calmidazolium has been researched along with Ache in 3 studies
calmidazolium: powerful inhibitor of or red blood cell Ca++-ATPase & Ca++ transport into inside-out red blood cell vesicles; RN refers to chloride; structure in first source; an antagonist of calmodulin
calmidazolium : An imidazolium ion that is imidazolium cation substituted by a bis(4-chlorophenyl)methyl group at position 1 and a 2-[(2,4-dichlorobenzyl)oxy]-2-(2,4-dichlorophenyl)ethyl group at position 3. It acts as an antagonist of calmodulin, a calcium binding messenger protein.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (66.67) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Oláh, Z | 1 |
Jósvay, K | 1 |
Pecze, L | 1 |
Letoha, T | 1 |
Babai, N | 1 |
Budai, D | 1 |
Otvös, F | 1 |
Szalma, S | 1 |
Vizler, C | 1 |
Menéndez, L | 2 |
Hidalgo, A | 2 |
Baamonde, A | 2 |
Alvarez-Vega, M | 1 |
Gutiérrez, M | 1 |
3 other studies available for calmidazolium and Ache
Article | Year |
---|---|
Anti-calmodulins and tricyclic adjuvants in pain therapy block the TRPV1 channel.
Topics: Animals; Antidepressive Agents, Tricyclic; Antipsychotic Agents; Calcium; Calmodulin; Capsaicin; Cel | 2007 |
Spinal calmodulin inhibitors reduce N-methyl-D-aspartate- and septide-induced nociceptive behavior.
Topics: alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid; Animals; Calcium-Calmodulin-Dependent Prot | 1997 |
Comparison of the effects of calmidazolium, morphine and bupivacaine on N-methyl-D-aspartate- and septide-induced nociceptive behaviour.
Topics: Analgesics; Animals; Bupivacaine; Imidazoles; Male; Morphine; N-Methylaspartate; Pain; Pain Measurem | 1998 |