null

SMILES Cl.Cc1ccc2c(N)c3CCCc3nc2c1

InChI Key

  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 = 50569760   

TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50569760(CHEMBL4857969)copy SMILES
Affinity DataIC50: 347nMAssay Description:Inhibition of human recombinant AChE assessed as reduction in cholinesterase activity using acetylthiocholine iodide as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC365GPubMed
LigandPNGBDBM50569760(CHEMBL4857969)copy SMILES
Affinity DataIC50: 1.56E+4nMAssay Description:Inhibition of human GluN1a/GluN2B receptor expressed in HEK293 cells assessed as inhibition of glycine/glutamate-induced current measured at -60 mV h...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC365GPubMed
TargetGlutamate receptor ionotropic, NMDA 1/2A(Homo sapiens (Human))TBA
LigandPNGBDBM50569760(CHEMBL4857969)copy SMILES
Affinity DataIC50: 7.68E+3nMAssay Description:Inhibition of human GluN1a/GluN2A receptor expressed in HEK293 cells assessed as inhibition of glycine/glutamate-induced current measured at -60 mV h...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC365GPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50569760(CHEMBL4857969)copy SMILES
Affinity DataIC50: 8.44E+3nMAssay Description:Inhibition of human plasmatic BuChE assessed as reduction in cholinesterase activity by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC365GPubMed