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Last Updated: 5 years ago

Possible Interaction: Arachidonic Acid and Masoprocol

supplement:

Arachidonic Acid

supplement:

Masoprocol

Research Papers that Mention the Interaction

“ Nordihydroguaiaretic acid , an inhibitor of the lipoxygenase pathway, significantly inhibited both hydrogen peroxide and arachidonic acid-stimulated c-Fos and c-Jun protein expression and AP-1 activity.”
The Journal of Biological Chemistry  •  1996  |  View Paper
“A LOX inhibitor, nordihydroguaiaretic acid , attenuated production of 15(S)-HETE and inhibited the phosphorylation of p38 MAPK following exposure to arachidonic acid.”
Journal of Biological Chemistry  •  2005  |  View Paper
“The ability of arachidonic acid to stimulate PI3K activity in neutrophils was suppressed by indomethacin and nordihydroguaiaretic acid , inhibitors of the cyclooxygenases and lipoxygenases, respectively, but not by 17-octadecynoic acid, an inhibitor of ω-hydroxylation of arachidonic acid by cytochrome P450 monooxygenases.”
The Journal of Biological Chemistry  •  2001  |  View Paper
“Esculetin and nordihydroguaiaretic acid inhibited formation of hepoxilin B3, 12-oxo-eicosatetraenoic acid , trioxilins, and 12-hydroxyeicosatetraenoic acid in a concentration-dependent manner.”
The Journal of investigative dermatology  •  2000  |  View Paper
“In contrast, the increase in adhesion to vitronectin induced by A23187 and AA was, at best, only partially inhibited by nordihydroguaiaretic acid treatment.”
Cancer research  •  1996  |  View Paper
“The increased rate in NNK oxidation by arachidonic acid or lipoxygenase was inhibited completely by nordihydroguaiaretic acid.”
Cancer research  •  1995  |  View Paper
“The arachidonic acid uptake activity was significantly reduced by the presence of indomethacin in platelets obtained from both under and over-forty year old subjects, and by the presence of nordihydroguaiaretic acid in platelets obtained from over-forty year old subjects.”
Revista espanola de fisiologia  •  1995  |  View Paper
“Pretreatment of LAN‐5 cells with nordihydroguaiaretic acid , a lipoxygenase inhibitor, or with indomethacin, a cyclooxygenase inhibitor, amplified the release of[3H]arachidonic acid and production of lysophosphatidylcholine induced by non‐saturating concentrations of IFN‐γ.”
FEBS letters  •  1992  |  View Paper
“For example, NDGA inhibited arachidonic acid-stimulated release with a 50% inhibitory concentration (IC50) of 0.39 microM for PGI2, 0.25 microM for 15-HETE, and 0.10 microM for 12-HETE.”
The American journal of physiology  •  1989  |  View Paper
“ Nordihydroguaiaretic acid and 5,8,11,14-eicosatetraynoic acid both inhibited the conversion of arachidonic acid to 15-HETE with respective 50% inhibitory concentrations of 2.0 microM and 0.9 microM, while ATP, GTP, and cyclic AMP had no effect on activity at pH 6.8-7.2.”
The Journal of investigative dermatology  •  1988  |  View Paper
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