Compile Data Set for Download or QSAR
Found 202 with Last Name = 'uliassi' and Initial = 'e'
TargetP2Y purinoceptor 14(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50512416(CHEMBL4447162)copy SMILEScopy InChI
Affinity DataKi:  0.0800nMAssay Description:Antagonist activity at human P2Y14R expressed in CHO cells assessed as inhibition of UDPG-mediated reduction of forskolin-induced [3H]cAMP production...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetP2Y purinoceptor 14(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50512416(CHEMBL4447162)copy SMILEScopy InChI
Affinity DataKi:  0.0800nMAssay Description:Antagonist activity at human P2Y14R expressed in CHO cells assessed as inhibition of UDPG-mediated reduction of forskolin-induced [3H]cAMP production...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50532693(CHEMBL4544251)copy SMILEScopy InChI
Affinity DataKi:  170nMAssay Description:Binding affinity to human H1 histamine receptor expressed in HEK cells by PDSP assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50532693(CHEMBL4544251)copy SMILEScopy InChI
Affinity DataKi:  170nMAssay Description:Binding affinity to human H1 histamine receptor expressed in HEK cells by PDSP assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetAlpha-2C adrenergic receptor(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50532693(CHEMBL4544251)copy SMILEScopy InChI
Affinity DataKi:  1.32E+3nMAssay Description:Binding affinity to human alpha2C receptor expressed in MDCK cells by PDSP assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetAlpha-2C adrenergic receptor(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50532693(CHEMBL4544251)copy SMILEScopy InChI
Affinity DataKi:  1.32E+3nMAssay Description:Binding affinity to human alpha2C receptor expressed in MDCK cells by PDSP assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetSigma non-opioid intracellular receptor 1(Cavia porcellus (Guinea pig))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50532691(CHEMBL4455037)copy SMILEScopy InChI
Affinity DataKi:  1.46E+3nMAssay Description:Binding affinity to guinea pig sigma1 receptor by PDSP assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetSigma non-opioid intracellular receptor 1(Cavia porcellus (Guinea pig))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50532691(CHEMBL4455037)copy SMILEScopy InChI
Affinity DataKi:  1.46E+3nMAssay Description:Binding affinity to guinea pig sigma1 receptor by PDSP assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50532693(CHEMBL4544251)copy SMILEScopy InChI
Affinity DataKi:  1.56E+3nMAssay Description:Binding affinity to human alpha2A receptor expressed in MDCK cells by PDSP assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetAlpha-2A adrenergic receptor(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50532693(CHEMBL4544251)copy SMILEScopy InChI
Affinity DataKi:  1.56E+3nMAssay Description:Binding affinity to human alpha2A receptor expressed in MDCK cells by PDSP assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
University of Bologna

Curated by ChEMBL
LigandPNGBDBM50278487(CHEMBL3585376)copy SMILEScopy InChI
Affinity DataKi:  2.30E+3nMAssay Description:Displacement of 125-I echistatin from Vitronectin receptor (alpha v beta3)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50B3PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50456168(CHEMBL1800685)copy SMILEScopy InChI
Affinity DataKi:  2.75E+3nMAssay Description:Binding affinity to human delta opioid receptor expressed in HEK cells by PDSP assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50456168(CHEMBL1800685)copy SMILEScopy InChI
Affinity DataKi:  2.75E+3nMAssay Description:Binding affinity to human delta opioid receptor expressed in HEK cells by PDSP assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetSigma intracellular receptor 2(Rattus norvegicus (Rat))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50532691(CHEMBL4455037)copy SMILEScopy InChI
Affinity DataKi:  3.60E+3nMAssay Description:Binding affinity to sigma 2 receptor in rat PC3 cells by PDSP assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetSigma intracellular receptor 2(Rattus norvegicus (Rat))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50532691(CHEMBL4455037)copy SMILEScopy InChI
Affinity DataKi:  3.60E+3nMAssay Description:Binding affinity to sigma 2 receptor in rat PC3 cells by PDSP assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
University of Bologna

Curated by ChEMBL
LigandPNGBDBM50278488(CHEMBL4159241)copy SMILEScopy InChI
Affinity DataKi:  4.00E+3nMAssay Description:Inhibition of Trypanosoma cruzi trypanothione reductase assessed as reduction in NADPH consumption using varying levels of trypanothione disulfide as...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50B3PubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
University of Bologna

Curated by ChEMBL
LigandPNGBDBM50278486(CHEMBL4160100)copy SMILEScopy InChI
Affinity DataKi:  5.60E+3nMAssay Description:Mixed-type inhibition of Trypanosoma cruzi trypanothione reductase assessed as reduction in NADPH consumption using varying levels of trypanothione d...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50B3PubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
University of Bologna

Curated by ChEMBL
LigandPNGBDBM77970(3-(2-chloranyl-5,6-dihydrobenzo[b][1]benzazepin-11...)copy SMILEScopy InChI
Affinity DataKi:  6.50E+3nMAssay Description:Inhibition of Trypanosoma cruzi trypanothione reductase assessed as reduction in NADPH consumption using varying levels of trypanothione disulfide as...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50B3PubMed
TargetD(3) dopamine receptor(Rattus norvegicus (Rat))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50456168(CHEMBL1800685)copy SMILEScopy InChI
Affinity DataKi:  6.79E+3nMAssay Description:Binding affinity to rat D3 dopamine receptor expressed in HEK293T cells by PDSP assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetD(3) dopamine receptor(Rattus norvegicus (Rat))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50456168(CHEMBL1800685)copy SMILEScopy InChI
Affinity DataKi:  6.79E+3nMAssay Description:Binding affinity to rat D3 dopamine receptor expressed in HEK293T cells by PDSP assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
University of Bologna

Curated by ChEMBL
LigandPNGBDBM50278489(CHEMBL4170316)copy SMILEScopy InChI
Affinity DataKi:  2.24E+4nMAssay Description:Non-competitive inhibition of Trypanosoma cruzi trypanothione reductase assessed as reduction in NADPH consumption using varying levels of trypanothi...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50B3PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50523376(CHEMBL4589980)copy SMILEScopy InChI
Affinity DataIC50: 0.00800nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetP2Y purinoceptor 14(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50456168(CHEMBL1800685)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:Antagonist activity human P2Y14R expressed in African green monkey COS7 cells assessed as inhibition of UDPG-induced [3H]inositol phosphate accumulat...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetP2Y purinoceptor 14(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50456168(CHEMBL1800685)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:Antagonist activity human P2Y14R expressed in African green monkey COS7 cells assessed as inhibition of UDPG-induced [3H]inositol phosphate accumulat...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50028685(CHEMBL3356536)copy SMILEScopy InChI
Affinity DataIC50: 0.720nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50028685(CHEMBL3356536)copy SMILEScopy InChI
Affinity DataIC50: 0.720nMAssay Description:Inhibition of human recombinant AChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50523394(CHEMBL4448188)copy SMILEScopy InChI
Affinity DataIC50: 0.730nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50231951(2,5-bis(6-((2-methoxybenzyl)(ethyl)amino)hexylamin...)copy SMILEScopy InChI
Affinity DataIC50: 1.60nMAssay Description:Inhibition of human recombinant AChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50028681(CHEMBL3356532)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMAssay Description:Inhibition of human recombinant AChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50028691(CHEMBL3356951)copy SMILEScopy InChI
Affinity DataIC50: 3.20nMAssay Description:Inhibition of human recombinant AChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetCholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50099602(CHEMBL3343931)copy SMILES
Affinity DataIC50: 3.90nMAssay Description:Inhibition of human recombinant BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50028682(CHEMBL3356533)copy SMILEScopy InChI
Affinity DataIC50: 5.40nMAssay Description:Inhibition of human recombinant AChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetCholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50028679(CHEMBL3356530)copy SMILEScopy InChI
Affinity DataIC50: 5.5nMAssay Description:Inhibition of human plasmatic BChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetP2Y purinoceptor 14(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50456168(CHEMBL1800685)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Displacement of 6-Amino-9-(2-carboxy-4-((6-(4-(4-(4-(4-(3-carboxy-6-(4-(trifluoromethyl)phenyl)-naphthalen-1-yl)phenyl)piperidin-1-yl)-butyl)-1H-1,2,...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetP2Y purinoceptor 14(Homo sapiens (Human))
National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL
LigandPNGBDBM50456168(CHEMBL1800685)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Displacement of 6-Amino-9-(2-carboxy-4-((6-(4-(4-(4-(4-(3-carboxy-6-(4-(trifluoromethyl)phenyl)-naphthalen-1-yl)phenyl)piperidin-1-yl)-butyl)-1H-1,2,...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5K34PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50523387(CHEMBL4556281)copy SMILEScopy InChI
Affinity DataIC50: 6.30nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50523391(CHEMBL4449083)copy SMILEScopy InChI
Affinity DataIC50: 6.90nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM8987(6-chloro-1,2,3,4-tetrahydroacridin-9-amine | 6-chl...)copy SMILEScopy InChI
Affinity DataIC50: 7.20nMAssay Description:Inhibition of human recombinant AChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50523377(CHEMBL4559593)copy SMILEScopy InChI
Affinity DataIC50: 7.40nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetCholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50523376(CHEMBL4589980)copy SMILEScopy InChI
Affinity DataIC50: 7.80nMAssay Description:Inhibition of human recombinant BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50028692(CHEMBL3356952)copy SMILEScopy InChI
Affinity DataIC50: 8.90nMAssay Description:Inhibition of human recombinant AChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetCholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50523387(CHEMBL4556281)copy SMILEScopy InChI
Affinity DataIC50: 9.10nMAssay Description:Inhibition of human recombinant BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50028686(CHEMBL3356537)copy SMILEScopy InChI
Affinity DataIC50: 9.20nMAssay Description:Inhibition of human recombinant AChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetCholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50523377(CHEMBL4559593)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Inhibition of human recombinant BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50028679(CHEMBL3356530)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Inhibition of human recombinant AChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetCholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50028684(CHEMBL3356535)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibition of human plasmatic BChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetCholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50028680(CHEMBL3356531)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:Inhibition of human plasmatic BChE after 5 mins by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HVDPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50523375(CHEMBL4555818)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM8987(6-chloro-1,2,3,4-tetrahydroacridin-9-amine | 6-chl...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
TargetCholinesterase(Homo sapiens (Human))
University of Hradec Kralove

Curated by ChEMBL
LigandPNGBDBM50523388(CHEMBL4556575)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Inhibition of human recombinant BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition and measured...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0S3XPubMed
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