Publication: Discovery of novel halogenated 8-hydroxyquinoline-based anti-MRSA agents: In vitro and QSAR studies
dc.contributor.author | Rungrot Cherdtrakulkiat | en_US |
dc.contributor.author | Apilak Worachartcheewan | en_US |
dc.contributor.author | Srisurang Tantimavanich | en_US |
dc.contributor.author | Ratana Lawung | en_US |
dc.contributor.author | Nujarin Sinthupoom | en_US |
dc.contributor.author | Supaluk Prachayasittikul | en_US |
dc.contributor.author | Somsak Ruchirawat | en_US |
dc.contributor.author | Virapong Prachayasittikul | en_US |
dc.contributor.other | Chulabhorn Research Institute | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.contributor.other | Ministry of Education | en_US |
dc.contributor.other | Chulabhorn Graduate Institute | en_US |
dc.date.accessioned | 2020-03-26T05:12:39Z | |
dc.date.available | 2020-03-26T05:12:39Z | |
dc.date.issued | 2020-02-01 | en_US |
dc.description.abstract | © 2019 Wiley Periodicals, Inc. Methicillin-resistant Staphylococcus aureus (MRSA) infection has been considered to be one of global health problems due to limited classes of effective antimicrobial drugs. Herein, 8-hydroxyquinoline (8HQ) and its derivatives (1-7) were investigated for their anti-MRSA and antioxidant activities. Cloxyquin (2), a halogenated 8HQ, exerted the highest antimicrobial activity (MIC50 ≤ 5.57 μM) with high safety index, whereas an amino-derivative 7 showed the strongest antioxidant activity. Additionally, quantitative structure-activity relationship (QSAR) study demonstrated that mass, polarizability, topological charge, and van der Waals volume are essential properties governing the anti-MRSA activity. Taken together, cloxyquin was highlighted as a promising compound for further development as a novel anti-MRSA agent. QSAR findings would also benefit for further rational design of novel 8HQ-based compounds to combat the MRSA resistance. | en_US |
dc.identifier.citation | Drug Development Research. Vol.81, No.1 (2020), 127-135 | en_US |
dc.identifier.doi | 10.1002/ddr.21611 | en_US |
dc.identifier.issn | 10982299 | en_US |
dc.identifier.issn | 02724391 | en_US |
dc.identifier.other | 2-s2.0-85074301327 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/53905 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85074301327&origin=inward | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Discovery of novel halogenated 8-hydroxyquinoline-based anti-MRSA agents: In vitro and QSAR studies | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85074301327&origin=inward | en_US |