thiazoles has been researched along with kni-727 in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Goto, T; Hamawaki, T; Hayashi, Y; Kimura, T; Kiso, Y; Kumagai, A; Matsumoto, H; Sano, K | 1 |
Freire, E; Kimura, T; Kiso, Y; Luque, I; Nezami, A | 1 |
Hayashi, Y; Ito, T; Kimura, T; Kiso, Y; Matsumoto, H; Sohma, Y | 1 |
Hamada, Y; Hayashi, Y; Kimura, T; Kiso, Y; Matsumoto, H; Yamaguchi, S | 1 |
4 other study(ies) available for thiazoles and kni-727
Article | Year |
---|---|
Design, synthesis, and biological evaluation of anti-HIV double-drugs. conjugates of HIV protease inhibitors with a reverse transcriptase inhibitor through spontaneously cleavable linkers.
Topics: Animals; Anti-HIV Agents; Drug Design; Drug Evaluation, Preclinical; HIV Protease Inhibitors; Humans; Prodrugs; Reverse Transcriptase Inhibitors; Structure-Activity Relationship; Thiazoles; Tumor Cells, Cultured; Zidovudine | 2001 |
Identification and characterization of allophenylnorstatine-based inhibitors of plasmepsin II, an antimalarial target.
Topics: Amides; Animals; Antimalarials; Aspartic Acid Endopeptidases; Binding Sites; Chromogenic Compounds; Enzyme Stability; Erythrocytes; Humans; Models, Molecular; Phenylbutyrates; Plasmodium falciparum; Protease Inhibitors; Protozoan Proteins; Substrate Specificity; Thermodynamics; Thiazoles | 2002 |
Development of water-soluble prodrugs of the HIV-1 protease inhibitor KNI-727: importance of the conversion time for higher gastrointestinal absorption of prodrugs based on spontaneous chemical cleavage.
Topics: Animals; Area Under Curve; Biological Availability; Carbamates; Cyclization; Drug Design; Duodenum; Furans; Half-Life; HIV Protease Inhibitors; Imides; Intestinal Absorption; Male; Organophosphates; Prodrugs; Rats; Rats, Sprague-Dawley; Solubility; Structure-Activity Relationship; Sulfonamides; Thiazoles; Water | 2003 |
Water-soluble prodrugs of dipeptide HIV protease inhibitors based on O-->N intramolecular acyl migration: Design, synthesis and kinetic study.
Topics: Acylation; Dipeptides; Drug Design; HIV Protease Inhibitors; Humans; Kinetics; Prodrugs; Solubility; Thiazoles; Water | 2004 |