BDBM50018303 11-[2-(2-Dipropylaminomethyl-piperidin-1-yl)-acetyl]-5,11-dihydro-benzo[e]pyrido[3,2-b][1,4]diazepin-6-one::CHEMBL46390

SMILES CCCN(CCC)CC1CCCCN1CC(=O)N1c2ccccc2C(=O)Nc2cccnc12

InChI Key InChIKey=LKNIGFDMQKJKEG-UHFFFAOYSA-N

Data  4 IC50

  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 = 50018303   

TargetMuscarinic acetylcholine receptor M2(RAT)
Dr. Karl Thomae

Curated by ChEMBL
LigandPNGBDBM50018303(11-[2-(2-Dipropylaminomethyl-piperidin-1-yl)-acety...)
Affinity DataIC50:  1.50E+3nMAssay Description:Binding affinity to the rat cardiac muscarinic acetylcholine receptor M2 using 0.3 nM [3H]-N-methylscopolamine as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMuscarinic acetylcholine receptor M3(RAT)
College Of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50018303(11-[2-(2-Dipropylaminomethyl-piperidin-1-yl)-acety...)
Affinity DataIC50:  6.00E+3nMAssay Description:Inhibition of rat submandibular muscarinic (M3) receptor isolated from tissue homogenatesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMuscarinic acetylcholine receptor M2(RAT)
Dr. Karl Thomae

Curated by ChEMBL
LigandPNGBDBM50018303(11-[2-(2-Dipropylaminomethyl-piperidin-1-yl)-acety...)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of muscarinic (M2) receptor isolated from rat atriaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMuscarinic acetylcholine receptor M3(RAT)
College Of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50018303(11-[2-(2-Dipropylaminomethyl-piperidin-1-yl)-acety...)
Affinity DataIC50:  6.00E+3nMAssay Description:Binding affinity for glandular muscarinic acetylcholine receptor M3 in rat assayed using 0.3 nM [3H]-N-methylscopolamine as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed