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Prostaglandin Receptor

Prostaglandin Receptor

Cat. No. Product Name CAS No. Information
CSN17319 Treprostinil Sodium 289480-64-4 Treprostinil sodium is a potent DP1 and EP2 agonist with EC50 values of 0.60.1 and 6.21.2 nM, respectively.
CSN12127 Travoprost   157283-68-6 Travoprost is a synthetic prostaglandin Fsub2sub analog as a potent and selective FP prostaglandin receptor agonist used for controlling the progression of glaucoma or ocular hypertension by reducing intraocular pressure
CSN17247 TG6-10-1 1415716-58-3 TG6-10-1 is an antagonist of prostaglandin E2 receptor subtype EP2
CSN17989 Terutroban 165538-40-9 Terutroban is a thromboxaneprostaglandin endoperoxide receptor antagonist
CSN22249 Taprenepag Isopropyl 1005549-94-9 Taprenepag isopropyl is a highly selective EP2 receptor agonist.
CSN18419 Taprenepag 752187-80-7 Taprenepag is an agonist of prostaglandin E2 receptor with EC50 of 28 nM with hypotensive activity
CSN16883 Setipiprant 866460-33-5 Setipiprant is an orally available, selective CRTH2 antagonist.
CSN23716 Rumodolin 81846-19-7 Rumodolinl a analog of prostacyclin is an agonist of IP receptor that used clinically to treat pulmonary arterial hypertension It is a vasodilator with antithrombotic and anti-inflammatory properties
CSN21394 RO1138452 221529-58-4 RO1138452 is a selective antagonist of prostacyclin (IP) receptor with pKi of 9.3 0.1 in human platelets.
CSN20322 Prostaglandin D2 41598-07-6 Prostaglandin D2 is the major eicosanoid product of mast cells and is released in large quantities during allergic and asthmatic anaphylaxis
CSN13785 PF-04418948 1078166-57-0 PF-04418948 is an antagonist of prostaglandin EP2 receptor with IC50 of 16 nM
CSN18259 ONO-AE3-208 402473-54-5 ONO-AE3-208 is an antagonist of EP4 with Ki of 13 nM and exhibits suppression the invasion and metastasis of prostate cancer cells
CSN22473 OBE022 2005486-31-5 OBE022 is an oral and selective prostaglandin F2 PGF2 receptor antagonist with Kis of 1 nM 26 nM for human and rat FP receptors respectively
CSN16825 NS-304   475086-01-2 NS-304 is an agonist of prostacyclin IP1 receptor with Ki of 260 nM. It is used for the treatment of pulmonary arterial hypertension.
CSN16760 MRE-269   475085-57-5 MRE-269 can act as an agonist of IP receptor and it is an active metabolite of selexipag
CSN17385 MK-2894 Sodium 1006036-88-9 MK-2894 sodium is a highly potent and selective second generation EP4 antagonist.
CSN17384 MK-2894 1006036-87-8 MK-2894 is a highly potent and selective second generation EP4 antagonist.
CSN16851 Misoprostol 59122-46-2 Misoprostol is a synthetic prostaglandin E1 PGE1 analog that is used to prevent gastric ulcers to treat missed miscarriage to induce labor and to induce abortion
CSN16233 MF498 915191-42-3 MF498 is a selective E prostanoid receptor 4 EP4 receptor antagonist displayed strong binding affinity for the EP4 receptor with Ki of 07 nM
CSN11301 Limaprost 74397-12-9 Limaprost is a PGE1 analog and potent platelet adhesion inhibitor.
CSN18339 Laropiprant 571170-77-9 Laropiprant is a potent, selective DP1 receptor antagonist with Ki value of 0.57 nM and exhibits 1,000 fold selectivity over DP2 receptor (Ki0.75 M).
CSN20466 L-798,106 244101-02-8 L-798106 is a potent and highly selective prostanoid EP3 receptor antagonist Ki values are 03 916 5000 and 5000 nM at EP3 EP4 EP1 and EP2 respectively and it can attenuate sulprostone-induced inhibition of EFS-evoked twitch and contractile responses in vivo
CSN11189 Iloprost 78919-13-8 Iloprost is a synthetic analogue of prostacyclin PGI2
CSN22113 Ifetroban 143443-90-7 Ifetroban is a long-acting thromboxane A2 receptor antagonist with antiplatelet activity
CSN18274 GW627368 439288-66-1 GW627368 is a potent and selective competitive antagonist of prostanoid EP4 receptor (Ki 100 nM) with additional human TP receptor affinity (Ki 150 nM).
CSN18265 Grapiprant 415903-37-6 Grapiprant is a selective EP4 receptor antagonist whose physiological ligand is prostaglandin E2 (PGE2).
CSN18130 Evatanepag 223488-57-1 Evatanepag is an EP2 receptor selective prostaglandin E2 PGE2 agonist that induces local bone formation with EC50 of 03 nM
CSN10940 Ethamsylate   2624-44-4 Ethamsylate acts as a haemostatic drug by increasing capillary endothelial resistance and promoting platelet adhesion
CSN20029 Esuberaprost Sodium 88475-69-8 Esuberaprost is a potential substance for treating pulmonary arterial hypertension (PAH).
CSN20026 Esuberaprost 94132-88-4 Esuberaprost is a potential substance for treating pulmonary arterial hypertension (PAH).
CSN10910 Enprostil 73121-56-9 Enprostil is a synthetic prostaglandin designed to resemble dinoprostone
CSN21111 E-7046 1369489-71-3 E7046 is a specific antagonist of the type 4 prostaglandin E2 (PGE2) receptor EP4. It possesses significant antitumor growth activity in multiple preclinical tumor models through modulating myeloid cells, including tumor-associated macrophages and myeloid-derived suppressor cells.
CSN11793 Dinoprost Tromethamine 38562-01-5 Dinoprost tromethamine is a natural prostaglandin used as an abortifacient.
CSN11792 Dinoprost 551-11-1 Dinoprost is a naturally occurring prostaglandin used in medicine to induce labor and as an abortifacient.
CSN13150 CJ-42794 847728-01-2 CJ-42794 is a selective prostaglandin E receptor subtype 4 (EP4) antagonist, inhibits 3H-PGE2 binding to the human EP4 receptor with a mean pKi of 8.5, a binding affinity that was at least 200-fold selective for the human EP4 receptor than other human EP receptor subtypes (EP1, EP2, and EP3).
CSN22111 Carbacyclin 69552-46-1 Carbacyclin is a PGI2 analogue, acts as a prostacyclin (PGI2) receptor agonist and vasodilator, and potently inhibits platelet aggregation.
CSN17217 Bimatoprost 155206-00-1 Bimatoprost, a analog of prostaglandin, can control the progression of glaucoma and ocular hypertension.
CSN19378 Alprostadil 745-65-3 Alprostadil is an analog of prostaglandin which is prostaglandin E1 agonist with vasodilatory properties and can be used to treat erectile dysfunction
CSN17196 AH 6809 33458-93-4 AH 6809 is an EP and DP receptor antagonist with nearly equal affinity for the cloned human EP1, EP2, EP3-III, and DP1 receptors.
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