Arglabin (English Wikipedia)

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

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doi.org

  • Csuk, René; Heinold, Anke; Siewert, Bianka; Schwarz, Stefan; Barthel, Alexander; Kluge, Ralph; Ströhl, Dieter (2012). "Synthesis and Biological Evaluation of Antitumor-Active Arglabin Derivatives". Archiv der Pharmazie. 345 (8): 215–222. doi:10.1002/ardp.201100065. PMID 21997763. S2CID 20190855.
  • Adekenov, S.M.; Mukhametzhanov, M.N.; Kagarlitskii, A.D.; Kupriyanov, A.N. (1982). "Arglabin - a new sesquiterpene lactone from Artemisia glabella". Chemistry of Natural Compounds. 18 (5): 623–624. doi:10.1007/BF00575063. S2CID 41159002.
  • Lone, Shabir H.; Bhat, Khursheed A.; Khuroo, Mohd A. (2015). "Arglabin: From isolation to antitumor evaluation". Chemico-Biological Interactions. 240 (5): 180–198. doi:10.1016/j.cbi.2015.08.015. PMID 26327249.
  • Zhai, Jia-Dai; Li, Dongmei; Long, Jing; Zhang, Hao-Liang; Lin, Jian-Ping; Qiu, Chuan-Jiang; Zhang, Quan; Chen, Yue (2012). "Biomimetic Semisynthesis of Arglabin from Parthenolide". The Journal of Organic Chemistry. 77 (16): 7103–7107. doi:10.1021/jo300888s. PMID 22849854.
  • Schall, Andreas; Reiser, Oliver (2008). "Synthesis of Biologically Active Guaianolides with trans-Annulated Lactone Moiety". European Journal of Organic Chemistry. 2008 (14): 2353–2364. doi:10.1002/ejoc.200700880.
  • Zhangabylov, N.S.; Dederer, L. Yu.; Gorbacheva, L.B.; Vasil'eva, S.V.; Terekhov, A.S.; Adekenov, S.M. (2004). "Sesquiterpene Lactone Arglabin Influences DNA Synthesis in P388 Leukemia Cells in vivo". Pharmaceutical Chemistry Journal. 38 (12): 651–653. doi:10.1007/s11094-005-0052-9. S2CID 7388281.
  • Zhang, Quan; Lu, Yaxin; Ding, Yahui; Zhai, Jiadai; Ji, Qing; Ma, Weiwei; Yang, Ming; Fan, Hongxia; Long, Jing (2012). "Guaianolide Sesquiterpene Lactones, a Source To Discover Agents That Selectively Inhibit Acute Myelogenous Leukemia Stem and Progenitor Cells". Journal of Medicinal Chemistry. 55 (20): 8757–8769. doi:10.1021/jm301064b. ISSN 0022-2623. PMID 22985027.
  • Abderrazak, Amna; Couchie, Dominique; Mahmood, Dler Faieeq Darweesh; Elhage, Rima; Vindis, Cécile; Laffargue, Muriel; Matéo, Véronique; Büchele, Berthold; Ayala, Monica Rubio (2015). "Anti-inflammatory and antiatherogenic effects of the NLRP3 inflammasome inhibitor arglabin in ApoE2.Ki mice fed a high-fat diet". Circulation. 131 (12): 1061–1070. doi:10.1161/CIRCULATIONAHA.114.013730. ISSN 1524-4539. PMID 25613820.
  • Ivanescu, Bianca; Miron, Anca; Corciova, Andreia (2015). "Sesquiterpene Lactones from Artemisia Genus: Biological Activities and Methods of Analysis". Journal of Analytical Methods in Chemistry. 2015: 247685. doi:10.1155/2015/247685. ISSN 2090-8865. PMC 4606394. PMID 26495156.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Csuk, René; Heinold, Anke; Siewert, Bianka; Schwarz, Stefan; Barthel, Alexander; Kluge, Ralph; Ströhl, Dieter (2012). "Synthesis and Biological Evaluation of Antitumor-Active Arglabin Derivatives". Archiv der Pharmazie. 345 (8): 215–222. doi:10.1002/ardp.201100065. PMID 21997763. S2CID 20190855.
  • Lone, Shabir H.; Bhat, Khursheed A.; Khuroo, Mohd A. (2015). "Arglabin: From isolation to antitumor evaluation". Chemico-Biological Interactions. 240 (5): 180–198. doi:10.1016/j.cbi.2015.08.015. PMID 26327249.
  • Zhai, Jia-Dai; Li, Dongmei; Long, Jing; Zhang, Hao-Liang; Lin, Jian-Ping; Qiu, Chuan-Jiang; Zhang, Quan; Chen, Yue (2012). "Biomimetic Semisynthesis of Arglabin from Parthenolide". The Journal of Organic Chemistry. 77 (16): 7103–7107. doi:10.1021/jo300888s. PMID 22849854.
  • Zhang, Quan; Lu, Yaxin; Ding, Yahui; Zhai, Jiadai; Ji, Qing; Ma, Weiwei; Yang, Ming; Fan, Hongxia; Long, Jing (2012). "Guaianolide Sesquiterpene Lactones, a Source To Discover Agents That Selectively Inhibit Acute Myelogenous Leukemia Stem and Progenitor Cells". Journal of Medicinal Chemistry. 55 (20): 8757–8769. doi:10.1021/jm301064b. ISSN 0022-2623. PMID 22985027.
  • Abderrazak, Amna; Couchie, Dominique; Mahmood, Dler Faieeq Darweesh; Elhage, Rima; Vindis, Cécile; Laffargue, Muriel; Matéo, Véronique; Büchele, Berthold; Ayala, Monica Rubio (2015). "Anti-inflammatory and antiatherogenic effects of the NLRP3 inflammasome inhibitor arglabin in ApoE2.Ki mice fed a high-fat diet". Circulation. 131 (12): 1061–1070. doi:10.1161/CIRCULATIONAHA.114.013730. ISSN 1524-4539. PMID 25613820.
  • Ivanescu, Bianca; Miron, Anca; Corciova, Andreia (2015). "Sesquiterpene Lactones from Artemisia Genus: Biological Activities and Methods of Analysis". Journal of Analytical Methods in Chemistry. 2015: 247685. doi:10.1155/2015/247685. ISSN 2090-8865. PMC 4606394. PMID 26495156.

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

  • Csuk, René; Heinold, Anke; Siewert, Bianka; Schwarz, Stefan; Barthel, Alexander; Kluge, Ralph; Ströhl, Dieter (2012). "Synthesis and Biological Evaluation of Antitumor-Active Arglabin Derivatives". Archiv der Pharmazie. 345 (8): 215–222. doi:10.1002/ardp.201100065. PMID 21997763. S2CID 20190855.
  • Adekenov, S.M.; Mukhametzhanov, M.N.; Kagarlitskii, A.D.; Kupriyanov, A.N. (1982). "Arglabin - a new sesquiterpene lactone from Artemisia glabella". Chemistry of Natural Compounds. 18 (5): 623–624. doi:10.1007/BF00575063. S2CID 41159002.
  • Zhangabylov, N.S.; Dederer, L. Yu.; Gorbacheva, L.B.; Vasil'eva, S.V.; Terekhov, A.S.; Adekenov, S.M. (2004). "Sesquiterpene Lactone Arglabin Influences DNA Synthesis in P388 Leukemia Cells in vivo". Pharmaceutical Chemistry Journal. 38 (12): 651–653. doi:10.1007/s11094-005-0052-9. S2CID 7388281.

worldcat.org

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