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EPOPROSTENOL Drug Record

  • Summary
  • Interactions
  • Claims
  • EPOPROSTENOL chembl:CHEMBL1139 Approved

    Alternate Names:

    PROSTAGLANDIN I2
    PROSTAGLANDIN X
    U-53217
    PGX
    PROSTACYCLIN
    FLOLAN
    PG-I2
    EPOPROSTENOL
    ACT-385781A
    PGI2

    Drug Info:

    FDA Approval 1995
    Drug Class small molecule
    Drug Indications Platelet Aggregation Inhibitors
    Drug Indications Antihypertensive Agents
    Drug Class platelet aggregation inhibitors
    Drug Class antihypertensive agents
    Year of Approval 1995
    Drug Categories prostacyclin analogues
    Drug Categories anticoagulants
    Drug Categories antiplatelet agents
    Drug Categories drugs that are mainly renally excreted
    Drug Categories prostacycline vasodilator
    Drug Categories vasodilating agents
    Drug Categories vasodilation
    (2 More Sources)

    Publications:

    Ibrahim et al., 2010, Dominant negative actions of human prostacyclin receptor variant through dimerization: implications for cardiovascular disease., Arterioscler. Thromb. Vasc. Biol.
    Chen et al., 2002, TTD: Therapeutic Target Database., Nucleic Acids Res.
    Kasza et al., 2009, Novel signaling pathways promote a paracrine wave of prostacyclin-induced vascular smooth muscle differentiation., J. Mol. Cell. Cardiol.
    Yang et al., 2002, Signaling through Gi family members in platelets. Redundancy and specificity in the regulation of adenylyl cyclase and other effectors., J. Biol. Chem.
    Kobsar et al., 2010, Prostacyclin receptor stimulation facilitates detection of human platelet P2Y(12) receptor inhibition by the PFA-100 system., Platelets
    Cattaneo et al., 2007, Inhibition of the platelet P2Y12 receptor for adenosine diphosphate potentiates the antiplatelet effect of prostacyclin., J. Thromb. Haemost.
    Nakayama, 2010, Genetic polymorphisms of prostacyclin synthase gene and cardiovascular disease., Int Angiol
    Ruan et al., 2008, Characterization of the substrate mimic bound to engineered prostacyclin synthase in solution using high-resolution NMR spectroscopy and mutagenesis: implication of the molecular mechanism in biosynthesis of prostacyclin., Biochemistry
  • EPOPROSTENOL   PTGIS

    Interaction Score: 17.04

    Interaction Types & Directionality:
    inducer (activating)

    Interaction Info:

    PMIDs:
    20357747 18081314


    Sources:
    DrugBank

  • EPOPROSTENOL   PTGIR

    Interaction Score: 5.68

    Interaction Types & Directionality:
    agonist (activating)

    Interaction Info:
    Direct Interaction? False
    Endogenous Drug? True
    Specific Action of the Ligand Agonist

    PMIDs:
    20522800 11752352 19302827 12297509


    Sources:
    TEND TdgClinicalTrial TTD DrugBank GuideToPharmacology

  • EPOPROSTENOL   P2RY12

    Interaction Score: 2.39

    Interaction Types & Directionality:
    agonist (activating)

    Interaction Info:

    PMIDs:
    20085435 12297509 17155953


    Sources:
    DrugBank

  • EPOPROSTENOL   PTGER4

    Interaction Score: 0.57

    Interaction Types & Directionality:
    agonist (activating)

    Interaction Info:
    Specific Action of the Ligand Full agonist
    Endogenous Drug? True

    PMIDs:
    None found


    Sources:
    GuideToPharmacology

  • EPOPROSTENOL   PTGER1

    Interaction Score: 0.54

    Interaction Types & Directionality:
    agonist (activating)

    Interaction Info:
    Direct Interaction? True
    Endogenous Drug? True
    Specific Action of the Ligand Full agonist

    PMIDs:
    None found


    Sources:
    GuideToPharmacology

  • DrugBank: DB01240

    • Version: 5.1.7

    Alternate Names:
    EPOPROSTENOL DrugBank Drug Name
    35121-78-9 CAS Number
    Caripul Drug Brand

    Drug Info:
    Drug Type small molecule
    Drug Groups approved
    Drug Categories anticoagulants

    Publications:
    Nakayama, 2010, Genetic polymorphisms of prostacyclin synthase gene and cardiovascular disease., Int Angiol
    Ruan et al., 2008, Characterization of the substrate mimic bound to engineered prostacyclin synthase in solution using high-resolution NMR spectroscopy and mutagenesis: implication of the molecular mechanism in biosynthesis of prostacyclin., Biochemistry
    Kobsar et al., 2010, Prostacyclin receptor stimulation facilitates detection of human platelet P2Y(12) receptor inhibition by the PFA-100 system., Platelets

  • TEND: EPOPROSTENOL

    • Version: 01-August-2011

    Alternate Names:
    EPOPROSTENOL Primary Drug Name

    Drug Info:
    Year of Approval 1995
    Drug Class antihypertensive agents
    Drug Class platelet aggregation inhibitors

    Publications:

  • TdgClinicalTrial: EPOPROSTENOL

    • Version: January-2014

    Alternate Names:

    Drug Info:
    Drug Indications Antihypertensive Agents
    Drug Indications Platelet Aggregation Inhibitors
    Drug Class small molecule

    Publications:

  • GuideToPharmacology: 135651541

    • Version: 29-September-2020

    Alternate Names:
    PGI2 GuideToPharmacology Ligand Name

    Drug Info:

    Publications:

  • TTD: Epoprostenol

    • Version: 2020.06.01

    Alternate Names:
    D0V0IX TTD Drug ID

    Drug Info:

    Publications:

  • ChemblDrugs: chembl:CHEMBL1139

    • Version: ChEMBL_27

    Alternate Names:

    Drug Info:

    Publications:

Disclaimer: This resource is intended for purely research purposes. It should not be used for emergencies or medical or professional advice.

A finding of a drug-gene interaction or potentially druggable category does not necessarily indicate effectiveness (or lack thereof) of any drug or treatment regimen. A finding of no interaction or no potentially druggable category does not necessarily indicate lack of effectiveness of any drug or treatment regimen. Drug-gene interactions or potentially druggable categories are not presented in ranked order of potential or predicted efficacy.

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DGIdb (v4.2.0 - sha1 afd9f30b) • Last updated 2020-10-21