On Sunday, April 20th 2025, starting 8:30am GMT, there will be maintenance work that will involve the website being unavailable during parts of the day. We apologize for any inconvenience this may cause and appreciate your understanding.
We noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
Printable Handouts
Navigable Slide Index
- Introduction
- Herpes simplex virus type-1 & type-2
- Labial herpes-cold sores
- Common diseases caused by HSV
- HSV infections are life-long
- All viruses are obligate intracellular parasites
- HSV-the first virus treated effectively with antivirals
- Animal models of HSV showed antivirals effectivity
- Findings for antiviral compounds
- Anticipated problems: latency and drug-resistance
- Productive replication cycle of herpes virus
- Inhibitors are compared by measuring their EC50
- Plaque-reduction assay for HSV-1 inhibitor
- Plaque reduction assay in tissue culture
- Virus sensitivity to two antiviral compounds
- Nucleoside analogues: successful HSV inhibitors
- Natural nucleosides
- Idoxuridine: first antiviral nucleoside analogue
- Nucleoside analogues disrupt HSV DNA synthesis
- Selective inhibition of HSV
- Herpes simplex virus thymidine kinase - HSV TK
- HSV TK phosphorylates the nucleoside analogue
- Further antiviral pyrimidine nucleoside analogues
- Adenine arabinoside
- A problem with "first generation" analogues
- Purine nucleoside analogues
- Normal conversion of deoxyguanosine
- Acyclovir conversion to acyclovir triphosphate
- ACV-TP binds to HSV DNA-pol in place of dGTP
- Acyclovir: anti HSV-1 activity in clinical isolates
- Achieving in vivo inhibitory concentrations
- Acyclovir & penciclovir have similar activity
- ACV and PCV: low aqueous solubility
- The solution to the oral bioavailability problem
- Prudrugs conversion yields active compounds
- Serum levels of acyclovir following valaciclovir
- Similar prodrug strategy for ganciclovir
- HSV infections in immunocompromised host
- Remaining problems in HSV disease management
- History of herpes simplex virus antiviral drugs
Topics Covered
- Herpes simplex virus type-1 & type-2
- Common diseases caused by HSV
- HSV infections are life-long
- All viruses are obligate intracellular parasites
- HSV-the first virus treated effectively with antivirals
- Findings for antiviral compounds
- Nucleoside analogues: successful HSV inhibitors
- Acyclovir & penciclovir have similar activity, low aqueous solubility
- Prudrugs conversion yields active compounds
- Remaining problems in HSV disease management
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Field, H.J. (2011, August 30). Herpes simplex virus antiviral chemotherapy [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved April 15, 2025, from https://doi.org/10.69645/PCLG9934.Export Citation (RIS)
Publication History
- Published on August 30, 2011
Financial Disclosures
- Dr. Hugh J. Field has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.