Compile Data Set for Download or QSAR
Found 310 with Last Name = 'del prado' and Initial = 'm'
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071491(4-(1H-Imidazol-4-yl)-butyramidine | CHEMBL72156 | ...)copy SMILEScopy InChI
Affinity DataKi:  1.20nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494356(CHEMBL3088070)copy SMILEScopy InChI
Affinity DataKi:  3nMAssay Description:Displacement of [3H]AMPA from homomeric recombinant GluA2 receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071496(CHEMBL73053 | N-(4-Chloro-benzyl)-2-[4-(1H-imidazo...)copy SMILEScopy InChI
Affinity DataKi:  7.20nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM22914(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)copy SMILEScopy InChI
Affinity DataKi:  7.30nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071492(CHEMBL312341 | N-(4-Chloro-benzyl)-4-(1H-imidazol-...)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494356(CHEMBL3088070)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071488(4-(1H-Imidazol-4-ylmethyl)-benzamidine | CHEMBL736...)copy SMILEScopy InChI
Affinity DataKi:  38nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494342(CHEMBL3088072)copy SMILEScopy InChI
Affinity DataKi:  90nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494350(CHEMBL3088064)copy SMILEScopy InChI
Affinity DataKi:  100nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071494(4-(1H-Imidazol-4-ylmethyl)-N-(4-trifluoromethyl-be...)copy SMILEScopy InChI
Affinity DataKi:  140nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494355(CHEMBL3085836)copy SMILEScopy InChI
Affinity DataKi:  160nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494365(CHEMBL3085837)copy SMILEScopy InChI
Affinity DataKi:  160nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071493(4-[2-(1H-Imidazol-4-yl)-ethyl]-benzamidine | CHEMB...)copy SMILEScopy InChI
Affinity DataKi:  165nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071498(CHEMBL75100 | N-(4-Chloro-benzyl)-3-[4-(1H-imidazo...)copy SMILEScopy InChI
Affinity DataKi:  175nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494358(CHEMBL3088058)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494364(CHEMBL3088054)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50207594(2,3-Dihydroxy-6-nitro-benzo[f]quinoxaline-7-sulfon...)copy SMILEScopy InChI
Affinity DataKi:  210nMAssay Description:Inhibition of [3H]-AMPA binding to human GluR2 receptors expressed in HEK 293 cellsMore data for this Ligand-Target Pair
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071497(3-[2-(1H-Imidazol-4-yl)-ethyl]-benzamidine | CHEMB...)copy SMILEScopy InChI
Affinity DataKi:  220nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50207594(2,3-Dihydroxy-6-nitro-benzo[f]quinoxaline-7-sulfon...)copy SMILEScopy InChI
Affinity DataKi:  260nMAssay Description:Ability to displace binding of [3H]AMPA to recombinant human Ionotropic glutamate receptor AMPA 2More data for this Ligand-Target Pair
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071495(3-(1H-Imidazol-4-ylmethyl)-benzamidine | CHEMBL753...)copy SMILEScopy InChI
Affinity DataKi:  310nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071499(3-(1H-Imidazol-4-yl)-benzamidine | CHEMBL72110)copy SMILEScopy InChI
Affinity DataKi:  350nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494351(CHEMBL3088060)copy SMILEScopy InChI
Affinity DataKi:  400nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494351(CHEMBL3088060)copy SMILEScopy InChI
Affinity DataKi:  400nMAssay Description:Displacement of [3H]AMPA from homomeric recombinant GluA2 receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071489(4-(1H-Imidazol-4-ylmethyl)-N-phenethyl-benzamidine...)copy SMILEScopy InChI
Affinity DataKi:  445nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494055(CHEMBL2440699)copy SMILEScopy InChI
Affinity DataKi:  500nMAssay Description:Binding affinity to GluK1 receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2862KDBPubMed
TargetHistamine H3 receptor(GUINEA PIG)
Schering-Plough Research Institute

Curated by ChEMBL
LigandPNGBDBM50071490(4-(1H-Imidazol-4-ylmethyl)-N-(4-methoxy-benzyl)-be...)copy SMILEScopy InChI
Affinity DataKi:  513nMAssay Description:Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WH3PubMed
TargetGlutamate receptor 4(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50207594(2,3-Dihydroxy-6-nitro-benzo[f]quinoxaline-7-sulfon...)copy SMILEScopy InChI
Affinity DataKi:  600nMAssay Description:Ability to displace binding of [3H]AMPA to recombinant human Ionotropic glutamate receptor AMPA 4More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2XP75N4PubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494367(CHEMBL3087685)copy SMILEScopy InChI
Affinity DataKi:  600nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494348(CHEMBL3088069)copy SMILEScopy InChI
Affinity DataKi:  700nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50168964((3S,4aR,6S,8aR)-6-[2-(1H-Tetrazol-5-yl)-phenylamin...)copy SMILEScopy InChI
Affinity DataKi:  800nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494068(CHEMBL2440688)copy SMILEScopy InChI
Affinity DataKi:  800nMAssay Description:Binding affinity to GluK1 receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2862KDBPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494061(CHEMBL2440689)copy SMILEScopy InChI
Affinity DataKi:  900nMAssay Description:Binding affinity to GluK1 receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2862KDBPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494352(CHEMBL3088059)copy SMILEScopy InChI
Affinity DataKi:  900nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor 3(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50207594(2,3-Dihydroxy-6-nitro-benzo[f]quinoxaline-7-sulfon...)copy SMILEScopy InChI
Affinity DataKi:  900nMAssay Description:Ability to displace binding of [3H]AMPA to recombinant human Ionotropic glutamate receptor AMPA 3More data for this Ligand-Target Pair
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494346(CHEMBL3088074)copy SMILEScopy InChI
Affinity DataKi:  900nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494347(CHEMBL3088071)copy SMILEScopy InChI
Affinity DataKi:  900nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494366(CHEMBL3088068)copy SMILEScopy InChI
Affinity DataKi:  1.00E+3nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494349(CHEMBL3088066)copy SMILEScopy InChI
Affinity DataKi:  1.10E+3nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494359(CHEMBL3088055)copy SMILEScopy InChI
Affinity DataKi:  1.10E+3nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494361(CHEMBL3088062)copy SMILEScopy InChI
Affinity DataKi:  1.10E+3nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50168965((3S,4aS,6S,8aR)-6-[2-(1H-Tetrazol-5-yl)-phenoxy]-d...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+3nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494051(CHEMBL2440702)copy SMILEScopy InChI
Affinity DataKi:  1.30E+3nMAssay Description:Binding affinity to GluK1 receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2862KDBPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494362(CHEMBL3088063)copy SMILEScopy InChI
Affinity DataKi:  1.40E+3nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494059(CHEMBL2440685)copy SMILEScopy InChI
Affinity DataKi:  1.50E+3nMAssay Description:Binding affinity to GluK1 receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2862KDBPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50168964((3S,4aR,6S,8aR)-6-[2-(1H-Tetrazol-5-yl)-phenylamin...)copy SMILEScopy InChI
Affinity DataKi:  1.55E+3nMAssay Description:Inhibition of [3H]-KA binding to iontropic glutamate receptor 5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3ZDMPubMed
TargetGlutamate receptor 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50207594(2,3-Dihydroxy-6-nitro-benzo[f]quinoxaline-7-sulfon...)copy SMILEScopy InChI
Affinity DataKi:  1.60E+3nMAssay Description:Ability to displace binding of [3H]AMPA to recombinant human Ionotropic glutamate receptor AMPA 1More data for this Ligand-Target Pair
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50168965((3S,4aS,6S,8aR)-6-[2-(1H-Tetrazol-5-yl)-phenoxy]-d...)copy SMILEScopy InChI
Affinity DataKi:  1.69E+3nMAssay Description:Inhibition of [3H]-KA binding to iontropic glutamate receptor 5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3ZDMPubMed
TargetGlutamate receptor ionotropic, kainate 1(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494360(CHEMBL3085838)copy SMILEScopy InChI
Affinity DataKi:  1.70E+3nMAssay Description:Displacement of [3H]ATPA from human Gluk1 receptorMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494348(CHEMBL3088069)copy SMILEScopy InChI
Affinity DataKi:  1.70E+3nMAssay Description:Displacement of [3H]AMPA from homomeric recombinant GluA2 receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Centro de Investigaci�n Lilly

Curated by ChEMBL
LigandPNGBDBM50494362(CHEMBL3088063)copy SMILEScopy InChI
Affinity DataKi:  2.00E+3nMAssay Description:Displacement of [3H]AMPA from homomeric recombinant GluA2 receptor (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XS5ZBWPubMed
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