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Prostaglandin Receptor Ligands

  • AH-6809
    A prostaglandin DP-receptor inhibitor. The compound has been reported to antagonize the anti-aggregatory activity of BW245C, 9 α, 11 β-PGF2, and PGD2.
    Katalog #CAS NummerSummenformelMenge
    sc-20134233458-93-4C17H14O55 mg/25 mg
  • AL 6598
    Katalog #CAS NummerSummenformelMenge
    sc-358796170291-06-2C23H39ClO5500 µg/1mg
  • AA 2414
    Thromboxane A2 (TP) receptor antagonist. Antiasthmatic agent; inhibits platelet aggregation and bronchoconstriction induced by a TXA2 mimetic in guinea pigs.
    Katalog #CAS NummerSummenformelMenge
    sc-203796112665-43-7C22H26O410 mg/50 mg
  • BAY-u 3405
    Suppresses PGD2-induced migration of human eosinophils (IC50 = 170 nM). Potent dual antagonist of TP/DP2 (CRTH2) prostanoid receptors (Ki values are 4.3, 4.5 and > 10000 nM for hDP2, hTP and hDP1 receptors respectively).
    Katalog #CAS NummerSummenformelMenge
    sc-203834116649-85-5C21H21FN2O4S10 mg/50 mg
  • Carbacyclin (Carbocyclic PGI2)
    Carbacyclin is a stable analog of prostacyclin shown to inhibit platelet aggregation.
    Katalog #CAS NummerSummenformelMenge
    sc-20125069552-46-1C21H34O41 mg/10 mg
  • 1-(7-Carboxyheptyl)imidazole
    Selective inhibitor of thromboxane synthetase.
    Katalog #CAS NummerSummenformelMenge
    sc-20591568887-68-3C11H18N2O210 mg/25 mg
  • cis-5,8,11,14,17-Eicosapentaenoic acid sodium salt
    This compound reduces thromboxane A2 production.
    Katalog #CAS NummerSummenformelMenge
    sc-21473573167-03-0C20H29NaO25 mg/10 mg
  • Cloprostenol Sodium
    A synthetic F series prostaglandin that functions as a potent agonist towards the FP receptor.
    Katalog #CAS NummerSummenformelMenge
    sc-20133855028-72-3C22H28O6Cl ·Na1 mg/10 mg
  • 16,16-Dimethyl-prostaglandin E2
    Prostaglandin E2 analog with potent cytoprotective activity and enhanced metabolic resistance yielding a longer half-life in vivo. Acts on all 4 EP receptors (EP1,2,3, and 4).
    Katalog #CAS NummerSummenformelMenge
    sc-20124039746-25-3C22H36O51 mg
  • 13,14-epoxy Travoprost
    An impurity generated in the production of fluprostenol isopropyl ester.
    Katalog #CAS NummerSummenformelMenge
    sc-287303n.n.C26H35F3O71 mg/5 mg
  • Fluprostenol
    Fluprostenol is a prostaglandin F (FP) receptor agonist that is more selective than PGF2α (sc-201227).
    Katalog #CAS NummerSummenformelMenge
    sc-20133640666-16-8C23H29F3O61 mg/10 mg
  • GW 627368X
    A selective and potent competitive antagonist of the EP4 receptor with additional human TP receptor affinity.
    Katalog #CAS NummerSummenformelMenge
    sc-221702439288-66-1C30H28N2O6S1 mg/5 mg
  • Latanoprost
    Latanoprost is a prodrug (isopropyl ester) of 17-phenyl-13,14-dihydro prostaglandin F2α. The free acid form is a potent agonist at FP receptors. It is in clinical use as a topical antiglaucoma agent and has been shown to reduce IOP (intraoccular pressure).
    Katalog #CAS NummerSummenformelMenge
    sc-201354130209-82-4C26H40O51 mg/5 mg
  • L-798,106
    Potent and highly selective prostanoid EP3 receptor antagonist (Ki values are 0.3, 916, > 5000 and > 5000 nM at EP3, EP4, EP1 and EP2 respectively). Attenuates sulprostone-induced inhibition of EFS-evoked twitch and contractile responses in vivo.
    Katalog #CAS NummerSummenformelMenge
    sc-204047244101-02-8C27H22BrNO4S10 mg/50 mg
  • L-655,240
    A potent inhibitor of contractions induced by prostaglandin endoperoxide analogs. Also reported to be an inhibitor of thromboxane receptors.
    Katalog #CAS NummerSummenformelMenge
    sc-201350103253-15-2C21H21ClFNO21 mg/5 mg
  • L-670,596
    An orally active potent and selective thromboxane A2/prostaglandin endoperoxide receptor antagonist. Inhibits human platelet aggregation in vitro and the U-44069-induced contractions of guinea-pig trachea. Also prevents thromboxane-mediated endothelial cell death.
    Katalog #CAS NummerSummenformelMenge
    sc-204041121083-05-4C22H21F2NO4S10 mg
  • Misoprostol (SC-29333)
    A synthetic E prostaglandin that has been shown to prevent tissue corrosion induced by certain anti-inflammatory compounds. Shown to have negative effects on the murine nervous system.
    Katalog #CAS NummerSummenformelMenge
    sc-20126459122-46-2C22H38O510 mg/100 mg
  • Ozagrel hydrochloride
    Potent and selective inhibitor of thromboxane (TXA2) synthetase (IC50 = 4 nM). Does not inhibit prostacyclin (PGI2) synthetase, cyclooxygenase or PGE2 isomerase (IC50 > 1 mM). Inhibits platelet aggregation in vitro and arachidonate-induced arterial contraction in vivo.
    Katalog #CAS NummerSummenformelMenge
    sc-20415374003-18-2C13H14N2O2.HCl10 mg/50 mg
  • Picotamide
    Picotamide is a dually active thromboxane A2 and thromboxane A2 synthase inhibitor. It has been shown to exhibit platelet inhibitory effects ex vivo and in vitro.
    Katalog #CAS NummerSummenformelMenge
    sc-20133432828-81-2C21H10N4O310 mg/50 mg
  • 17-Phenyl-trinor-prostaglandin E2
    A synthetic analog of PGE2 (sc-201225), found to be a selective EP1 and EP3 receptor agonist, unlike PGE2 which antagonizes a variety of EP receptors.
    Katalog #CAS NummerSummenformelMenge
    sc-20125538315-43-4C23H30O51 mg/10 mg
  • PTA2 (Pinane thromboxane A2)
    A chemically stable, carbocyclic analog of thromboxane A2, that has been shown to act as a TP receptor antagonist which leads to coronary artery contraction and platelet aggregation induced by prostaglandin endoperoxide analogs and arachidonic acid.
    Katalog #CAS NummerSummenformelMenge
    sc-20117771111-01-8C24H40O31 mg
  • SC-51089
    A selective antagonist of prostaglandin E2, which displays specificity towards the EP1 receptor subtype. This compound contains a diacylhydrazine moiety, which has often been observed to release hydrazine.
    Katalog #CAS NummerSummenformelMenge
    sc-201344146033-02-5C22H19ClN4O3 ·HCl5 mg/25 mg
  • SC-51322
    A potent and selective prostaglandin E2 antagonist (pA2=8.1). Displays in vivo analgesic activity in the mouse (ED50=0.9 mg/kg)1.
    Katalog #CAS NummerSummenformelMenge
    sc-205848n.n.C22H20ClN3O4S5 mg/25 mg
  • SQ-29548
    A compound that reversibly and competitively acts as a thromboxane A2/prostraglandin endoperoxide receptor antagonist.
    Katalog #CAS NummerSummenformelMenge
    sc-20133298672-91-4C21H29N3O41 mg/10 mg
  • Seratrodast
    A potent and selective thromboxane A2 receptor antagonist with antioxidant effects. Inhibits peroxide-induced vasoconstriction in human placenta and bronchoconstriction in guinea pigs.
    Katalog #CAS NummerSummenformelMenge
    sc-201352112665-43-7C22H26O410 mg/50 mg
  • Sulprostone
    A metabolism-resistant synthetic analog of PGE2, that is a selective EP3 prostanoid receptor agonist. Shown to be a potent stiumulator of uterine smooth muscle contractions.
    Katalog #CAS NummerSummenformelMenge
    sc-20134860325-46-4C23H31NO7S1 mg/5 mg
  • U-46619
    Shown to be a potent agonist of thromboxane A2 receptor and also reported to cause constriction of coronary arteries. When bound to TXA2 receptors, this compound inhibits the release of hippocampal noradrenaline.
    Katalog #CAS NummerSummenformelMenge
    sc-20124256985-40-1C21H34O41 mg/10 mg