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http://hdl.handle.net/1843/59321
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DC Field | Value | Language |
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dc.creator | Carmindo R. Borel | pt_BR |
dc.creator | Luiz Cláudio de Almeida Barbosa | pt_BR |
dc.creator | Célia Maltha | pt_BR |
dc.creator | Sergio Fernandes | pt_BR |
dc.creator | Larissa Santos | pt_BR |
dc.creator | Jacqueline Takahashi | pt_BR |
dc.date.accessioned | 2023-10-09T23:01:55Z | - |
dc.date.available | 2023-10-09T23:01:55Z | - |
dc.date.issued | 2017 | - |
dc.citation.volume | 40 | pt_BR |
dc.citation.issue | 9 | pt_BR |
dc.citation.spage | 1065 | pt_BR |
dc.citation.epage | 1073 | pt_BR |
dc.identifier.doi | https://doi.org/10.21577/0100-4042.20170118 | pt_BR |
dc.identifier.issn | 0100-4042 | pt_BR |
dc.identifier.uri | http://hdl.handle.net/1843/59321 | - |
dc.description.resumo | In this work a series of 2-(2- pyridyl)quinolines were prepared via a Povarov reaction between anilines, 2-pyridinocarbadehyde and ethyl vinyl ether under microwaves heating conditions. The optimized conditions herein reported allowed the preparation of several pyridylquinolines in yields in the range of 30-83%, some of them not previously accessible by this multicomponent process. The reported methodology has advantage over previous report due to its larger scope and short reaction time (2 hours). All quinolines obtained were assayed against five species of clinically important yeasts Candida sp and against Cryptococcus neoformans. Some of them possessed a broad spectrum of action including 2-(2-pyridyl)quinoline (20) and 6,8-dimethoxy-2-(pyridin-2-yl)quinolone (22) that were highly effective in inhibiting Candida species (IC50 < 1.95 µg/mL against C. tropicalis and C. krusei). Some compounds were more potent than commercial drugs Nistatin and Miconazole. | pt_BR |
dc.description.sponsorship | CNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico | pt_BR |
dc.description.sponsorship | FAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas Gerais | pt_BR |
dc.format.mimetype | pt_BR | |
dc.language | por | pt_BR |
dc.publisher | Universidade Federal de Minas Gerais | pt_BR |
dc.publisher.country | Brasil | pt_BR |
dc.publisher.department | ICX - DEPARTAMENTO DE QUÍMICA | pt_BR |
dc.publisher.initials | UFMG | pt_BR |
dc.relation.ispartof | Química Nova | pt_BR |
dc.rights | Acesso Aberto | pt_BR |
dc.subject | Pyridylquinoline | pt_BR |
dc.subject | Antifungal | pt_BR |
dc.subject | Povarov reaction | pt_BR |
dc.subject | Cycloaddition | pt_BR |
dc.subject | Candida spp | pt_BR |
dc.subject.other | Microondas | pt_BR |
dc.subject.other | Atividade antifúngicas | pt_BR |
dc.title | Síntese de 2-(2-piridil)quinolinas promovida por micro-ondas e suas atividades antifúngicas | pt_BR |
dc.title.alternative | Synthesis of 2-(2-pyridyl)quinolines promoted mby microwaves and their antigungal activities | pt_BR |
dc.type | Artigo de Periódico | pt_BR |
dc.url.externa | https://www.scielo.br/j/qn/a/jc7LwYFcTfXr3ztJ5YjZhpv/ | pt_BR |
dc.identifier.orcid | https://orcid.org/0000-0002-5395-9608 | pt_BR |
Appears in Collections: | Artigo de Periódico |
Files in This Item:
File | Description | Size | Format | |
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SÍNTESE DE 2-(2-PIRIDIL)QUINOLINAS PROMOVIDA POR MICRO-ONDAS E SUAS ATIVIDADES ANTIFÚNGICAS.pdf | 480.58 kB | Adobe PDF | View/Open |
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