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Synthesis and in vitro profile of 7-substituted quinoline chromanols as novel, non-acidic LTB4 antagonists
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, no. 8 (1995): 887-892
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Abstract
The development of novel LTB(4) antagonists from a class of quinolylmethyl LTD(4) antagonists is described. These alpha-methyl quinolylmethyl chromanols were found to have good in vitro activity.
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