» Articles » PMID: 7247370

Antiviral Activity of Win 41258-3, a Pyrazole Compound, Against Herpes Simplex Virus in Mouse Genital Infection and in Guinea Pig Skin Infection

Overview
Specialty Pharmacology
Date 1981 Mar 1
PMID 7247370
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Win 41258-3 (4-[6-(2-chloro-4-methoxyphenoxy)hexyl]-3,5-diethyl-1H-pyrazole methane sulfonate) has in vitro and in vivo activity against herpes simplex virus types 1 and 2. In cell culture, a concentration of 2 microgram/ml produced a greater than 50% inhibition of plaque formation of herpes simplex virus type 2, and 3 microgram/ml produced a 100% reduction of herpes simplex virus type 1. Win 41258-3 was effective against herpes simplex virus types 1 and 2 in mouse genital infection after intravaginal administration. Win 41258-3 was administered to mice at 4 h postinfection with solutions containing 1.25, 2.5, 5, or 10% of the compound in saturated tampons. Therapy resulted in a high survival rate (80 to 100%) of treated animals versus 20 to 30% of placebo-treated controls. Win 41258-3 was also effective in guinea pig skin infection produced by herpes simplex virus type 1. Solutions of 2.5, 5, and 10% Win 41258-3, applied to the skin starting 24 h postinfection, resulted in rapid suppression of development of herpetic vesicles and significant reduction of the virus titers in the lesion sites.

Citing Articles

DFT Study of Regio- and Stereoselective 13DC Reaction between Diazopropane and Substituted Chalcone Derivatives: Molecular Docking of Novel Pyrazole Derivatives as Anti-Alzheimer's Agents.

Al-Hazmy S, Zouaghi M, Amri N, Arfaoui Y, Alhagri I, Hamdi N Molecules. 2023; 28(4).

PMID: 36838888 PMC: 9964806. DOI: 10.3390/molecules28041899.


Topical treatment of cutaneous herpes simplex virus infection in hairless mice with (E)-5-(2-bromovinyl)-2'-deoxyuridine and related compounds.

De Clercq E Antimicrob Agents Chemother. 1984; 26(2):155-9.

PMID: 6486759 PMC: 284110. DOI: 10.1128/AAC.26.2.155.


Acyclovir. A review of its pharmacodynamic properties and therapeutic efficacy.

Richards D, Carmine A, Brogden R, Heel R, Speight T, Avery G Drugs. 1983; 26(5):378-438.

PMID: 6315332 DOI: 10.2165/00003495-198326050-00002.


Specific targets for antiviral drugs.

De Clercq E Biochem J. 1982; 205(1):1-13.

PMID: 6181775 PMC: 1158439. DOI: 10.1042/bj2050001.


Xylotubercidin against herpes simplex virus type 2 in mice.

De Clercq E, Robins M Antimicrob Agents Chemother. 1986; 30(5):719-24.

PMID: 3800347 PMC: 176520. DOI: 10.1128/AAC.30.5.719.


References
1.
Hubler Jr W, Felber T, TROLL D, Jarratt M . Guinea pig model for cutaneous herpes simplex virus infection. J Invest Dermatol. 1974; 62(2):92-5. DOI: 10.1111/1523-1747.ep12692222. View

2.
Kern E, Richards J, Overall Jr J, Glasgow L . Genital Herpesvirus homonis infection in mice. II. Treatment with phosphonoacetic acid, adenine arabinoside, and adenine arabinoside 5'-monophosphate. J Infect Dis. 1977; 135(4):557-67. DOI: 10.1093/infdis/135.4.557. View

3.
Diana G, SALVADOR U, Zalay E, Johnson R, Collins J, Johnson D . Antiviral activity of some beta-diketones. 1. Aryl alkyl diketones. In vitro activity against both RNA and DNA viruses. J Med Chem. 1977; 20(6):750-6. DOI: 10.1021/jm00216a003. View

4.
Diana G, SALVADOR U, Zalay E, CARABATEAS P, Williams G, Collins J . Antiviral activity of some beta-diketones. 2. Aryloxy alkyl diketones. In vitro activity against both RNA and DNA viruses. J Med Chem. 1977; 20(6):757-61. DOI: 10.1021/jm00216a004. View

5.
Diana G, CARABATEAS P, SALVADOR U, Williams G, Zalay E, Pancic F . Antiviral activity of some beta-diketones. 3. Aryl bis(beta-diketones). Antiherpetic activity. J Med Chem. 1978; 21(7):689-92. DOI: 10.1021/jm00205a019. View