Papain-Like Protease (PLpro) Inhibitory Effects of Cinnamic Amides from Tribulus terrestris Fruitsopen access
- Authors
- Song, Yeong Hun; Kim, Dae Wook; Curtis-Long, Marcus John; Yuk, Heung Joo; Wang, Yan; Zhuang, Ningning; Lee, Kon Ho; Jeon, Kwon Seok; Park, Ki Hun
- Issue Date
- Jun-2014
- Publisher
- PHARMACEUTICAL SOC JAPAN
- Keywords
- papain-like protease; Tribulus terrestris; cinnamic amide; carbinolamide
- Citation
- BIOLOGICAL & PHARMACEUTICAL BULLETIN, v.37, no.6, pp 1021 - 1028
- Pages
- 8
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- BIOLOGICAL & PHARMACEUTICAL BULLETIN
- Volume
- 37
- Number
- 6
- Start Page
- 1021
- End Page
- 1028
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/18962
- DOI
- 10.1248/bpb.b14-00026
- ISSN
- 0918-6158
1347-5215
- Abstract
- Tribulus terrestris fruits are well known for their usage in pharmaceutical preparations and food supplements. The methanol extract of T. terrestris fruits showed potent inhibition against the papain-like protease (PLpro), an essential proteolylic enzyme for protection to pathogenic virus and bacteria. Subsequent bioactivity-guided fractionation of this extract led to six cinnamic amides (1-6) and ferulic acid (7). Compound 6 emerged as new compound possessing the very rare carbinolamide motif. These compounds (1-7) were evaluated for severe acute respiratory syndrome coronavirus (SARS-CoV) PLpro inhibitory activity to identify their potencies and kinetic behavior. Compounds (1-6) displayed significant inhibitory activity with IC50 values in the range 15.8-70.1 mu M. The new cinnamic amide 6 was found to be most potent inhibitor with an IC50 of 15.8 mu M. In kinetic studies, all inhibitors exhibited mixed type inhibition. Furthermore, the most active PLpro inhibitors (1-6) were proven to be present in the native fruits in high quantities by HPLC chromatogram and liquid chromatography with diode array detection and electrospray ionization mass spectrometry (LC-DAD-ESI/MS).
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