2',3'-Dideoxyinosine (DDI) and 2',3'-dideoxy-2,6-diaminopurine riboside (ddDAPR) are potent and selective inhibitors of human immunodeficiency virus (HIV) replication in MT-4 cells. They are also inhibitory to the transformation of C3H/3T3 cells by Moloney murine sarcoma virus (MSV). In vivo, they are only marginally effective in delaying MSV-induced tumor formation, and mortality associated therewith in newborn NMRI mice. When combined with ribavirin, DDI and ddDAPR become much more effective in inhibiting MSV and HIV replication in vitro and MSV-induced tumor formation in vivo. These observations point to the potential role of ribavirin in potentiating the anti-HIV activity of DDI in AIDS patients.status: publishe
From our investigations the following compounds have emerged as particularly potent and selective in...
A large variety of compounds have been reported to inhibit the replication of human immunodeficiency...
9-(2-Phosphonylmethoxyethyl)adenine (PMEA) is a potent and selective inhibitor of the replication of...
Ribavirin enhances the anti-human immunodeficiency virus activity of 2',3'-dideoxyinosine (ddIno) in...
The combined antiviral effects of various 2',3'-dideoxynucleosides and ribavirin on the replication ...
The 2',3'-dideoxyriboside of 2,6-diaminopurine(ddDAPR) is, like 2',3'-dideoxyadenosine (ddAdo), a po...
Discovered 45 years ago, ribavirin still proves useful as a broad-spectrum anti-viral drug against d...
The efficacy and toxicity of ribavirin (25 or 1 25 mg/kg/day), 2’,3’-dideoxyinosine (ddl) (200 mg/kg...
Several sugar-modified 2,6-diaminopurine and guanine 2',3'-dideoxyribosides were synthesized and eva...
The epidemics caused by pathogenic viruses, such as HIV, hepatitis C virus (HCV) and most recently t...
It is not yet clear to what extent depletion of intracellular GTP pools contributes to the antiviral...
In the design of selective inhibitors of the human immunodeficiency virus (HIV), the etiologic agent...
Multiple clinical trials have demonstrated that herpes simplex virus 2 (HSV-2) suppressive therapy u...
The 2',3'-dideoxyriboside of 2,6-diaminopurine (ddDAPR) and its 2',3'-didehydro derivative (ddeDAPR)...
We examined the inhibitory effect of 20 antiviral compounds, including ribavirin, on the replication...
From our investigations the following compounds have emerged as particularly potent and selective in...
A large variety of compounds have been reported to inhibit the replication of human immunodeficiency...
9-(2-Phosphonylmethoxyethyl)adenine (PMEA) is a potent and selective inhibitor of the replication of...
Ribavirin enhances the anti-human immunodeficiency virus activity of 2',3'-dideoxyinosine (ddIno) in...
The combined antiviral effects of various 2',3'-dideoxynucleosides and ribavirin on the replication ...
The 2',3'-dideoxyriboside of 2,6-diaminopurine(ddDAPR) is, like 2',3'-dideoxyadenosine (ddAdo), a po...
Discovered 45 years ago, ribavirin still proves useful as a broad-spectrum anti-viral drug against d...
The efficacy and toxicity of ribavirin (25 or 1 25 mg/kg/day), 2’,3’-dideoxyinosine (ddl) (200 mg/kg...
Several sugar-modified 2,6-diaminopurine and guanine 2',3'-dideoxyribosides were synthesized and eva...
The epidemics caused by pathogenic viruses, such as HIV, hepatitis C virus (HCV) and most recently t...
It is not yet clear to what extent depletion of intracellular GTP pools contributes to the antiviral...
In the design of selective inhibitors of the human immunodeficiency virus (HIV), the etiologic agent...
Multiple clinical trials have demonstrated that herpes simplex virus 2 (HSV-2) suppressive therapy u...
The 2',3'-dideoxyriboside of 2,6-diaminopurine (ddDAPR) and its 2',3'-didehydro derivative (ddeDAPR)...
We examined the inhibitory effect of 20 antiviral compounds, including ribavirin, on the replication...
From our investigations the following compounds have emerged as particularly potent and selective in...
A large variety of compounds have been reported to inhibit the replication of human immunodeficiency...
9-(2-Phosphonylmethoxyethyl)adenine (PMEA) is a potent and selective inhibitor of the replication of...