Isolation and Characterization of New Anti-Inflammatory and Antioxidant Components from Deep Marine-Derived Fungus <i>Myrothecium</i> SP. Bzo-l062
In the present study, four new compounds including a pair of 2-benzoyl tetrahydrofuran enantiomers, namely, (−)-1<i>S</i>-myrothecol (<b>1a</b>) and (+)-1<i>R</i>-myrothecol (<b>1b</b>), a methoxy-myrothecol racemate (<b>2</b>), and an azap...
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doaj-4539edb8f4434700b69c4f6c46631c5b2020-11-27T08:11:48ZengMDPI AGMarine Drugs1660-33972020-11-011859759710.3390/md18120597Isolation and Characterization of New Anti-Inflammatory and Antioxidant Components from Deep Marine-Derived Fungus <i>Myrothecium</i> SP. Bzo-l062Xiaojie Lu0Junjie He1Yanhua Wu2Na Du3Xiaofan Li4Jianhua Ju5Zhangli Hu6Kazuo Umezawa7Liyan Wang8Shenzhen Key Laboratory of Marine Bioresource and Eco-environmental Science, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, ChinaShenzhen Key Laboratory of Marine Bioresource and Eco-environmental Science, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, ChinaDepartment of Molecular Target Medicine, Aichi Medical University School of Medicine, Nagakute 480-1195, JapanShenzhen Key Laboratory of Marine Bioresource and Eco-environmental Science, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, ChinaShenzhen Key Laboratory of Marine Bioresource and Eco-environmental Science, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, ChinaCAS Key Laboratory of Tropical Marine Bio-resources and Ecology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, Guangdong 510301, ChinaShenzhen Key Laboratory of Marine Bioresource and Eco-environmental Science, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, ChinaDepartment of Molecular Target Medicine, Aichi Medical University School of Medicine, Nagakute 480-1195, JapanShenzhen Key Laboratory of Marine Bioresource and Eco-environmental Science, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, ChinaIn the present study, four new compounds including a pair of 2-benzoyl tetrahydrofuran enantiomers, namely, (−)-1<i>S</i>-myrothecol (<b>1a</b>) and (+)-1<i>R</i>-myrothecol (<b>1b</b>), a methoxy-myrothecol racemate (<b>2</b>), and an azaphilone derivative, myrothin (<b>3</b>), were isolated along with four known compounds (<b>4</b>–<b>7</b>) from cultures of the deep-sea fungus <i>Myrothecium </i>sp. BZO-L062. Enantiomeric compounds <b>1a</b> and <b>1b </b>were separated through normal-phase chiral high-performance liquid chromatography. The absolute configurations of <b>1a</b>, <b>1b</b>, and <b>3</b> were assigned by ECD spectra. Among them, the new compound <b>1a</b> and its enantiomer <b>1b </b>exhibited anti-inflammatory activity, inhibited nitric oxide formation in lipopolysaccharide-treated RAW264.7 cells, and exhibited antioxidant activity in the 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) and oxygen radical absorbance capacity assays.https://www.mdpi.com/1660-3397/18/12/597deep sea marine-derived fungus<i>Myrothecium</i> sp.myrothecolnitric oxide (NO)antioxidant activity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xiaojie Lu Junjie He Yanhua Wu Na Du Xiaofan Li Jianhua Ju Zhangli Hu Kazuo Umezawa Liyan Wang |
spellingShingle |
Xiaojie Lu Junjie He Yanhua Wu Na Du Xiaofan Li Jianhua Ju Zhangli Hu Kazuo Umezawa Liyan Wang Isolation and Characterization of New Anti-Inflammatory and Antioxidant Components from Deep Marine-Derived Fungus <i>Myrothecium</i> SP. Bzo-l062 Marine Drugs deep sea marine-derived fungus <i>Myrothecium</i> sp. myrothecol nitric oxide (NO) antioxidant activity |
author_facet |
Xiaojie Lu Junjie He Yanhua Wu Na Du Xiaofan Li Jianhua Ju Zhangli Hu Kazuo Umezawa Liyan Wang |
author_sort |
Xiaojie Lu |
title |
Isolation and Characterization of New Anti-Inflammatory and Antioxidant Components from Deep Marine-Derived Fungus <i>Myrothecium</i> SP. Bzo-l062 |
title_short |
Isolation and Characterization of New Anti-Inflammatory and Antioxidant Components from Deep Marine-Derived Fungus <i>Myrothecium</i> SP. Bzo-l062 |
title_full |
Isolation and Characterization of New Anti-Inflammatory and Antioxidant Components from Deep Marine-Derived Fungus <i>Myrothecium</i> SP. Bzo-l062 |
title_fullStr |
Isolation and Characterization of New Anti-Inflammatory and Antioxidant Components from Deep Marine-Derived Fungus <i>Myrothecium</i> SP. Bzo-l062 |
title_full_unstemmed |
Isolation and Characterization of New Anti-Inflammatory and Antioxidant Components from Deep Marine-Derived Fungus <i>Myrothecium</i> SP. Bzo-l062 |
title_sort |
isolation and characterization of new anti-inflammatory and antioxidant components from deep marine-derived fungus <i>myrothecium</i> sp. bzo-l062 |
publisher |
MDPI AG |
series |
Marine Drugs |
issn |
1660-3397 |
publishDate |
2020-11-01 |
description |
In the present study, four new compounds including a pair of 2-benzoyl tetrahydrofuran enantiomers, namely, (−)-1<i>S</i>-myrothecol (<b>1a</b>) and (+)-1<i>R</i>-myrothecol (<b>1b</b>), a methoxy-myrothecol racemate (<b>2</b>), and an azaphilone derivative, myrothin (<b>3</b>), were isolated along with four known compounds (<b>4</b>–<b>7</b>) from cultures of the deep-sea fungus <i>Myrothecium </i>sp. BZO-L062. Enantiomeric compounds <b>1a</b> and <b>1b </b>were separated through normal-phase chiral high-performance liquid chromatography. The absolute configurations of <b>1a</b>, <b>1b</b>, and <b>3</b> were assigned by ECD spectra. Among them, the new compound <b>1a</b> and its enantiomer <b>1b </b>exhibited anti-inflammatory activity, inhibited nitric oxide formation in lipopolysaccharide-treated RAW264.7 cells, and exhibited antioxidant activity in the 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) and oxygen radical absorbance capacity assays. |
topic |
deep sea marine-derived fungus <i>Myrothecium</i> sp. myrothecol nitric oxide (NO) antioxidant activity |
url |
https://www.mdpi.com/1660-3397/18/12/597 |
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