BDBM50398840 CHEMBL2177529

SMILES C1NCC2CC1CC(=C2)c1ccc(nc1)-c1ccccc1

InChI Key InChIKey=ULUVSICUEWOINW-UHFFFAOYSA-N

Data  2 KI  2 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50398840   

LigandPNGBDBM50398840(CHEMBL2177529)
Affinity DataEC50:  9.66E+3nMAssay Description:Agonist activity at human alpha4beta2 nAChR low sensitivity form expressed in human SH-EP1 cells assessed as increase in calcium flux by FLIPRMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50398840(CHEMBL2177529)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at human alpha4beta2 nAChR high sensitivity form expressed in human SH-EP1 cells assessed as increase in calcium flux by FLIPRMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50398840(CHEMBL2177529)
Affinity DataKi:  105nMAssay Description:Displacement of [3H]nicotine from human alpha4beta2 nAChR expressed in human SH-EP1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50398840(CHEMBL2177529)
Affinity DataKi:  590nMAssay Description:Displacement of [3H]epibatidine from human alpha7 nAChR expressed in human HEK/RIC3 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed