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Authors = Abdullah Sulaiman Al-Ayed

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Open AccessArticle A New and Efficient Method for the Synthesis of Novel 3-Acetyl Coumarins Oxadiazoles Derivatives with Expected Biological Activity
Molecules 2014, 19(1), 911-924; doi:10.3390/molecules19010911
Received: 2 December 2013 / Revised: 30 December 2013 / Accepted: 30 December 2013 / Published: 14 January 2014
Cited by 6 | Viewed by 1769 | PDF Full-text (308 KB) | HTML Full-text | XML Full-text
Abstract
This paper presents the design of some novel 3-acetylcoumarin derivatives, based on minimal inhibitory concentration values (MICs) previously obtained against some microorganism cultures, Gram positive and negative bacteria and fungi. Some of these molecules exhibited antibacterial activity against S. aureus, comparable to
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This paper presents the design of some novel 3-acetylcoumarin derivatives, based on minimal inhibitory concentration values (MICs) previously obtained against some microorganism cultures, Gram positive and negative bacteria and fungi. Some of these molecules exhibited antibacterial activity against S. aureus, comparable to that of the standard used (impinem). The in vitro antioxidant activities of the novel 3-acetylcoumarin oxadiazoles were assayed by the quantitative 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity method. The compounds 5c,d proved to be the most active, showing the highest capacity to deplete the DPPH radicals. Structure elucidation of the products has been accomplished on the basis of IR, 1H-NMR, 13C-NMR, NOESY and HMBC NMR data. Full article
(This article belongs to the Section Medicinal Chemistry)

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