Antileishmanial Thioureas: Synthesis, Biological Activity and <i>in Silico</i> Evaluations of New Promising Derivatives-Reference-Cited by-同舟云学术

Antileishmanial Thioureas: Synthesis, Biological Activity and in Silico Evaluations of New Promising Derivatives

Published:2017 Issue:10 Volume:65 Page:911-919
ISSN:0009-2363
Container-title:Chemical and Pharmaceutical Bulletin
language:en
Short-container-title:CHEMICAL & PHARMACEUTICAL BULLETIN

Author:

Viana Gil Mendes¹,Soares Deivid Costa²,Santana Marcos Vinicius³,do Amaral Lilian Henriques¹,Meireles Paloma Wetler¹,Nunes Raquel Pinto¹,da Silva Luiz Cláudio Rodrigues Pereira¹,Aguiar Lúcia Cruz de Sequeira⁴,Rodrigues Carlos Rangel⁵,de Sousa Valeria Pereira¹,Castro Helena Carla³,Abreu Paula Alvarez⁶,Sathler Plínio Cunha¹,Saraiva Elvira Maria²,Cabral Lucio Mendes¹

Affiliation:

1. Universidade Federal do Rio de Janeiro, LabTIF, Faculdade de Farmácia, Ilha do Fundão

2. Universidade Federal do Rio de Janeiro, Laboratório de Imunobiologia das Leishmanioses, Instituto de Microbiologia Paulo de Góes

3. Universidade Federal Fluminense, LABiEMol, Departamento de Biologia Celular e Molecular, Outeiro de São João Baptista

4. Universidade Federal do Rio de Janeiro, Instituto de Química, Ilha do Fundão

5. Universidade Federal do Rio de Janeiro, ModMolQSAR, Faculdade de Farmácia, Ilha do Fundão

6. Laboratório de Modelagem Molecular e Pesquisa em Ciências Farmacêuticas, LaMCiFar. Universidade Federal do Rio de Janeiro-Campus Macaé

Publisher

Pharmaceutical Society of Japan

Subject

Drug Discovery,General Chemistry,General Medicine

Link

https://www.jstage.jst.go.jp/article/cpb/65/10/65_c17-00293/_pdf

Reference46 articles.

1. 1) Alvar J., Vélez I. D., Bern C., Herrero M., Desjeux P., Cano J., Jannin J., den Boer M., PLOS ONE, 7, e35671 (2012).

2. 2) de Menezes J. P. B., Guedes C. E. S., Petersen A. L. de O. A., Fraga D. B. M., Veras P. S. T., BioMed Res. Int., 2015, e815023 (2015). doi: 10.1155/2015/815023

3. 3) Sindermann H., Engel J., Trans. R. Soc. Trop. Med. Hyg., 100 (Suppl. 1), S17–S20 (2006).

4. 4) Barrett M. P., Croft S. L., Br. Med. Bull., 104, 175–196 (2012).

5. 5) C. de Sequeira Aguiar L., M. Viana G., V. dos Santos Romualdo M., V. Costa M., S. Bonato B., Lett. Org. Chem., 8, 540–544 (2011).

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. New Prospective Insecticidal Agents Based on N‐(arylcarbamothioyl)arylmide Derivatives Against Spodoptera frugiperda: Design, Synthesis, Toxicological, Biological, Biomedical Studies and Antibacterial Activity;Chemistry & Biodiversity;2024-09-09

2. Palladium(II) complexes of thiobenzamide derivative ligands: Synthesis, crystal structure, supramolecular architecture, Hirshfeld surface analysis, and in vitro antibacterial and antifungal activities;Journal of Molecular Structure;2024-07

3. Synthesis, Characterization, DFT Calculations and Anticoagulant Activity of Symmetrical and Unsymmetrical N-Aryl Thiourea Derivatives;J CHEM SOC PAKISTAN;2024

4. Synthesis, crystal structure analysis, computational modelling and evaluation of anti-cervical cancer activity of novel 1,5-dicyclooctyl thiocarbohydrazone;Physical Chemistry Chemical Physics;2024

5. Sulfur‐ and Amine‐ Promoted Multielectron Autoredox Transformation of Nitromethane: Multicomponent Access to Thiourea Derivatives;Chemistry – A European Journal;2023-12-12