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Prostaglandin Receptor
Prostaglandin Receptor Isoform Specific Products
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Prostaglandin Receptor Related Products (767)
Related Products (767)
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Antibodies (2)
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Prostaglandin Receptor Isoform Comparison
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Laropiprant sodium
0 ImagesCat. No.: HY-50175ACAS No.: 572874-50-1Synonyms: MK-0524 sodium -
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MK-8318
0 ImagesCat. No.: HY-112604CAS No.: 1416581-40-2MK-8318 is a potent and selective CRTh2 receptor antagonist with a Ki of 5.0 nM. -
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ARRY-502
0 ImagesCat. No.: HY-124065CAS No.: 1202891-16-4ARRY-502 is an orally active, potent and selective CRTh2 antagonist. ARRY-502 blocks PGD2-mediated Th2 inflammation (e.g., eosinophil activation, airway hyperresponsiveness). ARRY-502 is promising for research of Th2-related asthma. -
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ICI 185282
0 ImagesCat. No.: HY-101235CAS No.: 106393-80-0ICI 185282 is a potent, selective, orally active thromboxane A2 (TXA₂) receptor antagonist. ICI 185282 causes dose-dependent inhibition of U-46619 (HY-108566)-induced platelet aggregation ex-vivo in guinea-pig. ICI 185,282 inhibits bronchospasm induced by U-46619, PGD2 (HY-101988), PGF2α (HY-12956), arachidonic acid (HY-109590), LTD4 and PAF (HY-108635) in vivo. ICI 185282 can be used for bronchial asthma research. -
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ACT-774312
0 ImagesCat. No.: HY-182637CAS No.: 1809863-68-0ACT-774312 is a potent and selective CRTH2 antagonist with an IC50 of 4 nM. ACT-774312 blocks the activity and internalization of the CRTH2 receptor, and inhibits PGD2-induced morphological changes in eosinophils. ACT-774312 can be used in the research of nasal polyps and type 2 inflammatory diseases. -
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GSK345931A
0 ImagesCat. No.: HY-111258CAS No.: 869499-38-7GSK345931A is an EP1 receptor antagonist. GSK345931A shows measurable CNS penetration in the mouse and rat and potent analgesic efficacy in acute and sub-chronic models of inflammatory pain. -
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MK-1029
0 ImagesCat. No.: HY-123787CAS No.: 1242273-04-6MK-1029 is a DP2 antagonist. MK-1029 can be used in research on respiratory diseases such as asthma. -
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NVP-QAV680
0 ImagesCat. No.: HY-12284CAS No.: 872365-16-7NVP-QAV680 is a potent and selective CRTh2 receptor antagonist with low nanomolar (nM) functional potency to inhibit CRTh2-driven activation of human eosinophils and Th2 lymphocytes. NVP-QAV680 exhibits good oral bioavailability and demonstrates efficacy in CRTh2-dependent mechanisms and allergic disease models in rats. -
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(R)-Vorbipiprant
0 ImagesCat. No.: HY-163651CAS No.: 2502965-92-4Synonyms: (R)-CR6086(R)-Vorbipiprant ((R)-CR6086) is an orally active antagonist for prostaglandin E2 receptor 4 (EP4) with Ki of 16.6 nM for human EP4. (R)-Vorbipiprant inhibits PGE2 (HY-101952)-induced cAMP production with an IC50 of 22 nM. (R)-Vorbipiprant exhibits immunomodulatory and anti-angiogenic activities, and ameliorates the collagen-induced arthritis in mice. -
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TGI-15
0 ImagesCat. No.: HY-178792CAS No.: 3073601-32-5TGI-15 is a highly selective prostaglandin F receptor antagonist. TGI-15 inhibits downstream signaling pathways by blocking the binding of PGF2 α to FP receptors. TGI-15 can be used for research on fibrotic and inflammatory conditions. -
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EP1 receptor antagonist-1
0 ImagesCat. No.: HY-177544CAS No.: 330795-70-5EP1 receptor antagonist-1 (Compound Example 5a freebase) is an EP1 prostaglandin receptor antagonist. EP1 receptor antagonist-1 is promising for research of urinary system-related diseases. -
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ASP7657 free base
0 ImagesASP7657 free base is an orally active EP4 receptor antagonist, with Kis of 2.21 and 6.02 nM for the human and rat EP4 receptors. -
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(S)-Trimetoquinol hydrochloride
0 ImagesCat. No.: HY-108282CAS No.: 18559-59-6Synonyms: (S)-AQL 208 hydrochloride; (S)-TMQ hydrochloride(S)-Trimetoquinol hydrochloride (Compound 1) is a apotent, nonselective, nonclassical β-adrenergic agonist and nonprostanoid thromboxane A2/prostaglandin H2 antagonist. (S)-Trimetoquinol hydrochloride can be used for research of neurological and cardiovascular disease. -
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CGS-22652
0 ImagesCat. No.: HY-19132CAS No.: 134235-78-2CGS 22652 is a potent thromboxane A2 receptor antagonist. CGS 22652 has selective thromboxane A2 synthase inhibitory properties. CGS 22652 can be used in the research of coronary artery thrombosis. -
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I-SAP
0 ImagesCat. No.: HY-118044CAS No.: 133538-58-6I-SAP is a radioiodinated TXA2/PGH2 receptor antagonist. The bind between I-SAP and the receptors, is inhibited by the histidine modifying reagent diethyl-pyrocarbonate (DEPC). -
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AH22921
0 ImagesCat. No.: HY-115827CAS No.: 74480-23-2AH22921 is an EP4 prostaglandin receptor antagonist with the activity of antagonizing the activation of adenylate cyclase by prostaglandins in CHO cells. AH22921 can shift the PGE2 concentration-response curve to the right in CHO cells. It is a non-competitive antagonist that is selective for EP4 receptors and has an antagonistic effect on EP4 receptors in CHO cells, but does not affect the PGE2 concentration-response curve in NPE cells containing EP2 receptors. -
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MF266-1
0 ImagesCat. No.: HY-111304CAS No.: 848188-18-1MF266-1 is a selective E prostanoid receptor 1 (EP1) antagonist with an Ki value of 3.8 nM. MF266-1 also has moderate selectivity for thromboxane A2 receptor (TP). MF266-1 is promising for research of arthritis. -
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KF15766
0 ImagesCat. No.: HY-100570CAS No.: 124907-44-4KF15766 (compd 34E) is an orally active TXA2 and H1 dual antagonist with Kis of 740 and 20 nM. KF15766 can be used for antiallergic research. -
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Domitroban
0 ImagesCat. No.: HY-106891CAS No.: 112966-96-8Domitroban is a thromboxane A2 receptor (TBXA2R) antagonist. Domitroban can inhibit platelet aggregation. Domitroban can be used for the research of cardiovascular disease, such as thrombosis. -
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EP3 antagonist 4
0 ImagesCat. No.: HY-153256CAS No.: 2408297-80-1EP3 antagonist 4 (Compound 28) is an EP3 antagonist, with a Ki value of 2 nM for hEP. EP3 antagonist 4 shows low in vivo clearance, high oral AUC, and good bioavailability in the rat full PK studies. EP3 antagonist 4 can be used for research of beta cell dysfunction in diabetes. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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