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Inhibition of Human Neutrophil Elastase by Sesquiterpene Lactone Dimers from the Flowers of Inula britannica
Author(s) -
Kwan-Chul Kim,
Dae Jung Kim,
Myung Sun Lee,
Ji Yun Seo,
IckDong Yoo,
Ik Soo Lee
Publication year - 2018
Publication title -
journal of microbiology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 64
eISSN - 1738-8872
pISSN - 1017-7825
DOI - 10.4014/jmb.1807.07039
Subject(s) - elastase , ic50 , chemistry , stereochemistry , sesquiterpene , inula , sesquiterpene lactone , lactone , in vitro , dimer , inhibitory postsynaptic potential , biochemistry , enzyme , biology , organic chemistry , medicine , neuroscience , alternative medicine , traditional chinese medicine , pathology
A new sesquiterpene lactone dimer [1] , together with five known compounds (2-6) , was isolated from the flowers of Inula britannica . The structures of these compounds were established by extensive spectroscopic studies and chemical evidence. The inhibitory activities of these isolated compounds (1-6) against human neutrophil elastase (HNE) were also evaluated in vitro; compounds 1 and 6 exhibited significant inhibitory effects against HNE activity, with IC 50 values of 8.2 and 10.4 μM, respectively, comparable to that of epigallocatechin gallate (EGCG; IC 50 = 10.9 μM). In addition, compounds 3 and 5 exhibited moderate HNE inhibitory effects, with IC 50 values of 21.9 and 42.5 μM, respectively. In contrast, compounds 2 and 4 exhibited no such activity (IC 50 100 μM). The mechanism by which 1 and 3 inhibited HNE was noncompetitive inhibition, with inhibition constant ( K i ) values of 8.0 and 22.8 μM, respectively.

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