null

SMILES CCN(CC)CCCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34

InChI Key InChIKey=XNETYORDRXPMRM-UHFFFAOYSA-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 = 50365773   

TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
School of Chemistry& Chemical Engineering of Guangxi Normal University

Curated by ChEMBL
LigandPNGBDBM50365773(CHEMBL1956552)copy SMILEScopy InChI
Affinity DataKi:  260nMAssay Description:Non-competitive inhibition of Electrophorus electricus AChE assessed as hydrolysis of acetylthiocholineiodide after 15 mins incubation by spectrophot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HH6KJXPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
School of Chemistry& Chemical Engineering of Guangxi Normal University

Curated by ChEMBL
LigandPNGBDBM50365773(CHEMBL1956552)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HH6KJXPubMed
TargetCholinesterase(Equus caballus (Horse))
School of Chemistry& Chemical Engineering of Guangxi Normal University

Curated by ChEMBL
LigandPNGBDBM50365773(CHEMBL1956552)copy SMILEScopy InChI
Affinity DataIC50: 2.81E+3nMAssay Description:Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HH6KJXPubMed