Expedient synthesis and structure-activity relationships of phenanthroindolizidine and phenanthroquinolizidine alkaloids

Organic and Biomolecular Chemistry

Volumn 4, Issue 5, 2006, Pages 860-867

  Chuang, Ta Hsien ^a   Lee, Shiow Ju ^b   Yang, Cheng Wei ^b   Wu, Pei Lin ^a,c  

^a NATIONAL CHENG KUNG UNIVERSITY   (Taiwan)

^b NATIONAL HEALTH RESEARCH INSTITUTES   (Taiwan)

^c CHUNG HWA UNIVERSITY OF MEDICAL TECHNOLOGY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDES; CELLS; DISEASES;

CELL LINES; PHENANTHROQUINOLIZIDINE; POTENT INHIBITION;

ALKALI METAL ALLOYS;

ALKALOID; ANTINEOPLASTIC AGENT; INDOLIZINE DERIVATIVE; PHENANTHRENE DERIVATIVE; PHENANTHROINDOLIZIDINE; PHENANTHROLINE DERIVATIVE; PHENANTHROQUINOLIZIDINE; QUINOLIZINE DERIVATIVE; TYLOPHORINE;

ARTICLE; BIOCHEMISTRY; CHEMISTRY; DRUG SCREENING; HUMAN; METHODOLOGY; STRUCTURE ACTIVITY RELATION; SYNTHESIS; TUMOR CELL LINE;

ALKALOIDS; ANTINEOPLASTIC AGENTS; BIOCHEMISTRY; CELL LINE, TUMOR; DRUG SCREENING ASSAYS, ANTITUMOR; HUMANS; INDOLIZINES; PHENANTHRENES; PHENANTHROLINES; QUINOLIZINES; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 33644524990     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b516152e     Document Type: Article

References (34)

1. A. N. Ratnagiriswaran K. Venkatachalam Indian J. Med. Res. 22 433 441
2. G. R. Donaldson M. R. Atkinson A. W. Murray Biochem. Biophys. Res. Commun. 31 104 109
3. R. S. Gupta L. Siminovitch Biochemistry 16 3209 3214
4. T. R. Govindachari N. Viswanathan Heterocycles 11 587 613
5. K. N. Rao R. K. Bhattacharya S. R. Venkatachalam Cancer Lett. 128 183 188
6. E. Gellert R. Rudzats J. Med. Chem. 7 361 362
7. G. R. Pettit A. Goswami G. M. Cragg J. M. Schmidt J. C. Zou J. Nat. Prod. 47 913 919
8. F. Abe M. Hirokawa T. Yamauchi K. Honda N. Hayashi M. Ishii S. Imagawa M. Iwahana Chem. Pharm. Bull. 46 767 769
9. D. Stærk J. Christensen E. Lemmich J. Ø. Duus C. E. Olsen J. W. Jaroszewski J. Nat. Prod. 63 1584 1586
10. K. K. Bhutani G. L. Sharma M. Ali Planta Med. 53 532 536
11. B. Baumgartner C. A. J. Erdelmeier A. D. Wright T. Rali O. Sticher Phytochemistry 29 3327 3330
12. P. L. Wu K. V. Rao C. H. Su C. S. Kuoh T. S. Wu Heterocycles 57 2401 2408
13. A. G. Damu P. C. Kuo L. S. Shi C. Y. Li C. S. Kuoh P. L. Wu T. S. Wu J. Nat. Prod. 68 1071 1075
14. V. K. Mangla D. S. Bhakuni Tetrahedron 36 2489 2490
15. J. E. Cragg R. B. Herbert F. B. Jackson C. J. Moody I. T. Nicoison J. Chem. Soc., Perkin Trans. 1 2477 2485
16. H. Lida M. Tanaka C. Kibayashi J. Chem. Soc., Chem. Commun. 271 272
17. B. Chauncy E. Gellert Aust. J. Chem. 23 2503 2516
18. S. M. Weinreb N. A. Khatri J. Am. Chem. Soc. 101 5073 5074
19. A. J. Liepa R. E. Summons J. Chem. Soc., Chem. Commun. 826 827
20. M. Ihara M. Tsuruta K. Fukumoto T. Kametani J. Chem. Soc., Chem. Commun. 1159 1161
21. W. H. Pearson R. Walavalkar Tetrahedron 50 12293 12304
22. Y. M. Osornio L. D. Miranda R. Cruz-Almanza J. M. Muchowski Tetrahedron Lett. 45 2855 2858
23. A. L. J. Beckwith C. H. Schiesser Tetrahedron 41 3925 3941
24. T. R. Govindachari N. Viswanathan J. Radhakrishnan R. Charubala N. N. Rao B. R. Pai Indian J. Chem. 11 1215 1216
25. K. V. Rao L. S. Kapicak J. Heterocycl. Chem. 13 1073 1077
26. P. L. Wu T. H. Chuang Y. Chou J. Org. Chem. 66 6585 6594
27. S. Ono M. Uehara Bull. Univ. Osaka Prefect., Ser. A 6 167 171
28. D. M. Jorina J. R. L. Smith J. Chem. Soc., Perkin Trans. 1 1702 1706
29. T. F. Buckley H. Rapoport J. Org. Chem. 48 4222 4232
30. P. L. Wu C. H. Su Y. J. Gu J. Chin. Chem. Soc. 47 271 274
31. H. Iida Y. Watanabe M. Tanaka C. Kibayashi J. Org. Chem. 49 2412 2418
32. D. O. Shah K. N. Trivedi Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 15 599 602
33. E. Gellert T. R. Govindachari M. V. Lakshmikantham I. S. Ragade R. Rudzats N. Viswanathan J. Chem. Soc. 1008 1014
34. J. P. Liou Y. L. Chang F. M. Kuo C. W. Chang H. Y. Tseng C. C. Wang Y. N. Yang J. Y. Chang S. J. Lee H. P. Hsieh J. Med. Chem. 47 4247 4257