Potent, selective pyrimidinetrione-based inhibitors of MMP-13

被引:42
|
作者
Reiter, Lawrence A.
Freeman-Cook, Kevin D.
Jones, Christopher S.
Martinelli, Gary J.
Antipas, Amy S.
Berliner, Martin A.
Datta, Kaushik
Downs, James T.
Eskra, James D.
Forman, Michael D.
Greer, Elaine M.
Guzman, Roberto
Hardink, Joel R.
Janat, Fouad
Keene, Nandell F.
Laird, Ellen R.
Liras, Jennifer L.
Lopresti-Morrow, Lori L.
Mitchell, Peter G.
Pandit, Jayvardhan
Robertson, Donald
Sperger, Diana
Vaughn-Bowser, Marcie L.
Waller, Darra M.
Yocum, Sue A.
机构
[1] Pfizer, Global Res & Dev, Groton Labs, Groton, CT 06340 USA
[2] Pfizer Global Res & Dev, Ann Arbor Labs, Ann Arbor, MI 48105 USA
关键词
pyrimidinetrione; matrix metalloprotease; MMP-13; collagenase-3;
D O I
10.1016/j.bmcl.2006.08.066
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Using SAR from two related series of pyrimidinetrione-based inhibitors, compounds with potent MMP-13 inhibition and > 100-fold selectivity against other MMPs have been identified. Despite high molecular weights, c log Ps, and polar surface areas, the compounds are generally well absorbed and have excellent pharmacokinetic (PK) properties when dosed as sodium salts. In a rat fibrosis model, a compound from the series displayed no fibrosis at exposures many fold greater than its MMP-13 IC50. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5822 / 5826
页数:5
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