Herpes Simplex Viruses in Antiviral Drug Discovery

2006 ◽  
Vol 12 (11) ◽  
pp. 1357-1370 ◽  
Author(s):  
Luis Schang
Molecules ◽  
2021 ◽  
Vol 26 (16) ◽  
pp. 4927
Author(s):  
Anita Toscani ◽  
Rossana Denaro ◽  
Sergio Fernando Castillo Pacheco ◽  
Matteo Biolatti ◽  
Silvia Anselmi ◽  
...  

Current therapy against herpes simplex viruses (HSV) relies on the use of a few nucleoside antivirals such as acyclovir, famciclovir and valacyclovir. However, the current drugs are ineffective against latent and drug-resistant HSV infections. A series of amidinourea compounds, designed as analogues of the antiviral drug moroxydine, has been synthesized and evaluated as potential non-nucleoside anti-HSV agents. Three compounds showed micromolar activity against HSV-1 and low cytotoxicity, turning to be promising candidates for future optimization. Preliminary mode of action studies revealed that the new compounds act in an early stage of the HSV replication cycle, just after the viral attachment and the entry phase of the infection.


Antibiotics ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 159
Author(s):  
Floriana D’Angeli ◽  
Giuseppe Antonio Malfa ◽  
Adriana Garozzo ◽  
Giovanni Li Volti ◽  
Carlo Genovese ◽  
...  

The difficulty to treat resistant strains-related hospital-acquired infections (HAIs) promoted the study of phytoextracts, known sources of bioactive molecules. Accordingly, in the present study, the pharmacological activities of Juglans regia (L.) pellicle extract (WPE) were investigated. The antiviral effect was tested against Herpes simplex virus type 1 and 2, Poliovirus 1, Adenovirus 2, Echovirus 9, Coxsackievirus B1 through the plaque reduction assay. The antibacterial and antifungal activities were evaluated against medically important strains, by the microdilution method. DPPH and superoxide dismutase (SOD)s-like activity assays were used to determine the antioxidant effect. Besides, the extract was screened for cytotoxicity on Caco-2, MCF-7, and HFF1 cell lines by the 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) assay. The total phenolic and flavonoid contents were also evaluated. Interestingly, WPE inhibited Herpes simplex viruses (HSVs) replication, bacterial and fungal growth. WPE showed free radical scavenging capacity and inhibited superoxide anion formation in a dose-dependent manner. These effects could be attributed to the high content of phenols and flavonoids, which were 0.377 ± 0.01 mg GE/g and 0.292 ± 0.08 mg CE/g, respectively. Moreover, WPE was able to reduce Caco-2 cell viability, at both 48 h and 72 h. The promising results encourage further studies aimed to better elucidate the role of WPE in the prevention of human infectious diseases.


2012 ◽  
Vol 2 (5) ◽  
pp. 606-613 ◽  
Author(s):  
Benoît de Chassey ◽  
Laurène Meyniel-Schicklin ◽  
Anne Aublin-Gex ◽  
Patrice André ◽  
Vincent Lotteau

Author(s):  
Akshatha H. S ◽  
Gurubasavaraj V. Pujar ◽  
Arun Kumar Sethu ◽  
Meduri Bhagyalalitha ◽  
Manisha Singh

2004 ◽  
Vol 13 (8) ◽  
pp. 1065-1069 ◽  
Author(s):  
Wade Blair ◽  
Manos Perros

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