| 摘要 |
Inhibiting leucotriene synthesis in patients with novel substituted N-(quinolin-2-yl-methoxy)benzyl-sulphonyl-urea of the formula (I) in which A, B, D, E, G, K AND M each independently is H, OH, halogen, CF3, OCF3, COOH, alkyl, alkoxy, alkoxycarbonyl or aryl, R1 is alkyl or cycloalky,, R2 and R3 each independently is H or alkyl, and R4 is alkyl, aryl or a heterocyclic radical, and salts thereof. Le A 27 130
|
