Kita Y, Ohkubo K, Hirasawa Y, Katayama Y, Ohno M, Nishino S, Kato M, Yoshida K
New Drug Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Osaka, Japan.
Eur J Pharmacol. 1995 Mar 6;275(2):125-30. doi: 10.1016/0014-2999(94)00750-2.
We report that (+/-)-(E)-ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexeneamide (FK409) decomposes and releases nitric oxide (NO) spontaneously in solution. (+/-)-N-[(E)-4-Ethyl-3-[(Z)-hydroxyimino]-5-nitro-3-hexen-1- yl]-3- pyridinecarboxamide (FR144420) was synthesized with the aim of discovering a compound with longer duration of effects in vivo, compared with FK409. FR144420, like FK409, released NO spontaneously in solution, but the amount of NO released from FR144420 during a 5-min incubation was half the amount from FK409. In addition, FR144420 spontaneously decomposed and generated nitrite, which is an oxidative metabolite of NO, at half the rate of FK409. In a vasorelaxant study with isolated rat aorta, FR144420 had a weaker potency than FK409 (EC50 = 54 and 8.1 nM, respectively). In in vivo studies, FR144420 decreased mean blood pressure immediately after intravenous and oral administration to conscious rats. The maximum hypotensive effects of FR144420 were less than those of FK409. However, the durations of FR144420-induced (i.v. and p.o.) hypotensive effects were longer than those of FK409-induced effects. In conclusion, FR144420 is more stable and releases NO more slowly in solution than does FK409. In in vivo experiments, FR144420 showed a longer duration of effects than FK409. FR144420 may be very useful for investigating the in vivo actions of NO.
我们报告,(±)-(E)-乙基-2- [(E)-羟基亚氨基]-5-硝基-3-己烯酰胺(FK409)在溶液中会自发分解并释放一氧化氮(NO)。合成了(±)-N- [(E)-4-乙基-3- [(Z)-羟基亚氨基]-5-硝基-3-己烯-1-基]-3-吡啶甲酰胺(FR144420),目的是发现一种与FK409相比在体内作用持续时间更长的化合物。FR144420与FK409一样,在溶液中会自发释放NO,但在5分钟孵育期间从FR144420释放的NO量是FK409释放量的一半。此外,FR144420会自发分解并生成亚硝酸盐,亚硝酸盐是NO的一种氧化代谢产物,其生成速率是FK409的一半。在对离体大鼠主动脉的血管舒张研究中,FR144420的效力比FK409弱(EC50分别为54和8.1 nM)。在体内研究中,给清醒大鼠静脉内和口服给药后,FR144420会立即降低平均血压。FR144420的最大降压作用小于FK409。然而,FR144420诱导的(静脉内和口服)降压作用的持续时间比FK409诱导的作用持续时间更长。总之,与FK409相比,FR144420在溶液中更稳定,释放NO的速度更慢。在体内实验中,FR144420的作用持续时间比FK409更长。FR144420可能对研究NO的体内作用非常有用。