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Prostanoid Receptors

Products for  Prostanoid Receptors

  1. Cat.No. Product Name Information
  2. GC16838 (±)-Cloprostenol sodium salt

    prostaglandin F2α (PGF2α) analog,FP receptor agonist

    (±)-Cloprostenol sodium salt  Chemical Structure
  3. GC12750 (+)-Fluprostenol Prostaglandin F2α (FP) receptor agonist (+)-Fluprostenol  Chemical Structure
  4. GC11133 16,16-Dimethyl Prostaglandin E2

    derivative of prostaglandin E2

    16,16-Dimethyl Prostaglandin E2  Chemical Structure
  5. GC17224 AH 23848 (calcium salt) dual antagonist of TP1 and EP4 receptors AH 23848 (calcium salt)  Chemical Structure
  6. GC11820 BMY 45778 partial agonist at IP1 prostacyclin receptors BMY 45778  Chemical Structure
  7. GC12101 Epoprostenol Epoprostenol (Prostaglandin I2 (sodium salt)), the synthetic form of the natural prostaglandin derivative prostacyclin (prostaglandin I2), is registered worldwide for the treatment of Pulmonary arterial hypertension (PAH). Epoprostenol  Chemical Structure
  8. GC14812 GW 627368 prostanoid EP4 receptor antagonist GW 627368  Chemical Structure
  9. GC15911 Iloprost Prostacyclin (PGI2) analog;IP, EP1 and EP3 receptors agonist Iloprost  Chemical Structure
  10. GC14173 L-161,982 EP4 receptor antagonist L-161,982  Chemical Structure
  11. GC13067 L-655,240 thromboxane A2/prostaglandin endoperoxide receptor antagonist L-655,240  Chemical Structure
  12. GC13609 L-670,596 thromboxane A2/prostaglandin endoperoxide receptor antagonist L-670,596  Chemical Structure
  13. GC10304 L-798,106 prostanoid EP3 receptor antagonist L-798,106  Chemical Structure
  14. GC16639 NS 304 NS 304 (NS-304) is an orally available and potent agonist for the Prostacyclin (PGI2) receptor (IP receptor). NS 304  Chemical Structure
  15. GC11067 PF 04418948

    EP2 receptor antagonist

    PF 04418948  Chemical Structure
  16. GC15948 Prostaglandin E2

    Prostaglandin E2 is a major metabolite produced from arachidonic acid catalyzed by Cyclooxygenase (COX).

    Prostaglandin E2  Chemical Structure
  17. GC15622 Prostaglandin F2α Prostaglandin F2α (Prostaglandin F2α tromethamine salt) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Prostaglandin F2α  Chemical Structure
  18. GC17410 S18886 S18886 is a thromboxane-prostaglandin receptor antagonist. S18886  Chemical Structure
  19. GC14128 SC 19220 EP1 receptor antagonist SC 19220  Chemical Structure
  20. GC13165 SC 51089 EP1 prostanoid receptor antagonist SC 51089  Chemical Structure
  21. GC15157 SC 51322 EP1 prostanoid receptor antagonist SC 51322  Chemical Structure
  22. GC17861 Sulprostone

    EP3 and EP1 receptor agonist

    Sulprostone  Chemical Structure
  23. GC11122 TCS 2510

    EP4 agonist

    TCS 2510  Chemical Structure
  24. GC13732 TG4-155 brain penetrant EP2 antagonist TG4-155  Chemical Structure
  25. GC13205 U 46619

    Selective agonist of PGH2/TxA2 (TP) receptor

    U 46619  Chemical Structure
  26. GC18132 U-44069 TP receptor agonist U-44069  Chemical Structure

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