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Substituted N,N-bis-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity

机译:用于抑制胆固醇酯转移蛋白活性的取代的N,N-双苯基氨基醇化合物

摘要

The invention relates to substituted polycyclic aryl and heteroaryl tertiary-heteroalkylamine compounds useful as inhibitors of cholesteryl ester transfer protein (CETP; plasma lipid transfer protein-I) and compounds, compositions and methods for treating atherosclerosis and other coronary artery diseases. Preferred tertiary-heteroalkylamine compounds are substituted N,N-bis-phenyl aminoalcohols. A preferred specific N,N-bis-phenyl aminoalcohol is the compound: embedded image
机译:本发明涉及用作胆固醇酯转移蛋白(CETP;血浆脂质转移蛋白-I)抑制剂的取代的多环芳基和杂芳基叔杂烷基胺化合物,以及用于治疗动脉粥样硬化和其他冠状动脉疾病的化合物,组合物和方法。优选的叔杂烷基胺化合物是取代的N,N-双苯基氨基醇。优选的特定的N,N-双苯基氨基醇是该化合物:<化学ID =“ CHEM-US-00001”> <图像alt =“嵌入式图像” file =“ US06677382-20040113-C00001.GIF” he =“ 84.00105 “ id =” EMI-C00001“ imgContent =”未定义“ imgFormat =” GIF“ wi =” 152.66475“ />

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