BDBM8984 7-methyl-1,2,3,4-tetrahydroacridin-9-amine::Tacrine Analogue 1

SMILES Cc1ccc2nc3CCCCc3c(N)c2c1

InChI Key InChIKey=ZZKQNBNYCRCFCW-UHFFFAOYSA-N

Data  7 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 7 hits for monomerid = 8984   

TargetAcetylcholinesterase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM8984(7-methyl-1,2,3,4-tetrahydroacridin-9-amine | Tacri...)
Affinity DataIC50:  8.10E+3nMpH: 8.0 T: 2°CAssay Description:The cholinesterase assays were performed using colorimetric method reported by Ellman. The appearance of product was monitored at 412 nm for 5 min us...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM8984(7-methyl-1,2,3,4-tetrahydroacridin-9-amine | Tacri...)
Affinity DataIC50:  8.10E+3nMAssay Description:Inhibition of AChEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM8984(7-methyl-1,2,3,4-tetrahydroacridin-9-amine | Tacri...)
Affinity DataIC50:  8.13E+3nMAssay Description:Inhibitory activity against human erythrocyte acetylcholinesteraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuronal acetylcholine receptor subunit alpha-3/alpha-6/beta-4(Rattus norvegicus (Rat))
University Hospital Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM8984(7-methyl-1,2,3,4-tetrahydroacridin-9-amine | Tacri...)
Affinity DataIC50:  1.32E+4nMAssay Description:Inhibition of human GluN1a/GluN2B receptor expressed in HEK293 cells assessed as inhibition of glycine/glutamate-induced current measured at -60 mV h...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
University Hospital Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM8984(7-methyl-1,2,3,4-tetrahydroacridin-9-amine | Tacri...)
Affinity DataIC50:  1.37E+4nMAssay Description:Inhibition of human plasmatic BuChE assessed as reduction in cholinesterase activity by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate receptor ionotropic, NMDA 1/2A(Homo sapiens (Human))
University Hospital Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM8984(7-methyl-1,2,3,4-tetrahydroacridin-9-amine | Tacri...)
Affinity DataIC50:  1.23E+4nMAssay Description:Inhibition of human GluN1a/GluN2A receptor expressed in HEK293 cells assessed as inhibition of glycine/glutamate-induced current measured at -60 mV h...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University Of Bologna

LigandPNGBDBM8984(7-methyl-1,2,3,4-tetrahydroacridin-9-amine | Tacri...)
Affinity DataIC50:  1.55E+4nMAssay Description:Inhibition of human recombinant AChE assessed as reduction in cholinesterase activity using acetylthiocholine iodide as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed