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1.
Chinese Traditional and Herbal Drugs ; (24): 1546-1550, 2019.
Artigo em Chinês | WPRIM | ID: wpr-851221

RESUMO

Objective To study the chemical constituents from the aerial part of Euphorbia sikkimensis. Methods The chemical constituents were isolated and purified through various column chromatographies. The structures of all the isolated compounds were identified by combination of spectroscopic methods (MS, 1H, 13C NMR) with the literature data. Results Sixteen compounds were isolated from the aerial part of E. sikkimensis. They were 9-epi-blumenol C (1), blumenol A (2), 4-hydroxy-2,3-dimethyl-2-nonen- 4-olide (3), caulilide I (4), 6-methoxy-7,8-methylenedioxycoumarin (5), herniarin (6), ingenol (7), sakuranetin (8), naringenin (9), luteolin (10), taraxerone (11), glutinone (12), phytol (13), 9,12,15-linoleic acid (14), 9,12-linoleic acid (15), and α-monpalmitin (16). Conclusion All the isolated compounds, except compounds 9 and 14, are isolated from this plant for the first time.

2.
Osong Public Health and Research Perspectives ; (6): 415-420, 2017.
Artigo em Inglês | WPRIM | ID: wpr-644179

RESUMO

OBJECTIVES: Rhinoviruses (RVs) cause common cold and are associated with exacerbation of chronic inflammatory respiratory diseases. Until now, no clinically effective antiviral chemotherapeutic agents to treat diseases caused by human rhinoviruses (HRVs) have been reported. We assessed the anti-HRV3 activity of sakuranetin isolated from Sorbus commixta Hedl. in human epithelioid carcinoma cervix (HeLa) cells, to evaluate its anti-rhinoviral potential in the clinical setting. METHODS: Antiviral activity and cytotoxicity as well as the effect of sakuranetin on HRV3-induced cytopathic effects (CPEs) were evaluated using the sulforhodamine B (SRB) method using CPE reduction. The morphology of HRV3-infected cells was studied using a light microscope. RESULTS: Sakuranetin actively inhibited HRV3 replication and exhibited antiviral activity of more than 67% without cytotoxicity in HeLa cells, at 100 μg/mL. Ribavirin showed anti-HRV3 activity similar to that of sakuranetin. Treatment of HRV-infected HeLa cells with sakuranetin visibly reduced CPEs. CONCLUSION: The inhibition of HRV production by sakuranetin is mainly due to its general antioxidant activity through inhibition of viral adsorption. Therefore, the antiviral activity of sakuranetin should be further investigated to elucidate its mode of action and prevent HRV3-mediated diseases in pathological conditions.


Assuntos
Feminino , Humanos , Adsorção , Colo do Útero , Resfriado Comum , Células HeLa , Técnicas In Vitro , Métodos , Rhinovirus , Ribavirina , Sorbus
3.
Rev. bras. farmacogn ; 21(5): 915-920, Sept.-Oct. 2011. ilus, tab
Artigo em Inglês | LILACS | ID: lil-600972

RESUMO

The antiviral activity of extracts obtained from Ageratina havanensis (Kunth) R.M.King & H.Rob., Asteraceae, against rabbit vesivirus (RaV) (Caliciviridae) and human herpes simplex viruses type 1 and 2 (HSV-1, HSV-2) (Herpesviridae) were analyzed, and the main metabolites from the most active extract were isolated and characterized. The antiviral properties were investigated by measuring the inhibition of viral-induced cytopathic effect in Vero cells. The strongest inhibitory effects were found for ethyl acetate extract from leaves (SI=5 for RaV and SI=5.4 for HSV-1). The crude ethyl acetate extract was further fractionated by chromatographic methods and the structures of isolated compounds were established through comprehensive spectroscopic analyses, including IR, 2D NMR and MS. Four flavonoids were identified: 5,4'-dihydroxy-7-methoxyflavanone (sakuranetin), 3,5,4'-trihydroxy-7-methoxyflavanone (7-methoxyaromadendrin), 4'-O-β-D-glucosyl-5,3'-dihydroxy-7-methoxyflavanone (4'-O-β-D-glucosyl-7-methoxy-eriodictyol) and 4'-O-β-D-glucosyl-5-hydroxy-7-methoxyflavanone (4'-O-β-D-glucosylsakuranetin). This is the first report on antiviral activity for Ageratina havanensis.

4.
Chinese Traditional and Herbal Drugs ; (24)1994.
Artigo em Chinês | WPRIM | ID: wpr-575354

RESUMO

Objective To investigate the chemical constituents in the barks of Populus davidiana. Methods The constituents were isolated by column chromatography and their structures were determined on the basis of chemical and spectral data. Results Sixteen compounds were isolated and twelve of them were identified as 3?-acetoxyurs-12-en-28-oicacid (Ⅰ), ?-sitosterol (Ⅱ), 4-methoxyphenol (Ⅲ), 3-methoxyphenol (Ⅳ), sakuranetin (Ⅴ), scopoletin (Ⅵ), 2R, 3R-dihydro-7-methoxy-kaempferol (Ⅶ), salicyloyltremuloidin (Ⅷ), tremuloidin (Ⅸ), ?-sitosterol-3-O-glucoside (Ⅹ), salireposide (Ⅺ), and sakuranin ( ⅩⅡ ). Conclusion Compounds Ⅰ, Ⅴ, Ⅵ, and ⅩⅡ are isolated from the plants of Populus L. for the first time.

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