Yamaguchi Yasuchika, Menear Keith, Cohen Nissim-Claude, Mah Robert, Cumin Frédéric, Schnell Christian, Wood Jeanette M, Maibaum Jürgen
Faculty of Pharmaceutical Sciences, Nagasaki International University, Sasebo, Nagasaki 859-3298, Japan.
Bioorg Med Chem Lett. 2009 Aug 15;19(16):4863-7. doi: 10.1016/j.bmcl.2009.05.128. Epub 2009 Jun 26.
Novel nonpeptide small molecule renin inhibitors bearing an N-isopropyl P(1) motif were designed based on initial lead structures 1 and aliskiren (2). (P(3)-P(1))-Benzamide derivatives such as 9a and 34, as well as the corresponding P(1) basic tertiary amine derivatives 10 and 35 were found to display low nanomolar inhibition against human renin in vitro.
基于初始先导结构1和阿利吉仑(2)设计了带有N-异丙基P(1)基序的新型非肽小分子肾素抑制剂。发现(P(3)-P(1))-苯甲酰胺衍生物如9a和34以及相应的P(1)碱性叔胺衍生物10和35在体外对人肾素显示出低纳摩尔抑制作用。