BDBM50508998 CHEMBL3747907

SMILES Clc1ccc(OCCCCCCCN2CCCCC2)cc1

InChI Key InChIKey=BNRCWTHOFLFDDE-UHFFFAOYSA-N

Data  3 KI  5 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 8 hits for monomerid = 50508998   

TargetAcetylcholinesterase(Electric eel)
Julius Maximilian University of W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50508998(CHEMBL3747907)
Affinity DataIC50: 3.90E+3nMAssay Description:Inhibition of electric eel AChEMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/19/2021
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Julius Maximilian University of W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50508998(CHEMBL3747907)
Affinity DataIC50: 3.94E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/27/2021
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Jagiellonian University Medical College

Curated by ChEMBL
LigandPNGBDBM50508998(CHEMBL3747907)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine chloride as substrate preincubated for 5 mins followed by substrate addition measured after ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/27/2021
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Julius Maximilian University of W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50508998(CHEMBL3747907)
Affinity DataIC50: 3.94E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/27/2021
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Jagiellonian University Medical College

Curated by ChEMBL
LigandPNGBDBM50508998(CHEMBL3747907)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine chloride as substrate preincubated for 5 mins followed by substrate addition measured after ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/27/2021
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Julius Maximilian University of W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50508998(CHEMBL3747907)
Affinity DataKi:  128nMAssay Description:Inhibition of human histamine H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/19/2021
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Julius Maximilian University of W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50508998(CHEMBL3747907)
Affinity DataKi:  128nMAssay Description:Displacement of [3H]Nalpha-methylhistamine from human full length recombinant histamine H3 receptor expressed in HEK293 cell membranes after 90 mins ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/27/2021
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Julius Maximilian University of W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50508998(CHEMBL3747907)
Affinity DataKi:  128nMAssay Description:Displacement of [3H]Nalpha-methylhistamine from human full length recombinant histamine H3 receptor expressed in HEK293 cell membranes after 90 mins ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/27/2021
Entry Details Article
PubMed