Phenolic compounds from Nicotiana tabacum and their biological activities

Journal of Asian Natural Products Research

Volumn 14, Issue 5, 2012, Pages 450-456

  Chen, Yong Kuan ^a   Li, Xue Sen ^a,b   Yang, Guang Yu ^a   Chen, Zhang Yu ^a   Hu, Qiu Fen ^b   Miao, Ming Ming ^a  

^a YUNNAN ACADEMY OF TOBACCO SCIENCE   (China)

^b YUNNAN MINZU UNIVERSITY   (China)

Author keywords

anti HIV 1 activities; cytotoxicities; Nicotiana tabacum; nicotphenols A C; phenolic compounds

Indexed keywords

1 HYDROXY 1,3,5 BISABOLATRIEN 10 ONE; 4 O CAFFEOYLQUINIC ACID; 5 O CAFFEOYLQUINIC ACID; CAFFEIC ACID; CHLOROGENIC ACID; ESCULETIN; FERULIC ACID; NICOTIFLORIN; NICOTPHENOL A; NICOTPHENOL B; NICOTPHENOL C; PARA COUMARIC ACID; PHENOL DERIVATIVE; QUERCETIN; RUTOSIDE; SCOPOLETIN; SCOPOLINE; UNCLASSIFIED DRUG; VANILLIC ACID;

ANTIVIRAL ACTIVITY; ARTICLE; BIOLOGICAL ACTIVITY; CYTOTOXICITY; DRUG STRUCTURE; HUMAN IMMUNODEFICIENCY VIRUS 1; NONHUMAN; TOBACCO;

ANTI-HIV AGENTS; DRUGS, CHINESE HERBAL; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PHENOLS; PLANT LEAVES; TOBACCO;

HUMAN IMMUNODEFICIENCY VIRUS 1; NICOTIANA TABACUM;

EID: 84860518215     PISSN: 10286020     EISSN: 14772213     Source Type: Journal    
DOI: 10.1080/10286020.2012.669578     Document Type: Article

References (20)

1. The Editorial Committee of the Administration Bureau of Flora of China. 2005. Flora of China, Vol. 67, 153 Beijing: Beijing Science and Technology Press.
2. Cavender, A.P., and, Alban, M. 2009. J. Ethnobiol. Ethnomed., 5: 3
3. Feng, X., Wang, J.S., Luo, J., and, Kong, L.Y. 2010. J. Asian Nat. Prod. Res., 12: 252
4. Shinozaki, Y., Tobita, T., Mizutani, M., and, Matsuzaki, T. 1996. Biosci. Biotech. Biochem., 60: 903
5. Petterson, T., Eklund, A.M., and, Wahlberg, I. 1993. J. Agric. Food. Chem., 41: 2097
6. Wei, X.C., Sumithran, S.C., Deaciuc, A.G., Burton, H.R., Bush, L.P., Dwoskin, L.P., and, Crooks, P.A. 2005. Life Sci., 78: 495
7. Vereecke, D., Messens, E., Klarskov, K., Bruyn, A., Montagu, M., and, Goethals, K. 1997. Planta, 201: 342
8. Lu, Y.R., and, Yeap, F.L. 2002. Phytochemistry, 59: 117
9. Yu, D.Q., and, Yang, J.S. 1999. Handbook of Analytical Chemistry (7th volume), Nuclear Magnetic Resonance spectroscopy, 2nd ed., 449-457. Beijing: Chemical Industry Press.
10. Lee, C.K., and, Cheng, Y.S. 2001. J. Chin. Chem. Soc., 48: 1077
11. Fukagawa, N., and, Ishizu, A. 1991. J. Wood Chem. Tech., 11: 263
12. Yoshikawa, M., Morikawa, T., Xu, F., Ando, S., and, Matsuda, H. 2003. Heterocycles, 60: 1787
13. Cavalcante, S.H., Yoshida, M., and, Gottlieb, O.R. 1985. Phytochemistry, 24: 1051
14. Matsuda, N., and, Kikuchi, M. 1996. Chem. Pharm. Bull., 44: 1676
15. Zhang, X.J., Yang, G.Y., Wang, R.R., Pu, J.X., Sun, H.D., Xiao, W.L., and, Zheng, Y.T. 2010. Chem. Biodiv., 7: 2692
16. Pu, J.X., Yang, L.M., Xiao, W.L., Li, R.T., Lei, C., Gao, X.M., Huang, S.X., and, Sun, H.D. 2008. Phytochemistry, 69: 1266
17. Wang, J.H., Tam, S.C., Huang, H., Yang, D.Y., Wang, Y.Y., and, Zheng, Y.T. 2004. Biochem. Biophys. Res. Commun., 317: 965
18. Hahm, J.C., Lee, I.K., Kang, W.K., Kim, S.U., and, Ahn, Y.J. 2005. Planta Med., 71: 464
19. Amblard, F., Govindarajan, B., Lefkove, B., Rapp, K.L., Detorio, M., Arbiser, J.L., and, Schinazi, R.F. 2007. Bioorg. Med. Chem. Lett., 17: 4428
20. Mosmann, T. 1983. J. Immunol. Methods, 65: 55