Abstract
The design, synthesis, and biological evaluation of N-arylprolyl-dipeptide derivatives as small molecule VLA-4 antagonists is described. Potency against VLA-4 and alpha(4)beta(7) and rat pharmacokinetic evaluation revealed some advantages over the related N-(arylsulfonyl)-prolyl-dipeptide analogues.
MeSH terms
-
Animals
-
Dipeptides / blood
-
Dipeptides / chemical synthesis*
-
Dipeptides / pharmacokinetics
-
Dipeptides / pharmacology*
-
Half-Life
-
Integrin alpha4beta1 / antagonists & inhibitors*
-
Metabolic Clearance Rate
-
Molecular Structure
-
Rats
-
Rats, Sprague-Dawley
-
Structure-Activity Relationship
Substances
-
Dipeptides
-
Integrin alpha4beta1