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BMS-626529的系列稀释液的结合溶液（30μL）平衡，然后吸附至MicroBioSpin 6色谱柱。将柱离心（~14,000rpm）5分钟，收集洗脱液，用闪烁计数器测定放射性。为了测量解离动力学，将150nM [3H] BMS-626529或90nM [3H] BMS-488043与60nM gp120在环境温度下孵育1小时以实现平衡结合，然后大摩尔过量（14倍）加入可溶性CD4蛋白以驱动解离。以指定的时间间隔取出等分试样，吸附到离心柱上，并离心，并对洗脱液中的放射性进行定量。比较来自具有和不具有可溶性CD4攻击的平行样品的氚信号允许测定结合的化合物百分比[1]。",{"key":243,"value":244},"细胞实验","在连续稀释的BMS-626529存在下进行细胞毒性测定长达6天，并使用XTT测定法定量细胞活力。为了确定CC50值（杀死50％细胞所需的药物浓度），最初以0.1×10 6个细胞\u002F mL的密度接种实验室适应的外周血单核细胞（PBMC）。在没有化合物的情况下，6天后细胞密度通常达到1×106到1.2×106 \u002F mL [1]。",{"key":246,"value":247},"参考文献","[1].\nNowicka-Sans B, et al. In vitro antiviral characteristics of HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068. Antimicrobial Agents and Chemotherapy (2012), 56(7), 3498-3507.\n[2].\nNettles RE, et al. Pharmacodynamics, safety, and pharmacokinetics of BMS-663068, an oral HIV-1 attachment inhibitor in HIV-1-infected subjects. 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