Synthesis and biological activity of novel mycophenolic acid conjugates containing nitro-acridine/acridone derivatives
作者:Magdalena Malachowska-Ugarte、Grzegorz Cholewinski、Krystyna Dzierzbicka、Piotr Trzonkowski
DOI:10.1016/j.ejmech.2012.04.040
日期:2012.8
units. The type of heterocyclic part influenced their cytotoxic and anti-proliferative properties. Coupling of MPA 1 with 9-(ω-aminoalkyl)amino-1-nitroacridines 2 and 1-[(ω-aminoalkyl)-4-nitro-9(10H)]-acridones 3 was tested. Although all tested conjugates were active, compounds 4a–e exhibited the highest potency. Preliminary experiments with GMP suggested that the tested compounds acted as IMPDH inhibitors
合成了由麦考酚酸(MPA)和1-硝基ac啶/ 4-硝基ac啶酮衍生物组成的混合药效团抗增殖化合物,并已评估其为五种不同白血病细胞系的抑制剂(Jurkat,Molt-4,HL-60,CCRF-CEM (L1210)和来自健康供体的人外周血单个核细胞。这些缀合物在MPA和杂环单元之间具有不同长度的接头。杂环部分的类型影响了它们的细胞毒性和抗增殖特性。测试了MPA 1与9-(ω-氨基烷基)氨基-1-硝基ac啶2和1-[((ω-氨基烷基)-4-硝基-9(10 H)]-rid啶酮3的偶联。尽管所有测试的结合物均具有活性,但化合物4a – e表现出最高的效力。GMP的初步实验表明,所测试的化合物可作为IMPDH抑制剂。