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Ботиров (Botirov), Эркин (Erkin) Хожиакбарович (Hozhiakbarovich); Каримов (Karimov), Абдурашид (Abdurashid); Юлдашев (Yuldashev), Малик (Malik) Патахович (Patahovich) (2014)
Publisher: Altai State University
Journal: Khimiia rastitel'nogo syr'ia (Chemistry of plant raw material)
Languages: Russian
Types: Article
Subjects: Scutellaria adenostegia Briq., Lamiaceae, флавоны, флавонолы и флаваноны., Scutellaria adenostegia Briq., Lamiaceae, flavones, flavanones
The article is devoted to the phytochemical study of flavonoids of roots and above-ground part of Scutellaria adenostegia Briq. families of Lamiaceae. From the overgrown part of Scutellaria adenostegia Briq. the known flavonoids norvogonin, oroxylin А, quercetin, hispidulin, and from the roots – vogonin, chrysin-7-O-methylglucuronide, oroxyloside, vogonoside, (±)-5,21-dihydroxi-6,6′,7-trimethoxiflavanone, (-)-5,21-dihydroxi-6,6′,7,8-tetramethoxyflavanone are first abstracted. Foregoing flavonoids are identified on the basis of results of chemical transformations (acid and alkaline hydrolysis), data of IR, UV, 1Н-NMR and mass spectra, comparing of physical and chemical constants to literary information, and also direct comparing to the standards of flavonoids, abstracted from other types of Scutellaria L. It is set that in composition the flavonoids of Scutellaria adenostegia Briq. connections prevail with unsubstituted for the ring of В.
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    • 1. Shang X., He X., He X., Li M., Zhang R., Fan P., Zhang Q., Jia Z. J. Ethnopharmacol., 2010, vol. 128, p . 279-313.
    • 2. Rastitel'nye resursy SSSR. Tsvetkovye rasteniia, ikh khimicheskii sostav, ispol'zovanie. Semeistva HippuridaceaeLobeliacae. [Plant resources of the USSR. Flowering plants, their chemical composition, the use. Families Hippuridaceae-Lobeliacae]. St. Petersburg, 1991, pp. 85-90. (in Russ.).
    • 3. Flora Uzbekistana. [Flora of Uzbekistan]. Tashkent, 1961, vol. 5, pp. 270-292. (in Russ.).
    • 4. Tarakhovskii Iu.S., Kim Iu.A., Abdrasilov B.S., Muzafarov E.N. Flavonoidy: biokhimiia, biofizika, meditsina. [Flavonoids: biochemistry, biophysics and medicine]. Pushchino, 2013, 310 p. (in Russ.).
    • 5. Gol'dberg E.D., Dygai A.M., Litvinenko V.I., Popova T.P., Suslov N.I. Shlemnik baikal'skii. Fitokhimiia i farmakologicheskie svoistva. [Baikal skullcap. Phytochemistry and pharmacological properties]. Tomsk, 1994, 222 p. (in Russ.).
    • 6. Parajuli P., Joshee N., Rimando A., Mittal S., Yadav A. K. Planta Med., 2009, vol. 75, pp. 41-48.
    • 7. Li-Weber M. Cancer Treat. Rev., 2009, vol. 35, pp. 57-68.
    • 8. Gao Z., Huang K., Yang X., Xu H. Biochim. Biophys. Acta., 1999, vol. 1472, no. 3, pp. 643-650.
    • 9. Mamadalieva N.Z., Herrmann F., El-Readi M.Z., Tahrani ., Hamoud R., Egamberdieva D.R., Azimova S.S., Wink . J. Pharm. Pharmacol., 2011, vol. 63, no. 10, pp. 1346-1357.
    • 10. Chemesova I.I., Iinuma M., Budantsev A.L. Chemistry of Natural Compounds, 1993, vol. 29, pp. 133-134.
    • 11. Nasrullaev F.D. Flavony nekotorykh vidov Scutellaria i Lagochilus semeistvo Labiatae.: avtoef. diss. ... kand. khim. nauk. [Flavones and some species Scutellaria Lagochilus family Labiatae .: dissertation author's Candidate of Chemical Science]. Tashkent,1993, 24 p. (in Russ.).
    • 12. Malikov V.M, Iuldashev M.P. Khimiia prirodnykh soedinenii, 2002, no. 4, pp. 299-324; 2002, no. 5, pp. 385-407. (in Russ.).
    • 13. Iuldashev M.P., Botirov E.Kh., Malikov V.M. Khimiia prirodnykh soedinenii, 1994, no. 6, pp. 822-823. (in Russ.).
    • 14. Shamyanov I.D., E.Kh.Botirov, Yuldashev M.P., Mallabaev A. Chemistry of Natural Compounds, 1983, vol. 19, pp. 763-764.
    • 15. Iuldashev M.P., Batirov E.Kh., Malikov V.M. Khimiia prirodnykh soedinenii, 1996, no. 4, pp. 610-612. (in Russ.).
    • 16. Zhou Z.H., Zhang Y.J., Yang Ch.R. Advances in Plant Glycosides, Chemistry and Biology. Amsterdam: Elsevier. 1999, pp. 305-310.
    • 17. Karimov A., Iuldashev M.P., Botirov E.Kh. Khimiia rastitel'nogo syr'ia, 2012, no. 3, pp. 101-105. (in Russ.).
    • 18. Siddikov G.U., Iuldashev M.P., Botirov E.Kh., Abdullaev Sh.V. Khimiia prirodnykh soedinenii, 2006, no. 3, pp. 293. (in Russ.).
    • 19. Miyaichi Y., Imoto Y., Tomimori T., Lin C-C. Chem. Pharm. Bull., 1987, vol. 35, pp. 3720-3725.
    • Received September 16, 2014
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