Chemical Constituents of the Egg Cases of <i>Tenodera angustipennis</i> (Mantidis ootheca) with Intracellular Reactive Oxygen Species Scavenging Activity

As a traditional medicine with potential antioxidant effects, <i>Tenodera angustipennis</i> egg cases (Mantidis ootheca) are a potential source of new bioactive substances. Herein, three new <i>N</i>-acetyldopamine derivatives, namely, (+)-tenoderin A (<b>1a</b>),...

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প্রধান লেখক: Seung Mok Ryu, Hyeon-hwa Nam, Joong Sun Kim, Jun-ho Song, Young Hye Seo, Hyo Seon Kim, A Yeong Lee, Wook Jin Kim, Dongho Lee, Byeong Cheol Moon, Jun Lee
বিন্যাস: প্রবন্ধ
ভাষা:English
প্রকাশিত: MDPI AG 2021-04-01
মালা:Biomolecules
বিষয়গুলি:
অনলাইন ব্যবহার করুন:https://www.mdpi.com/2218-273X/11/4/556
বিবরন
সংক্ষিপ্ত:As a traditional medicine with potential antioxidant effects, <i>Tenodera angustipennis</i> egg cases (Mantidis ootheca) are a potential source of new bioactive substances. Herein, three new <i>N</i>-acetyldopamine derivatives, namely, (+)-tenoderin A (<b>1a</b>), (−)-tenoderin A (<b>1b</b>), and tenoderin B (<b>2</b>), along with thirteen known compounds (<b>3</b>–<b>15</b>), were isolated from a 70% EtOH extract of <i>T</i>. <i>angustipennis</i> egg cases. Compound <b>1</b> was isolated as a racemic mixture, and two enantiomers (<b>1a</b> and <b>1b</b>) were successfully separated by chiral-phase preparative HPLC. The chemical structures of the new compounds were established by NMR spectroscopy and high-resolution electrospray ionization mass spectrometry, and the absolute configurations of enantiomers <b>1a</b> and <b>1b</b> were determined by electronic circular dichroism spectroscopy. All the new compounds exhibited antioxidant activities with IC<sub>50</sub> values of 19.45–81.98 μM, as evaluated using free-radical scavenging assays, with the highest activity observed for compound <b>2</b>. In addition, compounds <b>1a</b>, <b>1b</b>, and <b>2</b> exhibited inhibitory activities on intracellular reactive oxygen species generation.
আইএসএসএন:2218-273X