作者:Karen E Sexton、Helen T Lee、Mark Massa、Janak Padia、William C Patt、Peggy Liao、Jason K Pontrello、Bruce D Roth、Mark A Spahr、Randy Ramharack
DOI:10.1016/j.bmc.2002.04.001
日期:2003.11
Compounds of the general structure A and B were investigated for their activity as lipoprotein(a), [Lp(a)], assembly (coupling) inhibitors. SAR around the amino acid derivatives (structure A) gave compound 14-6 as a potent coupling inhibitor. Oral closing of compound 14-6 to Lp(a) transgenic mice and cymologous monkeys resulted in a > 30% decrease in plasma Lp(a) levels after 1-2 weeks of treatment at 100 mg/kg/day.) (C) 2003 Elsevier Ltd. All rights reserved.