abacavir and entecavir

abacavir has been researched along with entecavir* in 2 studies

Other Studies

2 other study(ies) available for abacavir and entecavir

Article	Year
A library of nucleotide analogues terminate RNA synthesis catalyzed by polymerases of coronaviruses that cause SARS and COVID-19. Antiviral research, 2020, Volume: 180 Topics: Antiviral Agents; Betacoronavirus; Cidofovir; Coronavirus Infections; COVID-19; Dideoxynucleosides; Ganciclovir; Guanine; Nucleotides; Pandemics; Pneumonia, Viral; Prodrugs; RNA-Dependent RNA Polymerase; RNA, Viral; SARS-CoV-2; Severe Acute Respiratory Syndrome; Severe acute respiratory syndrome-related coronavirus; Stavudine; Valganciclovir	2020
A new and short convergent synthetic strategy to carbocyclic nucleosides. Nucleosides, nucleotides & nucleic acids, 2007, Volume: 26, Issue:8-9 An efficient synthesis for racemic cyclopent-3-en-1-yl nucleoside analogues has been developed starting from cyclopentadiene. The key step is the regioselective hydroboration of a mixture of intermediate alkylatede cyclopentadienes to give one cyclopentenol. Topics: Acids, Carbocyclic; Anti-HIV Agents; Antiviral Agents; Dideoxynucleosides; Drug Design; Guanine; Humans; Nucleosides	2007

Article

Year

A library of nucleotide analogues terminate RNA synthesis catalyzed by polymerases of coronaviruses that cause SARS and COVID-19.

Antiviral research, 2020, Volume: 180

Topics: Antiviral Agents; Betacoronavirus; Cidofovir; Coronavirus Infections; COVID-19; Dideoxynucleosides; Ganciclovir; Guanine; Nucleotides; Pandemics; Pneumonia, Viral; Prodrugs; RNA-Dependent RNA Polymerase; RNA, Viral; SARS-CoV-2; Severe Acute Respiratory Syndrome; Severe acute respiratory syndrome-related coronavirus; Stavudine; Valganciclovir

2020

A new and short convergent synthetic strategy to carbocyclic nucleosides.

Nucleosides, nucleotides & nucleic acids, 2007, Volume: 26, Issue:8-9

An efficient synthesis for racemic cyclopent-3-en-1-yl nucleoside analogues has been developed starting from cyclopentadiene. The key step is the regioselective hydroboration of a mixture of intermediate alkylatede cyclopentadienes to give one cyclopentenol.

Topics: Acids, Carbocyclic; Anti-HIV Agents; Antiviral Agents; Dideoxynucleosides; Drug Design; Guanine; Humans; Nucleosides

2007