Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14853
Title: Synthesis of bis, tris and tetra(dihydrocaffeoyl)polyamine conjugates as antibacterial agents against VRSA
Authors: Yingyongnarongkul B.-E.
Apiratikul N.
Aroonrerk N.
Suksamrarn A.
Keywords: 3,4-dihydroxyphenylpropionic acid
antiinfective agent
caffeic acid derivative
dihydrocaffeic acid
drug derivative
spermidine
animal
antibiotic resistance
article
cell survival
Cercopithecus
chemical structure
dose response
drug effect
growth, development and aging
IC 50
microbiological examination
penicillin resistance
Staphylococcus aureus
synthesis
Vero cell
Animals
Anti-Bacterial Agents
Caffeic Acids
Cell Survival
Cercopithecus aethiops
Dose-Response Relationship, Drug
Inhibitory Concentration 50
Methicillin Resistance
Microbial Sensitivity Tests
Molecular Structure
Spermidine
Staphylococcus aureus
Vancomycin Resistance
Vero Cells
Issue Date: 2008
Abstract: Bis, tris and tetra(dihydrocaffeoyl)polyamine conjugates were synthesized using solid phase synthesis technique. These compounds were screened for antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) (11 strains) and vancomycin-resistant S. aureus (VRSA) (4 strains). Bis, tris and tetra(dihydrocaffeoyl)polyamine analogues showed antibacterial activity against VRSA which were better than the reference drugs, vancomycin. Tetra(dihydrocaffeoyl) polyamine conjugate exhibited the highest activity. These compounds showed no cytotoxicity against vero cells. © 2008 The Pharmaceutical Society of Korea.
URI: https://ir.swu.ac.th/jspui/handle/123456789/14853
https://www.scopus.com/inward/record.uri?eid=2-s2.0-45749097459&doi=10.1007%2fs12272-001-1215-4&partnerID=40&md5=9d9df22ae5f6bc2755552008dc25c54d
ISSN: 2536269
Appears in Collections:Scopus 1983-2021

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