Compile Data Set for Download or QSAR
Found 96 with Last Name = 'dieckman' and Initial = 'dk'
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060725(2-[1,4']Bipiperidinyl-1'-yl-1-[2-(4-chloro-phenoxy...)copy SMILEScopy InChI
Affinity DataKi:  0.75nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060726(2-[1,4']Bipiperidinyl-1'-yl-1-[2-(4-chloro-phenoxy...)copy SMILEScopy InChI
Affinity DataKi:  1.40nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060725(2-[1,4']Bipiperidinyl-1'-yl-1-[2-(4-chloro-phenoxy...)copy SMILEScopy InChI
Affinity DataKi:  1.80nMAssay Description:Ability of the compound to reverse Neuropeptide Y receptor type 1-induced inhibition of forskolin-induced inhibition of forskolin-stimulated cAMPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060724(2-[1,4']Bipiperidinyl-1'-yl-1-[2-(4-chloro-phenoxy...)copy SMILEScopy InChI
Affinity DataKi:  1.90nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060721(2-(4-Chloro-phenoxymethyl)-1-methyl-3-(2-piperidin...)copy SMILEScopy InChI
Affinity DataKi:  4.60nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060722(2-[1,4']Bipiperidinyl-1'-yl-1-[2-(4-chloro-phenoxy...)copy SMILEScopy InChI
Affinity DataKi:  26nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetGlutamate receptor ionotropic, kainate 5(Homo sapiens (Human))
Eli Lilly and Company

Curated by PDSP Ki Database
LigandPNGBDBM86754(LY 466195 | LY-466195)copy SMILEScopy InChI
Affinity DataKi:  50nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060720(1'-{2-[2-(4-Chloro-phenoxymethyl)-1-methyl-1H-indo...)copy SMILEScopy InChI
Affinity DataKi:  93nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060730(1'-[2-(4-Chloro-phenoxymethyl)-1-(2-piperidin-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  98nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetGlutamate receptor 2(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:  260nMAssay Description:Ability to displace binding of [3H]AMPA to recombinant human Ionotropic glutamate receptor AMPA 2More data for this Ligand-Target Pair
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060723(1-[1,4']Bipiperidinyl-1'-yl-2-[2-(4-chloro-phenoxy...)copy SMILEScopy InChI
Affinity DataKi:  440nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060729(1'-[2-(4-Chloro-phenoxymethyl)-1-methyl-1H-indol-3...)copy SMILEScopy InChI
Affinity DataKi:  559nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
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 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86750(LY 302679 | LY-302679)copy SMILEScopy InChI
Affinity DataKi:  820nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
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
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060731(2-(2,4-Dichloro-phenoxymethyl)-1-methyl-3-piperidi...)copy SMILEScopy InChI
Affinity DataKi:  1.26E+3nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetGlutamate receptor ionotropic, kainate 5(Homo sapiens (Human))
Eli Lilly and Company

Curated by PDSP Ki Database
LigandPNGBDBM86749(LY 457691)copy SMILEScopy InChI
Affinity DataKi:  1.55E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
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 5(Homo sapiens (Human))
Eli Lilly and Company

Curated by PDSP Ki Database
LigandPNGBDBM86755(LY 458545 | LY-458545)copy SMILEScopy InChI
Affinity DataKi:  1.69E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060728((R)-2-(2,2-diphenylacetamido)-5-guanidino-N-(4-hyd...)copy SMILEScopy InChI
Affinity DataKi:  2.32E+3nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060727(2-(4-Chloro-phenoxymethyl)-1-methyl-3-piperidin-1-...)copy SMILEScopy InChI
Affinity DataKi:  2.32E+3nMAssay Description:Binding affinity for Neuropeptide Y receptor type 1 expressed in AV-12 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetGlutamate receptor ionotropic, kainate 5(Homo sapiens (Human))
Eli Lilly and Company

Curated by PDSP Ki Database
LigandPNGBDBM86752(LY 294486 | LY-294486)copy SMILEScopy InChI
Affinity DataKi:  3.06E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86751(CHEMBL14935 | LY 293558 | LY-293558)copy SMILEScopy InChI
Affinity DataKi:  3.20E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86751(CHEMBL14935 | LY 293558 | LY-293558)copy SMILEScopy InChI
Affinity DataKi:  3.20E+3nMAssay Description:Ability to displace binding of [3H]AMPA to recombinant human Ionotropic glutamate receptor AMPA 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2XP75N4PubMed
TargetGlutamate receptor ionotropic, kainate 5(Homo sapiens (Human))
Eli Lilly and Company

Curated by PDSP Ki Database
LigandPNGBDBM86750(LY 302679 | LY-302679)copy SMILEScopy InChI
Affinity DataKi:  3.41E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor ionotropic, kainate 5(Homo sapiens (Human))
Eli Lilly and Company

Curated by PDSP Ki Database
LigandPNGBDBM50168962((3S,4aR,6S,8aR)-6-(4-Carboxy-benzyl)-decahydro-iso...)copy SMILEScopy InChI
Affinity DataKi:  4.00E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor ionotropic, kainate 5(Homo sapiens (Human))
Eli Lilly and Company

Curated by PDSP Ki Database
LigandPNGBDBM86751(CHEMBL14935 | LY 293558 | LY-293558)copy SMILEScopy InChI
Affinity DataKi:  4.20E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86749(LY 457691)copy SMILEScopy InChI
Affinity DataKi:  5.50E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor ionotropic, kainate 5(Homo sapiens (Human))
Eli Lilly and Company

Curated by PDSP Ki Database
LigandPNGBDBM86756(LY 467711 | LY-467711)copy SMILEScopy InChI
Affinity DataKi:  7.40E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86755(LY 458545 | LY-458545)copy SMILEScopy InChI
Affinity DataKi:  8.30E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor ionotropic, kainate 3(Homo sapiens (Human))
Eli Lilly and Company

Curated by PDSP Ki Database
LigandPNGBDBM86754(LY 466195 | LY-466195)copy SMILEScopy InChI
Affinity DataKi:  8.90E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86751(CHEMBL14935 | LY 293558 | LY-293558)copy SMILEScopy InChI
Affinity DataKi:  9.20E+3nMAssay Description:Ability to displace binding of [3H]AMPA to recombinant human Ionotropic glutamate receptor AMPA 1More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2XP75N4PubMed
TargetGlutamate receptor 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50168962((3S,4aR,6S,8aR)-6-(4-Carboxy-benzyl)-decahydro-iso...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor 1(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86754(LY 466195 | LY-466195)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetNeuropeptide Y receptor type 4(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060727(2-(4-Chloro-phenoxymethyl)-1-methyl-3-piperidin-1-...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Affinity for human Neuropeptide Y receptor type 4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 4(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060724(2-[1,4']Bipiperidinyl-1'-yl-1-[2-(4-chloro-phenoxy...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Affinity for human Neuropeptide Y receptor type 4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 4(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060720(1'-{2-[2-(4-Chloro-phenoxymethyl)-1-methyl-1H-indo...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Affinity for human Neuropeptide Y receptor type 4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060729(1'-[2-(4-Chloro-phenoxymethyl)-1-methyl-1H-indol-3...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Affinity for human Neuropeptide Y receptor type 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060726(2-[1,4']Bipiperidinyl-1'-yl-1-[2-(4-chloro-phenoxy...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Affinity for human Neuropeptide Y receptor type 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 4(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060726(2-[1,4']Bipiperidinyl-1'-yl-1-[2-(4-chloro-phenoxy...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Affinity for human Neuropeptide Y receptor type 4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 4(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060728((R)-2-(2,2-diphenylacetamido)-5-guanidino-N-(4-hyd...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Affinity for human Neuropeptide Y receptor type 4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060729(1'-[2-(4-Chloro-phenoxymethyl)-1-methyl-1H-indol-3...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Affinity for human Neuropeptide Y receptor type 5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060727(2-(4-Chloro-phenoxymethyl)-1-methyl-3-piperidin-1-...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Affinity for human Neuropeptide Y receptor type 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50060727(2-(4-Chloro-phenoxymethyl)-1-methyl-3-piperidin-1-...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Affinity for human Neuropeptide Y receptor type 5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HQ3Z1PPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86752(LY 294486 | LY-294486)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50168962((3S,4aR,6S,8aR)-6-(4-Carboxy-benzyl)-decahydro-iso...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86754(LY 466195 | LY-466195)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86756(LY 467711 | LY-467711)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor 2(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86753(LY 525327 | LY-525327)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
TargetGlutamate receptor 4(Homo sapiens (Human))
Lilly Research Laboratories

Curated by ChEMBL
LigandPNGBDBM86751(CHEMBL14935 | LY 293558 | LY-293558)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP230DPubMed
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