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The Scientific World Journal
Volume 2014 (2014), Article ID 654193, 9 pages
http://dx.doi.org/10.1155/2014/654193
Research Article

Componential Profile and Amylase Inhibiting Activity of Phenolic Compounds from Calendula officinalis L. Leaves

Laboratory of Medical and Biological Research, Institute of General and Experimental Biology, Siberian Division, Russian Academy of Science, Sakh’yanovoy Street, 6, Ulan-Ude 670047, Russia

Received 15 November 2013; Accepted 22 December 2013; Published 9 February 2014

Academic Editors: V. C. Filho and C. R. Wilson

Copyright © 2014 Daniil N. Olennikov and Nina I. Kashchenko. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. K. A. Khalid and J. A. Teixeira da Silva, “Biology of Calendula officinalis Linn.: focus on pharmacology, biological activities and agronomic practices,” Medicinal and Aromatic Plant Science and Biotechnology, vol. 6, no. 1, pp. 12–27, 2012. View at Google Scholar
  2. H. Friedrich, “Untersuchungen über die Isorhamnetinglykoside aus den Blüten von Calendula officinalis L.,” Archiv der Pharmazie, vol. 295, no. 6, pp. 464–471, 1962. View at Google Scholar
  3. T. Ercetin, F. S. Senol, I. Erdogan Orhan, and G. Toker, “Comparative assessment of antioxidant and cholinesterase inhibitory properties of the marigold extracts from Calendula arvensis L. and Calendula officinalis L,” Industrial Crops and Products, vol. 36, no. 1, pp. 203–208, 2012. View at Publisher · View at Google Scholar · View at Scopus
  4. E. Bakó, J. Deli, and G. Tóth, “HPLC study on the carotenoid composition of Calendula products,” Journal of Biochemical and Biophysical Methods, vol. 53, no. 1-3, pp. 241–250, 2002. View at Publisher · View at Google Scholar · View at Scopus
  5. G. Adler and Z. Kasprzyk, “Free sterols, steryl esters, glucosides, acylated glucosides and water-soluble complexes in Calendula officinalis,” Phytochemistry, vol. 14, no. 3, pp. 627–631, 1975. View at Google Scholar · View at Scopus
  6. A. Szakiel, D. Ruszkowski, A. Grudniak et al., “Antibacterial and antiparasitic activity of oleanolic acid and its glycosides isolated from marigold (Calendula officinalis),” Planta Medica, vol. 74, no. 14, pp. 1709–1715, 2008. View at Publisher · View at Google Scholar · View at Scopus
  7. O. O. Okoh, A. P. Sadimenko, O. T. Asekun, and A. J. Afolayan, “The effects of drying on the chemical components of essential oils of Calendula officinalis L,” African Journal of Biotechnology, vol. 7, no. 10, pp. 1500–1502, 2008. View at Google Scholar · View at Scopus
  8. N. T. Ul'chenko, A. I. Glushenkova, and K. S. Mukhamedova, “Lipids of Calendula officinalis,” Chemistry of Natural Compounds, vol. 34, no. 3, pp. 272–274, 1998. View at Google Scholar · View at Scopus
  9. D. N. Olennikov and N. I. Kashchenko, “New isorhamnetin glucosides and other phenolic compounds from Calendula officinalis’,” Chemistry of Natural Compounds, vol. 49, no. 5, pp. 717–723, 2013. View at Google Scholar
  10. M. Yoshikawa, T. Murakami, A. Kishi, T. Kageura, and H. Matsuda, “Medicinal flowers. III. Marigold. (1): Hypoglycemic, gastric emptying inhibitory, and gastroprotective principles and new oleanane-type triterpene oligoglycosides, calendasaponins A, B, C, and D, from Egyptian Calendula officinalis,” Chemical and Pharmaceutical Bulletin, vol. 49, no. 7, pp. 863–870, 2001. View at Publisher · View at Google Scholar · View at Scopus
  11. R. Rhabasa-Lhoret and J. L. Chiasson, “Alpha-glucosidase inhibitors,” in International Textbook of Diabetes Mellitus, R. A. Defronzo, E. Ferrannini, H. Keen, and P. Zimmet, Eds., vol. 1, John Wiley, UK, 2004. View at Google Scholar
  12. D. N. Olennikov, A. V. Rokhin, and L. M. Tankhaeva, “Lamiaceae carbohydrates. VI. Water-soluble polysaccharides from Lophanthus chinensis,” Chemistry of Natural Compounds, vol. 45, no. 3, pp. 300–303, 2009. View at Publisher · View at Google Scholar · View at Scopus
  13. D. N. Olennikov, S. V. Agafonova, A. V. Rokhin, T. A. Penzina, and G. B. Borovskii, “Branched glucan from the fruiting bodies of Piptoporus betulinus (Bull.:Fr) Karst,” Applied Biochemistry and Microbiology, vol. 48, no. 1, pp. 65–70, 2012. View at Publisher · View at Google Scholar · View at Scopus
  14. K. Shetty, O. F. Curtis, R. E. Levin, R. Witkowsky, and W. Ang, “Prevention of vitrification associated with in vitro shoot culture of oregano (Origanum vulgare) by Pseudomonas spp,” Journal of Plant Physiology, vol. 147, no. 3-4, pp. 447–451, 1995. View at Google Scholar · View at Scopus
  15. N. K. Chirikova, D. N. Olennikov, and L. M. Tankhaeva, “Quantitative determination of flavonoid content in the aerial part of Baical scullcap (Scutellaria baicalensis Georgi),” Russian Journal of Bioorganic Chemistry, vol. 36, no. 7, pp. 915–922, 2010. View at Publisher · View at Google Scholar · View at Scopus
  16. D. N. Olennikov and L. M. Tankhaeva, “Biologically active substances from Cacalia hastata leaves. 5. Coumarins and triterpenes,” Chemistry of Natural Compounds, vol. 41, no. 5, pp. 600–601, 2005. View at Publisher · View at Google Scholar · View at Scopus
  17. D. N. Olennikov, L. M. Tankhaeva, and S. V. Agafonova, “Antioxidant components of Laetiporus sulphureus (Bull.: Fr.) Murr. fruit bodies,” Applied Biochemistry and Microbiology, vol. 47, no. 4, pp. 419–425, 2011. View at Publisher · View at Google Scholar · View at Scopus
  18. D. N. Olennikov, L. M. Tankhaeva, A. V. Stolbikova, and E. V. Petrov, “Phenylpropanoids and polysaccharides from Plantago depressa and P. media growing in Buryatia,” Chemistry of Natural Compounds, vol. 47, no. 2, pp. 165–169, 2011. View at Publisher · View at Google Scholar · View at Scopus
  19. T. Satake, K. Kamiya, Y. An, T. Oishi, and J. Yamamoto, “The anti-thrombotic active constituents from Centella asiatica,” Biological and Pharmaceutical Bulletin, vol. 30, no. 5, pp. 935–940, 2007. View at Publisher · View at Google Scholar · View at Scopus
  20. V. M. Malikov and A. I. Saudkhodzhaev, “Coumarins: plants, structures, properties,” Chemistry of Natural Compounds, vol. 34, no. 5, pp. 517–548, 1998. View at Google Scholar
  21. D. N. Olennikov and V. V. Partilkhaev, “Isolation and densitometric HPTLC analysis of rutin, narcissin, nicotiflorin, and isoquercitrin in Caragana spinosa shoots,” Journal of Planar Chromatography, vol. 25, no. 1, pp. 30–35, 2012. View at Publisher · View at Google Scholar · View at Scopus
  22. Y. B. Wang, J. X. Pu, H. Y. Ren et al., “New acetylated flavonol glycosides from Knoxia corymbosa,” Chinese Chemical Letters, vol. 14, no. 12, pp. 1268–1270, 2003. View at Google Scholar · View at Scopus
  23. Q. Du, Y. Xu, L. Li, Y. Zhao, G. Jerz, and P. Winterhalter, “Antioxidant constituents in the fruits of Luffa cylindrica (L.) Roem,” Journal of Agricultural and Food Chemistry, vol. 54, no. 12, pp. 4186–4190, 2006. View at Publisher · View at Google Scholar · View at Scopus
  24. D. N. Olennikov, I. N. Zilfikarov, and S. E. Khodakova, “Phenolic compounds from Serenoa repens fruit,” Chemistry of Natural Compounds, vol. 49, no. 3, pp. 526–529, 2013. View at Google Scholar
  25. J. W. Choi, K. H. Kim, I. K. Lee, S. U. Choi, and K. R. Lee, “Phytochemical constituents of Amomum xanthioides,” Natural Product Sciences, vol. 15, no. 1, pp. 44–49, 2009. View at Google Scholar · View at Scopus
  26. E. Vidal-Ollivier, R. Elias, F. Faure et al., “Flavonol glycosides from Calendula officinalis flowers,” Planta Medica, vol. 55, no. 1, pp. 73–74, 1989. View at Google Scholar
  27. Z. Yuan, Y. Tezuka, W. Fan, S. Kadota, and X. Li, “Constituents of the underground parts of Glehnia littoralis,” Chemical and Pharmaceutical Bulletin, vol. 50, no. 1, pp. 73–77, 2002. View at Publisher · View at Google Scholar · View at Scopus
  28. K. Takara, D. Matsui, K. Wada, T. Ichiba, and Y. Nakasone, “New antioxidative phenolic glycosides isolated from Kokuto non-centrifuged cane sugar,” Bioscience, Biotechnology and Biochemistry, vol. 66, no. 1, pp. 29–35, 2002. View at Google Scholar · View at Scopus
  29. X.-W. Yang, H.-P. He, Y.-L. Ma et al., “Three new vanilloid derivatives from the stems of baccaurea ramiflora,” Planta Medica, vol. 76, no. 1, pp. 88–90, 2010. View at Publisher · View at Google Scholar · View at Scopus
  30. K. M. Canuto, M. A. S. Lima, and E. R. Silveira, “Amburosides c-h and 6-o-protocatechuoyl coumarin from Amburana cearensis,” Journal of the Brazilian Chemical Society, vol. 21, no. 9, pp. 1746–1753, 2010. View at Google Scholar · View at Scopus
  31. T. Yuan, C. Wan, A. González-Sarrías, V. Kandhi, N. B. Cech, and N. P. Seeram, “Phenolic glycosides from sugar maple (Acer saccharum) bark,” Journal of Natural Products, vol. 74, no. 11, pp. 2472–2476, 2011. View at Publisher · View at Google Scholar · View at Scopus
  32. R. D. Quin, W. Cheng, Q. Y. Zhang, and H. Liang, “Phenolic acid derivatives from Alchornea trewioides,” Acta Pharmaceutica Sinica, vol. 47, no. 7, pp. 926–929, 2012. View at Google Scholar
  33. J. Xiao, X. Ni, G. Kai, and X. Chen, “A review on structure-activity relationship of dietary polyphenols inhibiting α-amylase,” Critical Reviews in Food Science and Nutrition, vol. 53, no. 5, pp. 497–506, 2013. View at Google Scholar
  34. Z. Bahadoran, P. Mirmiran, and F. Azizi, “Dietary polyphenols as potential nutraceuticals in management of diabetes: a review,” Journal of Diabetes and Metabolic Disorders, vol. 12, no. 43, 2013. View at Google Scholar
  35. P. M. de Sales, P. M. de Souza, L. A. Simeoni, P. D. O. Magalhães, and D. Silveira, “α-amylase inhibitors: a review of raw material and isolated compounds from plant source,” Journal of Pharmacy and Pharmaceutical Sciences, vol. 15, no. 1, pp. 141–183, 2012. View at Google Scholar · View at Scopus