GLPBio

Prostaglandin Receptor

Prostaglandin receptors are a group of g-protein coupled receptor that exhibited a variety of functions in regulation of blood pressure and renal function; smooth muscle contraction; inhibition of plate aggregation; immune response etc.

Products Related to Prostaglandin Receptor(174)

  • GC14173 structure
    GC14173L-161,982
    CAS: 147776-06-5
    Purity: >95.00%

    EP4 receptor antagonist

  • GC14212 structure
    GC14212BW 245C
    CAS: 72814-32-5
    Purity: >98.00%

    DP1 receptor agonist

  • GC14758 structure
    GC14758BM 567
    CAS: 284464-77-3
    Purity: >98%

    dual acting antithrombogenic agent, acting as an inhibitor of thromboxane A2 (TXA2) synthase and as an antagonist of the TP receptor

  • GC14812 structure
    GC14812GW 627368
    CAS: 439288-66-1
    Purity: >99.50%

    prostanoid EP4 receptor antagonist

  • GC14859 structure
    GC14859BW 246C
    CAS: 65705-83-1
    Purity: >98%

    DP receptor agonist

  • GC14879 structure
    GC14879AH 6809
    CAS: 33458-93-4
    Purity: >99.00%

    An EP and DP receptor antagonist

  • GC15157 structure
    GC15157SC 51322
    CAS: 146032-79-3
    Purity: >98.00%

    EP1 prostanoid receptor antagonist

  • GC15213 structure
    GC15213SQ 29,548
    CAS: 98672-91-4
    Purity: >98.00%

    TP receptor antagonist

  • GC15622 structure
    GC15622Dinoprost (Prostaglandin F2a) tromethamine salt
    CAS: 38562-01-5
    Purity: >98.00%

    Prostaglandin F2α (Prostaglandin F2α tromethamine salt) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist.

  • GC15640 structure
    GC15640BAY u3405
    CAS: 116649-85-5
    Purity: >99.00%

    BAY u3405 is a selective thromboxane A2 (TxA2, IC50=14 nM) antagonist, which also antagonizes CRTH2 (IC50=113 nM) by inhibiting PGD2 binding.

  • GC15662 structure
    GC15662ONO-AE3-208
    CAS: 402473-54-5
    Purity: >98.00%

    ONO-AE3-208 is a prostaglandin receptor (EP) 4-specific antagonist with K i values of 1.3nM, 30nM, 790nM, and 2400nM for EP4, EP3, PGF, and thromboxane receptors, respectively.

  • GC15911 structure
    GC15911Iloprost
    CAS: 78919-13-8
    Purity: >98.00%

    Iloprost is a prostacyclin (PGI2) analog that affects platelet aggregation.

  • GC15948 structure
    GC15948Prostaglandin E2
    CAS: 363-24-6
    Purity: >98.00%

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

  • GC16027 structure
    GC16027ONO-8711
    CAS: 216158-34-8
    Purity: >98.00%

    EP1 receptor antagonist

  • GC16170 structure
    GC16170Ethamsylate
    CAS: 2624-44-4
    Purity: >98.00%

    Haemostatic drug

  • GC16477 structure
    GC16477MK-2894
    CAS: 1006036-87-8
    Purity: >98.00%
  • GC16539 structure
    GC16539Butaprost
    CAS: 69685-22-9
    Purity: >98.00%

    A selective agonist for the EP 2 receptors

  • GC16566 structure
    GC16566AL 8810 isopropyl ester
    CAS: 208114-93-6
    Purity: >98%

    lipid soluble, esterified prodrug form of AL 8810, a FP receptor antagonist

  • GC16639 structure
    GC16639NS 304
    CAS: 475086-01-2
    Purity: >99.50%

    NS 304 (NS-304) is an orally available and potent agonist for the Prostacyclin (PGI2) receptor (IP receptor).

  • GC16800 structure
    GC16800MF498
    CAS: 915191-42-3
    Purity: >98.50%

    EP4 receptor antagonist

  • GC16838 structure
    GC16838(±)-Cloprostenol sodium salt
    CAS: 55028-72-3
    Purity: >98.50%

    prostaglandin F2α (PGF2α) analog,FP receptor agonist

  • GC16895 structure
    GC16895AL 8810
    CAS: 246246-19-5
    Purity: >98%

    Antagonist of prostaglandin F2α (FP) receptor.

  • GC17000 structure
    GC17000Nedocromil
    CAS: 69049-73-6
    Purity: >98.50%

    anti-inflammatory agent

  • GC17224 structure
    GC17224AH 23848 (calcium salt)
    CAS: 81496-19-7
    Purity: >98%

    dual antagonist of TP1 and EP4 receptors