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Synthesis of New Azulene Derivatives and Study of Their Effect on Lipid Peroxidation and Lipoxygenase Activity
- Source :
- ChemInform. 34
- Publication Year :
- 2003
- Publisher :
- Wiley, 2003.
-
Abstract
- The relationship between free radicals and acute or chronic inflammation has been well established. We have previously reported the significant antioxidant activity of the natural azulene derivatives chamazulene and guaiazulene. Furthermore, some synthetic azulene analogues have been found to possess anti-inflammatory activity. In this investigation we report the synthesis of five 3-alkyl or 3-(hydroxy)alkylazulene-1-carboxylic acids and esters, from tropolone, via the corresponding furanone. The synthesised compounds were tested for their effect on the peroxidation of rat hepatic microsomal membrane lipids, applying the 2-thiobarbituric acid test. Their anti-inflammatory activity was evaluated in vitro by the offered inhibition of soybean lipoxygenase. All the tested molecules were found to inhibit lipid peroxidation by 100% at 1 mM. They were also found to considerably inhibit lipoxygenase activity. The above results are discussed in relation to the structure and physicochemical properties of the examined azulene derivatives.
- Subjects :
- Male
Magnetic Resonance Spectroscopy
Antioxidant
Spectrophotometry, Infrared
Stereochemistry
Membrane lipids
medicine.medical_treatment
Thiobarbituric Acid Reactive Substances
Azulenes
Lipid peroxidation
chemistry.chemical_compound
Lipoxygenase
Drug Discovery
Guaiazulene
medicine
Animals
Lipoxygenase Inhibitors
Cycloheptanes
biology
Chamazulene
Anti-Inflammatory Agents, Non-Steroidal
Biological activity
General Chemistry
Free Radical Scavengers
General Medicine
Azulene
Tropolone
Rats, Inbred F344
Rats
chemistry
Biochemistry
Microsomes, Liver
biology.protein
Indicators and Reagents
Lipid Peroxidation
Subjects
Details
- ISSN :
- 09317597
- Volume :
- 34
- Database :
- OpenAIRE
- Journal :
- ChemInform
- Accession number :
- edsair.doi.dedup.....e19cae78ba3fab27f6ae2641492205d9
- Full Text :
- https://doi.org/10.1002/chin.200301073