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Limonoids Containing a C??O?C29 Moiety: Isolation, Structural Modification, and Antiviral Activity.


ABSTRACT: Five new limonoids named thaigranatins A?E (1?5), containing a C??O?C29 moiety, were isolated from seeds of the Thai Xylocarpus granatum, collected at the mangrove swamp of Trang Province, together with the known limonoid, granatumin L (6). The structures of these compounds were established by HR-ESIMS and extensive NMR spectroscopic data. The absolute configuration of 1 was unequivocally determined by single-crystal X-ray diffraction analysis, conducted with Cu K? radiation; whereas that of 2 or 6 was established to be the same as that of 1 by the similarity of their electronic circular dichroism (ECD) spectra. In view of the marked antiviral activity of 6, its structure was modified via hydrolysis with alkaline KOH, esterification with diazomethane and various organic acids, and oximization with hydroxyamine. Finally, 18 derivatives, viz. 7?10, 8a?8i, 9a?9b, and 10a?10c, were obtained. In vitro antiviral activities of these derivatives against human immunodeficiency virus 1 (HIV-1) and influenza A virus (IAV) were evaluated. Most notably, 8i exhibited marked inhibitory activity against HIV-1 with an IC50 value of 15.98 ± 6.87 ?M and a CC50 value greater than 100.0 ?M; whereas 10b showed significant inhibitory activity against IAV with an IC50 value of 14.02 ± 3.54 ?M and a CC50 value greater than 100.0 ?M.

SUBMITTER: Ren JL 

PROVIDER: S-EPMC6266505 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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Limonoids Containing a C₁⁻<i>O</i>⁻C<sub>29</sub> Moiety: Isolation, Structural Modification, and Antiviral Activity.

Ren Jing-Ling JL   Zou Xiao-Peng XP   Li Wan-Shan WS   Shen Li L   Wu Jun J  

Marine drugs 20181104 11


Five new limonoids named thaigranatins A⁻E (<b>1</b>⁻<b>5</b>), containing a C₁⁻<i>O</i>⁻C<sub>29</sub> moiety, were isolated from seeds of the Thai <i>Xylocarpus granatum</i>, collected at the mangrove swamp of Trang Province, together with the known limonoid, granatumin L (<b>6</b>). The structures of these compounds were established by HR-ESIMS and extensive NMR spectroscopic data. The absolute configuration of <b>1</b> was unequivocally determined by single-crystal X-ray diffraction analysis  ...[more]

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