Bi Xiangdong, Lopez Christina, Bacchi Cyrus J, Rattendi Donna, Woster Patrick M
Department of Pharmaceutical Sciences, Wayne State University, 259 Mack Ave, Detroit, MI 48202, USA.
Bioorg Med Chem Lett. 2006 Jun 15;16(12):3229-32. doi: 10.1016/j.bmcl.2006.03.048. Epub 2006 Apr 17.
A series of polyaminoguanidines and polyaminobiguanides were synthesized and evaluated as potential antitrypanosomal agents. These analogues inhibit trypanothione reductase (TR) with IC50 values as low as 0.95 microM, but do not inhibit the closely related human enzyme glutathione reductase (GR). The most effective analogues, 7a, 7b and 8d, inhibited parasitic growth in vitro with IC50 values of 0.18, 0.09 and 0.18 microM, respectively. These agents represent a promising new class of potential antitrypanosomal agents.
合成了一系列聚氨基胍和聚氨基双胍,并将其作为潜在的抗锥虫剂进行评估。这些类似物对锥虫硫氧还蛋白还原酶(TR)具有抑制作用,IC50值低至0.95微摩尔,但不抑制与之密切相关的人类酶谷胱甘肽还原酶(GR)。最有效的类似物7a、7b和8d在体外抑制寄生虫生长,IC50值分别为0.18、0.09和0.18微摩尔。这些药物代表了一类有前途的新型潜在抗锥虫剂。