Stephacidin (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Stephacidin" in English language version.

refsWebsite

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8nih.gov

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7doi.org

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doi.org

Qian-Cutrone J, Huang S, Shu YZ, Vyas D, Fairchild C, Menendez A, Krampitz K, Dalterio R, Klohr SE, Gao Q (December 2002). "Stephacidin A and B: two structurally novel, selective inhibitors of the testosterone-dependent prostate LNCaP cells". Journal of the American Chemical Society. 124 (49): 14556–14557. doi:10.1021/ja028538n. PMID 12465964.
Borthwick AD (2012). "2,5-Diketopiperazines: Synthesis, Reactions, Medicinal Chemistry, and Bioactive Natural Products". Chemical Reviews. 112 (7): 3641–3716. doi:10.1021/cr200398y. PMID 22575049.
von Nussbaum F (2003). "Stephacidin B-A new stage of complexity within prenylated indole alkaloids from fungi". Angewandte Chemie International Edition. 42 (27): 3068–3071. doi:10.1002/anie.200301646. PMID 12866092.
Wulff JE, Herzon SB, Siegrist R, Myers AG (April 2007). "Evidence for the rapid conversion of stephacidin B into the electrophilic monomer avrainvillamide in cell culture". Journal of the American Chemical Society. 129 (16): 4898–4899. doi:10.1021/ja0690971. PMC 3175819. PMID 17397160.
Sugie Y, Hirai H, Inagaki T, Ishiguro M, Kim YJ, Kojima Y, Sakakibara T, Sakemi S, Sugiura A, Suzuki Y, Brennan L (2001). "A new antibiotic CJ-17,665 from Aspergillus ochraceus". The Journal of Antibiotics. 54 (11): 911–916. doi:10.7164/antibiotics.54.911. PMID 11827033.
Baran PS, Hafensteiner BD, Ambhaikar NB, Guerrero CA, Gallagher JD (July 2006). "Enantioselective total synthesis of avrainvillamide and the stephacidins". Journal of the American Chemical Society. 128 (26): 8678–8693. doi:10.1021/ja061660s. PMID 16802835.
Escolano C (December 2005). "Stephacidin B, the avrainvillamide dimer: A formidable synthetic challenge". Angewandte Chemie International Edition. 44 (47): 7670–7673. doi:10.1002/anie.200502383. PMID 16252300.

nih.gov

pubmed.ncbi.nlm.nih.gov

Qian-Cutrone J, Huang S, Shu YZ, Vyas D, Fairchild C, Menendez A, Krampitz K, Dalterio R, Klohr SE, Gao Q (December 2002). "Stephacidin A and B: two structurally novel, selective inhibitors of the testosterone-dependent prostate LNCaP cells". Journal of the American Chemical Society. 124 (49): 14556–14557. doi:10.1021/ja028538n. PMID 12465964.
Borthwick AD (2012). "2,5-Diketopiperazines: Synthesis, Reactions, Medicinal Chemistry, and Bioactive Natural Products". Chemical Reviews. 112 (7): 3641–3716. doi:10.1021/cr200398y. PMID 22575049.
von Nussbaum F (2003). "Stephacidin B-A new stage of complexity within prenylated indole alkaloids from fungi". Angewandte Chemie International Edition. 42 (27): 3068–3071. doi:10.1002/anie.200301646. PMID 12866092.
Wulff JE, Herzon SB, Siegrist R, Myers AG (April 2007). "Evidence for the rapid conversion of stephacidin B into the electrophilic monomer avrainvillamide in cell culture". Journal of the American Chemical Society. 129 (16): 4898–4899. doi:10.1021/ja0690971. PMC 3175819. PMID 17397160.
Sugie Y, Hirai H, Inagaki T, Ishiguro M, Kim YJ, Kojima Y, Sakakibara T, Sakemi S, Sugiura A, Suzuki Y, Brennan L (2001). "A new antibiotic CJ-17,665 from Aspergillus ochraceus". The Journal of Antibiotics. 54 (11): 911–916. doi:10.7164/antibiotics.54.911. PMID 11827033.
Baran PS, Hafensteiner BD, Ambhaikar NB, Guerrero CA, Gallagher JD (July 2006). "Enantioselective total synthesis of avrainvillamide and the stephacidins". Journal of the American Chemical Society. 128 (26): 8678–8693. doi:10.1021/ja061660s. PMID 16802835.
Escolano C (December 2005). "Stephacidin B, the avrainvillamide dimer: A formidable synthetic challenge". Angewandte Chemie International Edition. 44 (47): 7670–7673. doi:10.1002/anie.200502383. PMID 16252300.

ncbi.nlm.nih.gov

Wulff JE, Herzon SB, Siegrist R, Myers AG (April 2007). "Evidence for the rapid conversion of stephacidin B into the electrophilic monomer avrainvillamide in cell culture". Journal of the American Chemical Society. 129 (16): 4898–4899. doi:10.1021/ja0690971. PMC 3175819. PMID 17397160.