Human neutrophil elastase (HNE) inhibitory polyprenylated acylphloroglucinols from the flowers of Hypericum ascyron
- Authors
- Li, Zuo Peng; Kim, Jeong Yoon; Ban, Yeong Jun; Park, 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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