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A Novel Cytotoxic Alkaloid of Lamellarin Class from a Marine Ascidian Didemnum sp.

  • Ham, Jung-Yeob (Marine Biotechnology Laboratory and Research Institute of Oceanography, School of Earth and Environmental Sciences, Seoul National University) ;
  • Kang, Heon-Joong (Marine Biotechnology Laboratory and Research Institute of Oceanography, School of Earth and Environmental Sciences, Seoul National University)
  • 발행 : 2002.01.20

초록

키워드

참고문헌

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피인용 문헌

  1. Bioactive Nitrogenous Metabolites from Ascidians vol.74, pp.1, 2007, https://doi.org/10.3987/REV-07-SR(W)2
  2. Anticancer Alkaloid Lamellarins Inhibit Protein Kinases vol.6, pp.4, 2008, https://doi.org/10.3390/md20080026
  3. ChemInform Abstract: A Novel Cytotoxic Alkaloid of Lamellarin Class from a Marine Ascidian Didemnum sp. vol.33, pp.28, 2010, https://doi.org/10.1002/chin.200228265
  4. Trifluoroacetic acid-promoted Michael addition–cyclization reactions of vinylogous carbamates vol.12, pp.21, 2014, https://doi.org/10.1039/C4OB00437J
  5. Modular Synthesis of Lamellarins via Regioselective Assembly of 3,4,5-Differentially Arylated Pyrrole-2-carboxylates vol.79, pp.2, 2014, https://doi.org/10.1021/jo402181w
  6. Facile and Divergent Synthesis of Lamellarins and Lactam-Containing Derivatives with Improved Drug Likeness and Biological Activities vol.10, pp.12, 2015, https://doi.org/10.1002/asia.201500611
  7. Designing New Analogs for Streamlining the Structure of Cytotoxic Lamellarin Natural Products vol.10, pp.4, 2015, https://doi.org/10.1002/asia.201403361
  8. Synthetic Approaches to the Lamellarins—A Comprehensive Review vol.12, pp.12, 2014, https://doi.org/10.3390/md12126142
  9. Cytotoxicities and Structure-Activity Relationships of Natural and Unnatural Lamellarins toward Cancer Cell Lines vol.4, pp.3, 2009, https://doi.org/10.1002/cmdc.200800339
  10. Further developments in the synthesis of lamellarin alkaloids via direct metal–halogen exchange vol.44, pp.7, 2002, https://doi.org/10.1016/s0040-4039(02)02887-3
  11. Antileukemic effects of Didemnum psammatodes (Tunicata: Ascidiacea) constituents vol.151, pp.3, 2002, https://doi.org/10.1016/j.cbpa.2007.02.011
  12. Design and Synthesis of Lamellarin D Analogues Targeting Topoisomerase I vol.74, pp.21, 2002, https://doi.org/10.1021/jo901589e
  13. Assessing the drug-likeness of lamellarins, a marine-derived natural product class with diverse oncological activities vol.45, pp.6, 2002, https://doi.org/10.1016/j.ejmech.2010.01.053
  14. A simple synthesis of the lamellarin analogues from 3-nitro-2-trifluoromethyl-2H-chromenes and 1-benzyl-3,4-dihydroisoquinolines vol.20, pp.6, 2002, https://doi.org/10.1016/j.mencom.2010.11.006
  15. Synthesis and Biological Activity of Lamellarin Alkaloids: An Overview vol.83, pp.3, 2002, https://doi.org/10.3987/rev-10-686
  16. Exploring the molecular basis for selective cytotoxicity of lamellarins against human hormone-dependent T47D and hormone-independent MDA-MB-231 breast cancer cells vol.142, pp.1, 2002, https://doi.org/10.1007/s00706-010-0409-y
  17. Rotational Energy Barrier around the C1-C11 Single Bond in Lamellarins: A Study by Variable-Temperature NMR vol.88, pp.2, 2002, https://doi.org/10.3987/com-13-s(s)69
  18. A Novel Bromoindole Alkaloid from a Korean Colonial Tunicate Didemnum sp. vol.21, pp.4, 2015, https://doi.org/10.20307/nps.2015.21.4.278
  19. A Synthesis of Lamellarins via Regioselective Assembly of 1,2,3-Differentially Substituted 5,6-Dihydropyrrolo[2,1-a]Isoquinoline Core vol.91, pp.4, 2015, https://doi.org/10.3987/com-15-13188
  20. Active methylenes in the synthesis of a pyrrole motif: an imperative structural unit of pharmaceuticals, natural products and optoelectronic materials vol.6, pp.43, 2002, https://doi.org/10.1039/c6ra03411j
  21. Synthesis of Lamellarin G Trimethyl Ether by von Miller–Plöchl‐Type Cyclocondensation vol.2018, pp.30, 2002, https://doi.org/10.1002/ejoc.201800611
  22. Secondary Metabolites of the Genus Didemnum : A Comprehensive Review of Chemical Diversity and Pharmacological Properties vol.18, pp.6, 2020, https://doi.org/10.3390/md18060307
  23. Recent Advances in the Synthesis of Pyrroles vol.24, pp.11, 2002, https://doi.org/10.2174/1385272824999200528125651
  24. Synthesis of lamellarin R, lukianol A, lamellarin O and their analogues vol.10, pp.70, 2002, https://doi.org/10.1039/d0ra09249e
  25. [3 + 2]-Annulation of pyridinium ylides with 1-chloro-2-nitrostyrenes unveils a tubulin polymerization inhibitor vol.19, pp.33, 2002, https://doi.org/10.1039/d1ob01141c
  26. Pyrrole‐Fused Benzoxazinones/Quinoxalinones: Molecular Dynamic Simulation, Antiproliferative and Antibacterial Activities vol.6, pp.40, 2002, https://doi.org/10.1002/slct.202103015