Amoebicidal effect of 5,5′-[(4-nitrophenyl)methylene]bis-6-hydroxy-2-mercapto-3-methyl-4(3H)-pyrimidinone), a new drug againstEntamoeba histolytica

被引:8
|
作者
Vique-Sanchez, Jose L. [1 ]
Jimenez-Pineda, Albertana [2 ]
Benitez-Cardoza, Claudia G. [2 ]
机构
[1] Univ Autonoma Baja California, Fac Med Mexicali, Mexicali, Baja California, Mexico
[2] Inst Politecn Nacl, ENMyH, Lab Invest Bioquim, Mexico City, DF, Mexico
关键词
amoebicidal effect; EhTIM inhibitor; Entamoeba histolytica; triosephosphate isomerase; CRUZI-TRIOSEPHOSPHATE ISOMERASE; ENTAMOEBA-HISTOLYTICA; INHIBITORS; IDENTIFICATION; SIMULATION; EXPRESSION; FALCIPARUM; RESISTANCE; INSIGHTS; SEARCH;
D O I
10.1002/ardp.202000263
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Entamoeba histolyticais a cosmopolitan protozoan parasite that can produce infections in the intestine and some organs (liver, lungs, and brain), with worldwide prevalence. There are treatments againstE. histolytica(antiparasitics), but as the drugs used in these treatments have presented some type of resistance and/or side effects, there are cases with complications of this disease. Therefore, it is necessary to develop new drugs aimed at a specific therapeutic target against this parasite. Here, we used the compound 5,5 '-[(4-nitrophenyl)methylene]bis(6-hydroxy-2-mercapto-3-methyl-4(3H)-pyrimidinone) in the patenting process (called D4). D4 has a reported specific use against a glycolytic enzyme, the triosephosphate isomerase ofTrichomonas vaginalis(TvTIM). We determined that D4 has an amoebicidal effect in in vitro cultures, with an IC(50)value of 18.5 mu M, and we proposed a specific site of interaction (Lys77, His110, Gln115, and Glu118) in the triosephosphate isomerase ofE. histolytica(EhTIM). Furthermore, compound D4 has favorable experimental and theoretical toxicity results. Therefore, D4 should be further investigated as a potential drug againstE. histolytica.
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页数:7
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