| 摘要 |
Imidazole derivatives of formula: [DPIM]-S(O)p-W-Y, wherein [DPIM] is of formula (I), wherein R and R<1> each represents hydrogen, halogen, alkyl or alkoxy, p is 0, 1 or 2, W represents alkylene, Y represents an optionally substituted 5- or 6-membered unsaturated ring containing 1 to 4 nitrogen atoms, and pharmaceutically acceptable acid addition salts thereof, are inhibitors of acyl coenzyme-A:cholesterol-O-acyle transferase and of the binding of thromboxane TxA2 to its receptors and are useful in therapy. |
