| 摘要 |
Inhibiting leucotriene synthesis in patients with novel substituted N-(quinolin-2-yl-methoxy)benzylsulphonyl-urea of the formula <IMAGE> (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 cycloalkyl, R2 and R3 each independently is H or alkyl, and R4 is alkyl, aryl or a heterocyclic radical, and salts thereof.
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