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SMILES Clc1ccc2Nc3ccccc3C(=Nc2c1)N1CCNCC1

InChI Key InChIKey=JNNOSTQEZICQQP-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50122054   

TargetMuscarinic acetylcholine receptor M1(Homo sapiens (Human))
Universit£ de Strasbourg

Curated by ChEMBL
LigandPNGBDBM50122054(8-Chloro-11-piperazin-1-yl-5H-dibenzo[b,e][1,4]dia...)copy SMILEScopy InChI
Affinity DataKi:  60.3nMAssay Description:Displacement of [3H]NMS from EGFP-fused human M1 receptor N-terminal truncated at 17 residues expressed in HEK293 cells after 22 hrs by liquid scinti...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XW4KZ2PubMed
TargetMuscarinic acetylcholine receptor M1(Homo sapiens (Human))
Universit£ de Strasbourg

Curated by ChEMBL
LigandPNGBDBM50122054(8-Chloro-11-piperazin-1-yl-5H-dibenzo[b,e][1,4]dia...)copy SMILEScopy InChI
Affinity DataEC50:  18nMAssay Description:Agonist activity at human muscarinic M1 receptor expressed in CHO-K1 cells assessed as increase of acetylcholine-induced calcium flux by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2765G9KPubMed
TargetMuscarinic acetylcholine receptor M1(Homo sapiens (Human))
Universit£ de Strasbourg

Curated by ChEMBL
LigandPNGBDBM50122054(8-Chloro-11-piperazin-1-yl-5H-dibenzo[b,e][1,4]dia...)copy SMILEScopy InChI
Affinity DataEC50:  48nMAssay Description:Agonist activity at muscarinic M1 receptor (unknown origin) expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C82F2TPubMed