3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid has been researched along with flunitrazepam in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (100.00) | 18.7374 |
1990's | 0 (0.00) | 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 |
---|---|
Bender, AS; Swinyard, EA; White, HS | 1 |
Boast, CA; Gerhardt, SC; Jarvis, MF; Murphy, DE; Williams, M | 1 |
Loo, PS; Sills, MA; Williams, M | 1 |
3 other study(ies) available for 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid and flunitrazepam
Article | Year |
---|---|
Effect of the selective N-methyl-D-aspartate receptor agonist 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid on [3H]flunitrazepam binding.
Topics: Animals; Binding, Competitive; Flunitrazepam; In Vitro Techniques; Piperazines; Receptors, N-Methyl-D-Aspartate; Receptors, Neurotransmitter; Temperature | 1988 |
The novel N-methyl-D-aspartate (NMDA) antagonist CGS 19755 prevents ischemia-induced reductions of adenosine A1, NMDA, and PCP receptors in gerbil brain.
Topics: Adenosine; Animals; Autoradiography; Female; Flunitrazepam; Gerbillinae; Image Processing, Computer-Assisted; Ischemic Attack, Transient; Pipecolic Acids; Piperazines; Piperidines; Receptors, N-Methyl-D-Aspartate; Receptors, Neurotransmitter; Receptors, Phencyclidine | 1988 |
The NMDA antagonists, CPP and CGS 19755, lack affinity for central benzodiazepine receptors.
Topics: Animals; Anticonvulsants; Aspartic Acid; Binding, Competitive; Brain; Flunitrazepam; In Vitro Techniques; N-Methylaspartate; Pipecolic Acids; Piperazines; Piperidines; Rats; Receptors, GABA-A | 1988 |