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Found 56 with Last Name = 'ryu' and Initial = 'ck'
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462020(CHEMBL515513)
Affinity DataIC50:  550nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462028(CHEMBL4226173)
Affinity DataIC50:  570nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)
Affinity DataIC50:  600nMAssay Description:Inhibition of Cyclin-dependent kinase 2 (CDK2/cyclin A)More data for this Ligand-Target Pair
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50106501(6,7-Dichloro-5,8-quinolinequinone | 6,7-Dichloro-q...)
Affinity DataIC50:  630nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462022(CHEMBL4227412)
Affinity DataIC50:  730nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462021(CHEMBL4227020)
Affinity DataIC50:  790nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462025(CHEMBL331941)
Affinity DataIC50:  830nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462019(CHEMBL259499)
Affinity DataIC50:  840nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus 14)
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462014(CHEMBL4224853)
Affinity DataIC50:  850nMAssay Description:Inhibition of recombinant human rhinovirus protease 3C using fluorogenic-Dabcyl-KTSAVLQSGFRKME-Edan as substrate after 5 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462026(CHEMBL4229177)
Affinity DataIC50:  900nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462023(CHEMBL4226298)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462015(CHEMBL4227149)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462018(CHEMBL4225972)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462014(CHEMBL4224853)
Affinity DataIC50:  1.70E+3nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462017(CHEMBL4229199)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086650(5-(4-Iodo-phenylamino)-2-methyl-benzothiazole-4,7-...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195190(6-chloro-5-(4-ethoxyphenylamino)-1H-indazole-4,7-d...)
Affinity DataIC50:  4.90E+3nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462016(CHEMBL3213811)
Affinity DataIC50:  5.40E+3nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086652(5-(4-Methoxy-phenylamino)-2-methyl-benzothiazole-4...)
Affinity DataIC50:  5.60E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086658(2-Methyl-5-phenylamino-benzothiazole-4,7-dione | C...)
Affinity DataIC50:  6.00E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086655(2-Methyl-5-p-tolylamino-benzothiazole-4,7-dione | ...)
Affinity DataIC50:  6.00E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462024(CHEMBL4225121)
Affinity DataIC50:  6.20E+3nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086656(5-(4-Fluoro-phenylamino)-2-methyl-benzothiazole-4,...)
Affinity DataIC50:  6.30E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086651(5-(4-Bromo-phenylamino)-2-methyl-benzothiazole-4,7...)
Affinity DataIC50:  6.70E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086654(5-(4-Hydroxy-phenylamino)-2-methyl-benzothiazole-4...)
Affinity DataIC50:  6.70E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086657(5-(4-Chloro-phenylamino)-2-methyl-benzothiazole-4,...)
Affinity DataIC50:  7.00E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM5718(2,6,9-Trisubstituted purine deriv. 26 | 2-{[6-(ben...)
Affinity DataIC50:  7.00E+3nMAssay Description:Inhibition of Cyclin-dependent kinase 2 (CDK2/cyclin A)More data for this Ligand-Target Pair
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462027(CHEMBL4227809)
Affinity DataIC50:  8.30E+3nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus 14)
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50462026(CHEMBL4229177)
Affinity DataIC50:  8.40E+3nMAssay Description:Inhibition of recombinant human rhinovirus protease 3C using fluorogenic-Dabcyl-KTSAVLQSGFRKME-Edan as substrate after 5 mins by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Coxsackievirus B3 (strain Nancy))
Korea Research Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM36895(1-(2,3-dihydro-1,4-benzodioxin-6-yl)-3-(1,2,4,5-te...)
Affinity DataIC50:  1.11E+4nMAssay Description:Inhibition of human coxsackievirus B3 protease 3C expressed in Escherichia coli (BL21) using fluorogenic-Dabcyl-KEALFQGPPQFE-Edans as substrate after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195189(6-chloro-5-(3-fluorophenylamino)-1H-indazole-4,7-d...)
Affinity DataIC50:  1.18E+4nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195193(6-chloro-5-(3,4-dichlorophenylthio)-1H-indazole-4,...)
Affinity DataIC50:  1.23E+4nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195186(6-chloro-5-(4-(trifluoromethyl)phenylamino)-1H-ind...)
Affinity DataIC50:  1.24E+4nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195195(5-(3-bromophenylamino)-6-chloro-1H-indazole-4,7-di...)
Affinity DataIC50:  1.39E+4nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDNA topoisomerase 2-alpha/2-beta(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50469780(CHEMBL115665)
Affinity DataIC50:  1.51E+4nMAssay Description:Inhibitory activity against topo II-mediated decatenation of DNAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195187(6-chloro-5-(2-fluorophenylamino)-1H-indazole-4,7-d...)
Affinity DataIC50:  1.58E+4nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195192(6-chloro-5-(2,4-difluorophenylamino)-1H-indazole-4...)
Affinity DataIC50:  1.60E+4nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDNA topoisomerase 2-alpha/2-beta(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50469781(CHEMBL325088)
Affinity DataIC50:  1.73E+4nMAssay Description:Inhibitory activity against topo II-mediated decatenation of DNAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086653(5-(4-Ethoxy-phenylamino)-2-methyl-benzothiazole-4,...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195188(2-thioxo-(1,3)ditholo[4,5-beta][1,4-dithine-5,6-di...)
Affinity DataIC50:  2.50E+4nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDNA topoisomerase 2-alpha/2-beta(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50469779(CHEMBL115302)
Affinity DataIC50:  4.05E+4nMAssay Description:Inhibitory activity against DNA topoisomerase IIMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195191(6-chloro-5-(4-fluorophenylamino)-1H-indazole-4,7-d...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195184(6-chloro-5-(3,5-dimethylphenylthio)-1H-indazole-4,...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195194(1H-indazole-4,7-diamine | CHEMBL376871)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Ildong Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50195185(6-chloro-5-(3,5-difluorophenylamino)-1H-indazole-4...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Akt1 activity assessed as decrease in GSK3 phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM7533((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086656(5-(4-Fluoro-phenylamino)-2-methyl-benzothiazole-4,...)
Affinity DataIC50: >2.00E+5nMAssay Description:Inhibition of Cyclin-dependent kinase 2 (CDK2/cyclin A)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086658(2-Methyl-5-phenylamino-benzothiazole-4,7-dione | C...)
Affinity DataIC50: >2.00E+5nMAssay Description:Inhibition of Cyclin-dependent kinase 2 (CDK2/cyclin A)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM50086657(5-(4-Chloro-phenylamino)-2-methyl-benzothiazole-4,...)
Affinity DataIC50: >2.00E+5nMAssay Description:Inhibition of Cyclin-dependent kinase 2 (CDK2/cyclin A)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Ewha Womans University

Curated by ChEMBL
LigandPNGBDBM5718(2,6,9-Trisubstituted purine deriv. 26 | 2-{[6-(ben...)
Affinity DataIC50: >2.00E+5nMAssay Description:Inhibition of Cyclin-dependent kinase 4 (CDK4/cyclin Dl)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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