Chemically Modified Uridine Molecules Incorporating Acyl Residues to Enhance Antibacterial and Cytotoxic Activities

• 作者: Abul F. M. Sanaullah Hamida A. Ara Imtiaj Hasan Mohammad A. Manchur Mohammed K. Hossain Sarkar M. A. Kawsar Shagir A. Chowdhury Sheikh Aftab Uddin Yasuhiro Koide Yasuhiro Ozeki Yuki Fujii Yukiko Ogawa
• 来源期刊: 有机化学国际期刊(英文)
• 学科: 化学
• 关键词: URIDINE Synthesis Structure Spectroscopy ANTIBACTERIAL CYTOTOXICITY
• 年，卷（期）: 2015,（4）
• 页码范围: 232-245
• 页数: 14页
• 分类号: O6

摘要

A new N-acetylsulfanilylation series of uridine have been synthesized in good yield using direct acylation method and afforded the 5’-O-N-acetylsulfanilyluridine. In order to obtain newer products, the 5’-O-N-acetylsulfanilyluridine derivative was further transformed to a series of 2’,3’-di-O-acyl derivatives containing a wide variety of functionalities in a single molecular framework. The chemical structures of the newly synthesized compounds were confirmed on the basis of their FTIR, 1H-NMR spectroscopy, physicochemical properties and elemental analysis. All the synthesized uridine derivatives were tested for their in vitro antibacterial activity against six human pathogenic bacterial strains and for comparison standard antibiotic Ampicillin was also determined. The study revealed that the selectively acylated deriva-tives 5’-O-N-acetylsulfanilyl-2’,3’-di-O-lauroyluridine and 5’-O-N-acetylsulfanilyl-2’,3’-di-O-pivaloyluridine showed highest inhibition against Staphylococcus aureus and Bacillus cereus, respectively. We also observed that the introduction of hexanoyl, decanoyl, lauroyl, myristoyl and pivaloyl groups, the antibacterial functionality of the compound uridine increases. Another noteworthy observation was that the uridine derivatives were found comparatively more effective against Gram-positive microorganisms than those of Gram-negative microorganisms. In addition, the test chemicals were also tested for cyto-toxicity by brine shrimp lethality bioassay and compounds showed different rate mortality with different concentrations.