BDBM10622 (-)-Phenserine::(3aS)-1,3a,8-trimethyl-1H,2H,3H,3aH,8H,8aH-pyrrolo[2,3-b]indol-5-yl N-phenylcarbamate::CHEMBL54727

SMILES CN1CC[C@]2(C)C1N(C)c1ccc(OC(=O)Nc3ccccc3)cc21

InChI Key InChIKey=PBHFNBQPZCRWQP-IJHRGXPZSA-N

Data  14 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 14 hits for monomerid = 10622   

TargetAcetylcholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  22nMAssay Description:The cholinesterase assays were performed using colorimetric method reported by Ellman. The absorbance changes at 412 nm were recorded for 5 min with ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  1.56E+3nMAssay Description:The cholinesterase assays were performed using colorimetric method reported by Ellman. The absorbance changes at 412 nm were recorded for 5 min with ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  24nMpH: 8.0 T: 2°CAssay Description:The cholinesterase assays were performed using colorimetric method reported by Ellman. The absorbance changes at 412 nm were recorded for 5 min with ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  1.30E+3nMAssay Description:The cholinesterase assays were performed using colorimetric method reported by Ellman. The absorbance changes at 412 nm were recorded for 5 min with ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  24nMAssay Description:Inhibition of human acetylcholinesterase from erythrocytes (RBC)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  1.30E+3nMAssay Description:Inhibition of human ButyrylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  1.56E+3nMAssay Description:Inhibition of human plasma BChE pretreated for 30 mins by Ellman techniqueMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  1.56E+3nMAssay Description:Ability to inhibit butyrylcholinesterase (BChE), freshly prepared from human plasmaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  350nMAssay Description:Inhibitory activity against AcetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  350nMAssay Description:Inhibition acetylcholinesterase (AChE) enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Rattus norvegicus (rat))
Meiji Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibition of BuChE in Wistar rat plasma using acetylthiocholine iodide as substrate after 0.5 hrs by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
Meiji Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  28.3nMAssay Description:Inhibition of AChE in Wistar rat brain homogenate using acetylthiocholine iodide as substrate after 0.5 hrs by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  24nMAssay Description:Inhibition of human whole RBC AChE pretreated for 30 mins by Ellman techniqueMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
National Institutes Of Health

LigandPNGBDBM10622((-)-Phenserine | (3aS)-1,3a,8-trimethyl-1H,2H,3H,3...)
Affinity DataIC50:  24nMAssay Description:Ability to inhibit acetylcholinesterase (AChE), freshly prepared from human erythrocytesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed