Chan C, Yin H, McKie J H, Fairlamb A H, Douglas K T
School of Pharmacy and Pharmaceutical Sciences, University of Manchester, Oxford Road, Manchester M13 9PL, U.K.
Amino Acids. 2002 Jun;22(4):297-308. doi: 10.1007/s007260200016.
One route to the design of lead compounds for rational drug design approaches to developing drugs against trypanosomiasis, Chagas' disease and leishmaniasis is to develop novel inhibitors of the parasite-specific enzyme trypanothione reductase. A lead inhibitor based on a peptoid structure was designed in the present study based on the known strong competitive inhibition of trypanothione reductase by N-benzoyl-Leu-Arg-Arg-beta-naphthylamide and N-benzyloxycarbonyl-Ala-Arg-Arg-4-methoxy- beta-naphthylamide. In the target peptoid the arginyl residues were replaced by alkylimidazolium units and the benzyloxycarbonyl group by the benzylaminocarbonyl function. The peptoid was synthesised using t-butoxycarbonyl protection chemistry and couplings were activated by 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate. The resulting peptoid was shown to be a competitive inhibitor of recombinant trypanothione reductase from Trypanosoma cruzi with a K(i) value of 179 microM and with only weak inhibition of human erythrocyte glutathione reductase (the inhibition of glutathione reductase was at least 291-fold weaker than of trypanothione reductase).
开发治疗锥虫病、恰加斯病和利什曼病药物的合理药物设计方法中,先导化合物设计的一条途径是开发寄生虫特异性酶——锥虫硫醇还原酶的新型抑制剂。基于已知的N-苯甲酰基-L-亮氨酰-精氨酰-精氨酰-β-萘酰胺和N-苄氧羰基-丙氨酰-精氨酰-精氨酰-4-甲氧基-β-萘酰胺对锥虫硫醇还原酶的强竞争性抑制作用,本研究设计了一种基于类肽结构的先导抑制剂。在目标类肽中,精氨酰残基被烷基咪唑鎓单元取代,苄氧羰基被苄氨基羰基官能团取代。该类肽采用叔丁氧羰基保护化学合成,偶联反应由2-(1H-苯并三唑-1-基)-1,1,3,3-四甲基脲六氟磷酸盐激活。结果表明,所得类肽是克氏锥虫重组锥虫硫醇还原酶的竞争性抑制剂,K(i)值为179 microM,对人红细胞谷胱甘肽还原酶的抑制作用较弱(对谷胱甘肽还原酶的抑制作用比对锥虫硫醇还原酶的抑制作用至少弱291倍)。