Compile Data Set for Download or QSAR
Found 88 with Last Name = 'kirk' and Initial = 'gw'
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105466((S)-6-Amino-2-[(R)-2-[(4-benzenesulfonyl-piperazin...)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMAssay Description:Inhibitory concentration of the compound towards binding of sst2 receptor using [125I]-somatostatin as radioligand in Neuro2A cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105472((S)-6-Amino-2-[(R)-2-[(1-benzenesulfonyl-piperidin...)copy SMILEScopy InChI
Affinity DataIC50: 3.20nMAssay Description:Inhibitory concentration of the compound towards binding of sst2 receptor using [125I]-somatostatin as radioligand in Neuro2A cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105465((4R,8S,11S,17S)-8-(4-Amino-butyl)-17-(2-amino-3-na...)copy SMILEScopy InChI
Affinity DataIC50: 4.10nMAssay Description:Inhibitory concentration of the compound towards binding of sst2 receptor using [125I]-somatostatin as radioligand in Neuro2A cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105470((S)-6-Amino-2-((R)-3-(1H-indol-3-yl)-2-{[4-(4-meth...)copy SMILEScopy InChI
Affinity DataIC50: 4.40nMAssay Description:Inhibitory concentration of the compound towards binding of sst2 receptor using [125I]-somatostatin as radioligand in Neuro2A cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105469((S)-6-Amino-2-((R)-3-(1H-indol-3-yl)-2-{[4-(2-oxo-...)copy SMILEScopy InChI
Affinity DataIC50: 6.5nMAssay Description:Antagonistic activity of the compound towards sst2 receptor in GH4C1 cells a concentration of 1-2 x 10e6/mL incubated for 20 minutesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105469((S)-6-Amino-2-((R)-3-(1H-indol-3-yl)-2-{[4-(2-oxo-...)copy SMILEScopy InChI
Affinity DataIC50: 6.5nMAssay Description:Antagonistic activity of the compound towards sst2 receptor in GH4C1 cells a concentration of 1-2 x 10e6/mL incubated for 20 minutesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105468((S)-6-Amino-2-[(R)-2-[(4-benzoyl-piperazine-1-carb...)copy SMILEScopy InChI
Affinity DataIC50: 6.90nMAssay Description:Inhibitory concentration of the compound towards binding of sst2 receptor using [125I]-somatostatin as radioligand in Neuro2A cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105468((S)-6-Amino-2-[(R)-2-[(4-benzoyl-piperazine-1-carb...)copy SMILEScopy InChI
Affinity DataIC50: 6.90nMAssay Description:Inhibitory concentration of the compound towards binding of sst2 receptor using [125I]-somatostatin as radioligand in Neuro2A cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105471((S)-6-Amino-2-((R)-3-(1H-indol-3-yl)-2-{[4-(toluen...)copy SMILEScopy InChI
Affinity DataIC50: 9.20nMAssay Description:Inhibitory concentration of the compound towards binding of sst2 receptor using [125I]-somatostatin as radioligand in Neuro2A cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105466((S)-6-Amino-2-[(R)-2-[(4-benzenesulfonyl-piperazin...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:Inhibitory concentration of the compound towards binding of sst2 receptor using [125I]-somatostatin as radioligand in Neuro2A cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137438(5-Methanesulfonyl-2-[5-(4-methoxy-phenyl)-3-triflu...)copy SMILEScopy InChI
Affinity DataIC50: 44nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137423(2-(4-Chloro-3-difluoromethyl-5-phenyl-pyrazol-1-yl...)copy SMILEScopy InChI
Affinity DataIC50: 44nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 1(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137420(2-[5-(4-Ethoxy-phenyl)-3-trifluoromethyl-pyrazol-1...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137442(2-[3-Difluoromethyl-5-(3-fluoro-4-methoxy-phenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137439(2-[5-(2-Fluoro-4-methoxy-phenyl)-3-trifluoromethyl...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137435(2-(4-Chloro-5-phenyl-3-trifluoromethyl-pyrazol-1-y...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137424(2-[4-Chloro-5-(3-chloro-4-methoxy-phenyl)-3-difluo...)copy SMILEScopy InChI
Affinity DataIC50: 62nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137411(2-[3-Difluoromethyl-5-(4-methoxy-phenyl)-pyrazol-1...)copy SMILEScopy InChI
Affinity DataIC50: 64nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105470((S)-6-Amino-2-((R)-3-(1H-indol-3-yl)-2-{[4-(4-meth...)copy SMILEScopy InChI
Affinity DataIC50: 67nMAssay Description:Antagonistic activity of the compound towards sst2 receptor in GH4C1 cells a concentration of 1-2 x 10e6/mL incubated for 20 minutesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137437(5-Methanesulfonyl-2-[5-(4-methylsulfanyl-phenyl)-3...)copy SMILEScopy InChI
Affinity DataIC50: 69nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137427(2-(4-Bromo-3-difluoromethyl-5-phenyl-pyrazol-1-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137428(2-[3-Difluoromethyl-5-(4-methylsulfanyl-phenyl)-py...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137414(2-[5-(4-Chloro-phenyl)-3-difluoromethyl-pyrazol-1-...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137440(CHEMBL176934 | {4-[2-(5-Methanesulfonyl-pyridin-2-...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105472((S)-6-Amino-2-[(R)-2-[(1-benzenesulfonyl-piperidin...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Antagonistic activity of the compound towards sst2 receptor in GH4C1 cells a concentration of 1-2 x 10e6/mL incubated for 20 minutesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137420(2-[5-(4-Ethoxy-phenyl)-3-trifluoromethyl-pyrazol-1...)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137412(5-Methanesulfonyl-2-(4-methyl-5-phenyl-3-trifluoro...)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137434(2-[3-Difluoromethyl-5-(4-methoxy-3-methyl-phenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137418(2-(3-Difluoromethyl-5-p-tolyl-pyrazol-1-yl)-5-meth...)copy SMILEScopy InChI
Affinity DataIC50: 180nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137432(2-(3-Difluoromethyl-4-methyl-5-phenyl-pyrazol-1-yl...)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 1(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137411(2-[3-Difluoromethyl-5-(4-methoxy-phenyl)-pyrazol-1...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137416(2-(5-(4-fluorophenyl)-3-(trifluoromethyl)-1H-pyraz...)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137413(2-[5-(4-Chloro-phenyl)-3-trifluoromethyl-pyrazol-1...)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
Pfizer Inc

Curated by ChEMBL
LigandPNGBDBM50105465((4R,8S,11S,17S)-8-(4-Amino-butyl)-17-(2-amino-3-na...)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:Antagonistic activity of the compound towards sst2 receptor in GH4C1 cells a concentration of 1-2 x 10e6/mL incubated for 20 minutesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8D5SPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137415(5-Methanesulfonyl-2-[5-(4-methoxy-3-methyl-phenyl)...)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137410(2-[5-(4-Bromo-phenyl)-3-difluoromethyl-pyrazol-1-y...)copy SMILEScopy InChI
Affinity DataIC50: 290nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137441(2-[5-(3-Chloro-4-methoxy-phenyl)-3-trifluoromethyl...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137429(2-[3-Difluoromethyl-5-(4-fluoro-phenyl)-pyrazol-1-...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137421(2-[5-(3-Fluoro-4-methoxy-phenyl)-3-trifluoromethyl...)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137425(2-(3-(difluoromethyl)-5-phenyl-1H-pyrazol-1-yl)-5-...)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 1(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137423(2-(4-Chloro-3-difluoromethyl-5-phenyl-pyrazol-1-yl...)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137436(2-[5-(3-Chloro-4-methoxy-phenyl)-3-difluoromethyl-...)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137422(2-[3-Difluoromethyl-5-(2-fluoro-4-methoxy-phenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 390nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137417(2-[3-Difluoromethyl-5-(4-ethyl-phenyl)-pyrazol-1-y...)copy SMILEScopy InChI
Affinity DataIC50: 400nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137433(5-(methylsulfonyl)-2-(5-phenyl-3-(trifluoromethyl)...)copy SMILEScopy InChI
Affinity DataIC50: 410nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137419(2-[5-(4-Bromo-phenyl)-3-trifluoromethyl-pyrazol-1-...)copy SMILEScopy InChI
Affinity DataIC50: 450nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50057583(4-[3-Difluoromethyl-5-(3-fluoro-4-methoxy-phenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 630nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 1(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137438(5-Methanesulfonyl-2-[5-(4-methoxy-phenyl)-3-triflu...)copy SMILEScopy InChI
Affinity DataIC50: 830nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 1(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM50137428(2-[3-Difluoromethyl-5-(4-methylsulfanyl-phenyl)-py...)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25B01WPPubMed
TargetProstaglandin G/H synthase 2(Canis familiaris)
Pfizer Inc.

Curated by ChEMBL
LigandPNGBDBM11639(4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyraz...)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:In vitro inhibitory activity against cannine prostaglandin G/H synthase 2.More data for this Ligand-Target Pair
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