Synthesis and paroxonase activities of novel bromophenols

References

• Gribble GW. The diversity of naturally occurring organobromine compounds. Chem Soc Rev 1999;28:335–346.
   Web of Science ®Google Scholar
• Liu M, Hansen PE, Lin X. Bromophenols in marine algae and their bioactivities. Mar Drugs 2011;9:1273–1292.
   PubMed Web of Science ®Google Scholar
• Lee HS, Lee TH, Lee JH, Chae CS, Chung SC, Shin DS et al. Inhibition of the pathogenicity of Magnaporthe grisea by bromophenols, isocitrate lyase inhibitors, from the red alga Odonthalia corymbifera. J Agric Food Chem 2007;55:6923–6928.
   PubMed Web of Science ®Google Scholar
• Xu X, Song F, Wang S, Li S, Xiao F, Zhao J et al. Dibenzyl bromophenols with diverse dimerization patterns from the brown alga Leathesia nana. J Nat Prod 2004;67:1661–1666.
   PubMed Web of Science ®Google Scholar
• Kurata K, Taniguchii K, Takashima K, Hayashi I, Suzuki M. Feeding-deterrent bromophenols from Odonthalia corymbifera. Phytochemistry 1997;45:485–487.
   Web of Science ®Google Scholar
• Oh KB, Lee JH, Chung SC, Shin J, Shin HJ, Kim HK et al. Antimicrobial activities of the bromophenols from the red alga Odonthalia corymbifera and some synthetic derivatives. Bioorg Med Chem Lett 2008;18:104–108.
   PubMed Web of Science ®Google Scholar
• Shi D, Li J, Guo S, Su H, Fan X. The antitumor effect of bromophenol derivatives in vitro and Leathesia nana extract in vivo. Chin J Ocean Lim 2009;27:277–282.
   Web of Science ®Google Scholar
• Balaydin HT, Gülçin Í, Menzek A, Göksu S, Sahin E. Synthesis and antioxidant properties of diphenylmethane derivative bromophenols including a natural product. J Enzyme Inhib Med Chem 2010;25:685–695.
   PubMed Web of Science ®Google Scholar
• Wang W, Okada Y, Shi H, Wang Y, Okuyama T. Structures and aldose reductase inhibitory effects of bromophenols from the red alga Symphyocladia latiuscula. J Nat Prod 2005;68:620–622.
   PubMed Web of Science ®Google Scholar
• Balaydin HT, Soyut H, Ekinci D, Göksu S, Beydemir S, Menzek A et al. Synthesis and carbonic anhydrase inhibitory properties of novel bromophenols including natural products. J Enzyme Inhib Med Chem 2012;27:43–50.
   PubMed Web of Science ®Google Scholar
• Harel M, Aharoni A, Gaidukov L, Brumshtein B, Khersonsky O, Meged R et al. Structure and evolution of the serum paraoxonase family of detoxifying and anti-atherosclerotic enzymes. Nat Struct Mol Biol 2004;11:412–419.
   PubMed Web of Science ®Google Scholar
• Alici HA, Ekinci D, Beydemir S. Intravenous anesthetics inhibit human paraoxonase-1 (PON1) activity in vitro and in vivo. Clin Biochem 2008;41:1384–1390.
   PubMed Web of Science ®Google Scholar
• Ates O, Azizi S, Alp HH, Kiziltunc A, Beydemir S, Cinici E et al. Decreased serum paraoxonase 1 activity and increased serum homocysteine and malondialdehyde levels in age-related macular degeneration. Tohoku J Exp Med 2009;217:17–22.
   PubMed Web of Science ®Google Scholar
• Isgör MM, Beydemir S. Some cardiovascular therapeutics inhibit paraoxonase 1 (PON1) from human serum. Eur J Pharmacol 2010;645:135–142.
   PubMed Web of Science ®Google Scholar
• Aviram M, Rosenblat M, Bisgaier CL, Newton RS, Primo-Parmo SL, La Du BN. Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions. A possible peroxidative role for paraoxonase. J Clin Invest 1998;101:1581–1590.
   PubMed Web of Science ®Google Scholar
• La Du BN. (1992). Pharmo genetics of drug metabolism. New York: Pergamon Press, 51–91.
   Google Scholar
• Mackness MI, Durrington PN. HDL, its enzymes and its potential to influence lipid peroxidation. Atherosclerosis 1995;115:243–253.
   PubMed Web of Science ®Google Scholar
• Hosangadi BD, Kasbekar AB, Nabar MJ, Desai RC. Novel reactions with polyphosphoric acid II. Decarboxylative acetylation, trans-carbonylation, and other reactions of substituted aromatic carboxylic acids. Ind J Chem 1973;11:711–713.
   Google Scholar
• Ekinci D, Beydemir S. Evaluation of the impacts of antibiotic drugs on PON 1; a major bioscavenger against cardiovascular diseases. Eur J Pharmacol 2009;617:84–89.
   PubMed Web of Science ®Google Scholar
• Ekinci D, Beydemir S. Effect of some analgesics on paraoxonase-1 purified from human serum. J Enzyme Inhib Med Chem 2009;24:1034–1039.
   PubMed Web of Science ®Google Scholar
• Senturk M, Ekinci D, Alıcı HA, Beydemir S. Paraoxonase-1, an organophosphate detoxifier and cardioprotective enzyme, is inhibited by anesthetics: An in vitro and in vivo insight. Pestic Biochem Phys 2011;101:206–211.
   Web of Science ®Google Scholar
• Yilmaz H, Ciftci M, Beydemir S, Bakan E. Purification of glucose 6-phosphate dehydrogenase from chicken erythrocytes. investigation of some kinetic properties. Prep Biochem Biotechnol 2002;32:287–301.
   PubMed Web of Science ®Google Scholar
• Soyut H, Beydemir S, Hisar O. Effects of some metals on carbonic anhydrase from brains of rainbow trout. Biol Trace Elem Res 2008;123:179–190.
   PubMed Web of Science ®Google Scholar
• Balaydin HT, Akbaba Y, Menzek A, Sahin E, Göksu S. First and short syntheses of biologically active, naturally occurring brominated mono- and dibenzyl phenols. Arkivoc 2009;XIV:75–87.
   Google Scholar
• Göksu S, Seçen H. Concise syntheses of 2-aminoindans via indan-2-ol. Tetrahedron 2005;61:6801–6807.
   Web of Science ®Google Scholar
• Göksu S, Uğuz MT, Özdemir H, Seçen H. A concise synthesis and the antibacterial activity of 5,6-dimethoxynaphthalene-2-carboxylic acid. Turk J Chem 2005;29:199–205.
   Web of Science ®Google Scholar
• Lu Y, Shi T, Wang Y, Yang H, Yan X, Luo X et al. Halogen bonding–a novel interaction for rational drug design? J Med Chem 2009;52:2854–2862.
   PubMed Web of Science ®Google Scholar
• Göksu S, Seçen H, Sütbeyaz Y. An alternative synthesis of the dopaminergic drug 2-amino-1,2,3,4-tetrahydronaphthalene-5,6-diol (5,6-ADTN). Helv Chim Acta 2006;89:270–273.
   Web of Science ®Google Scholar