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Biosynthesis of a Flavonol from a Flavanone by Establishing a One-pot Bienzymatic Cascade
Published on: August 14, 2019
Flavonoid derivatives and lignan enantiomers from Phanera championii Benth. and their anti-neuroinflammatory activity
Ya-Jie Hu1, Ning Diao1, Dong Liang1
1School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, 510006, China; Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Guangxi Key Laboratory of Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, 541004, China.
Abstract:
Nine undescribed compounds, including two sesquiterpenoid-substituted flavanols (1 and 2), a flavan glucoside (3), and three pairs of lignan enantiomers (4a/4b‒6a/6b), together with 22 known flavonoid derivatives (7a/7b and 8‒27) were isolated from an EtOH extract of the rattans of Phanera championii Benth. Compounds 1 and 2 are extremely rare, featuring a unique combination of flavan-3-ols linked with sesquiterpenoids. Chiral HPLC analysis with a Daicel Chiralpak AD-H column was applied to the separation of four pairs of lignan enantiomers. The absolute configurations of all the undescribed compounds were identified by alkaline hydrolysis, acid hydrolysis, experimental and calculated ECD methods. The results of anti-neuroinflammatory activity indicated that five compounds (16, 22, and 24‒26) exhibited potent inhibitory effects on nitric oxide release in BV-2 microglial cells induced by LPS, with IC50 values ranging from 0.5 to 12.7 μM. Their preliminary structure-activity relationships were discussed.
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