- 氢H氢H
- 氦He氦He
- 锂Li锂Li
- 铍Be铍Be
- 硼B硼B
- 碳C碳C
- 氮N氮N
- 氧O氧O
- 氟F氟F
- 氖Ne氖Ne
- 钠Na钠Na
- 镁Mg镁Mg
- 铝Al铝Al
- 硅Si硅Si
- 磷P磷P
- 硫S硫S
- 氯CI氯CI
- 氩Ar氩Ar
- 钾K钾K
- 钙Ca钙Ca
- 钪Sc钪Sc
- 钛Ti钛Ti
- 钒V钒V
- 铬Cr铬Cr
- 锰Mn锰Mn
- 铁Fe铁Fe
- 钴Co钴Co
- 镍Ni镍Ni
- 铜Cu铜Cu
- 锌Zn锌Zn
- 镓Ga镓Ga
- 锗Ge锗Ge
- 砷As砷As
- 硒Se硒Se
- 溴Br溴Br
- 氪Kr氪Kr
- 铷Rb铷Rb
- 锶Sr锶Sr
- 钇Y钇Y
- 锆Zr锆Zr
- 铌Nb铌Nb
- 钼Mo钼Mo
- 锝Tc锝Tc
- 钌Ru钌Ru
- 铑Rh铑Rh
- 钯Pd钯Pd
- 银Ag银Ag
- 镉Cd镉Cd
- 铟In铟In
- 锡Sn锡Sn
- 锑Sb锑Sb
- 碲Te碲Te
- 碘I碘I
- 氙Xe氙Xe
- 铯Cs铯Cs
- 钡Ba钡Ba
- 镧La镧La
- 铪Hf铪Hf
- 钽Ta钽Ta
- 钨W钨W
- 铼Re铼Re
- 锇Os锇Os
- 铱Ir铱Ir
- 铂Pt铂Pt
- 金Au金Au
- 汞Hg汞Hg
- 铊Tl铊Tl
- 铅Pb铅Pb
- 铋Bi铋Bi
- 钋Po钋Po
- 砹At砹At
- 氡Rn氡Rn
- 钫Fr钫Fr
- 镭Ra镭Ra
- 锕Ac锕Ac
- 鏕Rf鏕Rf
- DbDb
- SgSg
- BhBh
- HsHs
- MtMt
- DsDs
- RgRg
- Cn Cn
- UutUut
- UuqUuq
- UupUup
- UuhUuh
- UuhUuh
- UuoUuo
Hexamminecobalt (III) Chloride as a Broad-Spectrum Antiviral Complex
Eddie L. Chang1 *, Gene G. Olinger2 , Lisa E. Hensley2 , Calli M. Lear2 , Corinne E. Scully2 , Marie K. Mankowski3 , Roger G. Ptak3 , Dzung C. Thach4 and D. Andrew Knight5
1 Center for Bio/Molecular Science and Engineering, 4555 Overlook Avenue SW, Washington, DC20375, USA
2 United States Army Medical Research Institute of Infectious Diseases, Division of Virology, 1425 Porter Street, Frederick, Maryland, USA
3 Infectious Disease Research Department, Southern Research Institute, 431 Aviation Way, Frederick, MD, 21701, USA
4 Laboratory of Infectious Diseases, National Institute of Allergies and Infectious Diseases, NIH, Department of Health and Human Services, Bethesda, MD 20892, US
Abstract
Metal ion complexes have the potential to form novel types of antiviral compounds, due to their ability to form octahedral and square-planar molecular geometries and their intrinsic charge density. Previously it has been shown that hexamminecobalt(III) chloride (Cohex) has antiviral properties against Sindbis virus (SINV) and adenovirus. Here, we report that Cohex also exhibits activities against two isolates of human immunodeficiency virus (HIV) and the Zaire Ebola (ZEBOV) strain expressing green fluorescent protein (GFP). The therapeutic indices for antiviral activity against the HIV isolates were similar to that found for SINV. Cohex was also effective in decreasing the host translation of viral GFP in four different cell-lines infected with ZEBOV. Toxicity studies in mice found no deleterious effects at up to 8 mg/kg. The 8 mg/kg concentration also prolonged survival of mice infected with ZEBOV. These results point to the potential of Cohex as a new type of broad-spectrum antibiotic compounds