Secondary Metabolites with <i>α</i>-Glucosidase Inhibitory Activity from Mangrove Endophytic Fungus <i>Talaromyces</i> sp. CY-3
Eight new compounds, including two sambutoxin derivatives (<b>1</b>–<b>2</b>), two highly oxygenated cyclopentenones (<b>7</b>–<b>8</b>), four highly oxygenated cyclohexenones (<b>9</b>–<b>12</b>), together with four known sambu...
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doaj-7555660442d64a4594fd24c50b04b5922021-09-26T00:35:27ZengMDPI AGMarine Drugs1660-33972021-08-011949249210.3390/md19090492Secondary Metabolites with <i>α</i>-Glucosidase Inhibitory Activity from Mangrove Endophytic Fungus <i>Talaromyces</i> sp. CY-3Wencong Yang0Qi Tan1Yihao Yin2Yan Chen3Yi Zhang4Jianying Wu5Leyao Gao6Bo Wang7Zhigang She8School of Chemistry, Sun Yat-Sen University, Guangzhou 510275, ChinaSchool of Chemistry, Sun Yat-Sen University, Guangzhou 510275, ChinaSchool of Chemistry, Sun Yat-Sen University, Guangzhou 510275, ChinaSchool of Chemistry, Sun Yat-Sen University, Guangzhou 510275, ChinaResearch Institute for Marine Drugs and Nutrition, College of Food Science and Technology, Guangdong Ocean University, Zhanjiang 524088, ChinaSchool of Chemistry, Sun Yat-Sen University, Guangzhou 510275, ChinaSchool of Chemistry, Sun Yat-Sen University, Guangzhou 510275, ChinaSchool of Chemistry, Sun Yat-Sen University, Guangzhou 510275, ChinaSchool of Chemistry, Sun Yat-Sen University, Guangzhou 510275, ChinaEight new compounds, including two sambutoxin derivatives (<b>1</b>–<b>2</b>), two highly oxygenated cyclopentenones (<b>7</b>–<b>8</b>), four highly oxygenated cyclohexenones (<b>9</b>–<b>12</b>), together with four known sambutoxin derivatives (<b>3</b>–<b>6</b>), were isolated from semimangrove endophytic fungus <i>Talaromyces</i> sp. CY-3, under the guidance of molecular networking. The structures of new isolates were elucidated by analysis of detailed spectroscopic data, ECD spectra, chemical hydrolysis, <sup>13</sup>C NMR calculation, and DP4+ analysis. In bioassays, compounds <b>1</b>–<b>5</b> displayed better <i>α</i>-glucosidase inhibitory activity than the positive control 1-deoxynojirimycin (IC<sub>50</sub> = 80.8 ± 0.3 μM), and the IC<sub>50</sub> value was in the range of 12.6 ± 0.9 to 57.3 ± 1.3 μM.https://www.mdpi.com/1660-3397/19/9/492<i>Talaromyces</i> sp.molecular networkingsambutoxinpolyketides<i>α</i>-glucosidase |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wencong Yang Qi Tan Yihao Yin Yan Chen Yi Zhang Jianying Wu Leyao Gao Bo Wang Zhigang She |
spellingShingle |
Wencong Yang Qi Tan Yihao Yin Yan Chen Yi Zhang Jianying Wu Leyao Gao Bo Wang Zhigang She Secondary Metabolites with <i>α</i>-Glucosidase Inhibitory Activity from Mangrove Endophytic Fungus <i>Talaromyces</i> sp. CY-3 Marine Drugs <i>Talaromyces</i> sp. molecular networking sambutoxin polyketides <i>α</i>-glucosidase |
author_facet |
Wencong Yang Qi Tan Yihao Yin Yan Chen Yi Zhang Jianying Wu Leyao Gao Bo Wang Zhigang She |
author_sort |
Wencong Yang |
title |
Secondary Metabolites with <i>α</i>-Glucosidase Inhibitory Activity from Mangrove Endophytic Fungus <i>Talaromyces</i> sp. CY-3 |
title_short |
Secondary Metabolites with <i>α</i>-Glucosidase Inhibitory Activity from Mangrove Endophytic Fungus <i>Talaromyces</i> sp. CY-3 |
title_full |
Secondary Metabolites with <i>α</i>-Glucosidase Inhibitory Activity from Mangrove Endophytic Fungus <i>Talaromyces</i> sp. CY-3 |
title_fullStr |
Secondary Metabolites with <i>α</i>-Glucosidase Inhibitory Activity from Mangrove Endophytic Fungus <i>Talaromyces</i> sp. CY-3 |
title_full_unstemmed |
Secondary Metabolites with <i>α</i>-Glucosidase Inhibitory Activity from Mangrove Endophytic Fungus <i>Talaromyces</i> sp. CY-3 |
title_sort |
secondary metabolites with <i>α</i>-glucosidase inhibitory activity from mangrove endophytic fungus <i>talaromyces</i> sp. cy-3 |
publisher |
MDPI AG |
series |
Marine Drugs |
issn |
1660-3397 |
publishDate |
2021-08-01 |
description |
Eight new compounds, including two sambutoxin derivatives (<b>1</b>–<b>2</b>), two highly oxygenated cyclopentenones (<b>7</b>–<b>8</b>), four highly oxygenated cyclohexenones (<b>9</b>–<b>12</b>), together with four known sambutoxin derivatives (<b>3</b>–<b>6</b>), were isolated from semimangrove endophytic fungus <i>Talaromyces</i> sp. CY-3, under the guidance of molecular networking. The structures of new isolates were elucidated by analysis of detailed spectroscopic data, ECD spectra, chemical hydrolysis, <sup>13</sup>C NMR calculation, and DP4+ analysis. In bioassays, compounds <b>1</b>–<b>5</b> displayed better <i>α</i>-glucosidase inhibitory activity than the positive control 1-deoxynojirimycin (IC<sub>50</sub> = 80.8 ± 0.3 μM), and the IC<sub>50</sub> value was in the range of 12.6 ± 0.9 to 57.3 ± 1.3 μM. |
topic |
<i>Talaromyces</i> sp. molecular networking sambutoxin polyketides <i>α</i>-glucosidase |
url |
https://www.mdpi.com/1660-3397/19/9/492 |
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