Have a personal or library account? Click to login
The isolation of bioactive flavonoids from Jacaranda obtusifolia H. B. K. ssp. rhombifolia (G. F. W. Meijer) Gentry Cover

The isolation of bioactive flavonoids from Jacaranda obtusifolia H. B. K. ssp. rhombifolia (G. F. W. Meijer) Gentry

Open Access
|Jun 2012

References

  1. R. M. Ali and P. J. Houghton, A new phenolic fatty acid ester with lipoxygenase inhibitory activity from Jacaranda filicifolia, Planta Med. 65 (1999) 455-457; DOI: 10.1055/s-2006-960811.10.1055/s-2006-96081110418336
  2. M. S. Gachet and W. Schühly, Jacaranda - An ethnopharmacological and phytochemical review, J. Ethnopharmacol. 121 (2009) 14-27; DOI: 10.1016/j.jep.2008.10.015.10.1016/j.jep.2008.10.01519010407
  3. T. Smitinan and K. Larsen, Flora of Thailand, The Chutima Press, Bangkok 1987.
  4. S. Khamsan, S. Liawruangrath, A. Teerawutkulrag, S. G. Pyne, M. J. Garson and B. Liawruangrath, A new isoflavone from Jacaranda obtusifolia H.B.K. ssp. rhombifolia (G.F.W. Meijer) Gentry, Acta Pharm. Sci. 53 (2011) 181-188.
  5. J. O. Brien, I. Wilson, T. Orton and F. Pognan, Investigation of the alamar blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity, Eur. J. Biochem. 267 (2000) 5421-5426; DOI: 10.1046/j.1432-1327.2000.01606.x.10.1046/j.1432-1327.2000.01606.x10951200
  6. L. Hunt, M. Jordan, M. De Jesus and F. M. Wurm, GFP expressing mammalian cells for fast, sensitive, noninvasive cell growth assessment in a kinetic mode, Biotechnol. Bioeng. 65 (1999) 201-205; DOI: 10.1002/(SICI)1097-0290(19991020)65:2<; 201::AID-BIT10>3.0.CO;2-H.
  7. C.-J. Ma, G.-S. Li, D.-L. Zhang, K. Liu and X. Fan, One step isolation and purification of liquiritigenin and isoliquiritigenin from Glycyrrhiza uralensis Risch. using high-speed counter-current chromatography, J. Chromatogr. A 1078 (2005) 188-192; DOI: 10.1016/j.chroma.2005.01.053.10.1016/j.chroma.2005.01.05316007997
  8. N. I. Kulesh, N. A. Vasilevskaya, M. V. Veselova, V. A. Denisenko and S. A. Fedoreev, Minor polyphenols from Maackia amurensis wood, Chem. Nat. Compds. 44 (2008) 712-714; DOI: 10.1007/s10600-009-9195-3.10.1007/s10600-009-9195-3
  9. E. Garo, J.-L. Wolfender, K. Hostettmann, W. Hiller, S. Antus and S. Mavi, Prenylated flavanones from Monotes engleri. online structure elucidation by LC/UV/NMR, Helv. Chim. Acta 81 (1998) 754-763; DOI: 10.1002/hlca.19980810325.10.1002/hlca.19980810325
  10. J. Li, S. Kadota, Y. Kawata, M. Hattori, G. Xu and T. Namba, Constituents of the roots of Cynanchum bungei Decne. Isolation and structures of four new glucosides, bungeiside A, B, C, and D, Chem. Pharm. Bull. 40 (1992) 3133-3137.10.1248/cpb.40.31331294317
  11. W. Fan, Y. Tezuka, K. M. Ni and S. Kadota, Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis, Chem. Pharm. Bull. 49 (2001) 396-401.10.1248/cpb.49.39611310664
  12. B. Fu, H. Li, X. Wang, F. S. C Lee and S. Cui, Isolation and identification of flavonoids in licorice and a study of their inhibitory effects on tyrosinase, J. Ag. Food Chem. 53 (2005) 7408-7414; DOI: 10.1021/jf051258h.10.1021/jf051258h16159166
  13. T. Han, H. Li, Q. Zhang, H. Zheng and L. Qin, New thiazinediones and other components from Xanthium strumarium, Chem. Nat. Compds. 42 (2006) 567-570; DOI: 10.1007/s10600-006-0215-2.10.1007/s10600-006-0215-2
DOI: https://doi.org/10.2478/v10007-012-0014-1 | Journal eISSN: 1846-9558 | Journal ISSN: 1330-0075
Language: English
Page range: 181 - 190
Published on: Jun 28, 2012
Published by: Croatian Pharmaceutical Society
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
Related subjects:

© 2012 Sorachai Khamsan, Saisunee Liawruangrath, Aphiwat Teerawutkulrag, Stephen Pyne, Mary Garson, Boonsom Liawruangrath, published by Croatian Pharmaceutical Society
This work is licensed under the Creative Commons License.

Volume 62 (2012): Issue 2 (June 2012)