Rubiadyna (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Rubiadyna" in Polish language version.

refsWebsite
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doi.org (Global: 2nd place; Polish: 6th place)

doi.org

  • Edward Schunck. On Rubian and Its Products of Decomposition. „Phil. Trans. R. Soc. Lond.”. 143, s. 67–107, 1853. DOI: 10.1098/rstl.1853.0003. 
  • Guntupalli M. Mohana Rao, Chandana V. Rao, Palpu Pushpangadan, Annie Shirwaikar. Hepatoprotective effects of rubiadin, a major constituent of Rubia cordifolia Linn. „Journal of Ethnopharmacology”. 103 (3), s. 484–490, 2006. DOI: 10.1016/j.jep.2005.08.073. 
  • Kaoru Inoue, Midori Yoshida, Miwa Takahashi, Hitoshi Fujimoto. Possible contribution of rubiadin, a metabolite of madder color, to renal carcinogenesis in rats. „Food and Chemical Toxicology”. 47 (4), s. 752–759, 2009. DOI: 10.1016/j.fct.2009.01.003. 
  • L. Marchlewski. LXXXV.—The constitution of rubiadinglucoside and rubiadin. „J. Chem. Soc., Trans.”. 63, s. 1137–1142, 1893. DOI: 10.1039/CT8936301137. 
  • E. Schunck, L. Marchlewski. XIX.—Notes on madder colouring matters. „J. Chem. Soc., Trans.”. 65, s. 182–187, 1894. DOI: 10.1039/CT8946500182. 
  • Elfed Thomas Jones, Alexander Robertson. CCXXIII.—Syntheses of glucosides. Part V. Two new syntheses of rubiadin and syntheses of 1-O-methylrubiadin and of rubiadin glucoside. „J. Chem. Soc.”, s. 1699–1709, 1930. DOI: 10.1039/JR9300001699. 
  • Toshiyuki Takano, Tomomi Kondo, Fumiaki Nakatsubo. Facile synthesis of rubiadin by microwave heating. „Journal of Wood Science”. 52 (1), s. 90–92, 2006. DOI: 10.1007/s10086-005-0727-6. 
  • A.R. Burnett, R.H. Thomson. Naturally occurring quinones. Part XIII. Anthraquinones and related naphthalenic compounds in Galium spp. and in Asperula odorata. „J. Chem. Soc. C”, s. 854–857, 1968. DOI: 10.1039/J39680000854. 
  • Th. Mulder-Krieger, R. Verpoorte, M. van der Kreek, A. Baerheim Svendsen. Identification of Alkaloids and Anthraquinones in Cinchona pubescens Callus Cultures; the Effect of Plant growth Regulators and Light on the Alkaloid Content.. „Planta Med.”. 50 (1), s. 17–20, 1984. DOI: 10.1055/s-2007-969609. PMID: 17340239. 
  • J.H. Bowie, R.G. Cooke, P.E. Wilkin. Colouring Matters of Australian Plants. X. Anthraquinones from Coelospermum Species. „Australian Journal of Chemistry”. 15 (2), s. 336–341, 1962. DOI: 10.1071/CH9620336. 
  • Lindsay H. Briggs,, G.A. Nicholls, R.M.L. Paterson. 318. Chemistry of the Coprosma genus. Part VI. Minor anthraquinone colouring matters from Coprosma australis. „J. Chem. Soc.”, s. 1718–1722, 1952. DOI: 10.1039/JR9520001718. 
  • Lindsay H. Briggs, G.A. Nicholls. 269. Chemistry of the coprosma genus. Part IV. The non-glycosidic anthraquinone compounds from coprosma lucida. „J. Chem. Soc.”, s. 1241–1246, 1949. DOI: 10.1039/JR9490001241. 
  • E.J.C. Brew, R.H. Thomason. Naturally occurring quinones. Part XIX. Anthraquinones in hymenodictyon excelsum and damnacanthus major. „J. Chem. Soc. C”, s. 2001–2007, 1971. DOI: 10.1039/J39710002001. 
  • J. Kuiper, R.P. Labadie. Polyploid complexes within the genus Galium. „Planta Med.”. 42 (8), s. 390–399, 1981. DOI: 10.1055/s-2007-971661. PMID: 17401995. 
  • N.S. Zhuravlev, M.I. Borisov. Anthraquinones of Galium dasypodum. „Khimiya Prirodnykh Soedinenii”. 5 (2), s. 118, 1969. DOI: 10.1007/BF00633289. 
  • N.S. Zhuravlev. Anthraquinones of Galium semiamictum. „Khimiya Prirodnykh Soedinenii”. 10 (5), s. 656, 1974. DOI: 10.1007/BF00567871. 
  • J.H. Bowie, R.G. Cooke. Colouring Matters of Australian Plants. IX. Anthraquinones from Morinda Species. „Australian Journal of Chemistry”. 15 (2), s. 332–335, 1962. DOI: 10.1071/CH9620332. 
  • E.K. Adesogan. Anthraquinones and anthraquinols from Morinda lucida: The biogenetic significance of oruwal and oruwalol. „Tetrahedron”. 29 (24), s. 4099–4102, 1973. DOI: 10.1016/0040-4020(73)80244-3. 
  • A.R. Burnett, R.H. Thomson. Anthraquinones in Morinda umbellata L. „Phytochemistry”. 7 (8), s. 1421–1422, 1968. DOI: 10.1016/S0031-9422(00)85651-4. 
  • H.H. Lee. Colouring matters from Prismatomeris malayana. „Phytochemistry”. 8 (2), s. 501–503, 1969. DOI: 10.1016/S0031-9422(00)85455-2. 
  • Ch. Dosseh, A.M. Tessier, P. Delaveau. Nouvelles Quinones des Racines de Rubia cordifolia L., III. „Planta Med.”. 43 (12), s. 360–366, 1981. DOI: 10.1055/s-2007-971524. PMID: 17402060. 
  • A.R. Burnett, R.H. Thomson. Biogenesis of Anthraquinones in Rubiaceae. „Chem. Commun. (London)”, s. 1125–1126, 1967. DOI: 10.1039/C19670001125. 

dx.doi.org

  • Th. Mulder-Krieger i inni, Identification of the alkaloids and anthraquinones in Cinchona ledgeriana callus cultures, „Planta Med.”, 1, 46, 1982, s. 19–24, DOI10.1055/s-2007-970010, PMID17396932.
  • Lindsay H. Briggs i inni, Chemistry of the Coprosma genus. Part XIV. Constituents of five New Zealand species, „J. Chem. Soc., Perkin Trans. 1”, 1976, s. 1789–1792, DOI10.1039/P19760001789.

nih.gov (Global: 4th place; Polish: 7th place)

ncbi.nlm.nih.gov

  • Th. Mulder-Krieger i inni, Identification of the alkaloids and anthraquinones in Cinchona ledgeriana callus cultures, „Planta Med.”, 1, 46, 1982, s. 19–24, DOI10.1055/s-2007-970010, PMID17396932.
  • Th. Mulder-Krieger, R. Verpoorte, M. van der Kreek, A. Baerheim Svendsen. Identification of Alkaloids and Anthraquinones in Cinchona pubescens Callus Cultures; the Effect of Plant growth Regulators and Light on the Alkaloid Content.. „Planta Med.”. 50 (1), s. 17–20, 1984. DOI: 10.1055/s-2007-969609. PMID: 17340239. 
  • J. Kuiper, R.P. Labadie. Polyploid complexes within the genus Galium. „Planta Med.”. 42 (8), s. 390–399, 1981. DOI: 10.1055/s-2007-971661. PMID: 17401995. 
  • J.S. Jiang, Z.M. Feng, P.C. Zhang. Chemical constituents from root of Prismatomeris tetrandra. „Zhongguo Zhong Yao Za Zhi”. 30 (22), s. 1751–1753, 2005. PMID: 16468371. 
  • Ch. Dosseh, A.M. Tessier, P. Delaveau. Nouvelles Quinones des Racines de Rubia cordifolia L., III. „Planta Med.”. 43 (12), s. 360–366, 1981. DOI: 10.1055/s-2007-971524. PMID: 17402060. 

pubchem.ncbi.nlm.nih.gov

worldcat.org (Global: 5th place; Polish: 2nd place)