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Planta Med ; 66(5): 471-3, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10909271

ABSTRACT

The isolation and characterisation of (S)-(+)-6-methoxy-alpha-methyl-2-naphthaleneacetic acid, a well known synthetic non-steroidal anti-inflammatory drug (naproxene), from a natural source is described for the first time. We evaluated the ability of naproxene and its 7-methoxy isomer to abrogate constitutive COX-1 and inducible COX-2 activity in human A549 cells. Naproxene inhibited COX-1 (IC50 = 3.42 microM) and COX-2 (IC50 = 1.53 microM), whereas the 7-methoxy isomer had no appreciable effect on COX-1 (IC50 >> 100 microM) but also abrogated the activity of COX-2 enzyme (IC50 = 14.42 microM).


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/isolation & purification , Enzyme Inhibitors/isolation & purification , Isoenzymes/pharmacology , Naproxen/analogs & derivatives , Naproxen/isolation & purification , Prostaglandin-Endoperoxide Synthases/pharmacology , Zingiberales/chemistry , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Cyclooxygenase 1 , Cyclooxygenase 2 , Enzyme Inhibitors/chemistry , Enzyme Inhibitors/pharmacology , Humans , Isomerism , Magnetic Resonance Spectroscopy , Mass Spectrometry , Membrane Proteins , Naproxen/chemistry , Naproxen/pharmacology , Tumor Cells, Cultured
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