Carbazole alkaloids from the peels of Clausena lansium

Journal of Asian Natural Products Research

Volumn 16, Issue 10, 2014, Pages 1024-1028

  Deng, Hui Dong ^a,b   Mei, Wen Li ^a   Wang, Hui ^a   Guo, Zhi Kai ^a   Dong, Wen Hua ^a   Wang, Hao ^a   Li, Shao Peng ^b   Dai, Hao Fu ^a  

^a INSTITUTE OF TROPICAL BIOSCIENCE AND BIOTECHNOLOGY   (China)

^b HAINAN UNIVERSITY   (China)

Author keywords

antibacterial activity; carbazole alkaloids; Clausena lansium; Rutaceae; glucosidase inhibitory activity

Indexed keywords

ALKALOID DERIVATIVE; ALPHA GLUCOSIDASE INHIBITOR; ANTIINFECTIVE AGENT; CARBAZOLE 3 CARBOXYLIC ACID; CARBAZOLE DERIVATIVE; CLAULANSINE J; CLAULANSINE K; METHYL 8 HYDROXYCARBAZOLE 3 CARBOXYLATE; METHYL CARBAZOLE 3 CARBOXYLATE; MUKONAL; O DEMETHYLMURRAYANINE; UNCLASSIFIED DRUG; ALKALOID; GLYCOSIDASE INHIBITOR; HERBACEOUS AGENT;

ANTIBACTERIAL ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CLAUSENA; CLAUSENA LANSIUM; DRUG ISOLATION; DRUG STRUCTURE; DRUG SYNTHESIS; HETERONUCLEAR MULTIPLE BOND CORRELATION; HETERONUCLEAR MULTIPLE QUANTUM COHERENCE; IC50; IN VITRO STUDY; NONHUMAN; STAPHYLOCOCCUS AUREUS; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECTS; ISOLATION AND PURIFICATION; MICROBIAL SENSITIVITY TEST; NUCLEAR MAGNETIC RESONANCE; PLANT STEM;

ALKALOIDS; ANTI-BACTERIAL AGENTS; CARBAZOLES; CLAUSENA; DRUGS, CHINESE HERBAL; GLYCOSIDE HYDROLASE INHIBITORS; INHIBITORY CONCENTRATION 50; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PLANT STEMS; STAPHYLOCOCCUS AUREUS;

EID: 84911991820     PISSN: 10286020     EISSN: 14772213     Source Type: Journal    
DOI: 10.1080/10286020.2014.930442     Document Type: Article

References (24)

1. T.K. Lim, Edible Med. Non-Med. Plants 4, 871 (2012).
2. K.N. Prasad, H.H. Xie, J. Hao, B. Yang, S.X. Qiu, X.Y. Wei, F. Chen, and Y.M. Jiang, Food Chem. 118, 62 (2010).
3. W.S. Li, J.D. Mcchesney, and F.S. Elferaly, Phytochemistry 30, 343 (1991).
4. V. Kumar, K. Vallipuram, A.C. Adebajo, and J. Reisch, Phytochemistry 40, 1563 (1995).
5. W. Maneerat, T. Ritthiwigrom, S. Cheenpracha, and S. Laphookhieo, Phytochem. Lett. 5, 26 (2012).
6. H. Liu, C.J. Li, J.Z. Yang, N. Ning, Y.K. Si, N.H. Chen, Q. Zhao, and D.M. Zhang, J. Nat. Prod. 75, 677 (2012).
7. C. Ito, S. Katsuno, and H. Furukawa, Chem. Pharm. Bull. 46, 341 (1998).
8. W. Maneerat, U. Prawat, N. Saewan, and S. Laphookhieo, Brazil J. Chem. Soc. 21, 665 (2010).
9. D.Y. Shen, C.H. Chao, H.H. Chan, G.J. Huang, and T.L. Hwang, Phytochemistry 82, 110 (2012).
10. M.H. Yang, Y.Y. Chen, and L. Huang, Phytochemistry 27, 445 (1988).
11. V. Lakshmi, K. Raj, and R.S. Kapil, Phytochemistry 28, 943 (1989).
12. J.H. Lin, Phytochemistry 28, 621 (1989).
13. G.C. Wang, W. Li, Y. Wang, X.Q. Zhang, Y.L. Li, and W.C. Ye, Nat. Prod. Res. 27, 558 (2013).
14. Y. Han, L.C. Li, W.B. Hao, M. Tang, and S.Q. Zhang, Parasitol. Res. 112, 511 (2013).
15. A.C. Adebajo, E.O. Iwalewa, E.M. Obuotor, G.F. Ibikunle, N.O. Omisore, C.O. Adewunmi, O.O. Obaparusi, M. Klaes, G.E. Adetogun, T.J. Schmidt, and E.J. Verspohl, J. Ethnopharmacol. 122, 10 (2009).
16. Y.S. Wang, H.P. He, Y.M. Shen, X. Hong, and X.J. Hao, J. Nat. Prod. 66, 416 (2003).
17. H. Liu, C.J. Li, J.Z. Yang, N. Ning, Y.K. Si, N.H. Chen, Q. Zhao, and D.M. Zhang, J. Nat. Prod. 75, 680 (2012).
18. S. Desikachcri and P.K.J. Rajendra, Hetercycles 24, 711 (1986).
19. W.S. Li, J.D. Mcchesney, and F.S. Elferaly, Phytochemistry 30, 344 (1991).
20. B.T. Ngadjui, J.F. Ayafor, B.L. Sondengam, and J.D. Connolly, Phytochemistry 28, 1519 (1989).
21. P. Bhattacharyya and A. Chakraborty, Phytochemistry 23, 471 (1984).
22. A.N. Jong, M.R. Bhandari, and J. Kawabata, Food Chem. 103, 1319 (2007).
23. S.Y. Xu, R.L. Bian, and X. Chen, Methods of Pharmacology Experiment (People's Sanitation Press, Beijing, 2003), p. 1651.
24. S.S. Li, L.F. Hu, Y.X. Zhao, W.J. Zuo, Y. B. Zeng, X.N. Li, W.L. Mei, and H.F. Dai, Asian J. Nat. Prod. Res. 13, 964 (2011).