PT - JOURNAL ARTICLE AU - Keiichi Kuwano AU - Asami Hashino AU - Tetsuo Asaki AU - Taisuke Hamamoto AU - Tetsuhiro Yamada AU - Kaori Okubo AU - Kenji Kuwabara TI - 2-{4-[(5,6-Diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}-<em>N</em>-(methylsulfonyl)acetamide (NS-304), an Orally Available and Long-Acting Prostacyclin Receptor Agonist Prodrug AID - 10.1124/jpet.107.124248 DP - 2007 Sep 01 TA - Journal of Pharmacology and Experimental Therapeutics PG - 1181--1188 VI - 322 IP - 3 4099 - http://jpet.aspetjournals.org/content/322/3/1181.short 4100 - http://jpet.aspetjournals.org/content/322/3/1181.full SO - J Pharmacol Exp Ther2007 Sep 01; 322 AB - Prostacyclin (PGI2) and its analogs are useful for the treatment of various vascular disorders, but their half-lives are too short for widespread clinical application. To overcome this drawback, we have synthesized a novel diphenylpyrazine derivative, 2-{4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}-N-(methylsulfonyl)acetamide (NS-304), a prodrug of the active form {4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}acetic acid (MRE-269). NS-304 is an orally available and potent agonist for the PGI2 receptor (IP receptor). The inhibition constant (Ki) of MRE-269 for the human IP receptor was 20 nM; in contrast, the Ki values for other prostanoid receptors were &gt;2.6 μM. MRE-269 was therefore a highly selective agonist for the IP receptor. The plasma concentrations of MRE-269 remained near peak levels for more than 8 h after oral administration of NS-304 to rats and dogs, and NS-304 increased femoral skin blood flow in rats in a long-lasting manner without affecting the hemodynamics. These findings indicate that NS-304 acts as a long-acting IP receptor agonist in vivo. The continuous vasodilation evoked by NS-304 was not attenuated by repeated treatment, indicating that NS-304 is unlikely to cause severe desensitization of the IP receptor in rats. Moreover, a microdose pharmacokinetic study in which NS-304 was orally administered to healthy male volunteers showed conversion of NS-304 to MRE-269 and a long plasma elimination half-life for MRE-269 (7.9 h). In conclusion, NS-304 is an orally available and long-acting IP receptor agonist prodrug, and its active form, MRE-269, is highly selective for the IP receptor. Therefore, NS-304 is a promising drug candidate for various vascular diseases, especially pulmonary arterial hypertension and arteriosclerosis obliterans.