Chlorothiophenecarboxamides as P1 surrogates of inhibitors of blood coagulation factor Xa
摘要:
Neutral chlorothiophenecarboxamides bearing an amino acid and a substituted aniline were synthesized and investigated for their factor Xa inhibitory activity in vitro. From selected 2-methylphenyl morpholinones the solution properties were determined. The most soluble and active compounds were then investigated in different animal species to compare the pharmacokinetic parameters. This led to a potent, water soluble and orally bioavailable candidate for further development: EMD 495235. (C) 2004 Elsevier Ltd. All rights reserved.
Novel compounds of the formula (I), in which D, W, X, Y, T, m and R
1
have the meaning indicated in Patent claim
1
, are inhibitors of coagulation factor Xa and can be employed for the prophylaxis and/or therapy of thromboembolic diseases and for the treatment of tumours.
式 (I) 的新型化合物,其中 D、W、X、Y、T、m 和 R
1
具有专利权利要求
1
是凝血因子 Xa 的抑制剂,可用于血栓栓塞性疾病的预防和/或治疗以及肿瘤的治疗。