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Found 198 with Last Name = 'fillgrove' and Initial = 'kl'
TargetCytochrome P450 3A4(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50169690(CHEMBL3806137)
Affinity DataKi:  540nMAssay Description:Time dependent inhibition of CYP3A4 in human liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2B(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50145198(CHEMBL3765778)
Affinity DataKi:  1.90E+3nMAssay Description:Positive allosteric modulation of 5-HT2B receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50145198(CHEMBL3765778)
Affinity DataKi:  2.00E+3nMAssay Description:Positive allosteric modulation of platelet-activating factor receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406127(CHEMBL5290844)
Affinity DataIC50:  1nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406134(CHEMBL5275403)
Affinity DataIC50:  1.70nMAssay Description:Antagonistic activity against M2 muscarinic receptor in guinea pig left atrium derived by plotting log(DR - 1) vs log[antagonist]More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406126(CHEMBL5291288)
Affinity DataIC50:  6nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406123(CHEMBL5277419)
Affinity DataIC50:  7nMAssay Description:In vitro Oxytocin receptor antagonistic activity against rat uterine stripsMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50593123(GENZ-682452 | GZ-402671 | GZ/SAR402671 | GZ402671 ...)
Affinity DataIC50:  12nMAssay Description:In vitro inhibitory activity against bovine cathepsin DMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Mus musculus)TBA
LigandPNGBDBM50406134(CHEMBL5275403)
Affinity DataIC50:  17nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Mus musculus)TBA
LigandPNGBDBM50406130(CHEMBL5272946)
Affinity DataIC50:  21nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406132(CHEMBL5273314)
Affinity DataIC50:  21nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406136(CHEMBL5278676)
Affinity DataIC50:  32nMAssay Description:In vitro inhibitory activity against aspartic proteinases pepsin from porcineMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406137(CHEMBL5286066)
Affinity DataIC50:  32nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406134(CHEMBL5275403)
Affinity DataIC50:  32nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406133(CHEMBL5288633)
Affinity DataIC50:  32nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406138(CHEMBL5286071)
Affinity DataIC50:  33nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406130(CHEMBL5272946)
Affinity DataIC50:  34nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406131(CHEMBL5278405)
Affinity DataIC50:  35nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406135(CHEMBL5278640)
Affinity DataIC50:  37nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50593123(GENZ-682452 | GZ-402671 | GZ/SAR402671 | GZ402671 ...)
Affinity DataIC50:  44nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406119(CHEMBL5273405)
Affinity DataIC50:  85nMAssay Description:In vitro Oxytocin receptor antagonistic activity against rat uterine stripsMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406128(CHEMBL5270537)
Affinity DataIC50:  180nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
Target5-hydroxytryptamine receptor 3A(Homo sapiens (Human))TBA
LigandPNGBDBM50406130(CHEMBL5272946)
Affinity DataIC50:  224nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
Target5-hydroxytryptamine receptor 3A(Homo sapiens (Human))TBA
LigandPNGBDBM50406131(CHEMBL5278405)
Affinity DataIC50:  338nMAssay Description:ETA receptor antagonist activity was measured by inhibition of ET-1 induced vasoconstriction in isolated porcine coronary arteryMore data for this Ligand-Target Pair
In DepthDetails PubMed
Target5-hydroxytryptamine receptor 3A(Homo sapiens (Human))TBA
LigandPNGBDBM50406135(CHEMBL5278640)
Affinity DataIC50:  585nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406118(CHEMBL5281181)
Affinity DataIC50:  690nMAssay Description:In vitro Oxytocin receptor antagonistic activity against rat uterine stripsMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406128(CHEMBL5270537)
Affinity DataIC50:  1.00E+3nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
Target5-hydroxytryptamine receptor 3A(Homo sapiens (Human))TBA
LigandPNGBDBM50406132(CHEMBL5273314)
Affinity DataIC50:  1.59E+3nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
Target5-hydroxytryptamine receptor 3A(Homo sapiens (Human))TBA
LigandPNGBDBM50406134(CHEMBL5275403)
Affinity DataIC50:  1.97E+3nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
LigandPNGBDBM50406130(CHEMBL5272946)
Affinity DataIC50:  2.00E+3nMAssay Description:Antagonistic activity against M2 muscarinic receptor in guinea pig left atrium derived by plotting log(DR - 1) vs log[antagonist]More data for this Ligand-Target Pair
In DepthDetails PubMed
Target5-hydroxytryptamine receptor 3A(Homo sapiens (Human))TBA
LigandPNGBDBM50406137(CHEMBL5286066)
Affinity DataIC50:  2.19E+3nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
LigandPNGBDBM50406134(CHEMBL5275403)
Affinity DataIC50:  2.20E+3nMAssay Description:Antagonistic activity against M2 muscarinic receptor in guinea pig left atrium derived by plotting log(DR - 1) vs log[antagonist]More data for this Ligand-Target Pair
In DepthDetails PubMed
LigandPNGBDBM50406130(CHEMBL5272946)
Affinity DataIC50:  2.20E+3nMAssay Description:Antagonistic activity against M2 muscarinic receptor in guinea pig left atrium derived by plotting log(DR - 1) vs log[antagonist]More data for this Ligand-Target Pair
In DepthDetails PubMed
Target5-hydroxytryptamine receptor 3A(Homo sapiens (Human))TBA
LigandPNGBDBM50406138(CHEMBL5286071)
Affinity DataIC50:  2.47E+3nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
LigandPNGBDBM50406134(CHEMBL5275403)
Affinity DataIC50:  4.10E+3nMAssay Description:Antagonistic activity against M2 muscarinic receptor in guinea pig left atrium derived by plotting log(DR - 1) vs log[antagonist]More data for this Ligand-Target Pair
In DepthDetails PubMed
Target5-hydroxytryptamine receptor 3A(Homo sapiens (Human))TBA
LigandPNGBDBM50406133(CHEMBL5288633)
Affinity DataIC50:  4.21E+3nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406122(CHEMBL5286114)
Affinity DataIC50:  7.40E+3nMAssay Description:In vitro Oxytocin receptor antagonistic activity against rat uterine stripsMore data for this Ligand-Target Pair
In DepthDetails PubMed
Target5-hydroxytryptamine receptor 3A(Homo sapiens (Human))TBA
LigandPNGBDBM50406136(CHEMBL5278676)
Affinity DataIC50:  7.47E+3nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetMuscarinic acetylcholine receptor M5(Homo sapiens (Human))TBA
LigandPNGBDBM50406134(CHEMBL5275403)
Affinity DataIC50:  1.02E+4nMAssay Description:Antagonistic activity against M2 muscarinic receptor in guinea pig left atrium derived by plotting log(DR - 1) vs log[antagonist]More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetMuscarinic acetylcholine receptor M5(Homo sapiens (Human))TBA
LigandPNGBDBM50406130(CHEMBL5272946)
Affinity DataIC50:  1.02E+4nMAssay Description:Antagonistic activity against M2 muscarinic receptor in guinea pig left atrium derived by plotting log(DR - 1) vs log[antagonist]More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406117(CHEMBL5288301)
Affinity DataIC50:  1.25E+4nMAssay Description:Compound was evaluated for the inhibition of microsomal 2,3-oxidosqualene-lanosterol cyclase in Candida albicans microsomesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406125(CHEMBL5291482)
Affinity DataIC50: >2.80E+4nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406120(CHEMBL5267915)
Affinity DataIC50: >2.80E+4nMAssay Description:In vitro Oxytocin receptor antagonistic activity against rat uterine stripsMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCeramide glucosyltransferase(Homo sapiens (Human))TBA
LigandPNGBDBM50406124(CHEMBL5277877)
Affinity DataIC50: >2.80E+4nMAssay Description:In vitro inhibitory potency against human kidney renin.More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))TBA
LigandPNGBDBM50406134(CHEMBL5275403)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))TBA
LigandPNGBDBM50406130(CHEMBL5272946)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50406134(CHEMBL5275403)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50406130(CHEMBL5272946)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of Choline AcetyltransferaseMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))TBA
LigandPNGBDBM50406130(CHEMBL5272946)
Affinity DataIC50: >5.00E+4nMAssay Description:Antagonistic activity against M2 muscarinic receptor in guinea pig left atrium derived by plotting log(DR - 1) vs log[antagonist]More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))TBA
LigandPNGBDBM50406134(CHEMBL5275403)
Affinity DataIC50: >5.00E+4nMAssay Description:Antagonistic activity against M2 muscarinic receptor in guinea pig left atrium derived by plotting log(DR - 1) vs log[antagonist]More data for this Ligand-Target Pair
In DepthDetails PubMed
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