Compile Data Set for Download or QSAR
Found 255 with Last Name = 'patel' and Initial = 'hs'
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384584(CHEMBL2036807 | US9744172, Compound UNC607A)copy SMILEScopy InChI
Affinity DataKi:  0.560nMAssay Description:Inhibition of Mer using EFPIYDFLPAKKK-CONH2 as substrate by Michaelis-Menton equationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384583(CHEMBL2036806)copy SMILEScopy InChI
Affinity DataKi:  0.730nMAssay Description:Inhibition of Mer using EFPIYDFLPAKKK-CONH2 as substrate by Michaelis-Menton equationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384582(CHEMBL2036805)copy SMILEScopy InChI
Affinity DataKi:  1.40nMAssay Description:Inhibition of Mer using EFPIYDFLPAKKK-CONH2 as substrate by Michaelis-Menton equationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM17292((1S,10R,11S,14S,15S)-15-methyltetracyclo[8.7.0.0^{...)copy SMILEScopy InChI
Affinity DataKi:  2nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384585(CHEMBL2036809)copy SMILEScopy InChI
Affinity DataKi:  2nMAssay Description:Inhibition of Mer using EFPIYDFLPAKKK-CONH2 as substrate by Michaelis-Menton equationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50276802(4-OHT | Afimoxifene | TamoGel)copy SMILEScopy InChI
Affinity DataKi:  2.5nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50084948(CHEMBL195515 | GW7604)copy SMILEScopy InChI
Affinity DataKi:  2.5nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384581(CHEMBL2036804)copy SMILEScopy InChI
Affinity DataKi:  2.70nMAssay Description:Inhibition of Mer using EFPIYDFLPAKKK-CONH2 as substrate by Michaelis-Menton equationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50276802(4-OHT | Afimoxifene | TamoGel)copy SMILEScopy InChI
Affinity DataKi:  3.20nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM17292((1S,10R,11S,14S,15S)-15-methyltetracyclo[8.7.0.0^{...)copy SMILEScopy InChI
Affinity DataKi:  3.20nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384576(CHEMBL2036808)copy SMILEScopy InChI
Affinity DataKi:  4.30nMAssay Description:Inhibition of Mer using EFPIYDFLPAKKK-CONH2 as substrate by Michaelis-Menton equationMore data for this Ligand-Target Pair
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475356(CHEMBL195080)copy SMILEScopy InChI
Affinity DataKi:  7.90nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475363(CHEMBL194774)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50084948(CHEMBL195515 | GW7604)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475356(CHEMBL195080)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475364(CHEMBL370750)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475364(CHEMBL370750)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475361(CHEMBL363630)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475363(CHEMBL194774)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475361(CHEMBL363630)copy SMILEScopy InChI
Affinity DataKi:  25nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475360(CHEMBL193865)copy SMILEScopy InChI
Affinity DataKi:  25nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475360(CHEMBL193865)copy SMILEScopy InChI
Affinity DataKi:  25nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475357(CHEMBL370492)copy SMILEScopy InChI
Affinity DataKi:  63nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475358(CHEMBL192025)copy SMILEScopy InChI
Affinity DataKi:  100nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475357(CHEMBL370492)copy SMILEScopy InChI
Affinity DataKi:  126nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475358(CHEMBL192025)copy SMILEScopy InChI
Affinity DataKi:  251nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475359(CHEMBL194600)copy SMILEScopy InChI
Affinity DataKi:  631nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475362(CHEMBL193730)copy SMILEScopy InChI
Affinity DataKi:  1.59E+3nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475362(CHEMBL193730)copy SMILEScopy InChI
Affinity DataKi:  1.59E+3nMAssay Description:Binding affinity for human estrogen receptor betaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475359(CHEMBL194600)copy SMILEScopy InChI
Affinity DataKi:  3.16E+3nMAssay Description:Binding affinity for human estrogen receptor alphaMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384584(CHEMBL2036807 | US9744172, Compound UNC607A)copy SMILEScopy InChI
Affinity DataIC50: 0.150nMAssay Description:Inhibition of Mer expressed in Escherichia coli BL21 (DE3) cells using EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluid capillary electr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384583(CHEMBL2036806)copy SMILEScopy InChI
Affinity DataIC50: 0.25nMAssay Description:Inhibition of Mer expressed in Escherichia coli BL21 (DE3) cells using EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluid capillary electr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384582(CHEMBL2036805)copy SMILEScopy InChI
Affinity DataIC50: 0.760nMAssay Description:Inhibition of Mer expressed in Escherichia coli BL21 (DE3) cells using EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluid capillary electr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50084948(CHEMBL195515 | GW7604)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:pIC50 for 1 nM estradiol-induced Ishikawa cell proliferationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384584(CHEMBL2036807 | US9744172, Compound UNC607A)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay Description:Inhibition of Axl using KKKKEEIYFFF-CONH2 as substrate after 180 mins by microfluid capillary electrophoresis assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50276802(4-OHT | Afimoxifene | TamoGel)copy SMILEScopy InChI
Affinity DataIC50: 1.60nMAssay Description:pIC50 for 1 nM estradiol-induced Ishikawa cell proliferationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384581(CHEMBL2036804)copy SMILEScopy InChI
Affinity DataIC50: 1.80nMAssay Description:Inhibition of Mer expressed in Escherichia coli BL21 (DE3) cells using EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluid capillary electr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384576(CHEMBL2036808)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMAssay Description:Inhibition of Mer expressed in Escherichia coli BL21 (DE3) cells using EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluid capillary electr...More data for this Ligand-Target Pair
TargetTyrosine-protein kinase receptor TYRO3(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384583(CHEMBL2036806)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMAssay Description:Inhibition of Tyro3 using EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluid capillary electrophoresis assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384585(CHEMBL2036809)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of Mer expressed in Escherichia coli BL21 (DE3) cells using EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluid capillary electr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475356(CHEMBL195080)copy SMILEScopy InChI
Affinity DataIC50: 3.20nMAssay Description:pIC50 for 1 nM estradiol-induced Ishikawa cell proliferationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384582(CHEMBL2036805)copy SMILEScopy InChI
Affinity DataIC50: 3.70nMAssay Description:Inhibition of Axl using KKKKEEIYFFF-CONH2 as substrate after 180 mins by microfluid capillary electrophoresis assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475363(CHEMBL194774)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:pIC50 for 1 nM estradiol-induced Ishikawa cell proliferationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
GlaxoSmithKline Research & Development

Curated by ChEMBL
LigandPNGBDBM50475360(CHEMBL193865)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:pIC50 for 1 nM estradiol-induced Ishikawa cell proliferationMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24T6N42PubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50384583(CHEMBL2036806)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of Axl using KKKKEEIYFFF-CONH2 as substrate after 180 mins by microfluid capillary electrophoresis assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DMCPubMed
LigandPNGBDBM28674(2-({3-[(2-carboxy-4-chlorophenyl)carbamoyl]benzene...)copy SMILEScopy InChI
Affinity DataIC50: 4nM EC50:  1.26E+3nMpH: 7.0 T: 2°CAssay Description:Competition-binding curves for test compounds were determined with expressed human PPAR LBD. Plots of inhibitor concentration versus cpm of radioliga...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3XWSPubMed
LigandPNGBDBM28691(5-methyl-2-({3-[(7-methyl-1H-indole-1-)sulfonyl]be...)copy SMILEScopy InChI
Affinity DataIC50: 4nM EC50:  79nMAssay Description:Competition-binding curves for test compounds were determined with expressed human PPAR LBD. Plots of inhibitor concentration versus cpm of radioliga...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3XWSPubMed
LigandPNGBDBM28661(2-{2-methyl-4-[({4-methyl-2-[4-(trifluoromethyl)ph...)copy SMILEScopy InChI
Affinity DataIC50: 5nM EC50:  3nMpH: 7.0 T: 2°CAssay Description:Competition-binding curves for test compounds were determined with expressed human PPAR LBD. Plots of inhibitor concentration versus cpm of radioliga...More data for this Ligand-Target Pair
LigandPNGBDBM28669(2-{[3-(1,2,3,4-tetrahydroisoquinoline-2-sulfonyl)b...)copy SMILEScopy InChI
Affinity DataIC50: 5nM EC50:  158nMpH: 7.0 T: 2°CAssay Description:Competition-binding curves for test compounds were determined with expressed human PPAR LBD. Plots of inhibitor concentration versus cpm of radioliga...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3XWSPubMed
LigandPNGBDBM28670(4-bromo-2-{[3-(1,2,3,4-tetrahydroisoquinoline-2-su...)copy SMILEScopy InChI
Affinity DataIC50: 5nM EC50:  158nMpH: 7.0 T: 2°CAssay Description:Competition-binding curves for test compounds were determined with expressed human PPAR LBD. Plots of inhibitor concentration versus cpm of radioliga...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3XWSPubMed
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