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DC Field | Value | Language |
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dc.contributor.author | Samosorn S. | |
dc.contributor.author | Tanwirat B. | |
dc.contributor.author | Muhamad N. | |
dc.contributor.author | Casadei G. | |
dc.contributor.author | Tomkiewicz D. | |
dc.contributor.author | Lewis K. | |
dc.contributor.author | Suksamrarn A. | |
dc.contributor.author | Prammananan T. | |
dc.contributor.author | Gornall K.C. | |
dc.contributor.author | Beck J.L. | |
dc.contributor.author | Bremner J.B. | |
dc.date.accessioned | 2021-04-05T04:32:50Z | - |
dc.date.available | 2021-04-05T04:32:50Z | - |
dc.date.issued | 2009 | |
dc.identifier.issn | 9680896 | |
dc.identifier.other | 2-s2.0-65549100031 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/15176 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-65549100031&doi=10.1016%2fj.bmc.2009.04.028&partnerID=40&md5=7d9a30a9bf253d6997e94fd82643d982 | |
dc.description.abstract | Conjugation of the NorA substrate berberine and the NorA inhibitor 5-nitro-2-phenyl-1H-indole via a methylene ether linking group gave the 13-substituted berberine-NorA inhibitor hybrid, 3. A series of simpler arylmethyl ether hybrid structures were also synthesized. The hybrid 3 showed excellent antibacterial activity (MIC Staphylococcus aureus, 1.7 μM), which was over 382-fold more active than the parent antibacterial berberine, against this bacterium. This compound was also shown to block the NorA efflux pump in S. aureus. © 2009 Elsevier Ltd. | |
dc.subject | 5 nitro 2 phenyl 1h indole | |
dc.subject | 9,10 dimethoxy 13 [2 (5 nitro 1h indol 2 yl)benzyloxy] 5,6 dihydrobenzo[g] 1,3 benzodioxolo[5,6 a]quinolizinium bromide | |
dc.subject | berberine | |
dc.subject | berberine 5 nitro 2 phenyl 1h indole conjugate | |
dc.subject | inf 55 | |
dc.subject | NorA pump inhibitor | |
dc.subject | protein inhibitor | |
dc.subject | unclassified drug | |
dc.subject | antibacterial activity | |
dc.subject | article | |
dc.subject | bacterial strain | |
dc.subject | controlled study | |
dc.subject | drug conjugation | |
dc.subject | drug potency | |
dc.subject | drug structure | |
dc.subject | drug synthesis | |
dc.subject | minimum inhibitory concentration | |
dc.subject | nonhuman | |
dc.subject | Staphylococcus aureus | |
dc.subject | Anti-Bacterial Agents | |
dc.subject | Bacterial Proteins | |
dc.subject | Berberine | |
dc.subject | Enterococcus faecalis | |
dc.subject | Ether, Ethyl | |
dc.subject | Indoles | |
dc.subject | Intercalating Agents | |
dc.subject | Molecular Structure | |
dc.subject | Multidrug Resistance-Associated Proteins | |
dc.subject | Staphylococcus aureus | |
dc.subject | Bacteria (microorganisms) | |
dc.subject | Staphylococcus aureus | |
dc.title | Antibacterial activity of berberine-NorA pump inhibitor hybrids with a methylene ether linking group | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Bioorganic and Medicinal Chemistry. Vol 17, No.11 (2009), p.3866-3872 | |
dc.identifier.doi | 10.1016/j.bmc.2009.04.028 | |
Appears in Collections: | Scopus 1983-2021 |
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