Herron D K, Goodson T, Bollinger N G, Swanson-Bean D, Wright I G, Staten G S, Thompson A R, Froelich L L, Jackson W T
Lilly Research Laboratories, Eli Lilly & Company, Indianapolis, Indiana 46285-0001.
J Med Chem. 1992 May 15;35(10):1818-28. doi: 10.1021/jm00088a018.
A series of hydroxyacetophenones was prepared for evaluation as leukotriene B4 (LTB4) receptor antagonists, culminating in 1-[5-ethyl-2-hydroxy-4-[[6-methyl-6-(1H-tetrazol-5- yl)heptyl]oxy]phenyl]ethanone (compound 35, LY255283). Using an assay for inhibition of specific [3H]LTB4 binding to human PMN, we found that substitution of a nonpolar substituent in the 5-position was required for activity. Best activity was realized with hydrogen in the 3-position, hydroxyl in the 2-position, short chain alkyl ketone in the 1-position, and a six- or eight-carbon chain linking the oxygen in the 4-position with an unsaturated terminal function. Compound 35, having an IC50 of 87 nM in the binding assay, was chosen for further preclinical evaluation.
制备了一系列羟基苯乙酮作为白三烯B4(LTB4)受体拮抗剂进行评估,最终得到1-[5-乙基-2-羟基-4-[[6-甲基-6-(1H-四氮唑-5-基)庚基]氧基]苯基]乙酮(化合物35,LY255283)。通过检测特异性[3H]LTB4与人中性粒细胞的结合抑制情况,我们发现5位需要取代非极性取代基才能产生活性。3位为氢、2位为羟基、1位为短链烷基酮,以及4位的氧与不饱和末端官能团之间连接六碳或八碳链时活性最佳。化合物35在结合试验中的IC50为87 nM,被选作进一步的临床前评估。