Phenolic compounds from the branches of eucalyptus maideni

Chemistry and Biodiversity

Volumn 9, Issue 1, 2012, Pages 123-130

  Tian, Li Wen ^a,b   Xu, Min ^a   Li, Yan ^a   Li, Xing Yao ^a,b   Wang, Dong ^a   Zhu, Hong Tao ^a   Yang, Chong Ren ^a,c   Zhang, Ying Jun ^a  

^a KUNMING INSTITUTE OF BOTANY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c Weihe Biotech Research and Development Center   (China)

Author keywords

Cytotoxic activity; Eucalmaidin F; Eucalyptus maideni; Phenolic compounds

Indexed keywords

3 (4 HYDROXYPHENYL)PROP 2 ENOIC ACID; 3 HYDROXY 1 (4 HYDROXYPHENYL)PROPAN 1 ONE; 3,4,5 TRIHYDROXYPHENOL; 5 GUAIACYL 3 HYDROXYPENTANOIC ACID; 8 BETA C GLUCOPYRANOSYL 5,7 DIHYDROXY 2 ISOBUTYLCHROMONE; AROMADENDRIN; CAFFEIC ACID; CISPLATIN; EUCALMAIDIN F; FLAVONOID; GALLIC ACID; GARCIMANGOSONE; GLUCOSIDE; GLYCEROL DERIVATIVE; LIGNAN DERIVATIVE; LYORESINOL 3ALPHA O ALPHA LEVO RHAMNOPYRANOSIDE; MACROCAPAL A; MACROCAPAL G; OLEUROPEIC ACID; PHENOL DERIVATIVE; PHLOROCETOPHENONE 2' GLUCOPYRANOSIDE; PHLOROGLUCINOL DERIVATIVE; PICEATANNOL; RESVERATROL; TACHIASIDE; TAXIFOLIN; TAXIFOLIN 3ALPHA O ALPHA LEVO RHAMNOPYRANOSIDE; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

CANCER CELL CULTURE; CARBON NUCLEAR MAGNETIC RESONANCE; CELL STRAIN HL 60; CONTROLLED STUDY; DEGRADATION; DRUG CYTOTOXICITY; DRUG SCREENING; EUCALYPTUS; EUCALYPTUS MAIDENI; HETERONUCLEAR MULTIPLE BOND CORRELATION; HUMAN; HUMAN CELL; IC 50; MASS SPECTROMETRY; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; REVIEW;

CELL LINE, TUMOR; CELL SURVIVAL; CHROMONES; DRUG SCREENING ASSAYS, ANTITUMOR; EUCALYPTUS; FLAVONES; HUMANS; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY; MOLECULAR CONFORMATION; PHENOLS; PLANT STEMS;

EUCALYPTUS;

EID: 84862920509     PISSN: 16121872     EISSN: 16121880     Source Type: Journal    
DOI: 10.1002/cbdv.201100021     Document Type: Review

References (31)

1. E. L. Ghisalberti, Phytochemistry 1996, 41, 7.
2. W. W. Fu, C. J. Zhao, Y. P. Pei, R. J. Wang, D. Q. Zuo, Y. J. Chen, Guowai Yiyao: Zhiwuyao Fence (Foreign Medical Sciences: World Phytomedicines) 2003, 18, 51.
3. L.-W. Tian, Y.-J. Zhang, Y.-F. Wang, C.-C. Lai, C.-R. Yang, J. Nat. Prod. 2009, 72, 1608.
4. L.-W. Tian, Y.-J. Zhang, C. Qu, Y.-F. Wang, C.-R. Yang, J. Nat. Prod. 2010, 73, 160.
5. M. DellaGreca, A. Fiorentino, P. Monaco, L. Previtera, Synth. Commun. 1998, 28, 3693.
6. K. Ogawa, I. Aoki, Y. Sashida, Phytochemistry 1992, 31, 2897.
7. D. Q. Yu, J. S. Yang, 'Analytical Chemistry Manual', Chemical Industry Press, Beijing, 1999, p. 460 and 899.
8. G. Dad, A. Corbani, P. Manitto, G. Speranza, L. Lunazzi, J. Nat. Prod. 1989, 52, 1327.
9. M. K. Seikel, F. D. Hostettler, G. J. Niemann, Phytochemistry 1971, 10, 2249.
10. H. Fuchino, T. Satoh, N. Tanaka, Chem. Pharm. Bull. 1995, 43, 1937.
11. Y.-L. Huang, C.-C. Chen, Y.-J. Chen, R.-L. Huang, B.-J. Shieh, J. Nat. Prod. 2001, 64, 903.
12. E. Chosson, A. Chaboud, A. J. Chulia, J. Raynaud, Phytochemistry 1998, 47, 87.
13. Y. Lu, L. Y. Foo, Food Chem. 1999, 65, 1.
14. Y. H. Gong, L. S. Ding, 'Carbon Nuclear Magnetic Resonance Analyses', Yunnan Technology Press, Yunnan, 2006, p. 462.
15. G. S. Jayatilake, H. Jayasuriya, E. S. Lee, N. M. Koonchanok, R. L. Geahlen, C. L. Ashendel, J. L. McLaughlin, C.-J. Chang, J. Nat. Prod. 1993, 56, 1805.
16. Y. Kashiwada, G. Nonaka, I. Nishioka, Chem. Pharm. Bull. 1984, 32, 3501.
17. V. S. Parmar, S. Gupta, K. S. Bisht, S. Mukherijee, P. M. Boll, W. Errington, Acta Chem. Scand. 1996, 50, 558.
18. M. Nishizawa, M. Emura, Y. Kan, H. Yamada, K. Ogawa, N. Hamanaka, Tetrahedron Lett. 1992, 33, 2983.
19. T. Miyase, A. Ueno, N. Takizawa, H. Kobayashi, H. Oguchi, Chem. Pharm. Bull. 1987, 35, 3713.
20. H. Ito, M. Koreishi, H. Tokuda, H. Nishino, T. Yoshida, J. Nat. Prod. 2000, 63, 1253.
21. D. Manns, R. Hartmann, Planta Med. 1994, 60, 467.
22. H. Ito, N. Kasajima, H. Tokuda, H. Nishino, T. Yoshida, J. Nat. Prod. 2004, 67, 411.
23. T. Mosmann, J. Immunol. Methods 1983, 65, 55.
24. Q.-M. Guo, X.-W. Yang, Biochem. Syst. Ecol. 2006, 34, 543.
25. W. E. Hillis, A. Carle, Aust. J. Chem. 1963, 16, 147.
26. A. Eyles, N. W. Davies, C. Mohammed, J. Chem. Ecol. 2003, 29, 881.
27. M. Takasaki, T. Konoshima, K. Fujitani, S. Yoshida, H. Nishimura, H. Tokuda, H. Nishino, A. Iwashima, M. Kozuka, Chem. Pharm. Bull. 1990, 38, 2737.
28. M. Takasaki, T. Konoshima, M. Kozuka, H. Tokuda, Biol. Pharm. Bull. 1995, 18, 435.
29. M. Takasaki, T. Konoshima, H. Etoh, I. P. Singh, H. Tokuda, H. Nishino, Cancer Lett. 2000, 155, 61.
30. F. C. Buzzi, C. L. Franzoi, G. Antonini, M. Fracasso, V. Cechinel Filho, R. A. Yunes, R. Niero, Eur. J. Med. Chem. 2009, 44, 4596.
31. I. Ohtani, T. Kusumi, Y. Kashman, H. Kakisawa, J. Am. Chem. Soc. 1991, 113, 4092.