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Home >> Signaling Pathways >> GPCR/G protein >> Prostanoid Receptors

Prostanoid Receptors

Products for  Prostanoid Receptors

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

    (±)16mchlorophenoxy tetranor PGF2α, (±)16mchlorophenoxy tetranor Prostaglandin F2α, DLCloprostenol

    prostaglandin F2α (PGF2α) analog,FP receptor agonist

     (±)-Cloprostenol sodium salt Chemical Structure
  3. GC12750 (+)-Fluprostenol

    16mtrifluoromethylphenoxy tetranor Prostaglandin F2α

     Prostaglandin F2α (FP) receptor agonist (+)-Fluprostenol Chemical Structure
  4. GC11133 16,16-Dimethyl Prostaglandin E2

    16,16dimethyl PGE2

    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, PGI2, Prostacyclin

     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

    Ciloprost

     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

    CM 9, GW 671021

     prostanoid EP3 receptor antagonist L-798,106 Chemical Structure
  14. GC16639 NS 304

    ACT293987, Selexipag

     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

    Dinoprostone, PGE2

     Prostaglandin E2 is a major metabolite produced from arachidonic acid catalyzed by Cyclooxygenase (COX). Prostaglandin E2 Chemical Structure
  17. GC15622 Prostaglandin F2α

    Dinoprost, PGF2α

     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

    Terutroban,Triplion

     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

    CID132748

     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

    CAY10598

    EP4 agonist

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

    9,11-dideoxy-9α,11α-methanoepoxy PGF2α, 9,11-dideoxy-9α,11α-methanoepoxy Prostaglandin F2α

    Selective agonist of PGH2/TxA2 (TP) receptor

     U 46619 Chemical Structure
  26. GC18132 U-44069

    9,11-dideoxy-9α,11α-epoxymethano PGF2α,9,11-dideoxy-9α,11α-epoxymethano Prostaglandin F2α,9,11-epoxymethano Prostaglandin H2

     TP receptor agonist U-44069 Chemical Structure

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