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calmidazolium and Ache

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.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Oláh, Z1
Jósvay, K1
Pecze, L1
Letoha, T1
Babai, N1
Budai, D1
Otvös, F1
Szalma, S1
Vizler, C1
Menéndez, L2
Hidalgo, A2
Baamonde, A2
Alvarez-Vega, M1
Gutiérrez, M1

Other Studies

3 other studies available for calmidazolium and Ache

ArticleYear
Anti-calmodulins and tricyclic adjuvants in pain therapy block the TRPV1 channel.
    PloS one, 2007, Jun-20, Volume: 2, Issue:6

    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.
    European journal of pharmacology, 1997, Sep-17, Volume: 335, Issue:1

    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.
    Naunyn-Schmiedeberg's archives of pharmacology, 1998, Volume: 358, Issue:6

    Topics: Analgesics; Animals; Bupivacaine; Imidazoles; Male; Morphine; N-Methylaspartate; Pain; Pain Measurem

1998