null

SMILES O=C(CCC1CCN(Cc2ccccc2)CC1)c1ccc2CCCCNc2c1

InChI Key InChIKey=PMBLXLOXUGVTGB-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 6 hits for monomerid = 50037157   

TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50037157(3-(1-Benzyl-piperidin-4-yl)-1-(2,3,4,5-tetrahydro-...)copy SMILEScopy InChI
Affinity DataIC50: 195nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6FG0PubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
Takeda Chemical Industries, Ltd.

Curated by ChEMBL
LigandPNGBDBM50037157(3-(1-Benzyl-piperidin-4-yl)-1-(2,3,4,5-tetrahydro-...)copy SMILEScopy InChI
Affinity DataIC50: 98nMAssay Description:Inhibition concentration against rat acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JS9PHXPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50037157(3-(1-Benzyl-piperidin-4-yl)-1-(2,3,4,5-tetrahydro-...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:In vitro inhibition of human recombinant AChE.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CZ37Q4PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50037157(3-(1-Benzyl-piperidin-4-yl)-1-(2,3,4,5-tetrahydro-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of AChEMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7GFMPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universidade Federal do Rio de Janeiro (UFRJ)

Curated by ChEMBL
LigandPNGBDBM50037157(3-(1-Benzyl-piperidin-4-yl)-1-(2,3,4,5-tetrahydro-...)copy SMILEScopy InChI
Affinity DataEC50:  1.14E+3nMAssay Description:In vitro reversal of vecuronium-induced neuromuscular block in guinea pig hemi-diaphragm.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CZ37Q4PubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
Takeda Chemical Industries, Ltd.

Curated by ChEMBL
LigandPNGBDBM50037157(3-(1-Benzyl-piperidin-4-yl)-1-(2,3,4,5-tetrahydro-...)copy SMILEScopy InChI
Affinity DataIC50: 97.7nMAssay Description:Inhibition of acetylcholinesterase (AChE)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2SX6C8GPubMed