Compile Data Set for Download or QSAR
Found 170 Enz. Inhib. hit(s) with all data for entry = 50007595
TargetHistamine H3 receptor(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50281388(CHEMBL4173258)copy SMILEScopy InChI
Affinity DataKi:  11nMAssay Description:Displacement of [3H]-N-alpha-methylhistamine from human H3R expressed in HEK293 cell membranes incubated for 90 mins by liquid scintillation counting...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50458225(Ciproxifan)copy SMILEScopy InChI
Affinity DataKi:  46nMAssay Description:Displacement of [3H]-N-alpha-methylhistamine from human H3R expressed in HEK293 cell membranes incubated for 90 mins by liquid scintillation counting...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50359391(CHEMBL1929421)copy SMILEScopy InChI
Affinity DataKi:  84nMAssay Description:Displacement of [3H]-N-alpha-methylhistamine from human H3R expressed in HEK293 cell membranes incubated for 90 mins by liquid scintillation counting...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9006(6-(1,2,3,4-Tetrahydro-acridin-9-ylamino)-hexanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9011(6-(6,8-Dichloro-1,2,3,4-tetrahydro-acridin-9-ylami...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510865(CHEMBL4532770)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9018(6-(1,2,3,4-Tetrahydro-acridin-9-ylamino)-hexanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510867(CHEMBL4469239)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510868(CHEMBL4448350)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510869(CHEMBL4443426)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9009(7-(6-Chloro-1,2,3,4-tetrahydro-acridin-9-ylamino)-...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510870(CHEMBL4543251)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9016(6-(8-Chloro-1,2,3,4-tetrahydro-acridin-9-ylamino)-...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510837(CHEMBL4467284)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9012(7-(6,8-Dichloro-1,2,3,4-tetrahydro-acridin-9-ylami...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9007(7-(1,2,3,4-Tetrahydro-acridin-9-ylamino)-heptanoic...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510845(CHEMBL4556734)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9008(6-(6-Chloro-1,2,3,4-tetrahydro-acridin-9-ylamino)-...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510846(CHEMBL4590945)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510847(CHEMBL4455677)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9013(6-(1,2,3,4-Tetrahydro-acridin-9-ylamino)-hexanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9014(7-(1,2,3,4-Tetrahydro-acridin-9-ylamino)-heptanoic...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9015(6-(6-Chloro-1,2,3,4-tetrahydro-acridin-9-ylamino)-...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510848(CHEMBL4468781)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM9017(7-(6,8-Dichloro-1,2,3,4-tetrahydro-acridin-9-ylami...)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510849(CHEMBL4579667)copy SMILEScopy InChI
Affinity DataIC50: 0nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50359391(CHEMBL1929421)copy SMILEScopy InChI
Affinity DataIC50: 0.270nMAssay Description:Inhibition of recombinant human MAOA expressed in baculovirus infected BTI insect cells using p-tyramine as substrate preincubated for 30 mins follow...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM8963(CHEMBL32823 | Homodimeric Tacrine Analog 3b | N-[7...)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:Inhibition of rat brain Acetylcholinesterase using acetylthiocholine as substrate in presence of BChE inhibitor ethopropazine by spectrophotometric m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM8964(CHEMBL75274 | Homodimeric Tacrine Analog 3c | N-[8...)copy SMILEScopy InChI
Affinity DataIC50: 0.660nMAssay Description:Inhibition of rat brain Acetylcholinesterase using acetylthiocholine as substrate in presence of BChE inhibitor ethopropazine by spectrophotometric m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM10469(Bis-THA inhibitor 1c | Bis-THA inhibitor 8 | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 0.770nMAssay Description:Inhibition of rat brain Acetylcholinesterase using acetylthiocholine as substrate in presence of BChE inhibitor ethopropazine by spectrophotometric m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM10592(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)copy SMILEScopy InChI
Affinity DataIC50: 0.780nMAssay Description:Inhibition of human Acetylcholinesterase using acetylthiocholine as substrate incubated for 15 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM10592(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)copy SMILEScopy InChI
Affinity DataIC50: 0.780nMAssay Description:Inhibition of human Acetylcholinesterase using acetylthiocholine as substrate incubated for 15 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetCholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510840(CHEMBL4456928)copy SMILEScopy InChI
Affinity DataIC50: 0.860nMAssay Description:Inhibition of human serum butyrylcholinesterase using butyrylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510844(CHEMBL4451532)copy SMILEScopy InChI
Affinity DataIC50: 1.60nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate preincubated for 5 mins followed by substrate addition by E...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510843(CHEMBL4466652)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate preincubated for 5 mins followed by substrate addition by E...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510840(CHEMBL4456928)copy SMILEScopy InChI
Affinity DataIC50: 3.60nMAssay Description:Inhibition of human Acetylcholinesterase using acetylthiocholine as substrate preincubated for 20 mins followed by substrate addition by Ellman's met...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetCholinesterase(Equus caballus (Horse))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50433323(CHEMBL2376472)copy SMILEScopy InChI
Affinity DataIC50: 3.70nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated 5 mins followed by substrate addition and measured after 2 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Bos taurus (bovine))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM10592(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)copy SMILEScopy InChI
Affinity DataIC50: 4.20nMAssay Description:Inhibition of bovine erythrocyte acetylcholinesterase using acetylthiocholine as substrate incubated for 15 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Bos taurus (bovine))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM10592(7-chloro-15-methyl-10-azatetracyclo[11.3.1.0^{2,11...)copy SMILEScopy InChI
Affinity DataIC50: 4.23nMAssay Description:Inhibition of bovine erythrocyte acetylcholinesterase using acetylthiocholine as substrate incubated for 15 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetCholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM132072(US8841453, 2)copy SMILEScopy InChI
Affinity DataIC50: 4.30nMAssay Description:Inhibition of human plasma butyrylcholinesterase using butyrylthiocholine as substrate preincubated for 30 mins followed by substrate addition and me...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50006627(CHEMBL3235503)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of human acetylcholinesterase using acetylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition by Ellma...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510834(CHEMBL4569511)copy SMILEScopy InChI
Affinity DataIC50: 5.20nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate preincubated for 5 mins followed by substrate addition by E...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetCholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50006627(CHEMBL3235503)copy SMILEScopy InChI
Affinity DataIC50: 5.70nMAssay Description:Inhibition of human serum butyrylcholinesterase using butyrylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 5.70nMAssay Description:Inhibition of human acetylcholinesteraseMore data for this Ligand-Target Pair
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50510853(CHEMBL4563881)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of rat synaptosome SERT assessed as reduction in [3H]5-HT uptakeMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetSodium-dependent serotonin transporter(Rattus norvegicus (rat))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50175503(CHEMBL197696 | Dimethyl-carbamic acid (R)-2-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of rat synaptosome SERT assessed as reduction in [3H]5-HT uptakeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM8979(CHEMBL486901 | N-[2-(1-benzylpiperidin-4-yl)ethyl]...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of rat cortex homogenate acetylcholinesterase by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM50080157((RS)-tacrine(10)-hupyridone | 5-[10-(1,2,3,4-Tetra...)copy SMILEScopy InChI
Affinity DataIC50: 8.80nMAssay Description:Inhibition of rat cortex homogenate acetylcholinesterase using acetylthiocholine as substrate in presence of BChE inhibitor ethopropazine by Ellman's...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
TargetCholinesterase(Equus caballus (Horse))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM8961(1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...)copy SMILEScopy InChI
Affinity DataIC50: 11nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated followed by substrate addition and measured after 2 mins by ...More data for this Ligand-Target Pair
TargetCholinesterase(Homo sapiens (Human))
CSIR-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Inhibition of human CholinesteraseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87F3NPubMed
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