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المؤلفElkhalifa, Dana
المؤلفAl-Hashimi, Israa
المؤلفAl Moustafa, Ala-Eddin
المؤلفKhalil, Ashraf
تاريخ الإتاحة2023-01-23T05:30:12Z
تاريخ النشر2021
اسم المنشورJournal of Drug Targeting
المصدرScopus
معرّف المصادر الموحدhttp://dx.doi.org/10.1080/1061186X.2020.1853759
معرّف المصادر الموحدhttp://hdl.handle.net/10576/38679
الملخصSome viral outbreaks have plagued the world since antiquity, including the most recent COVID-19 pandemic. The continuous spread and emergence of new viral diseases have urged the discovery of novel treatment options that can overcome the limitations of currently marketed antiviral drugs. Chalcones are natural open chain flavonoids that are found in various plants and can be synthesised in labs. Several studies have shown that these small organic molecules exert a number of pharmacological activities, including antiviral, anti-inflammatory, antimicrobial and anticancer. The purpose of this review is to provide a summary of the antiviral activities of chalcones and their derivatives on a set of human viral infections and their potential for targeting the most recent COVID-19 disease. Accordingly, we herein review chalcones activities on the following human viruses: Middle East respiratory syndrome coronavirus, severe acute respiratory syndrome coronavirus, human immunodeficiency, influenza, human rhinovirus, herpes simplex, dengue, human cytomegalovirus, hepatitis B and C, Rift Valley fever and Venezuelan equine encephalitis. We hope that this review will pave the way for the design and development of potentially potent and broad-spectrum chalcone based antiviral drugs.
راعي المشروعOpen Access funding provided by the Qatar National Library. Our lab is supported by grants from Qatar University: # QUCG-CPH-20/21-4, QUHI-CMED-19/20-1, QUCG-CMED-20/21-2.
اللغةen
الناشرTaylor and Francis Ltd.
الموضوعapoptosis
breast cancer
cell proliferation
Haematococcus pluvialis microalgae
invasion
العنوانA comprehensive review on the antiviral activities of chalcones
النوعArticle
الصفحات403-419
رقم العدد4
رقم المجلد29
dc.accessType Open Access


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