Steganacyna (Polish Wikipedia)

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

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aacrjournals.org

cancerres.aacrjournals.org

doi.org

  • Kupchan et al. Tumor inhibitors. LXXXX. Steganacin and steganangin, novel antileukemic lignan lactones from Steganotaenia araliacea. „J Am Chem Soc”. 95 (4), s. 1335–6, luty 1973. DOI: 10.1021/ja00785a054. 
  • Wickramaratne et al. Novel Antimitotic Dibenzocyclo-Octadiene Llignan Constituents of the Stem Bark of Steganotaenia araliacea. „J Nat Prod”. 56 (12), s. 2083–90, grudzień 1993. DOI: 10.1021/np50102a009. 
  • DL Sackett. Podophyllotoxin, steganacin and combretastatin: natural products that bind at the colchicine site of tubulin. „Pharmacol Ther”. 59 (2), s. 163–228, sierpień 1993. DOI: 10.1016/0163-7258(93)90044-E. 
  • Houlbert et al. Preparation, Etude Stereochimique et Evaluation de l'Activite Antileucemique de Derives Glucosidiques du (-)-Steganol. „J Nat Prod”. 48 (3), s. 345–56, maj 1985. DOI: 10.1021/np50039a001. (fr.). 
  • Mont et al. Diversity Oriented Microwave-Assisted Synthesis of (-)-Steganacin Aza-Analogues. „J Org Chem”. 73 (19), s. 7509–16, 2008-08-28. DOI: 10.1021/jo801290j. 
  • Imperio et al. Replacement of the lactone moiety on podophyllotoxin and steganacin analogues with a 1,5-disubstituted 1,2,3-triazole via ruthenium-catalyzed click chemistry. „Bioorg Med Chem”. 15 (21), s. 6748–57, 2007-11-01. DOI: 10.1016/j.bmc.2007.08.020. PMID: 17765552. 
  • Laurent et al. New two-step sequence involving a hetero-Diels–Alder and a nonphenolic oxidative coupling reaction: a convergent access to analogs of steganacin. „Tetrahedron Letters”. 52 (14), s. 1608–11, 2011-04-06. DOI: 10.1016/j.tetlet.2011.01.097. 

nih.gov

ncbi.nlm.nih.gov

  • Ishiguro et al. Stereoselective reactions. VIII. Stereochemical requirement for the benzylic oxidation of lignan lactone. A highly selective synthesis of the antitumor lignan lactone steganacin by the oxidation of stegane. „Chem Pharm Bull (Tokyo)”. 33 (2), s. 609–17, luty 1985. PMID: 2990746. 
  • AS Kende, LS Liebeskind. Letter: Total synthesis of (+/-)-steganacin. „Am Chem Soc”. 98 (1), s. 267–8, 1976-01-07. PMID: 1244373. 
  • D Becker, LR Hughes, RA Raphael. Total synthesis of the antileukaemic lignan (+/-)-steganacin. „Chem Soc Perkin 1”. 14, s. 1674–81, 1977. PMID: 561104. 
  • PB Schiff, AS Kende, SB Horwitz. Steganacin: an inhibitor of HeLa cell growth and microtubule assembly in vitro. „Biochem Biophys Res Commun”. 85 (2), s. 737–46, 1978-11-29. PMID: 736931. 
  • Bergemann et al. Novel B-ring modified allocolchicinoids of the NCME series: design, synthesis, antimicrotubule activity and cytotoxicity. „Bioorg Med Chem”. 11 (7), s. 1269–81, 2003-04-03. PMID: 12628654. 
  • Imperio et al. Replacement of the lactone moiety on podophyllotoxin and steganacin analogues with a 1,5-disubstituted 1,2,3-triazole via ruthenium-catalyzed click chemistry. „Bioorg Med Chem”. 15 (21), s. 6748–57, 2007-11-01. DOI: 10.1016/j.bmc.2007.08.020. PMID: 17765552.