Page last updated: 2024-08-24

l-697661 and efavirenz

l-697661 has been researched along with efavirenz in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Corbett, JW; Cordova, BC; Erickson-Viitanen, SK; Klabe, RM; Kresge, KJ; Pan, S; Rodgers, JD	1
Dornadula, G; Grobler, JA; Hazuda, DJ; Miller, MD; Rice, MR; Simcoe, AL	1

Other Studies

2 other study(ies) available for l-697661 and efavirenz

Article	Year
Trifluoromethyl-containing 3-alkoxymethyl- and 3-aryloxymethyl-2-pyridinones are potent inhibitors of HIV-1 non-nucleoside reverse transcriptase. Bioorganic & medicinal chemistry letters, 2001, Feb-12, Volume: 11, Issue:3 Topics: Anti-HIV Agents; Combinatorial Chemistry Techniques; Cytopathogenic Effect, Viral; Enzyme Inhibitors; Fluorine; HIV Reverse Transcriptase; HIV-1; Inhibitory Concentration 50; Mutation; Pyridones; Structure-Activity Relationship	2001
HIV-1 reverse transcriptase plus-strand initiation exhibits preferential sensitivity to non-nucleoside reverse transcriptase inhibitors in vitro. The Journal of biological chemistry, 2007, Mar-16, Volume: 282, Issue:11 Topics: Alkynes; Anti-HIV Agents; Benzoxazines; Benzoxazoles; Cyclopropanes; DNA; Dose-Response Relationship, Drug; Drug Resistance, Viral; Enzyme Inhibitors; HIV Reverse Transcriptase; In Vitro Techniques; Inhibitory Concentration 50; Ligands; Models, Genetic; Oxazines; Pyridones; Reverse Transcriptase Inhibitors; Stochastic Processes; Transcription, Genetic; Virus Replication	2007

Article

Year

Trifluoromethyl-containing 3-alkoxymethyl- and 3-aryloxymethyl-2-pyridinones are potent inhibitors of HIV-1 non-nucleoside reverse transcriptase.

Bioorganic & medicinal chemistry letters, 2001, Feb-12, Volume: 11, Issue:3

Topics: Anti-HIV Agents; Combinatorial Chemistry Techniques; Cytopathogenic Effect, Viral; Enzyme Inhibitors; Fluorine; HIV Reverse Transcriptase; HIV-1; Inhibitory Concentration 50; Mutation; Pyridones; Structure-Activity Relationship

2001

HIV-1 reverse transcriptase plus-strand initiation exhibits preferential sensitivity to non-nucleoside reverse transcriptase inhibitors in vitro.

The Journal of biological chemistry, 2007, Mar-16, Volume: 282, Issue:11

Topics: Alkynes; Anti-HIV Agents; Benzoxazines; Benzoxazoles; Cyclopropanes; DNA; Dose-Response Relationship, Drug; Drug Resistance, Viral; Enzyme Inhibitors; HIV Reverse Transcriptase; In Vitro Techniques; Inhibitory Concentration 50; Ligands; Models, Genetic; Oxazines; Pyridones; Reverse Transcriptase Inhibitors; Stochastic Processes; Transcription, Genetic; Virus Replication

2007