Evaluation of Biological Activities of Quinone-4-oxoquinoline Derivatives against Pathogens of Clinical Importance

Author:

Juliana Martins Francislene1ORCID,Savacini Sagrillo Fernanda2,Josianne Vinturelle Medeiros Rafaelle1,Gonçalves de Souza Alan2,Rodrigues Pinto Costa Amanda2,Silva Novais Juliana3,Alves Miceli Leonardo4,Campos Vinícius2,Marie Sá Figueiredo Agnes5,Claudia Cunha Anna2,Lidmar von Ranke Natalia4,Lamim Bello Murilo4,Abrahim-Vieira Bárbara4,De Souza Alessandra4,Ratcliffe Norman6,da Costa Santos Boechat Fernanda2,Cecília Bastos Vieira de Souza Maria2,Rangel Rodrigues Carlos4,Carla Castro Helena1

Affiliation:

1. Institute of Biology, Postgraduate Program in Science and Biotechnology, Federal Fluminense University, Niterói, Rio de Janeiro, Brazil

2. Department of Organic Chemistry, Chemistry Institute, Federal Fluminense University, Niterói, Rio de Janeiro, Brazil

3. Medical School, Postgraduate Program in Pathology, Federal Fluminense University, Niterói, Rio de Janeiro, Brazil | Faculty of Pharmacy, Estácio de Sá University (UNESA), São Gonçalo, Rio de Janeiro, Brazil

4. Department of Drugs and Medicines, Faculty of Pharmacy, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil

5. Department of Medical Microbiology, Paulo Goes Institute of Microbiology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil

6. Department of Biosciences, College of Science Swansea University, SA2 8PP, UK

Abstract

Background:Microbial resistance has become a worldwide public health problem, and may lead to morbidity and mortality in affected patients.Objective:Therefore, this work aimed to evaluate the antibacterial activity of quinone-4-oxoquinoline derivatives.Method:These derivatives were evaluated against Gram-positive and Gram-negative bacteria by their antibacterial activity, anti-biofilm, and hemolytic activities and by in silico assays.Results:The quinone-4-oxoquinoline derivatives presented broad-spectrum antibacterial activities, and in some cases were more active than commercially available reference drugs. These compounds also inhibited bacterial adhesion and the assays revealed seven non-hemolytic derivatives. The derivatives seem to cause damage to the bacterial cell membrane and those containing the carboxyl group at the C-3 position of the 4-quinolonic nucleus were more active than those containing a carboxyethyl group.Conclusion:The isoquinoline-5,8-dione nucleus also favored antimicrobial activity. The study showed that the target of the derivatives must be a non-conventional hydrophobic allosteric binding pocket on the DNA gyrase enzyme.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,General Medicine

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