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Synthesis, characterization and utilization of a new series of 1,2,3-triazole derivatives to neutralize some toxic activities of Bothrops jararaca snake venom
Amorim, Nayanna de Mello; Pereira Junior, Luiz Carlos Simas; Sanchez, Eladio Flores; Aquino, Gabriel Alves de; Ferreira, Vitor Francisco; Ferreira, Sabrina Baptista; Fuly, André Lopes; Oliveira, Eduardo Coriolano de.
  • Amorim, Nayanna de Mello; Federal Fluminense University. Institute of Biology. Department of Molecular and Cellular Biology. Niterói. BR
  • Pereira Junior, Luiz Carlos Simas; Federal Fluminense University. Institute of Biology. Department of Molecular and Cellular Biology. Niterói. BR
  • Sanchez, Eladio Flores; Ezequiel Dias Foundation. Research and Development Center. Belo Horizonte. BR
  • Aquino, Gabriel Alves de; Federal University of Rio de Janeiro. Institute of Chemistry. Department of Organic Chemistry. Rio de Janeiro. BR
  • Ferreira, Vitor Francisco; Federal Fluminense University. Faculty of Pharmacy. Department of Pharmaceutical Technology. Niterói. BR
  • Ferreira, Sabrina Baptista; Federal University of Rio de Janeiro. Institute of Chemistry. Department of Organic Chemistry. Rio de Janeiro. BR
  • Fuly, André Lopes; Federal Fluminense University. Institute of Biology. Department of Molecular and Cellular Biology. Niterói. BR
  • Oliveira, Eduardo Coriolano de; Federal Fluminense University. Institute of Biology. Department of Molecular and Cellular Biology. Niterói. BR
Braz. J. Pharm. Sci. (Online) ; 58: e201143, 2022. tab, graf
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1420361
ABSTRACT
Abstract Snake envenomation is a public health problem, and while serum therapy prevents death, the local effects of venoms can lead to amputations or morbidities. Thus, alternative treatments deserve attention. In this study, we tested eight derivatives of 1,2,3-triazole against some toxic activities of Bothrops jararaca venom. The derivatives were synthesized, and their structures analyzed by infrared and nuclear magnetic resonance. After that, the ability of compounds to inhibit hemolysis, coagulation, proteolysis, hemorrhaging, edema, and lethal activities of B. jararaca venom was investigated. The derivatives were incubated with B. jararaca venom (incubation protocol), administered before (prevention protocol) or after (treatment protocol) injecting venom into the mice. Then, hemorrhaging assay occurred. As a result, most of the derivatives inhibited the activities, even if they were incubated, injected before or after B. jararaca venom. However, the derivatives TRI 07 and TRI 18 seemed to be the most efficient in impairing hemorrhaging. The derivatives showed a low drug score of toxicity based on an in silico technique. Therefore, the derivatives fulfilled physicochemical and biological requirements to become drugs, and they may be a brand new initiative for designing antivenom molecules to complement antivenom therapy to efficiently block tissue necrosis or any other local effects.


Texto completo: DisponíveL Índice: LILACS (Américas) Tipo de estudo: Guia de Prática Clínica Idioma: Inglês Revista: Braz. J. Pharm. Sci. (Online) Assunto da revista: Farmacologia / Terapˆutica / Toxicologia Ano de publicação: 2022 Tipo de documento: Artigo País de afiliação: Brasil Instituição/País de afiliação: Ezequiel Dias Foundation/BR / Federal Fluminense University/BR / Federal University of Rio de Janeiro/BR

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Texto completo: DisponíveL Índice: LILACS (Américas) Tipo de estudo: Guia de Prática Clínica Idioma: Inglês Revista: Braz. J. Pharm. Sci. (Online) Assunto da revista: Farmacologia / Terapˆutica / Toxicologia Ano de publicação: 2022 Tipo de documento: Artigo País de afiliação: Brasil Instituição/País de afiliação: Ezequiel Dias Foundation/BR / Federal Fluminense University/BR / Federal University of Rio de Janeiro/BR