emivirine has been researched along with tnk-651 in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Esnouf, RM; Hopkins, AL; Jones, EY; Miyasaka, T; Ren, J; Ross, C; Stammers, DK; Stuart, DI; Tanaka, H; Walker, RT; Willcox, BE | 1 |
| Kang, X; Kollman, PA; Kuntz, ID; Wang, J | 1 |
| Huang, Y; Jiang, S; Li, L; Liu, C; Liu, J; Ma, L; Ouyang, Y; Qiao, K; Shao, Y; Wang, R; Wang, X; Xu, W; Zhang, J; Zhang, L; Zhang, Z | 1 |
| Danel, K; La Colla, P; Larsen, LM; Loddo, R; Pedersen, EB; Sanna, G | 1 |
| El-Brollosy, NR; Loddo, R | 1 |
5 other study(ies) available for emivirine and tnk-651
| Article | Year |
|---|---|
Complexes of HIV-1 reverse transcriptase with inhibitors of the HEPT series reveal conformational changes relevant to the design of potent non-nucleoside inhibitors.
Topics: Antiviral Agents; HIV Reverse Transcriptase; HIV-1; Humans; Hydrogen Bonding; Protein Conformation; Reverse Transcriptase Inhibitors; RNA-Directed DNA Polymerase; Structure-Activity Relationship | 1996 |
Hierarchical database screenings for HIV-1 reverse transcriptase using a pharmacophore model, rigid docking, solvation docking, and MM-PB/SA.
Topics: Allosteric Site; Anti-HIV Agents; Crystallography, X-Ray; Databases, Factual; Drug Design; HIV Reverse Transcriptase; Models, Molecular; Molecular Conformation; Molecular Structure; Protein Binding; Quantitative Structure-Activity Relationship; Reverse Transcriptase Inhibitors; Statistics as Topic; Thermodynamics | 2005 |
Design, synthesis, and biological evaluation of 1-[(2-benzyloxyl/alkoxyl)methyl]-5-halo-6-aryluracils as potent HIV-1 non-nucleoside reverse transcriptase inhibitors with an improved drug resistance profile.
Topics: Anti-HIV Agents; Cell Line, Tumor; Drug Design; Drug Resistance, Viral; HIV Reverse Transcriptase; HIV-1; Humans; Hydrogen Bonding; Models, Molecular; Structure-Activity Relationship; Uracil | 2012 |
Synthesis and antiviral activity of new dimeric inhibitors against HIV-1.
Topics: Anti-HIV Agents; Dimerization; HIV-1; Humans; Mutation; Pyrimidines; Uracil; Zidovudine | 2008 |
Synthesis and Antiviral Evaluation of 1-[(2-Phenoxyethyl)oxymethyl] and 6-(3,5-Dimethoxybenzyl) Analogues of HIV Drugs Emivirine and TNK-651.
Topics: Anti-HIV Agents; Cell Line; HIV-1; Microbial Sensitivity Tests; Molecular Structure; Mutation; Pyrimidines; Structure-Activity Relationship; Uracil | 2016 |