Name | levibuprofen |
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Synonyms |
Inoven
Lebrufen (RS)-ibuprofen Ibumetin Femadon 2-(4-Isobutylphenyl)propionic acid QVY1&R D1Y1&1 l-Ibuprofen Para-Isobutylhydratropic Acid Ibuprofen (2R)-2-(4-Isobutylphenyl)propanoic acid (R)-2-(4-Isobutylphenyl)propanoic acid Benzeneacetic acid, α-methyl-4-(2-methylpropyl)- (±)-ibuprofen Novogent N Ibutid fenbid 2-(4-Isobutylphenyl)propanoic acid MOTRIN Dolgirid (R)-Ibuprofen Amibufen (-)-ibuprofen Nurofen (R)-(-)-Ibuprofen Racemic ibuprofen (2R)-2-[4-(2-methylpropyl)phenyl]propanoic acid Advil Brufen Dolo-Dolgit Seclodin UNII:WK2XYI10QM Benzeneacetic acid, α-methyl-4-(2-methylpropyl)-, (αR)- IbU Panafen |
Description | (R)-(-)-Ibuprofen is the R enantiomer of Ibuprofen, inactive on COX, inhibits NF-κB activation; (R)-(-)-Ibuprofen exhibits anti-inflammatory and antinociceptive effects. |
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Related Catalog | |
Target |
NF-κB |
In Vitro | (R)-(-)-Ibuprofen is the R enantiomer of Ibuprofen, with no inhibitory effect on COX, but is involved in pathways of lipid metabolism and is incorporated into triglycerides along with endogenous fatty acids[1]. (R)-(-)-Ibuprofen (1 μM) significantly reduces NF-κB activation and completely prevents NF-κB induction at 10 μM. (R)-(-)-Ibuprofen inhibits NF-κB luciferase activity with an IC50 of 121.8 μM, weaker than that of S(+)-ibuprofen (IC50, 61.7 μM). Furthermore, (R)-(-)-Ibuprofen (10 mM) has no effect on HSF[2]. |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 319.6±11.0 °C at 760 mmHg |
Melting Point | 41-42ºC |
Molecular Formula | C13H18O2 |
Molecular Weight | 206.281 |
Flash Point | 216.7±14.4 °C |
Exact Mass | 206.130676 |
PSA | 37.30000 |
LogP | 3.72 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.519 |
HS Code | 2916399090 |
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Precursor 9 | |
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DownStream 1 | |
HS Code | 2916399090 |
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Summary | 2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0% |