| Autor: |
Quan, M. L., Liauw, A. Y., Ellis, C. D., Pruitt, J. R., Carini, D. J., Bostrom, L. L., Huang, P. P., Harrison, K., Knabb, R. M., Thoolen, M. J., Wong, P. C., Wexler, R. R. |
| Zdroj: |
Journal of Medicinal Chemistry; July 29, 1999, Vol. 42 Issue: 15 p2752-2759, 8p |
| Abstrakt: |
Thrombosis is a major cause of mortality in the industrialized world. Therefore, the prevention of blood coagulation has become a major target for new therapeutic agents. One attractive approach is the inhibition of factor Xa (FXa), the enzyme directly responsible for prothrombin activation. We report a series of novel biaryl-substituted isoxazoline derivatives in which the biaryl moiety was designed to interact with the S4 aryl-binding domain of the FXa active site. Several of the compounds herein have low nanomolar affinity for FXa, have good in vitro selectivity for FXa, and show potent antithrombotic efficacy in vivo. The three most potent compounds (33, 35, and 37) have inhibition constants for human FXa of 3.9, 2.3, and 0.83 nM, respectively, and ID50's ranging from 0.15 to 0.26 μmol/kg/h in the rabbit arterio-venous thrombosis model. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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