Thiosemicarbazone derivatives: Evaluation as cruzipain inhibitors and molecular modeling study of complexes with cruzain

被引:13
作者
Jasinski, Gabriel [1 ,2 ]
Salas-Sarduy, Emir [3 ]
Vega, Daniel [4 ,5 ]
Fabian, Lucas [2 ]
Martini, Maria Florencia [1 ,2 ]
Moglioni, Albertina G. [1 ,2 ]
机构
[1] Univ Buenos Aires, Fac Farm & Bioquim, Catedra Quim Med, CABA, RA-C1113AAD Buenos Aires, Argentina
[2] Univ Buenos Aires, Inst Quim & Metab Farmaco IQUIMEFA, CONICET, CABA, RA-1113 Buenos Aires, Argentina
[3] Univ San Martin UNSAM, Inst Invest Biotecnol Dr Rodolfo Ugalde IIBIO, CONICET, San Martin, 1650 Buenos Aires, Argentina
[4] CNEA, GIyA, CAC, Dept Fis Mat Condensada, RA-B1650KNA Buenos Aires, Argentina
[5] UNSAM, Escuela Ciencia & Tecnol, RA-B1650KNA Buenos Aires, Argentina
关键词
Chagas Disease; Thiosemicarbazones; Cruzipain Inhibitors; Molecular Docking; INTERFERENCE COMPOUNDS PAINS; TRYPANOSOMA-CRUZI; CYSTEINE PROTEASE; DFT CALCULATIONS; ASSAY; MECHANISM; DOCKING; HISTIDINE-159; IONIZATION; ACTIVATION;
D O I
10.1016/j.bmc.2022.116708
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of cruzipain inhibitors represents one of the most attractive challenges in the search for drugs for the treatment of Chagas disease. A recombinant form of this enzyme, cruzain, has been crystallized with numerous inhibitors, excluding thiosemicarbazones. These compounds have been established as potent inhibitors of cruzain, although there is very little data in the literature of thiosemicarbazones tested on cruzipain. In this work, we present the results of the evaluation of eleven thiosemicarbazones on cruzipain, isolated from T. cruzi epimastigotes, six of them previously evaluated on cruzain. For these latter, we studied through computational methods, the mode of interaction with the active site of cruzain and the contribution of geometric parameters to the possible mechanism of action involved in the observed inhibition. Finally, from some geometric parameters analyzed on modeled TSC-cruzain complexes, a semi-quantitative relationship was established that could explain the inhibitory activity of thiosemicarbazones on cruzipain, the enzyme actually present in the parasite.
引用
收藏
页数:14
相关论文
共 81 条
[1]  
Ackley J. Freeland, 2012, INHIBITORS CYSTEINE, V2
[2]   H++3.0: automating pK prediction and the preparation of biomolecular structures for atomistic molecular modeling and simulations [J].
Anandakrishnan, Ramu ;
Aguilar, Boris ;
Onufriev, Alexey V. .
NUCLEIC ACIDS RESEARCH, 2012, 40 (W1) :W537-W541
[3]  
[Anonymous], 1997, An Introduction to Hydrogen Bonding
[4]  
[Anonymous], theorists who have neglected the entanglements of nationalism and gender
[5]   Computational Study of the Michaelis Complex Formation and the Effect on the Reaction Mechanism of Cruzain Cysteine Protease [J].
Arafet, Kemel ;
Swiderek, Katarzyna ;
Moliner, Vicent .
ACS OMEGA, 2018, 3 (12) :18613-18622
[6]   Paleoparasitology of Chagas disease - A Review [J].
Araujo, Adauto ;
Jansen, Ana Maria ;
Reinhard, Karl ;
Ferreira, Luiz Fernando .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2009, 104 :9-16
[7]   Synthesis, biological assay in vitro and molecular docking studies of new Schiff base derivatives as potential urease inhibitors [J].
Aslam, Muhammad Adil S. ;
Mahmood, Shams-ul ;
Shahid, Mohammad ;
Saeed, Aamer ;
Iqbal, Jamshed .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2011, 46 (11) :5473-5479
[8]   Seven Year Itch: Pan-Assay Interference Compounds (PAINS) in 2017-Utility and Limitations [J].
Baell, Jonathan B. ;
Nissink, J. Willem M. .
ACS CHEMICAL BIOLOGY, 2018, 13 (01) :36-44
[9]   Feeling Nature's PAINS: Natural Products, Natural Product Drugs, and Pan Assay Interference Compounds (PAINS) [J].
Baell, Jonathan B. .
JOURNAL OF NATURAL PRODUCTS, 2016, 79 (03) :616-628
[10]   Observations on screening-based research and some concerning trends in the literature [J].
Baell, Jonathan B. .
FUTURE MEDICINAL CHEMISTRY, 2010, 2 (10) :1529-1546