selfotel has been researched along with organophosphonates in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Berge, OG; Claesson, A; Edvinsson, KM; Kallin, E; Larsson, U; Molin, H; Pelcman, B; Swahn, BM | 1 |
Abou-Gharbia, M; Bramlett, DR; Garrison, DT; Kinney, WA; Kowal, DM; Miller, TL; Moyer, JA; Schmid, J; Tasse, RP; Zaleska, MM | 1 |
2 other study(ies) available for selfotel and organophosphonates
Article | Year |
---|---|
Two non-racemic preparations of a piperidine-based NMDA antagonist with analgesic activity.
Topics: Analgesics; Animals; Binding Sites; Binding, Competitive; Excitatory Amino Acid Antagonists; Kinetics; Mice; N-Methylaspartate; Organophosphonates; Pain Measurement; Pipecolic Acids; Rats; Receptors, N-Methyl-D-Aspartate; Stereoisomerism | 1997 |
Design and synthesis of [2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7)-en-2-yl)-ethyl]phosphonic acid (EAA-090), a potent N-methyl-D-aspartate antagonist, via the use of 3-cyclobutene-1,2-dione as an achiral alpha-amino acid bioisostere.
Topics: Animals; Azabicyclo Compounds; Bridged Bicyclo Compounds, Heterocyclic; Cyclobutanes; Disease Models, Animal; Excitatory Amino Acid Antagonists; Excitatory Amino Acids; Ischemic Attack, Transient; Mice; Models, Chemical; N-Methylaspartate; Organophosphonates; Pipecolic Acids; Piperazines; Rats | 1998 |