TY - JOUR
T1 - Plant-derived lignans as potential antiviral agents
T2 - a systematic review
AU - Xu, Xin Ya
AU - Wang, Dong Ying
AU - Li, Yi Ping
AU - Deyrup, Stephen T.
AU - Zhang, Hong Jie
N1 - Funding Information:
This work was supported by the Research Grants Council of the Hong Kong Special Administrative Region, China (Nos. HKBU12103618 and HKBU12103917), the Innovation and Technology Commission of Hong Kong Special Administrative Region, China (MHP/105/19), the Research Grants Council of the Hong Kong Baptist University (HKBU), Interdisciplinary Research Matching Scheme (No. RC-IRMS/15-16/02), the Hong Kong Scholars Program Foundation (No. XJ2015047), and Mr. Kwok Yat Wai and Madam Kwok Chung Bo Fun Graduate School Development Fund (WANG Dong-Ying).
Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature B.V. 2021
PY - 2022/2
Y1 - 2022/2
N2 - Medicinal plants are one of the most important sources of antiviral
agents and lead compounds. Lignans are a large class of natural
compounds comprising two phenyl propane units. Many of them have
demonstrated biological activities, and some of them have even been
developed as therapeutic drugs. In this review, 630 lignans, including
those obtained from medicinal plants and their chemical derivatives,
were systematically reviewed for their antiviral activity and mechanism
of action. The compounds discussed herein were published in articles
between 1998 and 2020. The articles were identified using both database
searches (e.g., Web of Science, Pub Med and Scifinder) using key words
such as: antiviral activity, antiviral effects, lignans, HBV, HCV, HIV,
HPV, HSV, JEV, SARS-CoV, RSV and influenza A virus, and directed
searches of scholarly publisher’s websites including ACS, Elsevier,
Springer, Thieme, and Wiley. The compounds were classified on their
structural characteristics as 1) arylnaphthalene lignans, 2)
aryltetralin lignans, 3) dibenzylbutyrolactone lignans, 4)
dibenzylbutane lignans, 5) tetrahydrofuranoid and tetrahydrofurofuranoid
lignans, 6) benzofuran lignans, 7) neolignans, 8) dibenzocyclooctadiene
lignans and homolignans, and 9) norlignans and other lignoids. Details
on isolation and antiviral activities of the most active compounds
within each class of lignan are discussed in detail, as are studies of
synthetic lignans that provide structure–activity relationship
information.
AB - Medicinal plants are one of the most important sources of antiviral
agents and lead compounds. Lignans are a large class of natural
compounds comprising two phenyl propane units. Many of them have
demonstrated biological activities, and some of them have even been
developed as therapeutic drugs. In this review, 630 lignans, including
those obtained from medicinal plants and their chemical derivatives,
were systematically reviewed for their antiviral activity and mechanism
of action. The compounds discussed herein were published in articles
between 1998 and 2020. The articles were identified using both database
searches (e.g., Web of Science, Pub Med and Scifinder) using key words
such as: antiviral activity, antiviral effects, lignans, HBV, HCV, HIV,
HPV, HSV, JEV, SARS-CoV, RSV and influenza A virus, and directed
searches of scholarly publisher’s websites including ACS, Elsevier,
Springer, Thieme, and Wiley. The compounds were classified on their
structural characteristics as 1) arylnaphthalene lignans, 2)
aryltetralin lignans, 3) dibenzylbutyrolactone lignans, 4)
dibenzylbutane lignans, 5) tetrahydrofuranoid and tetrahydrofurofuranoid
lignans, 6) benzofuran lignans, 7) neolignans, 8) dibenzocyclooctadiene
lignans and homolignans, and 9) norlignans and other lignoids. Details
on isolation and antiviral activities of the most active compounds
within each class of lignan are discussed in detail, as are studies of
synthetic lignans that provide structure–activity relationship
information.
KW - Antiviral
KW - HBV
KW - HIV
KW - HSV
KW - Lignans
KW - Medicinal plants
UR - http://www.scopus.com/inward/record.url?scp=85107279648&partnerID=8YFLogxK
U2 - 10.1007/s11101-021-09758-0
DO - 10.1007/s11101-021-09758-0
M3 - Review article
AN - SCOPUS:85107279648
SN - 1568-7767
VL - 21
SP - 239
EP - 289
JO - Phytochemistry Reviews
JF - Phytochemistry Reviews
IS - 1
ER -