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1.
Mem Inst Oswaldo Cruz ; 115: e200254, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-33027420

RESUMEN

Coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a highly contagious infection that may break the healthcare system of several countries. Here, we aimed at presenting a critical view of ongoing drug repurposing efforts for COVID-19 as well as discussing opportunities for development of new treatments based on current knowledge of the mechanism of infection and potential targets within. Finally, we also discuss patent protection issues, cost effectiveness and scalability of synthetic routes for some of the most studied repurposing candidates since these are key aspects to meet global demand for COVID-19 treatment.


Asunto(s)
Infecciones por Coronavirus/tratamiento farmacológico , Descubrimiento de Drogas , Reposicionamiento de Medicamentos , Neumonía Viral/tratamiento farmacológico , Betacoronavirus , COVID-19 , Humanos , Pandemias , SARS-CoV-2 , Tratamiento Farmacológico de COVID-19
2.
Z Naturforsch C J Biosci ; 77(11-12): 459-471, 2022 Nov 25.
Artículo en Inglés | MEDLINE | ID: mdl-35767726

RESUMEN

Snakebite envenoming is a health concern and has been a neglected tropical disease since 2017, according to the World Health Organization. In this study, we evaluated the ability of ten 1,2,3-triazole derivatives AM001 to AM010 to inhibit pertinent in vitro (coagulant, hemolytic, and proteolytic) and in vivo (hemorrhagic, edematogenic, and lethal) activities of Bothrops jararaca venom. The derivatives were synthesized, and had their molecular structures fully characterized by CHN element analysis, Fourier-transform infrared spectroscopy and Nuclear magnetic resonance. The derivatives were incubated with the B. jararaca venom (incubation protocol) or administered before (prevention protocol) or after (treatment protocol) the injection of B. jararaca venom into the animals. Briefly, the derivatives were able to inhibit the main toxic effects triggered by B. jararaca venom, though with varying efficacies, and they were devoid of toxicity through in vivo, in silico or in vitro analyses. However, it seemed that the derivatives AM006 or AM010 inhibited more efficiently hemorrhage or lethality, respectively. The derivatives were nontoxic. Therefore, the 1,2,3-triazole derivatives may be useful as an adjuvant to more efficiently treat the local toxic effects caused by B. jararaca envenoming.


Asunto(s)
Bothrops , Venenos de Crotálidos , Animales , Venenos de Crotálidos/química , Antivenenos/farmacología , Triazoles , Hemorragia , Relación Estructura-Actividad
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