BDBM50413824 CHEMBL473093

SMILES CCCN1CCN(CC1)c1ncc(CCN(C)CCCc2ccccc2)s1

InChI Key InChIKey=LHFFBQAOSCEDBC-UHFFFAOYSA-N

Data  1 KI  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50413824   

TargetHistamine H3 receptor(Human)
Heinrich Heine University D£Sseldorf

Curated by ChEMBL
LigandPNGBDBM50413824(CHEMBL473093)
Affinity DataKi:  3.20nMAssay Description:Displacement of [3H]-Nalpha-methylhistamine from human histamine H3 receptor expressed in HEK293T cell membranes after 60 mins by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/17/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Central University of Punjab

Curated by ChEMBL
LigandPNGBDBM50413824(CHEMBL473093)
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of Electrophorus electricus AchE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and me...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/21/2023
Entry Details
PubMed
TargetCholinesterase(Horse)
Central University of Punjab

Curated by ChEMBL
LigandPNGBDBM50413824(CHEMBL473093)
Affinity DataIC50: 1.46E+4nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured aft...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/21/2023
Entry Details
PubMed