isoxazoles has been researched along with oxazolone in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (80.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Barrett, JF; Bronson, JJ; D'Andrea, SV; DenBleyker, KL; Frosco, M; Fung-Tomc, JC; Gill, P; Marinier, A; Martel, A; Mate, R; Meng, Z; Quesnelle, CA; Snyder, LB | 1 |
Ahmad, G; Gupta, P; Maurya, R; Mishra, PK; Srivastava, AK; Tamrakar, AK; Tiwari, P; Yadav, PP | 1 |
Bros, M; Jarman, ER; Knop, J; Reske-Kunz, AB; Sudowe, S; Weigmann, B | 1 |
Buckheit, RW; Cushman, M; De Clercq, E; Deng, BL; Hartman, TL; Pannecouque, C | 1 |
He, J; He, L; She, X; Sun, Y; Tang, S | 1 |
5 other study(ies) available for isoxazoles and oxazolone
Article | Year |
---|---|
Discovery of isoxazolinone antibacterial agents. Nitrogen as a replacement for the stereogenic center found in oxazolidinone antibacterials.
Topics: Anti-Bacterial Agents; Gram-Negative Bacteria; Gram-Positive Bacteria; Isoxazoles; Microbial Sensitivity Tests; Models, Molecular; Nitrogen; Oxazolidinones; Oxazolone; Pyrroles; Stereoisomerism; Structure-Activity Relationship | 2004 |
Synthesis of novel benzofuran isoxazolines as protein tyrosine phosphatase 1B inhibitors.
Topics: Benzofurans; Benzopyrans; Drug Design; Enzyme Inhibitors; Hypoglycemic Agents; Isoxazoles; Millettia; Models, Chemical; Oxazolone; Protein Binding; Protein Tyrosine Phosphatase, Non-Receptor Type 1; Protein Tyrosine Phosphatases | 2006 |
Induction of regulatory T cells by leflunomide in a murine model of contact allergen sensitivity.
Topics: Allergens; Animals; CD4-Positive T-Lymphocytes; CD8-Positive T-Lymphocytes; Cytokines; Dermatitis, Allergic Contact; Dinitrofluorobenzene; Disease Models, Animal; Female; Immunosuppressive Agents; Interleukin-10; Isoxazoles; Leflunomide; Lymphocyte Activation; Male; Mice; Mice, Inbred BALB C; Oxazolone; RNA, Messenger | 2006 |
Replacement of the metabolically labile methyl esters in the alkenyldiarylmethane series of non-nucleoside reverse transcriptase inhibitors with isoxazolone, isoxazole, oxazolone, or cyano substituents.
Topics: Animals; Anti-HIV Agents; Cell Line; Cyanides; Drug Design; Esters; Humans; In Vitro Techniques; Isoxazoles; Microbial Sensitivity Tests; Molecular Structure; Oxazolone; Rats; Reverse Transcriptase Inhibitors; Stereoisomerism; Structure-Activity Relationship | 2006 |
Efficient and regioselective synthesis of 5-hydroxy-2-isoxazolines: versatile synthons for isoxazoles, beta-lactams, and gamma-amino alcohols.
Topics: Amino Alcohols; beta-Lactams; Computer Simulation; Hydroxylation; Isoxazoles; Magnetic Resonance Spectroscopy; Molecular Structure; Oxazolone; Stereoisomerism; Thermodynamics | 2010 |