Prostaglandin Receptor
Prostaglandin Receptor(前列腺素受体)
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.
Prostaglandin Receptor 相关产品(170)
- GC15622Dinoprost (Prostaglandin F2a) tromethamine saltCAS: 38562-01-5纯度: >98.00%
A water soluble derivative of PGF 2α
- GC16838(±)-Cloprostenol sodium saltCAS: 55028-72-3纯度: >98.50%
A water soluble form of a PGF 2α analog
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC14173 | L-161,982 | 147776-06-5 | >95.00% | |
A potent, selective EP 4 receptor antagonist | ||||
| GC14212 | BW 245C | 72814-32-5 | >98.00% | |
A selective DP 1 receptor agonist | ||||
| GC14758 | BM 567 | 284464-77-3 | - | |
A dual thromboxane synthase inhibitor/TP receptor antagonist | ||||
| GC14812 | GW 627368 | 439288-66-1 | >99.50% | |
A potent EP 4 receptor antagonist | ||||
| GC14859 | BW 246C | 65705-83-1 | - | |
The less active C-8 diastereomer of BW 245C | ||||
| GC14879 | AH 6809 | 33458-93-4 | >99.00% | |
An EP and DP receptor antagonist | ||||
| GC15157 | SC 51322 | 146032-79-3 | >98.00% | |
A selective EP 1 antagonist | ||||
| GC15213 | SQ 29,548 | 98672-91-4 | >98.00% | |
A selective TP receptor antagonist | ||||
| GC15622 | Dinoprost (Prostaglandin F2a) tromethamine salt | 38562-01-5 | >98.00% | |
A water soluble derivative of PGF 2α | ||||
| GC15640 | BAY u3405 | 116649-85-5 | >99.00% | |
A dual TP and DP 2 /CRTH 2 receptor antagonist | ||||
| GC15662 | ONO-AE3-208 | 402473-54-5 | >98.00% | |
An EP 4 receptor antagonist | ||||
| GC15911 | Iloprost | 78919-13-8 | >98.00% / >99.00% | |
Iloprost是一种前列环素（PGI2）类似物，能够影响血小板聚集。 | ||||
| GC15948 | Prostaglandin E2 | 363-24-6 | >98.00% | |
Prostaglandin E2是花生四烯酸在环氧合酶(COX)催化下产生的主要代谢物。 | ||||
| GC16027 | ONO-8711 | 216158-34-8 | >98.00% | |
A potent EP 1 receptor antagonist | ||||
| GC16170 | Ethamsylate | 2624-44-4 | >98.00% | |
Ethamsylate 是一种止血药，也抑制这些前列腺素的生物合成和作用。 | ||||
| GC16477 | MK-2894 | 1006036-87-8 | >98.00% | |
MK-2894 是一种有效、选择性、口服活性和高亲和力 (Ki=0.56 nM) 的全拮抗剂，针对 E prostanoid receptor 4 (EP4 receptor) (IC50=2.5 nM)。 | ||||
| GC16539 | Butaprost | 69685-22-9 | >98.00% | |
A selective agonist for the EP 2 receptors | ||||
| GC16566 | AL 8810 isopropyl ester | 208114-93-6 | - | |
A lipid soluble, esterified prodrug of AL 8810 | ||||
| GC16639 | NS 304 | 475086-01-2 | >99.50% | |
An IP receptor agonist prodrug | ||||
| GC16800 | MF498 | 915191-42-3 | >98.50% | |
A selective EP 4 antagonist | ||||
| GC16838 | (±)-Cloprostenol sodium salt | 55028-72-3 | >98.50% | |
A water soluble form of a PGF 2α analog | ||||
| GC16895 | AL 8810 | 246246-19-5 | - | |
A potent, selective FP receptor antagonist | ||||
| GC17000 | Nedocromil | 69049-73-6 | >98.50% | |
A mast cell stabilizer | ||||
| GC17224 | AH 23848 (calcium salt) | 81496-19-7 | - | |
Dual antagonist of TP and EP 4 receptors | ||||