Compile Data Set for Download or QSAR
Found 76 with Last Name = 'lin' and Initial = 'kk'
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50084137(2-Methyl-6-(phenylethynyl)pyridine | 2-Methyl-6-ph...)copy SMILEScopy InChI
Affinity DataKi:  5.70nMAssay Description:Displacement of [3H]MPEP from mGlu5 receptor in rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216746(3-fluoro-5-(2-methylquinolin-7-yl)benzonitrile | C...)copy SMILEScopy InChI
Affinity DataKi:  22nMAssay Description:Displacement of [3H]MPEP from mGlu5 receptor in rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50210964(3-(2-methylquinolin-7-yl)benzonitrile | CHEMBL2447...)copy SMILEScopy InChI
Affinity DataKi:  72nMAssay Description:Displacement of [3H]MPEP from mGlu5 receptor in rat brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetGlycogen [starch] synthase, muscle(Homo sapiens (Human))
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50527393(CHEMBL4446895)copy SMILEScopy InChI
Affinity DataKi:  1.31E+3nMAssay Description:Competitive inhibition of C-terminal 6His-tagged human GYS1 using UDPG as substrate in presence of G-6-P by 14C-glucose incorporation based Michaelis...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MS3X64PubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50084137(2-Methyl-6-(phenylethynyl)pyridine | 2-Methyl-6-ph...)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Washington University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50391056(CHEMBL2088421)copy SMILEScopy InChI
Affinity DataIC50: 0.280nMAssay Description:Agonist activity at PPARalpha-LBD expressed in HEK293 cells co-expressing GAL4-DBD after 16 to 19 hrs by beta lactamase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66SFPubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Washington University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50099491(2-(4-(2-(3-cyclohexyl-1-(4-cyclohexylbutyl)ureido)...)copy SMILEScopy InChI
Affinity DataIC50: 0.460nMAssay Description:Agonist activity at PPARalpha-LBD expressed in HEK293 cells co-expressing GAL4-DBD after 16 to 19 hrs by beta lactamase reporter gene assayMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Washington University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50391057(CHEMBL2088422)copy SMILEScopy InChI
Affinity DataIC50: 0.590nMAssay Description:Agonist activity at PPARalpha-LBD expressed in HEK293 cells co-expressing GAL4-DBD after 16 to 19 hrs by beta lactamase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66SFPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216746(3-fluoro-5-(2-methylquinolin-7-yl)benzonitrile | C...)copy SMILEScopy InChI
Affinity DataIC50: 0.800nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216762(3-chloro-5-(2-methylquinolin-7-yl)benzonitrile | C...)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216758(3-methyl-5-(2-methylquinolin-7-yl)benzonitrile | C...)copy SMILEScopy InChI
Affinity DataIC50: 1.60nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Washington University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50099489(2-(4-{2-[1-(4-Cyclohexyl-butyl)-3-(2-methoxy-pheny...)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMAssay Description:Agonist activity at PPARalpha-LBD expressed in HEK293 cells co-expressing GAL4-DBD after 16 to 19 hrs by beta lactamase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25M66SFPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216750(5-(2-methylquinolin-7-yl)isophthalonitrile | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216749(3-(methoxymethyl)-5-(2-methylquinolin-7-yl)benzoni...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216761(3-methoxy-5-(2-methylquinolin-7-yl)benzonitrile | ...)copy SMILEScopy InChI
Affinity DataIC50: 2.40nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50210964(3-(2-methylquinolin-7-yl)benzonitrile | CHEMBL2447...)copy SMILEScopy InChI
Affinity DataIC50: 7.70nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216741(3-bromo-5-(2-methylquinolin-7-yl)benzonitrile | CH...)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216770(3-ethoxy-5-(2-methylquinolin-7-yl)benzonitrile | C...)copy SMILEScopy InChI
Affinity DataIC50: 17nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216745(5-(2-methylquinolin-7-yl)nicotinonitrile | CHEMBL2...)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216752(3-(ethylthio)-5-(2-methylquinolin-7-yl)benzonitril...)copy SMILEScopy InChI
Affinity DataIC50: 72nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216766(3-(2-methylquinolin-7-yl)-5-(trifluoromethoxy)benz...)copy SMILEScopy InChI
Affinity DataIC50: 75nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216768(3-(2-methoxyethoxy)-5-(2-methylquinolin-7-yl)benzo...)copy SMILEScopy InChI
Affinity DataIC50: 82nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216767(3-isopropoxy-5-(2-methylquinolin-7-yl)benzonitrile...)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216737(3-hydroxy-5-(2-methylquinolin-7-yl)benzonitrile | ...)copy SMILEScopy InChI
Affinity DataIC50: 360nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216769(2-(3-(2-methylquinolin-7-yl)phenyl)acetonitrile | ...)copy SMILEScopy InChI
Affinity DataIC50: 430nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetNADPH oxidase 4(Homo sapiens (Human))
Emory University

Curated by ChEMBL
LigandPNGBDBM50455025(CHEMBL4208156)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibition of Nox4 in HASMCs assessed as reduction in TGFbeta-induced increase in smooth muscle alpha actin level pretreated for 30 mins followed by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VD722WPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216747(2-methyl-7-(pyridin-3-yl)quinoline | CHEMBL231763)copy SMILEScopy InChI
Affinity DataIC50: 510nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216748(7-(3-methoxyphenyl)-2-methylquinoline | CHEMBL3948...)copy SMILEScopy InChI
Affinity DataIC50: 860nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216764(3-(ethylsulfonyl)-5-(2-methylquinolin-7-yl)benzoni...)copy SMILEScopy InChI
Affinity DataIC50: 1.09E+3nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216759(7-(3-fluorophenyl)-2-methylquinoline | CHEMBL23176...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetGlycogen [starch] synthase, muscle(Homo sapiens (Human))
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50527393(CHEMBL4446895)copy SMILEScopy InChI
Affinity DataIC50: 2.75E+3nMAssay Description:Inhibition of C-terminal 6His-tagged wild type human GYS1 using UDPG as substrate in presence of 1 mM G-6-P by 14C-glucose incorporation assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MS3X64PubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216755(2-methyl-7-m-tolylquinoline | CHEMBL231765)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+3nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetNADPH oxidase 4(Homo sapiens (Human))
Emory University

Curated by ChEMBL
LigandPNGBDBM50455023(CHEMBL4204145)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibition of Nox4 in HASMCs assessed as reduction in TGFbeta-induced increase in smooth muscle alpha actin level pretreated for 30 mins followed by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VD722WPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216754(7-(2-methoxyphenyl)-2-methylquinoline | CHEMBL2319...)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216740(1-(3-(2-methylquinolin-7-yl)phenyl)ethanone | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 4.76E+3nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216757(7-(3-(methoxymethyl)phenyl)-2-methylquinoline | CH...)copy SMILEScopy InChI
Affinity DataIC50: 5.80E+3nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetGlycogen [starch] synthase, muscle(Homo sapiens (Human))
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50527392(CHEMBL4540791)copy SMILEScopy InChI
Affinity DataIC50: 6.54E+3nMAssay Description:Inhibition of C-terminal 6His-tagged wild type human GYS1 using UDPG as substrate in presence of 1 mM G-6-P by 14C-glucose incorporation assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MS3X64PubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216753((3-(2-methylquinolin-7-yl)phenyl)methanol | CHEMBL...)copy SMILEScopy InChI
Affinity DataIC50: 8.70E+3nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216765(2-methyl-7-phenylquinoline | CHEMBL244418)copy SMILEScopy InChI
Affinity DataIC50: 9.00E+3nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216756(2-(2-methylquinolin-7-yl)benzonitrile | CHEMBL4345...)copy SMILEScopy InChI
Affinity DataIC50: 9.80E+3nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetGlycogen [starch] synthase, muscle(Homo sapiens (Human))
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50527395(CHEMBL4475137)copy SMILEScopy InChI
Affinity DataIC50: 9.82E+3nMAssay Description:Inhibition of C-terminal 6His-tagged wild type human GYS1 using UDPG as substrate in presence of 1 mM G-6-P by 14C-glucose incorporation assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MS3X64PubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216751(2-methyl-7-(3-(trifluoromethyl)phenyl)quinoline | ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216742(4-(2-methylquinolin-7-yl)benzonitrile | CHEMBL2321...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216760(3-(2-methylquinolin-7-yl)benzamide | CHEMBL231989)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216739(2-methyl-7-(3-(trifluoromethoxy)phenyl)quinoline |...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetGlycogen [starch] synthase, muscle(Homo sapiens (Human))
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50527401(CHEMBL4542006)copy SMILEScopy InChI
Affinity DataIC50: 1.01E+4nMAssay Description:Inhibition of C-terminal 6His-tagged wild type human GYS1 using UDPG as substrate in presence of 1 mM G-6-P by 14C-glucose incorporation assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MS3X64PubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216744(3-isobutoxy-5-(2-methylquinolin-7-yl)benzonitrile ...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetGlycogen [starch] synthase, muscle(Homo sapiens (Human))
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50527391(CHEMBL4557551)copy SMILEScopy InChI
Affinity DataIC50: 1.37E+4nMAssay Description:Inhibition of C-terminal 6His-tagged wild type human GYS1 using UDPG as substrate in presence of 1 mM G-6-P by 14C-glucose incorporation assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MS3X64PubMed
TargetMetabotropic glutamate receptor 5(Rattus norvegicus (Rat))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50216743(7-(3-chlorophenyl)-2-methylquinoline | CHEMBL23198...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMAssay Description:Activity at rat mGlu5 receptor expressed in CHO cells assessed as inhibition of quisqualate-stimulated calcium mobilization by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KDCPubMed
TargetGlycogen [starch] synthase, muscle(Homo sapiens (Human))
Indiana University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50527397(CHEMBL4566254)copy SMILEScopy InChI
Affinity DataIC50: 1.41E+4nMAssay Description:Inhibition of C-terminal 6His-tagged wild type human GYS1 using UDPG as substrate in presence of 1 mM G-6-P by 14C-glucose incorporation assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MS3X64PubMed
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