PGD2 是直接从 PGH2 衍生的五种主要酶促前列腺素之一。PGD2 的许多生物效应在体内是由经典的 7 跨膜 GPCR(DP1 受体)1 转导的。然而,第二种受体(与趋化因子相关的 CRTH2 受体)也能结合 PGD2。目前还没有关于 11-脱氧-11-亚甲基-15-酮 PGD2 药理特性的公开研究。
11-deoxy-11-methylene-15-keto Prostaglandin D2 (CAS 958759-75-6) 参考文献
1 Boie, Y., Sawyer, N., Slipetz, D.M., et al. Molecular cloning and characterization of the human prostanoid DP receptor. J Biol Chem 270 18910-18916 (1995). 2 Gervais, F.G., Cruz, R., Chateauneuf, A., et al. Selective modulation of chemokinesis, degranulation, and apoptosis in eosinophils through the PGD2 receptors CRTH2 and DP. J Allergy Clin Immunol 108(6) 982-988 (2002). 3 Monneret, G., Gravel, S., Diamond, M., et al. Prostaglandin D2 is a potent chemoattractant for human eosinophils that acts via a novel DP receptor. Blood 98(6) 1942-1948 (2001). 4 Hirai, H., Tanaka, K., Yoshie, O., et al. Prostaglandin D2 selectivity induces chemotaxis in T helper type 2 cells, eosinophils, and basophils via seven-transmembrane receptor CRTH2. J Exp Med 193(2) 255-261 (2001).