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Efficient and divergent enantioselective syntheses of DHPVs and anti-inflammatory effect on IEC-6 cells

Authors
Kim H.S.Chung S.Song M.-Y.Lim C.Shin H.Hur J.Kwon H.Suh Y.-G.Kim E.-H.Shin D.Kim S.-H.
Issue Date
May-2020
Publisher
MDPI AG
Keywords
Anti-inflammatory effect; Asymmetric dihydroxylation; DHPV; Divergent synthesis; IκBα; NF-κB
Citation
Molecules, v.25, no.9
Journal Title
Molecules
Volume
25
Number
9
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/51598
DOI
10.3390/molecules25092215
ISSN
1420-3049
Abstract
Despite numerous reports on the beneficial effects of catechin or epicatechin contained in tea and cacao extract on human health, a conclusive and precise molecular mechanism has not been elucidated. Metabolism of chemical compounds in gut microbiota recently gained significant attention, and extensive studies have been devoted in this field. In conjunction with these results, our group focused on the anti-inflammatory effects of both enantiomers of DHPV (5-(3',4'-dihydroxyphenyl)-γ-valerolactone), produced in the intestine by microbiota metabolism, on IEC-6 cells. Divergent and efficient enantioselective synthesis of (S)- and (R)-DHPV was efficiently achieved by cross-metathesis and Sharpless asymmetric dihydroxylation as a key reaction for four steps in 16% and 14% overall yields, respectively. The anti-inflammatory effects of two enantiomers were tested on IEC-6 cells, and we found that (S)-DHPV was more active than (R)-DHPV. This result implicates that the metabolite produced in the gut has beneficial effects on IEC-6 cells of rat intestines, and the chirality of the metabolite is important for its anti-inflammatory activity. This also provided information for the future discovery of novel small molecular therapeutics for the treatment of inflammatory bowel disease. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
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