Maryanoff Bruce E, McComsey David F, Costanzo Michael J, Yabut Stephen C, Lu Tianbao, Player Mark R, Giardino Edward C, Damiano Bruce P
Vascular Research Team, Johnson & Johnson Pharmaceutical Research & Development, Spring House, PA 19477-0776, USA.
Chem Biol Drug Des. 2006 Jul;68(1):29-36. doi: 10.1111/j.1747-0285.2006.00408.x.
Compound 2 (RWJ-445167; 3DP-10017), a dual inhibitor of thrombin and factor Xa, was advanced into human clinical studies. However, its oral bioavailability in humans proved to be below acceptable limits. To address this issue, we explored a prodrug approach involving numerous guanidine derivatives. Prodrug candidates of classes A (carbamate derivatives), B (imidate derivatives), and C (alkyl and acyl derivatives), compounds 3-6, were synthesized and evaluated for anticoagulant activity at 2 h after oral administration to rats. In comparison to the parent drug (2), little worthwhile improvement was observed for the prodrug candidates.
化合物2(RWJ-445167;3DP-10017)是一种凝血酶和Xa因子的双重抑制剂,已进入人体临床研究。然而,其在人体中的口服生物利用度被证明低于可接受的限度。为了解决这个问题,我们探索了一种涉及多种胍衍生物的前药方法。合成了A类(氨基甲酸酯衍生物)、B类(亚氨酯衍生物)和C类(烷基和酰基衍生物)的前药候选物,即化合物3-6,并在给大鼠口服给药2小时后评估其抗凝活性。与母体药物(2)相比,前药候选物几乎没有观察到有价值的改善。