Compounds > quantacure qtx
Page last updated: 2024-11-07

quantacure qtx

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

Description

Quantacure QTX: structure given in first source; water-soluble photo-polymerization initiator; improves the bond strength between composite and tooth substrate [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID128383
SCHEMBL ID476928
MeSH IDM0216925

Synonyms (11)

Synonym
quantacure qtx
2-hydroxy-3-(3,4-dimethyl-9-oxo-9h-thioxanthen-2-yloxy)-n,n,n-trimethyl-1-propanaminium chloride
103430-24-6
1-propanaminium, 3-((3,4-dimethyl-9-oxo-9h-thioxanthen-2-yl)oxy)-2-hydroxy-n,n,n-trimethyl-, chloride
SCHEMBL476928
(3-(3,4-dimethyl-9-oxo-9h-thioxanthen-2- yloxy)-2-oh-propyl)tri-me-ammon cl 97
[3-(3,4-dimethyl-9-oxo-9h-thioxanthene-2-yloxy)-2-hydroxypropyl]trimethylammonium chloride
[3-[(3,4-dimethyl-9-oxo-9h-thioxanthen-2-yl)oxy]-2-hydroxypropyl]trimethylammonium chloride
[3-(3,4-dimethyl-9-oxothioxanthen-2-yl)oxy-2-hydroxypropyl]-trimethylazanium;chloride
3-[(3,4-dimethyl-9-oxo-9h-thioxanthen-2-yl)oxy]-2-hydroxy-n,n,n-trimethylpropan-1-aminium chloride
DTXSID10908402
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's3 (60.00)29.6817
2010's0 (0.00)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: 12.66

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.66 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.45 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.66)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
citric acid, anhydrous
Citric Acid: A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.. citric acid : A tricarboxylic acid that is propane-1,2,3-tricarboxylic acid bearing a hydroxy substituent at position 2. It is an important metabolite in the pathway of all aerobic organisms.		1.9810tricarboxylic acidantimicrobial agent;
chelator;
food acidity regulator;
fundamental metabolite
camphor, (+-)-isomer
[no description available]		210bornane monoterpenoid;
cyclic monoterpene ketone		plant metabolite
edetic acid
Edetic Acid: A chelating agent that sequesters a variety of polyvalent cations such as CALCIUM. It is used in pharmaceutical manufacturing and as a food additive.		1.9810ethylenediamine derivative;
polyamino carboxylic acid;
tetracarboxylic acid		anticoagulant;
antidote;
chelator;
copper chelator;
geroprotector
hydroxyethyl methacrylate
hydroxyethyl methacrylate: many of cited refs are for gel which refers to polymeric form of above cpd: POLYHYDROXYETHYL METHACRYLATE. 2-hydroxyethyl methacrylate : An enoate ester that is the monomethacryloyl derivative of ethylene glycol.		2.4120enoate esterallergen;
polymerisation monomer
camphoroquinone
camphoroquinone: a natural monoterpene, non-aromatic quinone; structure given in first source. bornane-2,3-dione : A bornane monoterpenoid that is bicyclo[2.2.1]heptane substituted by methyl groups at positions 1, 7 and 7 and oxo groups at positions 2 and 3.		2.0210bornane monoterpenoid;
carbobicyclic compound
methacryloyloxydecyl dihydrogen phosphate
methacryloyloxydecyl dihydrogen phosphate: structure given in first source		210
n-phenyliminodiacetic acid
[no description available]		2.0210
ConditionIndicatedRelationship StrengthStudiesTrials