Compile Data Set for Download or QSAR
Found 199 of ic50 for UniProtKB: P43119
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50095207(CHEMBL430154 | [6-(4-Benzhydryl-pyrazol-1-ylmethyl...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Compound was tested for its binding affinity against Prostaglandin I2 receptor using conventional ligand assay by the displacement of [3H]-iloprost f...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22807KH
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM23954(5-[(2E,3aS,4R,5R,6aS)-5-hydroxy-4-[(1E,3S)-3-hydro...)copy SMILEScopy InChI
Affinity DataIC50: 8.40nMAssay Description:Binding affinity to human PGI2 receptor by radioligand displacement assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JH3NKCPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM23954(5-[(2E,3aS,4R,5R,6aS)-5-hydroxy-4-[(1E,3S)-3-hydro...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM23954(5-[(2E,3aS,4R,5R,6aS)-5-hydroxy-4-[(1E,3S)-3-hydro...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Displacement of [3H]iloprost from human recombinant IP receptor expressed in HEK293 cells measured after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CF9S3SPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM23954(5-[(2E,3aS,4R,5R,6aS)-5-hydroxy-4-[(1E,3S)-3-hydro...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Displacement of [3H]iloprost from human recombinant Prostanoid IP receptor expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67JS7PubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50284372(CHEMBL11211 | {5-[2-(N',N'-Diphenyl-hydrazinocarbo...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Compound was tested for prostacyclin (PGI-2) binding by displacement of [3H]-iloprost from human platelets using conventional ligand binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q261108S
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235375(CHEMBL3975122)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50163291(CHEMBL3793903)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Agonist activity at human IP receptor in platelet rich plasma assessed as inhibition of ADP-induced platelet aggregation preincubated for 1 min follo...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q52RJWPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM23954(5-[(2E,3aS,4R,5R,6aS)-5-hydroxy-4-[(1E,3S)-3-hydro...)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Binding affinity to PGI2 receptor (unknown origin) by radioligand displacement assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87C5QPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235370(CHEMBL3933704)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50284377(CHEMBL11746 | {5-[2-(4-Benzhydryl-pyrazol-1-yl)-et...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Compound was tested for its binding affinity against Prostaglandin I2 receptor using conventional ligand assay by the displacement of [3H]-iloprost f...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22807KH
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235378(CHEMBL3981509)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50284370(CHEMBL10836 | [6-(N',N'-Diphenyl-hydrazinocarbonyl...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Compound was tested for prostacyclin (PGI-2) binding by displacement of [3H]-iloprost from human platelets using conventional ligand binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q261108S
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235368(CHEMBL3893346)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235373(CHEMBL3928729)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Compound was tested for its inhibitory activity against cathepsin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235376(CHEMBL3926078)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50016954(CHEMBL1628262)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Agonist activity at prostanoid IP receptor (unknown origin) by functional assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5VXZPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235367(CHEMBL3952237)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM23954(5-[(2E,3aS,4R,5R,6aS)-5-hydroxy-4-[(1E,3S)-3-hydro...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Prostaglandin I2 receptor binding by displacement of [3H]-iloprost from human plateletsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FF3S9T
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM23954(5-[(2E,3aS,4R,5R,6aS)-5-hydroxy-4-[(1E,3S)-3-hydro...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Displacement of [3H]-iloprost from Prostaglandin I2 receptor of human plateletsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29P31MX
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235389(CHEMBL3983767)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM85602((R)-BUTAPROST | Butaprost (Free Acid) | CAS_69648-...)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:Agonist activity at prostanoid IP receptor (unknown origin) by functional assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5VXZPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235385(APD-811 | Ralinepag)copy SMILEScopy InChI
Affinity DataIC50: 38nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50191135(CHEMBL215442 | sodium 2-(3-(((1S,2R)-2-(4,5-diphen...)copy SMILEScopy InChI
Affinity DataIC50: 39nMAssay Description:Agonist activity at human PGI2 receptor assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R49QD9PubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235374(CHEMBL3935924)copy SMILEScopy InChI
Affinity DataIC50: 39nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50284378(CHEMBL11765 | [6-(4-Benzhydryl-pyrazol-1-ylmethyl)...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Compound was tested for its binding affinity against Prostaglandin I2 receptor using conventional ligand assay by the displacement of [3H]-iloprost f...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22807KH
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235379(CHEMBL3932106 | US10668033, Compound 55)copy SMILEScopy InChI
Affinity DataIC50: 43nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50191133(CHEMBL439357 | sodium (R)-2-(3-((2-(4,5-diphenylox...)copy SMILEScopy InChI
Affinity DataIC50: 48nMAssay Description:Agonist activity at human PGI2 receptor assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R49QD9PubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50191134(CHEMBL379203 | sodium 2-(3-(((1S,2S)-2-(4,5-diphen...)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Agonist activity at human PGI2 receptor assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R49QD9PubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM23960(5-(4-phenylbenzyl)oxazole-4-carboxamide, 6g | 5-{[...)copy SMILEScopy InChI
Affinity DataIC50: 53nM EC50:  51nMpH: 7.4 T: 2°CAssay Description:IP receptor binding activity was quantified via a filter binding assay measuring displacement of [3H]-Iloprost binding to human platelet membranes. R...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0M0HPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235372(CHEMBL3966307)copy SMILEScopy InChI
Affinity DataIC50: 54nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235384(CHEMBL3900038)copy SMILEScopy InChI
Affinity DataIC50: 54nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50191132(CHEMBL438092 | sodium (S)-2-(3-((2-(4,5-diphenylox...)copy SMILEScopy InChI
Affinity DataIC50: 58nMAssay Description:Agonist activity at human PGI2 receptor assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R49QD9PubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50136234(CHEMBL132589 | FR-181157 | Sodium; {3-[(R)-2-(4,5-...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Agonist activity at human PGI2 receptor assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R49QD9PubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235383(ACT-293987 | NS-304 | Selexipag | Uptravi)copy SMILEScopy InChI
Affinity DataIC50: 62nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50103396(CHEMBL3398236)copy SMILEScopy InChI
Affinity DataIC50: 62nMAssay Description:Agonist activity at human IP receptor in human platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057HQMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50103395(CHEMBL3398235)copy SMILEScopy InChI
Affinity DataIC50: 62nMAssay Description:Agonist activity at human IP receptor in human platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057HQMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50103394(CHEMBL3398229)copy SMILEScopy InChI
Affinity DataIC50: 64nMAssay Description:Agonist activity at human IP receptor in human platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057HQMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM23953(5-(4-phenylbenzyl)oxazole-4-carboxamide, 6a | 5-{[...)copy SMILEScopy InChI
Affinity DataIC50: 77nMpH: 7.4 T: 2°CAssay Description:IP receptor binding activity was quantified via a filter binding assay measuring displacement of [3H]-Iloprost binding to human platelet membranes. R...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RV0M0HPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50095203(CHEMBL94751 | [(S)-6-(3-Benzhydryl-6-oxo-6H-pyrida...)copy SMILEScopy InChI
Affinity DataIC50: 81nMAssay Description:Agonist activity at PGI2 receptor in Homo sapiens (human) platelets assessed as inhibition of ADP-induced aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0KD3
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50095203(CHEMBL94751 | [(S)-6-(3-Benzhydryl-6-oxo-6H-pyrida...)copy SMILEScopy InChI
Affinity DataIC50: 81nMAssay Description:Agonist activity at PGI2 in human platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81G2ZPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50103404(CHEMBL3398228)copy SMILEScopy InChI
Affinity DataIC50: 87nMAssay Description:Agonist activity at human IP receptor in human platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057HQMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235371(CHEMBL3922000)copy SMILEScopy InChI
Affinity DataIC50: 93nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50191137(CHEMBL212943 | sodium 2-(3-(((1S,2R)-2-(4,5-diphen...)copy SMILEScopy InChI
Affinity DataIC50: 114nMAssay Description:Agonist activity at human PGI2 receptor assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R49QD9PubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50191138(CHEMBL405770 | sodium 2-(3-(((1S,2S)-2-(4,5-diphen...)copy SMILEScopy InChI
Affinity DataIC50: 115nMAssay Description:Agonist activity at human PGI2 receptor assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R49QD9PubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50163296(CHEMBL3793911)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Agonist activity at human IP receptor in platelet rich plasma assessed as inhibition of ADP-induced platelet aggregation preincubated for 1 min follo...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q52RJWPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50235377(CHEMBL3890685)copy SMILEScopy InChI
Affinity DataIC50: 142nMAssay Description:Agonist activity at IP receptor in human primary platelets assessed as inhibition of ADP-induced platelet aggregationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VX0JSMPubMed
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50284366((6-{2-[(E)-Benzhydryloxyimino]-butyl}-5,6,7,8-tetr...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Displacement of [3H]-iloprost from Prostaglandin I2 receptor of human plateletsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29P31MX
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50095205((6-{2-[(E)-Benzhydryloxyimino]-pentyl}-5,6,7,8-tet...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Displacement of [3H]-iloprost from Prostaglandin I2 receptor of human plateletsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29P31MX
TargetProstacyclin receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50002401(8-(4,5-Diphenyl-pyrazol-1-yl)-octanoic acid | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay Description:IC50 value of the compound was evaluated by measuring the displacement of [3H]-iloprost from Prostaglandin I2 receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29K4966PubMed
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