Inhibition of African swine fever virus protease by myricetin and myricitrin
- 주제(키워드) African swine fever virus protease , antiviral , flavonoid , fret , inhibitory compounds
- 주제(기타) Biochemistry & Molecular Biology
- 주제(기타) Chemistry, Medicinal
- 설명문(일반) [Shin, Dong Hae; Kim, Mi-Sun] Ewha W Univ, Coll Pharm, Seoul 03760, South Korea; [Shin, Dong Hae; Kim, Mi-Sun] Ewha W Univ, Graduates Sch Pharmaceut Sci, Seoul, South Korea
- 등재 SCIE, SCOPUS
- OA유형 gold, Green Published
- 발행기관 TAYLOR & FRANCIS LTD
- 발행년도 2020
- 총서유형 Journal
- URI http://www.dcollection.net/handler/ewha/000000168915
- 본문언어 영어
- Published As https://dx.doi.org/10.1080/14756366.2020.1754813
- PubMed https://pubmed.ncbi.nlm.nih.gov/32299265
초록/요약
African swine fever (ASF) caused by the ASF virus (ASFV) is the most hazardous swine disease. Since a huge number of pigs have been slaughtered to avoid a pandemic spread, intense studies on the disease should be followed quickly. Recent studies reported that flavonoids have various antiviral activity including ASFV. In this report, ASFV protease was selected as an antiviral target protein to cope with ASF. With a FRET (Fluorescence resonance energy transfer) method, ASFV protease was assayed with a flavonoid library which was composed of sixty-five derivatives classified based on ten different scaffolds. Of these, the flavonols scaffold contains a potential anti-ASFV protease activity. The most prominent flavonol was myricetin with IC50 of 8.4 mu M. Its derivative, myricitrin, with the rhamnoside moiety was also showed the profound inhibitory effect on ASFV protease. These two flavonols apparently provide a way to develop anti-ASFV agents based on their scaffold.
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