Compile Data Set for Download or QSAR
Found 35 with Last Name = 'culic' and Initial = 'o'
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50133496((2R)-3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydr...)copy SMILEScopy InChI
Affinity DataKi:  7.50E+3nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells at 10 umol/L by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50133496((2R)-3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydr...)copy SMILEScopy InChI
Affinity DataKi:  1.02E+4nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells at 30 umol/L by ELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50059889((staurosporine)3-methoxy-2-methyl-4-methylamino-(2...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 1 min by ELISA in presence of 1 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50059889((staurosporine)3-methoxy-2-methyl-4-methylamino-(2...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 20 mins by ELISA in presence of 1 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50059889((staurosporine)3-methoxy-2-methyl-4-methylamino-(2...)copy SMILEScopy InChI
Affinity DataIC50: 36nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 1 min by ELISA in presence of 10 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50059889((staurosporine)3-methoxy-2-methyl-4-methylamino-(2...)copy SMILEScopy InChI
Affinity DataIC50: 83nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 20 mins by ELISA in presence of 10 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50059889((staurosporine)3-methoxy-2-methyl-4-methylamino-(2...)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 1 min by ELISA in presence of 100 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393736(CHEMBL2159140)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibition of human recombinant CYP3A4 using DEF as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50059889((staurosporine)3-methoxy-2-methyl-4-methylamino-(2...)copy SMILEScopy InChI
Affinity DataIC50: 510nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 20 mins by ELISA in presence of 100 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393730(CHEMBL2159131)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:Inhibition of human recombinant CYP3A4 using DEF as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393731(CHEMBL2159136)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:Inhibition of human recombinant CYP3A4 using DEF as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393734(CHEMBL2159133)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using DEF as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393733(CHEMBL2159134)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using DEF as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50133496((2R)-3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 20 mins by ELISA in presence of 1 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393729(CHEMBL2159130)copy SMILEScopy InChI
Affinity DataIC50: 1.33E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using DEF as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393732(CHEMBL2159135)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using DEF as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393738(CHEMBL2159138)copy SMILEScopy InChI
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50133496((2R)-3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 20 mins by ELISA in presence of 10 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393731(CHEMBL2159136)copy SMILEScopy InChI
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393736(CHEMBL2159140)copy SMILEScopy InChI
Affinity DataIC50: 5.70E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393735(CHEMBL2159132)copy SMILEScopy InChI
Affinity DataIC50: 7.80E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using DEF as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393737(CHEMBL2159139)copy SMILEScopy InChI
Affinity DataIC50: 7.90E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using DEF as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393730(CHEMBL2159131)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393733(CHEMBL2159134)copy SMILEScopy InChI
Affinity DataIC50: 9.80E+3nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393729(CHEMBL2159130)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393734(CHEMBL2159133)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393737(CHEMBL2159139)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50373918(AZITHROMYCIN | Azasite)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMedDrugBank
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393735(CHEMBL2159132)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50393732(CHEMBL2159135)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CYP3A4 using 7-BQ as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50373918(AZITHROMYCIN | Azasite)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CYP3A4 using DEF as substrate preincubated for 5 to 10 mins before substrate additionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5NX3PubMedDrugBank
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50133496((2R)-3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 20 mins by ELISA in presence of 100 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50133496((2R)-3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+4nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 1 min by ELISA in presence of 1 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50133496((2R)-3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 6.30E+4nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 1 min by ELISA in presence of 100 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed
TargetTyrosine-protein kinase Fyn(Homo sapiens (Human))
GlaxoSmithKline Research Centre Zagreb

Curated by ChEMBL
LigandPNGBDBM50133496((2R)-3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 7.40E+4nMAssay Description:Inhibition of human Fyn expressed in Sf9 cells after 1 min by ELISA in presence of 10 umol/L ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190H4PubMed