Compile Data Set for Download or QSAR
Found 33 with Last Name = 'bodman' and Initial = 'm'
TargetThromboxane A2 receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50035622((5Z,13E,15S)-9alpha,11alpha,15-trihydroxyprosta-5,...)copy SMILEScopy InChI
Affinity DataIC50: 0.00100nMAssay Description:In vitro binding of the compound at TP human prostaglandin receptor using [3H]-SQ-29,548 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin F2-alpha receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106547(7-[3,5-Dihydroxy-2-(3-hydroxy-4-phenoxy-but-1-enyl...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:In vitro binding of the compound at FP human prostaglandin receptor using [3H]-PGF-2 alpha as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin F2-alpha receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50035622((5Z,13E,15S)-9alpha,11alpha,15-trihydroxyprosta-5,...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro binding of the compound at FP human prostaglandin receptor using [3H]-PGF-2 alpha as radioligandMore data for this Ligand-Target Pair
TargetProstaglandin E2 receptor EP1 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106547(7-[3,5-Dihydroxy-2-(3-hydroxy-4-phenoxy-but-1-enyl...)copy SMILEScopy InChI
Affinity DataIC50: 38nMAssay Description:Functional activity in RAT-1 cells, transiently transfected with human prostaglandin EP1 receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin F2-alpha receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106548(CHEMBL440164 | {6-[3,5-Dihydroxy-2-(3-hydroxy-4-ph...)copy SMILEScopy InChI
Affinity DataIC50: 42nMAssay Description:In vitro binding of the compound at FP human prostaglandin receptor using [3H]-PGF-2 alpha as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP3 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50035622((5Z,13E,15S)-9alpha,11alpha,15-trihydroxyprosta-5,...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:In vitro binding of the compound at EP3 human prostaglandin receptor using [3H]-PGE-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin F2-alpha receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106546(CHEMBL134546 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 114nMAssay Description:In vitro binding of the compound at FP human prostaglandin receptor using [3H]-PGF-2 alpha as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP3 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106547(7-[3,5-Dihydroxy-2-(3-hydroxy-4-phenoxy-but-1-enyl...)copy SMILEScopy InChI
Affinity DataIC50: 186nMAssay Description:Functional activity in RAT-1 cells, transiently transfected with human prostaglandin EP3 receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP1 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50035622((5Z,13E,15S)-9alpha,11alpha,15-trihydroxyprosta-5,...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:In vitro binding of the compound at EP1 human prostaglandin receptor using [3H]-PGE-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin F2-alpha receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106549(CHEMBL336781 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 311nMAssay Description:In vitro binding of the compound at FP human prostaglandin receptor using [3H]-PGF-2 alpha as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetThromboxane A2 receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106547(7-[3,5-Dihydroxy-2-(3-hydroxy-4-phenoxy-but-1-enyl...)copy SMILEScopy InChI
Affinity DataIC50: 510nMAssay Description:Functional activity in RAT-1 cells, transiently transfected with human prostaglandin TP receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin F2-alpha receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106553(CHEMBL336543 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:In vitro binding of the compound at FP human prostaglandin receptor using [3H]- PGF-2 alpha as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin F2-alpha receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106552(CHEMBL133945 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 4.10E+3nMAssay Description:In vitro binding of the compound at FP human prostaglandin receptor using [3H]-PGF-2 alpha as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP4 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50035622((5Z,13E,15S)-9alpha,11alpha,15-trihydroxyprosta-5,...)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:In vitro binding of the compound at EP4 human prostaglandin receptor using [3H]-PGE-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin D2 receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50035622((5Z,13E,15S)-9alpha,11alpha,15-trihydroxyprosta-5,...)copy SMILEScopy InChI
Affinity DataIC50: 4.50E+3nMAssay Description:In vitro binding of the compound at DP human prostaglandin receptor using [3H]- PGD-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin F2-alpha receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106551(Butyl-{6-[3,5-dihydroxy-2-(3-hydroxy-oct-1-enyl)-c...)copy SMILEScopy InChI
Affinity DataIC50: 6.70E+3nMAssay Description:In vitro binding of the compound at FP human prostaglandin receptor using [3H]-PGF-2 alpha as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetThromboxane A2 receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106548(CHEMBL440164 | {6-[3,5-Dihydroxy-2-(3-hydroxy-4-ph...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at TP human prostaglandin receptor using [3H]-SQ-29,548 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP3 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106548(CHEMBL440164 | {6-[3,5-Dihydroxy-2-(3-hydroxy-4-ph...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at EP3 human prostaglandin receptor using [3H]-PGE-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP2 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106546(CHEMBL134546 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at EP2 human prostaglandin receptor using [3H]-PGE-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin D2 receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106548(CHEMBL440164 | {6-[3,5-Dihydroxy-2-(3-hydroxy-4-ph...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at DP human prostaglandin receptor using [3H]- PGD-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP3 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106546(CHEMBL134546 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at EP3 human prostaglandin receptor using [3H]-PGE-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP1 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106546(CHEMBL134546 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at EP1 human prostaglandin receptor using [3H]-PGE-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP1 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106548(CHEMBL440164 | {6-[3,5-Dihydroxy-2-(3-hydroxy-4-ph...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at EP1 human prostaglandin receptor using [3H]-PGE-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin D2 receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106546(CHEMBL134546 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at DP human prostaglandin receptor using [3H]- PGD-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin F2-alpha receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106550(CHEMBL334810 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at FP human prostaglandin receptor using [3H]- PGF-2 alpha as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetThromboxane A2 receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106546(CHEMBL134546 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at TP human prostaglandin receptor using [3H]-SQ-29,548 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP4 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106548(CHEMBL440164 | {6-[3,5-Dihydroxy-2-(3-hydroxy-4-ph...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at EP4 human prostaglandin receptor using [3H]-PGE-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP2 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106548(CHEMBL440164 | {6-[3,5-Dihydroxy-2-(3-hydroxy-4-ph...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at EP2 human prostaglandin receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106548(CHEMBL440164 | {6-[3,5-Dihydroxy-2-(3-hydroxy-4-ph...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at prostanoid IP receptor using [3H]-Iloprost as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstaglandin E2 receptor EP4 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106546(CHEMBL134546 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at EP4 human prostaglandin receptor using [3H]-PGE-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50106546(CHEMBL134546 | {6-[3,5-Dihydroxy-2-(3-hydroxy-oct-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro binding of the compound at prostanoid IP receptor using [3H]-Iloprost as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50035622((5Z,13E,15S)-9alpha,11alpha,15-trihydroxyprosta-5,...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro binding of the compound at prostanoid IP receptor using [3H]-Iloprost as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMedDrugBank
TargetProstaglandin E2 receptor EP2 subtype(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50035622((5Z,13E,15S)-9alpha,11alpha,15-trihydroxyprosta-5,...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro binding of the compound at EP2 human prostaglandin receptor using [3H]-PGE-2 as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2HT2NNPPubMed