STRUCTURE OF POLYPHENOLS OF LEAVES TANNING SUMAC RHUS CORIARIA L.

UDC 547.982/83/84

  • Zhamollitdin Fazlitdinovich Ziyavitdinov Institute of Bioorganic Chemistry Academician A.S. Sadykov AS RUz Email: Jamolitdin@mail.ru
  • Yuliya Igorevna Oshchepkova Institute of Bioorganic Chemistry Academician A.S. Sadykov AS RUz Email: joshepkova05@rambler.ru
  • Nodira Gulyamzhanovna Abdulladzhanova Institute of Bioorganic Chemistry Academician A.S. Sadykov AS RUz Email: anodira73@rambler.ru
  • Shavkat Ismailovich Salikhov Institute of Bioorganic Chemistry Academician A.S. Sadykov AS RUz Email: joshepkova05@rambler.ru
Keywords: Rhus coriaria L., Anacardiaceae family, chromatography, mass spectrum, structure, fragmentation, polyphenols

Abstract

The aim of this work is to study the composition and structural characteristics of the polyphenols of the tanning sumac Rhus coriaria L. of the Anacardiaceae family, growing in Uzbekistan, using a high-performance liquid chromatograph with a diode-matrix detector (HPLC-DAD) and a tandem temple mass-spectrometer (HPLC– Q-TOF-MS / MS).

The phenolic compounds of the aerial part (leaves) of Rhus coriaria L. plants of the Anacardiaceae family were studied. For the first time, polyphenol fractions were isolated from tanning sumac leaves using stepwise hydrophobic chromatography. By HPLC, as a result of semi-preparative chromatography from the fraction eluted with 30% ethanol, 9 individual compounds were obtained, in the amount of: R-1 – 0.5 mg, R-2 – 0.8 mg, R-3 – 2.3 mg, R-4 – 12.6 mg, R-5 – 34.5 mg, R-6 – 15 mg, R-7 – 8 mg, R-8 – 7.1 mg, R-9 – 45.5 mg As a result of mass spectrometric analyzes and NMR spectroscopy for individual polyphenols, it was established that the polyphenols isolated in the individual state consist of gallic acid and glucose, interconnected by an ester bond: mono-, di-, tri-, tetra-, penta- , hexa-, hepta-, octa- and non-O-galloyl-β-D-glucose.

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Author Biographies

Zhamollitdin Fazlitdinovich Ziyavitdinov, Institute of Bioorganic Chemistry Academician A.S. Sadykov AS RUz

кандидат химических наук, заместитель директора по науке и инновациям

Yuliya Igorevna Oshchepkova, Institute of Bioorganic Chemistry Academician A.S. Sadykov AS RUz

доктор химических наук, заведующая лабораторией химии белков и пептидов

Nodira Gulyamzhanovna Abdulladzhanova, Institute of Bioorganic Chemistry Academician A.S. Sadykov AS RUz

доктор химических наук, ведущий научный сотрудник лаборатории ЭТЛ

Shavkat Ismailovich Salikhov, Institute of Bioorganic Chemistry Academician A.S. Sadykov AS RUz

академик, директор

References

Ali-Shtayeh M.S., Al-Assali A.A., Jamous R.M. African Journal of Microbiology Research, 2013, no. 7, pр. 2560–2573.

Shafiei M., Nobakht M., Moazzam A.A. Pharmazie, 2011, no. 66, pр. 988–992.

Wetherilt H., Pala M. G. Charalambous, ed., Spices, Herbs and Edible Fungi: Developments in Food Science, Elsevier Science BV. Amsterdam, 1994, pp. 285–307.

Ozcan M. Journal of Medicinal Food, 2003, vol. 6, no. 1, pp. 63–66. DOI: 10.1089/109662003765184769.

Bozan B. et al. Acta Alimentaria, 2003, vol. 32, no. 1, pp. 53–61. DOI: 10.1556/AAlim.32.2003.1.7.

Candan F. Journal of Enzyme Inhibition and Medicinal Chemistry, 2003, vol. 18, no. 1, pp. 59–62. DOI: 10.1080/1475636031000069273.

Candan F., Sökmen A. Phytotherapy Research, 2004, vol. 18, no. 1, pp. 84–86. DOI: 10.1002/ptr.1228.

Pourahmad J. et al. Food and Chemical Toxicology, 2010, vol. 48, no. 3, pp. 854–858. DOI: 10.1016/j.fct.2009.12.021.

Bursal E., Köksal E. Food Research International, 2011, vol. 44, no. 7, pp. 2217–2221. DOI: 10.1016/j.foodres.2010.11.001.

Mohammadi S. et al. Journal of Pharmaceutical Sciences, 2010, vol. 18, pp. 270–275.

Giancarlo S. et al. Natural Product Research, 2006, vol. 20, no. 9, pp. 882–886. DOI: 10.1080/14786410500520186.

Lee S.H. et al. Planta Medica, 2003, vol. 69, no. 11, pp. 990–994. DOI: 10.1055/s-2003-45143.

Lee J.C. et al. Food and Chemical Toxicology, 2004, vol. 42, no. 9, pp. 1383–1388. DOI: 10.1016/j.fct.2004.03.012.

Park K.Y. et al. Journal of Ethnopharmacology, 2004, vol. 90, no. 1, pp. 73–79. DOI: 10.1016/j.jep.2003.09.043.

Panico A. et al. Journal of Medicinal Plants Research, 2009, vol. 3, pp. 855–861.

Fazeli M.O. et al. Food Control, 2007, vol. 18, no. 6, pp. 646–649. DOI: 10.1016/j.foodcont.2006.03.002.

Mohamea Khalil M.K. Journal of King Saud University, 2010, vol. 8, pp. 257–267.

Nimri L.F. et al. Pharmaceutical Biology, 1999, vol. 37, pp. 196–201. DOI: 10.1076/phbi.37.3.196.6308.

Adwan G. et al. Turkish Journal of Biology, 2010, vol. 30, pp. 239–242.

Abu-Shanab B. et al. Journal of the Islamic University of Gaza (Natural Sciences Series), 2005, vol. 13, pp. 147–153.

Gündüz G.T. et al. International Journal of Food Microbiology, 2010, vol. 141, no. 1–2, pp. 39–44. DOI: 10.1016/j.ijfoodmicro.2010.04.021.

Lin Y.M. et al. Planta Medica, 1999, vol. 65, no. 2, pp. 120–125. DOI: 10.1055/s-1999-13971.

Ahmed M.S. et al. Phytochemistry, 2001, vol. 58, no. 4, pp. 599–602. DOI: 10.1016/S0031-9422(01)00244-8.

McCutcheon A.R. et al. Journal of Ethnopharmacology, 1994, vol. 44, no. 3, pp. 157–169. DOI: 10.1016/0378-8741 (94) 01183-4.

Abu-Reidah I.M., Ali-Shtayeh M.S., Jamous R.M., Arráez-Román D., Segura-Carretero A. Food Chemistry, 2015, vol. 166, pp. 179–191.

Al-Boushi M.A., Hamdo H.H., Herbali J. International Journal of ChemTech Research, 2014, vol. 6, no. 4, pp. 2414–2420.

Kossah R., Nsabimana C., Zhang H., Chen W. Research Journal of Phytochemistry, 2010, vol. 4, pp. 146–153.

Ziyavitdinov Zh.F., Inogamov U.K., Sagdiyev N.Zh., Salikhov Sh.I. Khimiya prirodnykh soyedineniy, 1995, no. 6, pp. 862–866 (in Russ.).

Published
2020-03-05
How to Cite
1. Ziyavitdinov Z. F., Oshchepkova Y. I., Abdulladzhanova N. G., Salikhov S. I. STRUCTURE OF POLYPHENOLS OF LEAVES TANNING SUMAC RHUS CORIARIA L. // chemistry of plant raw material, 2020. № 1. P. 133-140. URL: http://journal.asu.ru/cw/article/view/6316.
Section
Low-molecular weight compounds