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Found 60 with Last Name = 'filipek' and Initial = 's'
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098189(CHEMBL3588930)
Affinity DataIC50:  50nMAssay Description:Allosteric antagonist activity against FPR2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Central University Of Rajasthan

Curated by ChEMBL
LigandPNGBDBM50580887(CHEMBL1496098)
Affinity DataIC50:  55nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50097999(CHEMBL3590218)
Affinity DataIC50:  80nMAssay Description:Antagonist activity against FPR2 (unknown origin) pre-treated for 5 mins before addition of Wpep by Fluo4 florescence based intracellular Ca2+ mobili...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098001(CHEMBL3590217)
Affinity DataIC50:  90nMAssay Description:Antagonist activity against human FPR2 expressed in rat RBL-2H3 cells pre-treated for 15 mins before addition of WKYMVm or C1 by intracellular Ca2+ m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098007(CHEMBL3590216)
Affinity DataIC50:  170nMAssay Description:Antagonist activity against human FPR2 expressed in rat RBL-2H3 cells pre-treated for 15 mins before addition of WKYMVm or C1 by intracellular Ca2+ m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Central University Of Rajasthan

Curated by ChEMBL
LigandPNGBDBM50580886(CHEMBL5083646)
Affinity DataIC50:  1.08E+3nMAssay Description:Inhibition of GSK3beta (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098046(CHEMBL3590215)
Affinity DataIC50:  6.65E+3nMAssay Description:Antagonist activity against human FPR2 expressed in rat RBL-2H3 cells pre-treated for 15 mins before addition of WKYMVm or C1 by intracellular Ca2+ m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Central University Of Rajasthan

Curated by ChEMBL
LigandPNGBDBM50580886(CHEMBL5083646)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CDK5 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Central University Of Rajasthan

Curated by ChEMBL
LigandPNGBDBM50580886(CHEMBL5083646)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CDK9 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDual specificity protein kinase CLK1(Homo sapiens (Human))
Central University Of Rajasthan

Curated by ChEMBL
LigandPNGBDBM50580886(CHEMBL5083646)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CLK1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Homo sapiens (Human))
Central University Of Rajasthan

Curated by ChEMBL
LigandPNGBDBM50580886(CHEMBL5083646)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of DYRK1A (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase haspin(Homo sapiens (Human))
Central University Of Rajasthan

Curated by ChEMBL
LigandPNGBDBM50580886(CHEMBL5083646)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of HASPIN (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
Central University Of Rajasthan

Curated by ChEMBL
LigandPNGBDBM50580886(CHEMBL5083646)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of PIM1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCasein kinase I delta/epsilon(Homo sapiens (Human))
Central University Of Rajasthan

Curated by ChEMBL
LigandPNGBDBM50580886(CHEMBL5083646)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of CK-1 delta/epsilon (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495303(CHEMBL3103184)
Affinity DataIC50:  1.44E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495302(CHEMBL3103314)
Affinity DataIC50:  1.76E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495287(CHEMBL3103312)
Affinity DataIC50:  2.18E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495289(CHEMBL3103308)
Affinity DataIC50:  2.37E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495293(CHEMBL3103313)
Affinity DataIC50:  2.63E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50134399(1,7-Dihydro-pyrrolo[2,3-d]pyrimidine-2,4-dione | 7...)
Affinity DataIC50:  3.87E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495286(CHEMBL3103180)
Affinity DataIC50:  4.06E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495292(CHEMBL3103178)
Affinity DataIC50:  4.06E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495300(CHEMBL3103317)
Affinity DataIC50:  4.64E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495290(CHEMBL3103185)
Affinity DataIC50:  5.47E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495301(CHEMBL3103315)
Affinity DataIC50:  5.82E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495295(CHEMBL3103182)
Affinity DataIC50:  6.93E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495294(CHEMBL3103310)
Affinity DataIC50:  8.32E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495288(CHEMBL3103311)
Affinity DataIC50:  8.44E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495291(CHEMBL3103177)
Affinity DataIC50:  8.72E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495299(CHEMBL3103318)
Affinity DataIC50:  8.87E+4nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495284(CHEMBL3103307)
Affinity DataIC50:  1.04E+5nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495298(CHEMBL3103181)
Affinity DataIC50:  1.17E+5nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495296(CHEMBL3103179)
Affinity DataIC50:  1.18E+5nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495304(CHEMBL3103183)
Affinity DataIC50:  1.31E+5nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495297(CHEMBL3103309)
Affinity DataIC50:  1.34E+5nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetThymidine phosphorylase(Escherichia coli)
Institute Of Information Technology

Curated by ChEMBL
LigandPNGBDBM50495285(CHEMBL3103316)
Affinity DataIC50:  1.73E+5nMAssay Description:Inhibition of Escherichia coli thymidine phosphorylase using thymidine 5' mono phosphate as substrate after 10 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098056(CHEMBL3590212)
Affinity DataEC50:  7.30E+3nMAssay Description:Agonist activity against human FPR2 expressed in human HL60 cells by Fluo-4AM dye based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098055(CHEMBL3590213)
Affinity DataEC50:  8.00E+3nMAssay Description:Agonist activity against human FPR2 expressed in human HL60 cells by Fluo-4AM dye based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098048(CHEMBL1290698)
Affinity DataEC50:  4.70E+3nMAssay Description:Agonist activity against human FPR2 expressed in human HL60 cells by Fluo-4AM dye based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098047(CHEMBL3590214)
Affinity DataEC50:  1.00E+4nMAssay Description:Agonist activity against human FPR2 expressed in human HL60 cells by Fluo-4AM dye based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098007(CHEMBL3590216)
Affinity DataEC50:  1.48E+3nMAssay Description:Agonist activity at human FPR2 expressed in rat RBL-2H3 cells by intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098001(CHEMBL3590217)
Affinity DataEC50:  470nMAssay Description:Agonist activity at human FPR2 expressed in rat RBL-2H3 cells by intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098000(CHEMBL3588922)
Affinity DataEC50:  140nMAssay Description:Agonist activity at FPR2 (unknown origin) by Fluo4 florescence based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098058(CHEMBL3590211)
Affinity DataEC50:  3.20E+3nMAssay Description:Agonist activity against human FPR2 expressed in human HL60 cells by Fluo-4AM dye based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098059(CHEMBL3590210)
Affinity DataEC50:  6.00E+3nMAssay Description:Agonist activity against human FPR2 expressed in human HL60 cells by Fluo-4AM dye based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098060(CHEMBL3590209)
Affinity DataEC50:  4.03E+3nMAssay Description:Agonist activity against human FPR2 expressed in human HL60 cells by Fluo-4AM dye based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098111(CHEMBL3590208)
Affinity DataEC50:  250nMAssay Description:Agonist activity against human FPR2 expressed in human HL60 cells by Fluo-4AM dye based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098172(CHEMBL3590207)
Affinity DataEC50:  160nMAssay Description:Agonist activity against human FPR2 expressed in human HL60 cells by Fluo-4AM dye based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098173(CHEMBL3590206)
Affinity DataEC50:  7nMAssay Description:Agonist activity against human FPR2 expressed in human HL60 cells by Fluo-4AM dye based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
University Of Warsaw

Curated by ChEMBL
LigandPNGBDBM50098174(CHEMBL3588929)
Affinity DataEC50:  4nMAssay Description:Agonist activity against human FPR2 expressed in human HL60 cells by Fluo-4AM dye based intracellular Ca2+ mobilization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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