Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14991
Title: Solid-phase synthesis and antibacterial activity of hydroxycinnamic acid amides and analogues against methicillin-resistant Staphylococcus aureus and vancomycin-resistant S. aureus
Authors: Yingyongnarongkul B.-e.
Apiratikul N.
Aroonrerk N.
Suksamrarn A.
Keywords: hydrocinnamic acid derivative
meticillin
oxacillin
vancomycin
antibacterial activity
antibiotic resistance
article
bacterial strain
controlled study
drug potency
drug screening
drug synthesis
methicillin resistant Staphylococcus aureus
minimum inhibitory concentration
nonhuman
solid phase synthesis
Staphylococcus aureus
Amides
Anti-Bacterial Agents
Caffeine
Combinatorial Chemistry Techniques
Coumaric Acids
Drug Combinations
Ethanol
Methicillin Resistance
Oxacillin
Staphylococcus aureus
Vancomycin Resistance
methicillin resistant Staphylococcus aureus
Staphylococcus aureus
Issue Date: 2006
Abstract: A library of hydroxycinnamic acid amides (HCAAs) and analogues were synthesized using solid-phase synthesis technique. These compounds were screened for antibacterial against methicillin-resistant Staphylococcus aureus (MRSA) (11 strains) and vancomycin-resistant S. aureus (VRSA) (4 strains). Dihydrocaffeoyl analogues showed activity against VRSA which were better than the reference drugs, vancomycin and oxacillin. These compounds also exhibited antibacterial activity against MRSA, which were more potent than oxacillin. © 2006 Elsevier Ltd. All rights reserved.
URI: https://ir.swu.ac.th/jspui/handle/123456789/14991
https://www.scopus.com/inward/record.uri?eid=2-s2.0-33749434812&doi=10.1016%2fj.bmcl.2006.08.062&partnerID=40&md5=39c9287b3f1fcba02da89c016669696b
ISSN: 0960894X
Appears in Collections:Scopus 1983-2021

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