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