null

SMILES CN1C[C@@H]2C[C@H]1CN2c1ccc(nn1)-c1ccc2sccc2c1

InChI Key InChIKey=SLGFKQGLWGSOOE-GJZGRUSLSA-N

  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 3 hits for monomerid = 50319938   

TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Abbott Park

Curated by ChEMBL
LigandPNGBDBM50319938((1S,4S)-2-(6-(benzo[b]thiophen-5-yl)pyridazin-3-yl...)copy SMILEScopy InChI
Affinity DataKi:  1.80nMAssay Description:Displacement of [3H]dofetidile from human ERG by whole-cell patch clampMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC905NPubMed
TargetNeuronal acetylcholine receptor subunit alpha-7(Rattus norvegicus (Rat))
Abbott Park

Curated by ChEMBL
LigandPNGBDBM50319938((1S,4S)-2-(6-(benzo[b]thiophen-5-yl)pyridazin-3-yl...)copy SMILEScopy InChI
Affinity DataKi:  3.10nMAssay Description:Displacement of [3H]A585539 from alpha7 nACHR in rat brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC905NPubMed
TargetNeuronal acetylcholine receptor subunit alpha-7(Homo sapiens (Human))
Abbott Park

Curated by ChEMBL
LigandPNGBDBM50319938((1S,4S)-2-(6-(benzo[b]thiophen-5-yl)pyridazin-3-yl...)copy SMILEScopy InChI
Affinity DataEC50:  1.50E+3nMAssay Description:Agonist activity at human alpha7 nACHR expressed in Xenopus oocyte assessed as activation of current by voltage clamp methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MC905NPubMed