Compile Data Set for Download or QSAR
Found 148 with Last Name = 'kovács' and Initial = 'l'
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102880(8,9,10-Trihydroxy-7-hydroxymethyl-6-oxa-1,3-diaza-...)copy SMILEScopy InChI
Affinity DataKi:  4.20E+3nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, muscle form(Homo sapiens (Human))
Lajos Kossuth University

Curated by ChEMBL
LigandPNGBDBM50215446(CHEMBL3351144)copy SMILEScopy InChI
Affinity DataKi:  4.20E+3nMAssay Description:Inhibitor constant was measured against Liver phosphorylase b in ratMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W66M82PubMed
TargetGlycogen phosphorylase, muscle form(Homo sapiens (Human))
Lajos Kossuth University

Curated by ChEMBL
LigandPNGBDBM50215446(CHEMBL3351144)copy SMILEScopy InChI
Affinity DataKi:  4.20E+3nMAssay Description:Inhibitor constant was measured against Muscle phosphorylase b in rabbitMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W66M82PubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102880(8,9,10-Trihydroxy-7-hydroxymethyl-6-oxa-1,3-diaza-...)copy SMILEScopy InChI
Affinity DataKi:  4.20E+3nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50263769((5S,7R,8S,9S,10R)-8,9,10-Trihydroxy-7-hydroxymethy...)copy SMILEScopy InChI
Affinity DataKi:  5.10E+3nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, muscle form(Homo sapiens (Human))
Lajos Kossuth University

Curated by ChEMBL
LigandPNGBDBM50263769((5S,7R,8S,9S,10R)-8,9,10-Trihydroxy-7-hydroxymethy...)copy SMILEScopy InChI
Affinity DataKi:  5.10E+3nMAssay Description:Inhibitor constant was measured against Muscle phosphorylase b in rabbitMore data for this Ligand-Target Pair
TargetGlycogen phosphorylase, liver form(Rattus norvegicus)
Lajos Kossuth University

Curated by ChEMBL
LigandPNGBDBM50263769((5S,7R,8S,9S,10R)-8,9,10-Trihydroxy-7-hydroxymethy...)copy SMILEScopy InChI
Affinity DataKi:  7.00E+3nMAssay Description:Inhibitor constant was measured against Liver phosphorylase b in ratMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W66M82PubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50263769((5S,7R,8S,9S,10R)-8,9,10-Trihydroxy-7-hydroxymethy...)copy SMILEScopy InChI
Affinity DataKi:  7.00E+3nMAssay Description:Inhibitory activity against liver Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50263769((5S,7R,8S,9S,10R)-8,9,10-Trihydroxy-7-hydroxymethy...)copy SMILEScopy InChI
Affinity DataKi:  1.09E+4nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase aMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, muscle form(Homo sapiens (Human))
Lajos Kossuth University

Curated by ChEMBL
LigandPNGBDBM50263769((5S,7R,8S,9S,10R)-8,9,10-Trihydroxy-7-hydroxymethy...)copy SMILEScopy InChI
Affinity DataKi:  1.09E+4nMAssay Description:Inhibitor constant was measured against Muscle phosphorylase a in rabbitMore data for this Ligand-Target Pair
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102880(8,9,10-Trihydroxy-7-hydroxymethyl-6-oxa-1,3-diaza-...)copy SMILEScopy InChI
Affinity DataKi:  1.28E+4nMAssay Description:Inhibitory activity against liver Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, liver form(Rattus norvegicus)
Lajos Kossuth University

Curated by ChEMBL
LigandPNGBDBM50215446(CHEMBL3351144)copy SMILEScopy InChI
Affinity DataKi:  1.28E+4nMAssay Description:Inhibitor constant was measured against Liver phosphorylase b in ratMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W66M82PubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102880(8,9,10-Trihydroxy-7-hydroxymethyl-6-oxa-1,3-diaza-...)copy SMILEScopy InChI
Affinity DataKi:  1.65E+4nMAssay Description:Inhibitory activity against liver Glycogen Phosphorylase aMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, liver form(Rattus norvegicus)
Lajos Kossuth University

Curated by ChEMBL
LigandPNGBDBM50215446(CHEMBL3351144)copy SMILEScopy InChI
Affinity DataKi:  1.65E+4nMAssay Description:Inhibitor constant was measured against Liver phosphorylase a in ratMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W66M82PubMed
TargetGlycogen phosphorylase, liver form(Rattus norvegicus)
Lajos Kossuth University

Curated by ChEMBL
LigandPNGBDBM50215446(CHEMBL3351144)copy SMILEScopy InChI
Affinity DataKi:  1.65E+4nMAssay Description:Inhibitor constant was measured against Liver phosphorylase b in ratMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W66M82PubMed
TargetGlycogen phosphorylase, muscle form(Homo sapiens (Human))
Lajos Kossuth University

Curated by ChEMBL
LigandPNGBDBM50215446(CHEMBL3351144)copy SMILEScopy InChI
Affinity DataKi:  2.60E+4nMAssay Description:Inhibitor constant was measured against Muscle phosphorylase a in rabbitMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W66M82PubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102880(8,9,10-Trihydroxy-7-hydroxymethyl-6-oxa-1,3-diaza-...)copy SMILEScopy InChI
Affinity DataKi:  2.60E+4nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase aMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50263769((5S,7R,8S,9S,10R)-8,9,10-Trihydroxy-7-hydroxymethy...)copy SMILEScopy InChI
Affinity DataKi:  2.98E+4nMAssay Description:Inhibitory activity against liver Glycogen Phosphorylase aMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, liver form(Rattus norvegicus)
Lajos Kossuth University

Curated by ChEMBL
LigandPNGBDBM50263769((5S,7R,8S,9S,10R)-8,9,10-Trihydroxy-7-hydroxymethy...)copy SMILEScopy InChI
Affinity DataKi:  2.98E+4nMAssay Description:Inhibitor constant was measured against Liver phosphorylase a in ratMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W66M82PubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50240802(1-N-ACETYL-BETA-D-GLUCOSAMINE | CHEMBL335315 | N-(...)copy SMILEScopy InChI
Affinity DataKi:  3.10E+4nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50240802(1-N-ACETYL-BETA-D-GLUCOSAMINE | CHEMBL335315 | N-(...)copy SMILEScopy InChI
Affinity DataKi:  3.20E+4nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50240801(CHEMBL131967 | N-((2R,3R,4S,5S,6R)-3,4,5-trihydrox...)copy SMILEScopy InChI
Affinity DataKi:  8.10E+4nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102884(8,9,10-Trihydroxy-7-hydroxymethyl-6-oxa-1,3-diaza-...)copy SMILEScopy InChI
Affinity DataKi:  1.05E+5nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102884(8,9,10-Trihydroxy-7-hydroxymethyl-6-oxa-1,3-diaza-...)copy SMILEScopy InChI
Affinity DataKi:  1.05E+5nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50240801(CHEMBL131967 | N-((2R,3R,4S,5S,6R)-3,4,5-trihydrox...)copy SMILEScopy InChI
Affinity DataKi:  1.44E+5nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102891(3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...)copy SMILEScopy InChI
Affinity DataKi:  3.70E+5nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102890(3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...)copy SMILEScopy InChI
Affinity DataKi:  4.40E+5nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102885(2,2,2-Trifluoro-N-(3,4,5-trihydroxy-6-hydroxymethy...)copy SMILEScopy InChI
Affinity DataKi:  7.10E+5nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102882(6-Hydroxymethyl-tetrahydro-pyran-2,3,4,5-tetraol |...)copy SMILEScopy InChI
Affinity DataKi:  1.70E+6nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102888(2,3,4,5-Tetrahydroxy-6-hydroxymethyl-tetrahydro-py...)copy SMILEScopy InChI
Affinity DataKi:  3.10E+6nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM34103(D-glucose | dextrose | glucose)copy SMILEScopy InChI
Affinity DataKi:  7.40E+6nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102892(8,9,10-Trihydroxy-2-thioxo-6-oxa-1,3-diaza-spiro[4...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+7nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102883(8,9,10-Trihydroxy-6-oxa-1,3-diaza-spiro[4.5]decane...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+7nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetGlycogen phosphorylase, brain form(Homo sapiens (Human))
University of Debrecen

Curated by ChEMBL
LigandPNGBDBM50102886(8,9,10-Trihydroxy-6-oxa-1,3-diaza-spiro[4.5]decane...)copy SMILEScopy InChI
Affinity DataKi:  1.15E+7nMAssay Description:Inhibitory activity against muscle Glycogen Phosphorylase bMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9JZQPubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM50062351((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM50062351((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetInterstitial collagenase(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM50062351((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
Target72 kDa type IV collagenase(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM50062351((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...)copy SMILEScopy InChI
Affinity DataIC50: 1nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256139(US9487462, 22)copy SMILEScopy InChI
Affinity DataIC50: 280nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256127(US9487462, 9)copy SMILEScopy InChI
Affinity DataIC50: 1.24E+3nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256131(US9487462, 13)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256128(US9487462, 10)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256125(US9487462, 6)copy SMILEScopy InChI
Affinity DataIC50: 1.76E+3nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256141(US9487462, 30)copy SMILEScopy InChI
Affinity DataIC50: 1.76E+3nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256120(US9487462, 1)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256133(US9487462, 15)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256126(US9487462, 7)copy SMILEScopy InChI
Affinity DataIC50: 3.20E+3nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256141(US9487462, 30)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+3nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetCollagenase 3(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256121(US9487462, 2)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+3nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
TargetInterstitial collagenase(Homo sapiens (Human))
PharmaHungary 2000 Kft.; TargetEx Kft.

US Patent
LigandPNGBDBM256141(US9487462, 30)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+3nMpH: 7.5 T: 2°CAssay Description:Stock solution of substrate (Mca-Lys-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) was prepared in DMSO at a concentration of 6 mM. Assays were performed in an as...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W094VZUS Patent
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