Drug class
Antiviral-HIV Cytidine Analogue Nucleoside RT Inhibitors
Antiviral-HIV cytidine analogue nucleoside reverse transcriptase inhibitors (NRTIs) are a structural subcategory of antiretroviral agents, most prominently represented by lamivudine and emtricitabine. Read more about Antiviral-HIV Cytidine Analogue Nucleoside RT Inhibitors
77 drugs in this class 36 manufacturers
Drugs in Antiviral-HIV Cytidine Analogue Nucleoside RT Inhibitors
EFAVIRENZ-EMTRIC-TENOFOV DISOP (efavirenz/emtricitabine/tenofovir disoproxil fumarate)
ABACAVIR-LAMIVUDINE (abacavir sulfate/lamivudine)
LAMIVUDINE
EMTRICITABINE-RILPIVIRNE-TENOF (emtricitabine/rilpivirine HCl/tenofovir disoproxil fumarate)
Antiviral-HIV cytidine analogue nucleoside reverse transcriptase inhibitors (NRTIs) are a structural subcategory of antiretroviral agents, most prominently represented by lamivudine and emtricitabine.
These agents mimic the endogenous pyrimidine nucleoside cytidine and, following intracellular phosphorylation into active triphosphate metabolites, compete with deoxycytidine triphosphate for incorporation into nascent viral DNA by HIV reverse transcriptase.
Because they lack a 3'-hydroxyl group, their incorporation causes premature viral DNA chain termination and prevents replication.
They serve as foundational backbone components in combination antiretroviral therapy for the management and prevention of human immunodeficiency virus type 1 (HIV-1) infection, and frequently possess concurrent therapeutic activity against hepatitis B virus (HBV) infection.
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thebodypro.com
Antiviral-HIV cytidine analogue nucleoside reverse transcriptase inhibitors (NRTIs) are a structural subcategory of antiretroviral agents, most prominently represented by lamivudine and emtricitabine
-
hiv.gov
Antiviral-HIV cytidine analogue nucleoside reverse transcriptase inhibitors (NRTIs) are a structural subcategory of antiretroviral agents, most prominently represented by lamivudine and emtricitabine
-
nih.gov
These agents mimic the endogenous pyrimidine nucleoside cytidine and, following intracellular phosphorylation into active triphosphate metabolites, compete with deoxycytidine triphosphate for incorporation into nascent viral DNA by HIV reverse transcriptase They serve as foundational backbone components in combination antiretroviral therapy for the management and prevention of human immunodeficiency virus type 1 (HIV-1) infection, and frequently possess concurrent therapeutic activity against he...
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drugbank.com
These agents mimic the endogenous pyrimidine nucleoside cytidine and, following intracellular phosphorylation into active triphosphate metabolites, compete with deoxycytidine triphosphate for incorporation into nascent viral DNA by HIV reverse transcriptase
-
nih.gov
Because they lack a 3′-hydroxyl group, their incorporation causes premature viral DNA chain termination and prevents replication
-
expasy.org
Because they lack a 3′-hydroxyl group, their incorporation causes premature viral DNA chain termination and prevents replication
-
selleckchem.com
They serve as foundational backbone components in combination antiretroviral therapy for the management and prevention of human immunodeficiency virus type 1 (HIV-1) infection, and frequently possess concurrent therapeutic activity against hepatitis B virus (HBV) infection
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