Loading…
Antiphytoviral toxins of Actinidia chinensis root bark (ACRB) extract: laboratory and semi‐field trials
BACKGROUND Actinidia chinensis Planch, which is distributed only in China, has been used to treat hepatitis and cancer. The objective of the present work was to identify the antiviral active ingredient of A. chinensis root bark (ACRB). RESULTS Bioassay‐guided isolation of the most active fraction, t...
Saved in:
Published in: | Pest management science 2018-07, Vol.74 (7), p.1630-1636 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | BACKGROUND
Actinidia chinensis Planch, which is distributed only in China, has been used to treat hepatitis and cancer. The objective of the present work was to identify the antiviral active ingredient of A. chinensis root bark (ACRB).
RESULTS
Bioassay‐guided isolation of the most active fraction, the EtOAc extract, led to the identification of seven compounds, (+)‐catechins‐7‐phytol (1), 5‐methoxy‐coumarin‐7‐β‐D‐glycosidase (2), (+)‐catechins (3), fupenzic acid (4), spathodic acid‐28‐O‐β‐D‐glucopyranoside (5), 3‐oxo‐9, 12‐diene‐30‐oic acid (6), and 3‐β‐(2‐carboxy benzoyloxy) oleanolic acid (7). Of these, 5‐methoxy‐coumarin‐7‐β‐D‐glycosidase (2) possessed the highest antiviral activity, followed by spathodic acid‐28‐O‐β‐D‐glucopyranoside (5). Thus, compounds 2 and 5 were the main active constituents, with potential for further development as biological antiviral agents.
CONCLUSION
The results suggest that ACRB possesses great potential value for development of an antiviral agent to control phytoviral diseases. © 2018 Society of Chemical Industry
An extract of Actinidia chinensis root bark (ACRB) displayed antiphytoviral effects in both laboratory and field trials. Bioassay‐guided fractionation led to the identification of two active compounds from the ACRB extract. |
---|---|
ISSN: | 1526-498X 1526-4998 |
DOI: | 10.1002/ps.4854 |