Unknown

Dataset Information

0

Inhibitory Activity of Quercetin 3-O-Arabinofuranoside and 2-Oxopomolic Acid Derived from Malus domestica on Soluble Epoxide Hydrolase.


ABSTRACT: Flavonoids and triterpenoids were revealed to be the potential inhibitors on soluble epoxide hydrolase (sEH). The aim of this study is to reveal sEH inhibitors from Fuji apples. A flavonoid and three triterpenoids derived from the fruit of Malus domestica were identified as quercetin-3-O-arabinoside (1), ursolic acid (2), corosolic acid (3), and 2-oxopomolic acid (4). They had half-maximal inhibitory concentration of the inhibitors (IC50) values of 39.3 ± 3.4, 84.5 ± 9.5, 51.3 ± 4.9, and 11.4 ± 2.7 ?M, respectively, on sEH. The inhibitors bound to allosteric sites of enzymes in mixed (1) and noncompetitive modes (2-4). Molecular simulations were carried out for inhibitors 1 and 4 to calculate the binding force of ligands to receptors. The inhibitors bound to the left (1) and right (4) pockets next to the enzyme's active site. Based on analyses of their molecular docking and dynamics, it was shown that inhibitors 1 and 4 can stably bind sEH at 1 bar and 300 K. Finally, inhibitors 1 and 4 are promising candidates for further studies using cell-based assays and in vivo cardiovascular tests.

SUBMITTER: Cho IS 

PROVIDER: S-EPMC7576482 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

Inhibitory Activity of Quercetin 3-<i>O</i>-Arabinofuranoside and 2-Oxopomolic Acid Derived from <i>Malus domestica</i> on Soluble Epoxide Hydrolase.

Cho In Sook IS   Kim Jang Hoon JH   Lin Yunjia Y   Su Xiang Dong XD   Kang Jong Seong JS   Yang Seo Young SY   Kim Young Ho YH  

Molecules (Basel, Switzerland) 20200922 18


Flavonoids and triterpenoids were revealed to be the potential inhibitors on soluble epoxide hydrolase (sEH). The aim of this study is to reveal sEH inhibitors from Fuji apples. A flavonoid and three triterpenoids derived from the fruit of <i>Malus domestica</i> were identified as quercetin-3-<i>O</i>-arabinoside (<b>1</b>), ursolic acid (<b>2</b>), corosolic acid (<b>3</b>), and 2-oxopomolic acid (<b>4</b>). They had half-maximal inhibitory concentration of the inhibitors (IC<sub>50</sub>) valu  ...[more]

Similar Datasets

| S-EPMC6331899 | biostudies-literature
| S-EPMC6151598 | biostudies-literature
| S-EPMC3597810 | biostudies-literature
| S-EPMC2728155 | biostudies-literature
| S-EPMC2533064 | biostudies-literature
| S-EPMC6210075 | biostudies-literature
| S-EPMC7004070 | biostudies-literature