Antioxidant and α-glucosidase inhibitory activities of Achillea tenorii

References

• Al-Hindawi M, Al-Deen IH, Nabi MH, Ismail MA. (1989). Anti-inflammatory activity of some Iraqi plants using intact rats. J Ethnopharmacol 26:163–8
   PubMed Web of Science ®Google Scholar
• Ardestani A, Yazdanparast R. (2007). Antioxidant and free radical scavenging potential of Achillea santolina extracts. Food Chem 104:21–9
   Web of Science ®Google Scholar
• Arnao MB, Cano A, Alcolea JF, Acosta M. (2001). Estimation of free radical-quenching activity of leaf pigment extracts. Phytochem Anal 12:138–43
   PubMed Web of Science ®Google Scholar
• Bai G, Cao X, Zhang H, et al. (2011). Direct screening of G-quadruplex ligands from Kalopanax septemlobus (Thunb.) Koidz extract by high performance liquid chromatography. J Chromatogr A 1218:6433–8
   PubMedGoogle Scholar
• Barış D, Kızıl M, Aytekin Ç, et al. (2011). In vitro antimicrobial and antioxidant activity of ethanol extract of three Hypericum and three Achillea species from Turkey. Int J Food Prop 14:339–55
   Web of Science ®Google Scholar
• Baron AD. (1998). Postprandial hyperglycaemia and alpha-glucosidase inhibitors. Diabetes Res Clin Pr 40:S51–5
   PubMed Web of Science ®Google Scholar
• Beker KI, Güçlü K, Demirata B, Apak R. (2010). A novel antioxidant assay of reducing capacity measured using ferrozine as the colour forming complexation reagent. Anal Methods 2:1770–8
   Google Scholar
• Benedek B, Gjoncaj N, Saukel J, Kopp B. (2007). Distribution of phenolic compounds in Middleeuropean taxa of the Achillea millefolium L. aggregate. Chem Biodivers 4:849–57
   PubMed Web of Science ®Google Scholar
• Benzie IFF, Strain JJ. (1996). The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: The FRAP assay. Anal Biochem 239:70–6
   PubMed Web of Science ®Google Scholar
• Brand-Williams W, Cuvelier ME, Berset C. (1995). Use of a free radical method to evaluate antioxidant activity. Lebensm Wiss Technol 28:25–30
   Web of Science ®Google Scholar
• Candana F, Unlub M, Tepec B, et al. (2003). Antioxidant and antimicrobial activity of the essential oil and methanol extracts of Achillea millefolium subsp. millefolium Afan. (Asteraceae). J Ethnopharmacol 87:215–20
   PubMedGoogle Scholar
• Conti F, Abbate G, Alessandrini A, Blasi C. (2005). An Annotated Checklist of the Italian Vascular Flora. Rome: Palombi Press
   Google Scholar
• dos Santos AR, Pereira de Barros M, Santin SM, et al. (2004). Polar constituents of the leaves of Machaonia brasiliensis (Rubiaceae). Quim Nova 27:525–7
   Google Scholar
• Elbein AD. (1991). Glycosidase inhibitors as antiviral and/or antitumor agents. Semin Cell Biol 2:309–17
   PubMedGoogle Scholar
• El-Kaissi S, Sherbeeni S. (2011). Pharmacological management of type 2 diabetes mellitus: An update. J Curr Diabetes Rev 7:392–405
   PubMedGoogle Scholar
• Ha TJ, Lee JH, Lee MH, et al. (2012). Isolation and identification of phenolic compounds from the seeds of Perilla frutescens (L.) and their inhibitory activities against α-glucosidase and aldose reductase. Food Chem 135:1397–403
   PubMed Web of Science ®Google Scholar
• Huo CH, Li Y, Zhang ML, et al. (2013). Cytotoxic flavonoids from the flowers of Achillea millefolium. Chem Nat Compd 48:958–62
   Google Scholar
• Ivancheva S, Kuzmanov B. (1986). Flavonoids in genus Achillea, A. nobilis-group. Bull Liaison – Groupe Polyphenols 13:577–9
   Google Scholar
• Kasaj D, Krenn L, Reznicek G, et al. (2001). Flavonoids in Achillea collina. Sci Pharm 69:75–83
   Google Scholar
• Kato E, Oikawa K, Takahashi K, Kawabata J. (2012). Synthesis and the intestinal glucosidase inhibitory activity of 2-aminoresorcinol derivatives toward an investigation of its binding site. Biosci Biotech Biochem 76:1044–6
   PubMed Web of Science ®Google Scholar
• Li T, Zhang XD, Song YW, Liu JW. (2005). A microplate-based screening method for α-glucosidase inhibitors. Chin J Clin Pharmacol Ther 10:1128–34
   Google Scholar
• Marchart E, Hattenberger A, Krenn L, Kopp B. (2003). Analysis of flavonoids in Achillea nobilis L. by capillary electrophoresis. Sci Pharm 71:133–45
   Google Scholar
• Nemeth E, Bernath J. (2008). Biological activities of yarrow species (Achillea spp.). Curr Pharm Des 14:3151–67
   PubMed Web of Science ®Google Scholar
• Oyama K, Kondo T. (2004). Total synthesis of apigenin 7,4′-di-O-β-glucopyranoside, a component of blue flower pigment of Salvia patens, and seven chiral analogs. Tetrahedron 60:2025–34
   Web of Science ®Google Scholar
• Park Y. (2007). Spectral assignments and reference data: 1H and 13C-NMR data of hydroxyflavone derivatives. Magn Reson Chem 45:674–9
   PubMed Web of Science ®Google Scholar
• Pignatti S. (1982). Flora d’Italia, vol. 3. Bologna, Italy: Edagricole, 84
   Google Scholar
• Solomko OV, Dzhumyrko SF, Kompantsev VA. (1978). Flavonoids of Achillea nobilis. Khim Prir Soedin 2:266–7
   Google Scholar
• Taylor R, Johnson AB. (1996). Does suppression of postprandial blood glucose excursions by the alpha-glucosidase inhibitor miglitol improve insulin sensitivity in diet-treated type II diabetic patients? Diabetes Care 19:559–63 .
   PubMedGoogle Scholar
• Van Loo P, De Bruyn A, Budesinsky M. (1986). Reinvestigation of the structural assignment of signals in the proton and carbon-13 NMR spectra of the flavone apigenin. Magn Reson Chem 24:879–82
   Web of Science ®Google Scholar
• Wada H. (1985). Chemical and chemotaxonomic study of pteridophytes. LIX. Studies of the chemical constituents of Alsophila spinulosa Tryon. Chem Pharm Bull 33:4182–7
   Google Scholar
• Westley AM, Westley J. (1996). Enzyme inhibition in open systems. Superiority of uncompetitive agents. J Biol Chem 271:5347–52
   PubMed Web of Science ®Google Scholar
• Yazdanparast R, Ardestani A, Jamshidi S. (2007). Experimental diabetes treated with Achillea santolina: Effect on pancreatic oxidative parameters. J Ethnopharmacol 112:13–18
   PubMed Web of Science ®Google Scholar
• Zapesochnaya GG, Ban’kovskii AI. (1976). Flavonoid from Achillea cartilaginea. Khim Prir Soedin (6):814–15
   Google Scholar