urea has been researched along with dmp 850 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 | 4 (80.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Anderson, PS; Bacheler, LT; Chang, CH; Cordova, B; Erickson-Viitanen, S; Garber, S; Johnson, BL; Klabe, RM; Ko, SS; Lam, PY; Li, R; Reid, C; Rodgers, JD; Ru, Y; Seitz, SP; Trainor, GL; Wang, H; Wright, MR | 1 |
| Aungst, BJ; Bulgarelli, JP; Nguyen, NH; Oates-Lenz, K | 1 |
| Bacheler, LT; Cordova, BC; Erickson-Viitanen, S; Garber, S; Harris, GD; Kaltenbach, RF; Klabe, RM; Logue, K; Patel, M; Stone, BR; Trainor, GL; Waltermire, RE; Wright, MR | 1 |
| Chrusciel, RA; Strohbach, JW | 1 |
| Bai, DL; He, XC; Yang, QG | 1 |
2 review(s) available for urea and dmp 850
| Article | Year |
|---|---|
Non-peptidic HIV protease inhibitors.
Topics: Anti-HIV Agents; Disulfides; Drug Resistance, Viral; Furans; Heterocyclic Compounds, 4 or More Rings; HIV; HIV Infections; HIV Protease Inhibitors; Humans; Molecular Structure; Mutation; Pyridines; Pyrones; Sulfonamides; Triazines; Urea | 2004 |
[Current status of HIV protease inhibitors].
Topics: 4-Hydroxycoumarins; Anti-HIV Agents; Atazanavir Sulfate; HIV Protease Inhibitors; Humans; Molecular Structure; Oligopeptides; Pyridines; Saquinavir; Urea | 2005 |
3 other study(ies) available for urea and dmp 850
| Article | Year |
|---|---|
Design and selection of DMP 850 and DMP 851: the next generation of cyclic urea HIV protease inhibitors.
Topics: Animals; Anti-HIV Agents; Crystallography, X-Ray; Dogs; Drug Design; HIV; HIV Protease Inhibitors; Molecular Structure; Mutation; Protein Binding; Urea; Virus Replication | 1998 |
The influence of donor and reservoir additives on Caco-2 permeability and secretory transport of HIV protease inhibitors and other lipophilic compounds.
Topics: Acetamides; Albumins; Azepines; Caco-2 Cells; Carbamates; Cell Membrane Permeability; Furans; HIV Protease Inhibitors; Humans; Indinavir; Intestinal Absorption; Nelfinavir; Ritonavir; Solvents; Structure-Activity Relationship; Sulfonamides; Urea | 2000 |
Synthesis, antiviral activity and pharmacokinetics of P1/P1' substituted 3-aminoindazole cyclic urea HIV protease inhibitors.
Topics: Administration, Oral; Animals; Biological Availability; Dogs; Drug Resistance; Heterocyclic Compounds, 4 or More Rings; HIV; HIV Protease Inhibitors; Hydrophobic and Hydrophilic Interactions; Protein Binding; Structure-Activity Relationship; Urea | 2003 |