Discovery of potent antagonists of leukocyte function-associated antigen-1/intercellular adhesion molecule-1 interaction. 3. Amide (C-ring) structure-activity relationship and improvement of overall properties of arylthio cinnamides

被引:22
作者
Pei, ZH
Xin, ZL
Liu, G
Li, YH
Reilly, EB
Lubbers, NL
Huth, JR
Link, JT
von Geldern, TW
Cox, BF
Leitza, S
Gao, Y
Marsh, KC
DeVries, P
Okasinski, GF
机构
[1] Abbott Labs, Dept Metab Dis Res, Div Pharmaceut Prod, Abbott Pk, IL 60064 USA
[2] Abbott Labs, Dept Integrat Pharmacol, Div Pharmaceut Prod, Abbott Pk, IL 60064 USA
[3] Abbott Labs, Dept Adv Technol, Div Pharmaceut Prod, Abbott Pk, IL 60064 USA
[4] Abbott Labs, Dept Drug Anal, Div Pharmaceut Prod, Abbott Pk, IL 60064 USA
关键词
D O I
10.1021/jm010059w
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The interaction of LFA-1 and ICAM-1 plays an important role in the cell adhesion process. On the basis of previously reported SAR and structural information on the binding of our p-arylthiocinnamide series to LFA-1, we have identified the cyclic amide (C-ring) as a site for modification. Improvement in potency and, more importantly, in the physical properties and pharmacokinetic profiles of the leading compounds resulted from this modification. One of the best compounds (11f) is also shown to reduce myocardial infarct size in rat.
引用
收藏
页码:2913 / 2920
页数:8
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