A review on the development of urease inhibitors as antimicrobial agents against pathogenic bacteria

被引:100
作者
Rego, Yuri F. [1 ]
Queiroz, Marcelo P. [1 ]
Brito, Tiago O. [2 ]
Carvalho, Priscila G. [2 ]
de Queiroz, Vagner T. [3 ]
de Fatima, Angelo [1 ]
Macedo, Fernando, Jr. [2 ]
机构
[1] Univ Fed Minas Gerais, Inst Ciencias Exatas, Dept Quim, Belo Horizonte, MG, Brazil
[2] Univ Estadual Londrina, Ctr Ciencias Exatas, Dept Quim, Londrina, PR, Brazil
[3] Univ Fed Espirito Santo, Ctr Ciencias Exatas Nat & Saude, Dept Quim & Fis, Alegre, ES, Brazil
关键词
Urease inhibitors; Urea; Thiourea; Heterocycles; Phosphorated compounds; URINARY-TRACT-INFECTION; STAPHYLOCOCCUS-SAPROPHYTICUS UREASE; THIOBARBITURIC ACID-DERIVATIVES; HELICOBACTER-PYLORI INFECTION; ASSISTED PARALLEL SYNTHESIS; TRANSFERASE P1-1 ACTIVITY; IN-VITRO; YERSINIA-ENTEROCOLITICA; BIOLOGICAL EVALUATION; MOLECULAR DOCKING;
D O I
10.1016/j.jare.2018.05.003
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ureases are enzymes that hydrolyze urea into ammonium and carbon dioxide. They have received considerable attention due to their impacts on living organism health, since the urease activity in microorganisms, particularly in bacteria, are potential causes and/or factors contributing to the persistence of some pathogen infections. This review compiles examples of the most potent antiurease organic substances. Emphasis was given to systematic screening studies on the inhibitory activity of rationally designed series of compounds with the corresponding SAR considerations. Ureases of Canavalia ensiformis, the usual model in antiureolytic studies, are emphasized. Although the active site of this class of hydrolases is conserved among bacteria and vegetal ureases, the same is not observerd for allosteric site. Therefore, inhibitors acting by participating in interactions with the allosteric site are more susceptible to a potential lack of association among their inhibitory profile for different ureases. The information about the inhibitory activity of different classes of compounds can be usefull to guide the development of new urease inhibitors that may be used in future in small molecular therapy against pathogenic bacteria. (C) 2018 Production and hosting by Elsevier B.V. on behalf of Cairo University.
引用
收藏
页码:69 / 100
页数:32
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