Page last updated: 2024-11-13

choline magnesium trisalicylate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Cross-References

ID SourceID
PubMed CID54682045
MeSH IDM0069124

Synonyms (20)

Synonym
tegunor
((1,2-ethanediylbis(carbamodithioato))(2-))manganese, mixt. with ((1,2-ethanediylbis(carbamodithioato))(2-))zinc & 2(or 4)-isooctyl-4,6(or 2,6)-dinitrophenyl 2-buten oate
ethanaminium, 2-hydroxy-n,n,n-trimethyl-, salt with 2-hydroxybenzoic acid (1:1), mixt. with 2-hydroxybenzoic acid magnesium salt (2:1)
choline magnesium trisalicylate
DB01401
tricosal (tn)
D07694
64425-90-7
unii-djj95fjp1h
choline magnesium salicylate
nsc 751675
tricolsal
djj95fjp1h ,
trisalicylate-choline
choline magnesium trisalicylate [who-dd]
ethanaminium, 2-hydroxy-n,n,n-trimethyl-, 2-hydroxybenzoate (1:1), mixt. with (t-4)-bis(2-(hydroxy-.kappa.o)benzoato-.kappa.o)magnesium
FQCQGOZEWWPOKI-UHFFFAOYSA-K
cholinemagnesiumtrisalicylate
Q20817211
DTXSID901344133

Research Excerpts

Overview

Choline magnesium trisalicylate is a non-acetylated salicylates used widely as a nonsteroidal anti-inflammatory drug.

ExcerptReferenceRelevance
"Choline magnesium trisalicylate is a non-acetylated salicylate used widely as a nonsteroidal anti-inflammatory drug. "( Eosinophilic hepatitis after ingestion of choline magnesium trisalicylate.
Nadkarni, MM; Peller, CA; Retig, J, 1992
)
1.99

Pharmacokinetics

ExcerptReferenceRelevance
" Salicylate levels were not sustained between doses and elimination rates and half-life were similar for both preparations."( A pharmacokinetic comparison of choline magnesium trisalicylate and soluble aspirin.
Berry, D; Gibson, T; Helliwell, M; Volans, G, 1984
)
0.55

Dosage Studied

Claims that twice-daily dosage of choline magnesium trisalicylate (CMT) may alter salicylates disposal kinetics and result in sustained plasma levels were examined. 18 healthy volunteers were administered single doses of commercially available solid dosage forms of aspirin, magnesium salicyllate (I), and choline magridate (II)

ExcerptRelevanceReference
" These data show that NSAIDs can affect the disposition of methotrexate, possibly increasing the potential for toxicity and necessitating dosage adjustments."( The effects of a salicylate, ibuprofen, and naproxen on the disposition of methotrexate in patients with rheumatoid arthritis.
Bradley, JD; Brater, DC; Hall, SD; Jones, DR; Krohn, K; Tracy, TS, 1992
)
0.28
" The 24-h area under the salicylate curve (AUC0-24 h) after the final 3000-mg salicylate dose averaged about twice the mean 12-h AUC after the last 1500-mg dose, indicating that the two dosing regimens were equally bioavailable."( Choline magnesium trisalicylate: comparative pharmacokinetic study of once-daily and twice-daily dosages.
Kann, J; Levitt, MJ, 1984
)
1.71
"Claims that twice-daily dosage of choline magnesium trisalicylate (CMT) may alter salicylate disposal kinetics and result in sustained plasma levels were examined."( A pharmacokinetic comparison of choline magnesium trisalicylate and soluble aspirin.
Berry, D; Gibson, T; Helliwell, M; Volans, G, 1984
)
0.83
"Eighteen healthy volunteers were administered single doses of commercially available solid dosage forms of aspirin, magnesium salicylate (I), and choline magnesium trisalicylate (II), equivalent to approximately 500 mg of salicylic acid, in a randomized, complete crossover design."( Comparative plasma salicylate and urine salicylurate levels following administration of aspirin, magnesium salicylate, and choline magnesium trisalicylate.
Mason, WD, 1980
)
0.67
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Pathways (1)

PathwayProteinsCompounds
Trisalicylate-Choline Action Pathway2967

Research

Studies (34)

TimeframeStudies, This Drug (%)All Drugs %
pre-199023 (67.65)18.7374
1990's8 (23.53)18.2507
2000's2 (5.88)29.6817
2010's1 (2.94)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 27.07

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index27.07 (24.57)
Research Supply Index3.97 (2.92)
Research Growth Index4.22 (4.65)
Search Engine Demand Index52.27 (26.88)
Search Engine Supply Index3.41 (0.95)

This Compound (27.07)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials17 (48.57%)5.53%
Reviews1 (2.86%)6.00%
Case Studies3 (8.57%)4.05%
Observational0 (0.00%)0.25%
Other14 (40.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (3)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Pilot Study of Nuclear Factor-kappa B (NFkB) Inhibition During Induction Chemotherapy for Patients With Acute Myelogenous Leukemia (AML) [NCT00156299]Phase 115 participants (Actual)Interventional2003-03-31Terminated(stopped due to Replaced by another study)
A Randomized Phase II Study of Nuclear Factor-kappa B (NF-κB) Inhibition During Induction Chemotherapy for Patients With Acute Myelogenous Leukemia [NCT02144675]Phase 227 participants (Actual)Interventional2009-01-31Completed
A Phase II Study of 12-O-tetradecanoylphorbol-13-acetate (TPA) Plus Dexamethasone & Choline Magnesium Trisalicylate in the Treatment of Patients With Relapsed/Refractory Acute Myelogenous Leukemia [NCT01009931]Phase 21 participants (Actual)Interventional2011-03-31Terminated(stopped due to Study was terminated early due to lack of experimental medication (supply issues))
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT02144675 (1) [back to overview]Inhibition of NF-kB Target Transcripts and/or Inhibition of Drug Efflux in at Least 50% of Patients

Inhibition of NF-kB Target Transcripts and/or Inhibition of Drug Efflux in at Least 50% of Patients

The clinical trial will be based on a sequential monitoring so that we will have a 90% confidence that choline magnesium trisalicylate (CMT) based modulation of NF-kB transcriptional targets and/or drug efflux occurs in at least 50% of patients. (NCT02144675)
Timeframe: 24 hours

InterventionParticipants (Count of Participants)
Arm I (Choline Magnesium Trisalicylate and Chemotherapy)13
Arm II (Chemotherapy)14

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