data for this Ligand-Target Pair
Affinity DataKi: 16nMAssay Description:Binding affinity to human Oxytocin receptor assessed as inhibition constantMore data for this Ligand-Target Pair
Affinity DataKi: 40nMAssay Description:Displacement of [3H]AVP from human Vasopressin V2 receptor assessed as dissociation constant by Cheng-Prusoff equation analysisMore data for this Ligand-Target Pair
Affinity DataKi: 40nMAssay Description:Inhibition of farnesyl transferase in NIH3T3 cell based assay in non-reducing (-DTT) conditionsMore data for this Ligand-Target Pair
