Synthesis and antiproliferative activity of conjugates of adenosine with muramyl dipeptide and nor-muramyl dipeptide derivatives

被引:8
|
作者
Samsel, Monika [1 ]
Dzierzbicka, Krystyna [1 ]
Trzonkowski, Piotr [2 ]
机构
[1] Gdansk Univ Technol, Dept Organ Chem, PL-80233 Gdansk, Poland
[2] Med Univ Gdansk, Dept Clin Immunol & Transplantol, PL-80211 Gdansk, Poland
关键词
Muramyl dipeptide conjugates; MDP(D; D); Nor-MDP(D; Adenosine; Synthesis; Biological activity; BIOLOGICAL-ACTIVITY; IMMUNE-RESPONSE; ADJUVANT; EXPRESSION; INDUCTION; TUFTSIN; ANALOGS;
D O I
10.1016/j.bmcl.2014.05.043
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We synthesized a series of MDP(D,D) and nor-MDP(D,D) derivatives conjugated with adenosine through a spacer as potential immunosuppressants. New conjugates 8a-k were evaluated on two leukemia cell lines (Jurkat and L1210) and PBMC from healthy donors. The conjugates 8a-k and MDP(D,D)/nor-MDP(D,D) derivatives 7e, f, i,j were active against L1210 cell line. Unconjugated nor-MDP(D,D) had better antiproliferative properties, but the conjugates 8b, f, g had the highest values of selectivity index. Both cell lines as well as PBMC were resistant to analogs 11a, b with the 6-aminohexanoic linker. (C) 2014 Published by Elsevier Ltd.
引用
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页码:3587 / 3591
页数:5
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