Anti-viral Activity of 5,6-Dichloro-1-(2'-Deoxy-beta-D-Ribofuranosyl)Benzimidazole and Related Derivatives

Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06510 * Department of Chemistry, University of Utah, Salt Lake City, Utah, U.S.A. Several derivatives of benzimidazole were tested for antiviral activity; of these the 1- - D -2'-deoxyriboside of 5,6-dichloro...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of general virology 1968-12, Vol.3 (3), p.393-402
Hauptverfasser: Diwan, A, Gowdy, Cellissa N, Robins, R. K, Prusoff, W. H
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06510 * Department of Chemistry, University of Utah, Salt Lake City, Utah, U.S.A. Several derivatives of benzimidazole were tested for antiviral activity; of these the 1- - D -2'-deoxyriboside of 5,6-dichlorobenzimidazole and the and anomers of 5,6-dimethyl-1-(2'-deoxy- D -ribofuranosyl)benzimidazole inhibited the reproduction in vitro of two DNA viruses, herpes simplex virus and polyoma virus; 5,6-dichloro-1-(2'-deoxy- - D -ribofuranosyl)benzimidazole (dDBZ) was the most inhibitory compound. Pretreatment of the host cells with dDBZ, subsequently removed by washing, did not affect the yield of these viruses. dDBZ did not have any direct inactivation effect on herpes simplex virus. Growth curves of herpes virus in the presence of dDBZ indicated that a reduced yield of the virus was obtained after a considerable lag, the first progeny virus being detected 24 hr after infection. Marked inhibition could be demonstrated when the compound was added as late as 15 hr after infection. Attempts to prevent the inhibition by dDBZ by addition of the following compounds failed: deoxyadenosine, deoxyguanosine, deoxycytidine, thymidine, adenine and adenosine. 5,6-Dichlorobenzimidazole, its ribonucleoside (5,6-dichloro-1-( - D -ribofuranosyl)benzimidazole (DRB)) and the corresponding deoxyribonucleoside (dDBZ) were compared for their relative antiviral activity against a DNA virus (herpes simplex virus) and RNA viruses (three strains of polio virus). All three compounds inhibited herpes simplex virus; the 5,6-dichlorobenzimidazole inhibited two strains of polio virus; and DRB inhibited all three strains of polio virus. dDBZ had the least inhibitory activity for two of the three strains of polio virus and did not inhibit the LSC 1 2 AB strain of polio virus. dDBZ at a concentration required to inhibit viral replication inhibited the synthesis of RNA and to a lesser extent that of DNA and protein of uninfected green monkey kidney cells. Received 12 March 1968; accepted 21 May 1968.
ISSN:0022-1317
1465-2099
DOI:10.1099/0022-1317-3-3-393