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プロストラチン (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "プロストラチン" in Japanese language version.

refsWebsite
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6nih.gov
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5doi.org
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2aidsresearch.org
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1time.com
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1archive.is
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1lbl.gov
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1news-medical.net
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1stanford.edu
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1prweb.com
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1aacrjournals.org
8,869th place
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aacrjournals.org

cancerres.aacrjournals.org

aidsresearch.org

archive.is

doi.org

  • Cashmore, A. R.; Seelye, R. N.; Cain, B. F.; Mack, H.; Schmidt, R.; Hecker, E. (1976). “The structure of prostratin : a toxic tetracyclic diterpene ester from Pimelea Prostrata”. Tetrahedron Lett. 17 (20): 1737-1738. doi:10.1016/S0040-4039(00)92940-X. 
  • Gustafson, K. R.; Cardellina, J. H. 2nd; McMahon, J. B.; Gulakowski, R. J.; Ishitoya, J.; Szallasi, Z.; Lewin, N. E.; Blumberg, P. M.; Weislow, O. S.; Beutler, J. A.; Buckheit, R. W., Jr.; Cragg, G. M.; Cox, P. A.; Bader, J. P.; Boyd, M. R. (1992). “A nonpromoting phorbol from the samoan medicinal plant Homalanthus nutans inhibits cell killing by HIV-1”. J. Med. Chem. 35 (11): 1978-1986. doi:10.1021/jm00089a006. PMID 1597853. 
  • Cox, P. A. (2001). “Ensuring Equitable Benefits: The Falealupo Covenant and the Isolation of Anti-Viral Drug Prostratin from a Samoan Medicinal Plant”. Pharm. Biol. 39, Supplement 1. doi:10.1076/phbi.39.7.33.5875.  Source: Pharmaceutical Biology (Formerly International Journal of Pharmacognosy), Volume 39, Supplement 1, Supplement 1/2001 , pp. 33-40(8)
  • Kirby, J.; Nishimoto, M.; Park, J. G.; Withers, S. T.; Nowroozi, F.; Behrendt, D.; Rutledge, E. J.; Fortman, J. L.; Johnson, H. E.; Anderson, J. V.; Keasling, J. D. (2010). “Cloning of casbene and neocembrene synthases from Euphorbiaceae plants and expression in Saccharomyces cerevisiae”. Phytochemistry 71 (13): 1466-1473. doi:10.1016/j.phytochem.2010.06.001. PMID 20594566. 
  • Paul A. Wender, Jung-Min Kee, Jeffrey M. Warrington (May 2008). “Practical Synthesis of Prostratin, DPP, and Their Analogs, Adjuvant Leads Against Latent HIV”. Science 320 (5876): 649–652. doi:10.1126/science.1154690. PMC 2704988. PMID 18451298. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2704988/. 

lbl.gov

keaslinglab.lbl.gov

news-medical.net

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Gustafson, K. R.; Cardellina, J. H. 2nd; McMahon, J. B.; Gulakowski, R. J.; Ishitoya, J.; Szallasi, Z.; Lewin, N. E.; Blumberg, P. M.; Weislow, O. S.; Beutler, J. A.; Buckheit, R. W., Jr.; Cragg, G. M.; Cox, P. A.; Bader, J. P.; Boyd, M. R. (1992). “A nonpromoting phorbol from the samoan medicinal plant Homalanthus nutans inhibits cell killing by HIV-1”. J. Med. Chem. 35 (11): 1978-1986. doi:10.1021/jm00089a006. PMID 1597853. 
  • Kirby, J.; Nishimoto, M.; Park, J. G.; Withers, S. T.; Nowroozi, F.; Behrendt, D.; Rutledge, E. J.; Fortman, J. L.; Johnson, H. E.; Anderson, J. V.; Keasling, J. D. (2010). “Cloning of casbene and neocembrene synthases from Euphorbiaceae plants and expression in Saccharomyces cerevisiae”. Phytochemistry 71 (13): 1466-1473. doi:10.1016/j.phytochem.2010.06.001. PMID 20594566. 
  • Paul A. Wender, Jung-Min Kee, Jeffrey M. Warrington (May 2008). “Practical Synthesis of Prostratin, DPP, and Their Analogs, Adjuvant Leads Against Latent HIV”. Science 320 (5876): 649–652. doi:10.1126/science.1154690. PMC 2704988. PMID 18451298. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2704988/. 
  • Szallasi, Z.; Krsmanovic, L.; Blumberg, P. M. (1993). “Nonpromoting 12-deoxyphorbol 13-esters inhibit phorbol 12-myristate 13-acetate induced tumor promotion in CD-1 mouse skin”. Cancer Res. 53 (11): 2507-2512. PMID 8495413. http://cancerres.aacrjournals.org/content/53/11/2507.abstract. 

ncbi.nlm.nih.gov

pmc.ncbi.nlm.nih.gov

prweb.com

stanford.edu

news.stanford.edu

time.com