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Corticostatine (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Corticostatine" in French language version.

refsWebsite
Global rank French rank
6nih.gov
4th place
12th place
6doi.org
2nd place
3rd place
1issn.org
57th place
4th place

doi.org

dx.doi.org

  • Aoki, Watanabe, Sanagawa et Setiawan, « Cortistatins A, B, C, and D, anti-angiogenic steroidal alkaloids, from the marine sponge Corticium simplex », Journal of the American Chemical Society, vol. 128, no 10,‎ , p. 3148–9 (PMID 16522087, DOI 10.1021/ja057404h)
  • Aoki, Watanabe, Tanabe et Arai, « Structure-activity relationship and biological property of cortistatins, anti-angiogenic spongean steroidal alkaloids », Bioorganic & Medicinal Chemistry, vol. 15, no 21,‎ , p. 6758–62 (PMID 17765550, DOI 10.1016/j.bmc.2007.08.017)
  • Pelish, Liau, Nitulescu et Tangpeerachaikul, « Mediator kinase inhibition further activates super-enhancer-associated genes in AML », Nature, vol. 526, no 7572,‎ , p. 273–276 (PMID 26416749, PMCID 4641525, DOI 10.1038/nature14904)
  • Mousseau, Clementz, Bakeman et Nagarsheth, « An Analog of the Natural Steroidal Alkaloid Cortistatin a Potently Suppresses Tat-Dependent HIV Transcription », Cell Host & Microbe, vol. 12, no 1,‎ , p. 97–108 (PMID 22817991, PMCID 3403716, DOI 10.1016/j.chom.2012.05.016)
  • Lee, Nieto-Oberhuber et Shair, « Enantioselective Synthesis of (+)-Cortistatin A, a Potent and Selective Inhibitor of Endothelial Cell Proliferation », Journal of the American Chemical Society, vol. 130, no 50,‎ , p. 16864–16866 (ISSN 0002-7863, PMID 19053422, DOI 10.1021/ja8071918)
  • Shenvi, Guerrero, Shi et Li, « Synthesis of (+)-Cortistatin A », Journal of the American Chemical Society, vol. 130, no 23,‎ , p. 7241–7243 (PMID 18479104, PMCID 2652360, DOI 10.1021/ja8023466)

issn.org

portal.issn.org

  • Lee, Nieto-Oberhuber et Shair, « Enantioselective Synthesis of (+)-Cortistatin A, a Potent and Selective Inhibitor of Endothelial Cell Proliferation », Journal of the American Chemical Society, vol. 130, no 50,‎ , p. 16864–16866 (ISSN 0002-7863, PMID 19053422, DOI 10.1021/ja8071918)

nih.gov

ncbi.nlm.nih.gov

  • Aoki, Watanabe, Sanagawa et Setiawan, « Cortistatins A, B, C, and D, anti-angiogenic steroidal alkaloids, from the marine sponge Corticium simplex », Journal of the American Chemical Society, vol. 128, no 10,‎ , p. 3148–9 (PMID 16522087, DOI 10.1021/ja057404h)
  • Aoki, Watanabe, Tanabe et Arai, « Structure-activity relationship and biological property of cortistatins, anti-angiogenic spongean steroidal alkaloids », Bioorganic & Medicinal Chemistry, vol. 15, no 21,‎ , p. 6758–62 (PMID 17765550, DOI 10.1016/j.bmc.2007.08.017)
  • Pelish, Liau, Nitulescu et Tangpeerachaikul, « Mediator kinase inhibition further activates super-enhancer-associated genes in AML », Nature, vol. 526, no 7572,‎ , p. 273–276 (PMID 26416749, PMCID 4641525, DOI 10.1038/nature14904)
  • Mousseau, Clementz, Bakeman et Nagarsheth, « An Analog of the Natural Steroidal Alkaloid Cortistatin a Potently Suppresses Tat-Dependent HIV Transcription », Cell Host & Microbe, vol. 12, no 1,‎ , p. 97–108 (PMID 22817991, PMCID 3403716, DOI 10.1016/j.chom.2012.05.016)
  • Lee, Nieto-Oberhuber et Shair, « Enantioselective Synthesis of (+)-Cortistatin A, a Potent and Selective Inhibitor of Endothelial Cell Proliferation », Journal of the American Chemical Society, vol. 130, no 50,‎ , p. 16864–16866 (ISSN 0002-7863, PMID 19053422, DOI 10.1021/ja8071918)
  • Shenvi, Guerrero, Shi et Li, « Synthesis of (+)-Cortistatin A », Journal of the American Chemical Society, vol. 130, no 23,‎ , p. 7241–7243 (PMID 18479104, PMCID 2652360, DOI 10.1021/ja8023466)