Page last updated: 2024-12-06

miroprofen

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

Description

miroprofen : A monocarboxylic acid that is propionic acid in which one of the hydrogens at position 2 is substituted by a 4-(imidazo[1,2-a]pyridin-2-yl)phenyl group. A non-steroidal anti-inflammatory drug that also exhibits analgesic, antipyretic and platelet aggregation inhibition properties. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID68752
CHEMBL ID2106551
CHEBI ID76249
SCHEMBL ID26767
MeSH IDM0069160

Synonyms (40)

Synonym
y-9213 ,
miroprofen
propionic acid, 2-(4-(imidazo(1,2-a)pyridin-2-yl)phenyl)-
miroprofene [inn-french]
miroprofen [inn]
p-imidazo(1,2-a)pyridin-2-ylhydratropic acid
y 9213
benzeneacetic acid, 4-imidazo(1,2-a)pyridin-2-yl-alpha-methyl-
miroprofeno [inn-spanish]
2-(4-(imidazo(1,2-a)pyridin-2-yl)phenyl)propionic acid
brn 0888858
2-(p-(2-imidazo(1,2-a)pyridiyl)phenyl)propionsaeure [german]
miroprofenum [inn-latin]
antopen
2-(p-(2-imidazo(1,2-a)pyridyl)phenyl)propionic acid
1-methoxy-3-(2-nitro-1-imidazolyl)-2-propanol
propionic acid, 2-(p-(imidazo(1,2-a)pyridin-2-yl)phenyl)-
55843-86-2
4-imidazo(1,2-a)pyridin-2-yl-alpha-methylbenzeneacetic acid
2-(4-imidazo[1,2-a]pyridin-2-ylphenyl)propanoic acid
miroprofenum
miroprofene
miroprofeno
s00i5xg484 ,
2-(p-(2-imidazo(1,2-a)pyridiyl)phenyl)propionsaeure
unii-s00i5xg484
2-[4-(imidazo[1,2-a]pyridin-2-yl)phenyl]propanoic acid
chebi:76249 ,
CHEMBL2106551
miroprofen [jan]
SCHEMBL26767
2-[4-(imidazo[1,2-a]pyridin-2-yl)phenyl]propionic acid
OJGQFYYLKNCIJD-UHFFFAOYSA-N
2-[p-(2-imidazo[1,2-a]pyridyl)phenyl]propionic acid
bdbm50486822
Q3858912
y 0213; y 9213
2-(4-(IMIDAZO[1,2-A]PYRIDIN-2-YL)PHENYL)PROPANOIC ACID
DTXSID30866515
AKOS040753062

Research Excerpts

[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (4)

RoleDescription
non-steroidal anti-inflammatory drugAn anti-inflammatory drug that is not a steroid. In addition to anti-inflammatory actions, non-steroidal anti-inflammatory drugs have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins.
antipyreticA drug that prevents or reduces fever by lowering the body temperature from a raised state. An antipyretic will not affect the normal body temperature if one does not have fever. Antipyretics cause the hypothalamus to override an interleukin-induced increase in temperature. The body will then work to lower the temperature and the result is a reduction in fever.
non-narcotic analgesicA drug that has principally analgesic, antipyretic and anti-inflammatory actions. Non-narcotic analgesics do not bind to opioid receptors.
platelet aggregation inhibitorA drug or agent which antagonizes or impairs any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
imidazopyridine
monocarboxylic acidAn oxoacid containing a single carboxy group.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)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: 21.55

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 Index21.55 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.45 (4.65)
Search Engine Demand Index18.60 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (21.55)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials2 (33.33%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other4 (66.67%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]