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Design, synthesis and cruzain docking of 3-(4-substituted-aryl)-1,2,4-oxadiazole-N-acylhydrazones as anti-Trypanosoma cruzi agents

机译：3-（4-取代芳基）-1,2,4-二氧化氮酰腙作为抗锥体瘤Cruzi试剂的设计，合成和克鲁锌对接

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José Mauricio dos Santos Filho; Ana Cristina Lima Leite; Boaz Galdino de Oliveira; Diogo Rodrigo Magalhães Moreira; Milena S. Lima; Milena Botelho Pereira Soares; Lucia Fernanda C.C. Leite;
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1. Design, synthesis and cruzain docking of 3-(4-substituted-aryl)-1,2,4-oxadiazole-N-acylhydrazones as anti-Trypanosoma cruzi agents. [J] . dos Santos Filho JM, Leite AC, de Oliveira BG Bioorganic and medicinal chemistry . 2009,第18期

机译：3-（4-取代-芳基）-1,2,4-恶二唑-N-酰基hydr的设计，合成和Cruzain对接，作为克鲁氏锥虫的抗药性。
2. Synthesis, Biological Evaluation, and Structure-Activity Relationships of Potent Noncovalent and Nonpeptidic Cruzain Inhibitors as Anti-Trypanosoma cruzi Agents [J] . Rafaela S. Ferreira, Marco A. Dessoy, Ivani Pauli, Journal of Medicinal Chemistry . 2014,第6期

机译：强大的非共价和非肽克鲁萨因抑制剂作为抗锥虫的有效成分的合成，生物学评价和构效关系
3. Synthesis, Biological Evaluation and Molecular Docking of New Benzenesulfonylhydrazone as Potential anti-Trypanosoma cruzi Agents [J] . Elizondo-Jimenez Silvia, Moreno-Herrera Antonio, Reyes-Olivares Rogelio, Medicinal chemistry . 2017,第2期

机译：新苯磺酰腙的合成，生物学评价和分子对接，作为潜在的抗锥虫瘤Cruzi代理剂
4. Artificial Neural Network and Docking Study in Design and Synthesis of Xanthenes as Antimicrobial Agents [C] . Elma Veljovic, Selma Spirtovic-Halilovic, Samija Muratovic International Conference on Medical and Biological Engineering . 2017

机译：人工神经网络与对接研究和X.Santhenes作为抗微生物剂的合成研究
5. Modeling, design, and development of potential inhibitors of gamma-glutamylamine cyclotransferase and inhibitors of cruzain as therapeutic agents for Chagas' disease. [D] . Chen, Shen-En. 2008

机译：建模，设计和开发潜在的γ-谷氨酰胺环转移酶抑制剂和克鲁萨因抑制剂作为南美锥虫病的治疗剂。
6. Structure-Based and Molecular Modeling Studies for the Discovery of Cyclic Imides as Reversible Cruzain Inhibitors With Potent Anti-Trypanosoma cruzi Activity [O] . Rafael A. A. Ferreira, Ivani Pauli, Thiago S. Sampaio, 2019

机译：基于结构和分子建模研究用于发现循环酰亚胺的可逆性抗蛋白酶瘤Cruzi活性
7. Synthesis, biological evaluation, and structure-activity relationships of potent noncovalent and nonpeptidic cruzain inhibitors as anti-Trypanosoma cruzi agents [O] . Ferreira Rafaela S., Dessoy Marco A., Pauli Ivani, 2014

机译：高效的非共价和非肽克鲁萨因抑制剂作为抗锥虫克鲁兹氏菌的合成，生物学评估和构效关系
8. Synthesis and Molecular Structure of (3-(PPh3)-3,3-(NO3)-3,1,2-RhC2B9H11), a Versatile Metallocarborane Reagent. [R] . Demidowicz, Z., Teller, R. G., Hawthorne, M. F. 1979

机译：通用金属碳硼烷试剂（3-（pph3）-3,3-（NO3）-3,1,2-RhC2B9H11）的合成和分子结构。

Design, synthesis and cruzain docking of 3-(4-substituted-aryl)-1,2,4-oxadiazole-N-acylhydrazones as anti-Trypanosoma cruzi agents

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