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Human neutrophil elastase (HNE) inhibitory polyprenylated acylphloroglucinols from the flowers of Hypericum ascyron

Authors
Li, Zuo PengKim, Jeong YoonBan, Yeong JunPark, Ki Hun
Issue Date
Sep-2019
Publisher
Academic Press
Keywords
Hypericum ascyron; Human neutrophil elastase; Polycyclic polyprenylated acylphloroglucinols; Enzyme kinetics
Citation
Bioorganic Chemistry, v.90
Indexed
SCI
SCIE
SCOPUS
Journal Title
Bioorganic Chemistry
Volume
90
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/8807
DOI
10.1016/j.bioorg.2019.103075
ISSN
0045-2068
1090-2120
Abstract
In the course of an investigation of human neutrophil elastase (HNE) associated with inflammation, the extract of the flower parts of Hypericum ascyron showed a significant influence to HNE. The responsible metabolites to HNE inhibition were found to be eight polyprenylated acylphloroglucinols, PPAPs (1-8) which showed IC50 ranges between 2.4 and 19.9 mu M. This is the first report to demonstrate that PPAP skeleton exhibits potent HNE inhibition. The compounds 1-3 were characterized and newly named as ascyronone E (IC50=4.3 mu M), ascyronone F (IC50=19.9 mu M), ascyronone G (IC50=4.5 mu M) based on 2D-NMR spectroscopic data. In the kinetic analysis of double reciprocal plots, all the compounds showed noncompetitive behaviors to HNE enzyme with the remaining of K-m and the increase of V-max. The binding affinity levels (K-SV) by using fluorescence were sufficient to be able to prove that PPAPs (1-8) had compliant interaction with inhibitory potencies.
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