Chemopreventive flavonoids from Millettia pulchra Kurz var-laxior (Dunn) Z.Wei (Yulangsan) function as Michael reaction acceptors

Bioorganic and Medicinal Chemistry Letters

Volumn 25, Issue 5, 2015, Pages 1078-1081

  Wang, Wenli ^a   Wang, Jian ^a   Li, Ning ^a   Zhang, Xiangrong ^a   Zhao, Weihong ^a   Li, Jiayuan ^a   Si, Yingying ^a  

^a SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

Author keywords

(Dunn) Z.Wei; Cancer chemoprevention; Flavonoids; Millettia pulchra Kurz var laxior; Molecular docking; NQO1; Yulangsan

Indexed keywords

ANTINEOPLASTIC AGENT; CHALCONE; FLAVANONE; FLAVONOID; ISOFLAVAN DERIVATIVE; NQO1 PROTEIN, HUMAN; NQO1 PROTEIN, MOUSE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE (PHOSPHATE) DEHYDROGENASE (QUINONE);

ANTINEOPLASTIC ACTIVITY; ARTICLE; CHEMOPROPHYLAXIS; COLUMN CHROMATOGRAPHY; CONTROLLED STUDY; DRUG IDENTIFICATION; DRUG STRUCTURE; ELECTROPHILICITY; ENZYME ACTIVITY; ENZYME INHIBITION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN CELL; HYDROGEN BOND; HYDROPHOBICITY; IN VITRO STUDY; MICHAEL ADDITION; MILLETTIA; MILLETTIA PULCHRA; MOLECULAR DOCKING; PLANT ROOT; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ULTRA PERFORMANCE LIQUID CHROMATOGRAPHY; ANIMAL; CHEMISTRY; DRUG EFFECTS; ENZYME ACTIVATION; ISOLATION AND PURIFICATION; METABOLISM; MOUSE; TUMOR CELL LINE;

MILLETTIA PULCHRA;

ANIMALS; ANTICARCINOGENIC AGENTS; CELL LINE, TUMOR; ENZYME ACTIVATION; FLAVONOIDS; HUMANS; MICE; MILLETTIA; MOLECULAR DOCKING SIMULATION; NAD(P)H DEHYDROGENASE (QUINONE);

EID: 84922759380     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2015.01.009     Document Type: Article

References (37)

1. J.K. Gary, T.H. Ernest, and C.S. Caroline Cancer chemoprevention Strategies for cancer chemoprevention Vol. 2 2005 Totowa Humana press New Jersey 22
2. X.L. Tan, M. Shi, H. Tang, W.G. Han, and S.D. Spivack J. Nutr. 140 2010 1404
3. W.K. Hong, and M.B. Sporn Science 278 1997 1073
4. P. Talalay Biofactors 12 2000 5
5. A.T. Dinkova-Kostova, and P. Talalay Free Radical Biol. Med. 29 2000 231
6. P. Nioi, and J.D. Hayes Mutat. Res. 555 2004 149
7. M. Cuendet, C.P. Otehan, R.C. Moon, and J.M. Pezzuto J. Nat. Prod. 69 2006 460
8. C.W. Boone, V.E. Steele, and G.J. Kelloff Mutat. Res. 267 1992 251
9. L.L. Song, J.W. Kosmeder, S.K. Lee, C. Gerhauser, D. Lantvit, and R.C. Moon Cancer Res. 59 1999 578
10. C.J. Henderson, A.G. Smith, J. Ure, K. Brown, E.J. Bacon, and C.R. Wolf Proc. Natl. Acad. Sci. U.S.A. 95 1998 5275
11. D.J. Long II, R.L. Waikel, X.J. Wang, D.R. Roop, and A.K. Jaiswal J. Natl. Cancer. Inst. 93 2001 1166
12. D.J. Long II, A. Gaikwad, A. Multani, S. Pathak, C.A. Montgomery, F.J. Gonzalez, and A.K. Jaiswal Cancer Res. 62 2002 3030
13. K.J. Ritchie, C.J. Henderson, X.J. Wang, O. Vassieva, D. Carrie, P.B. Farmer, M. Gaskell, K. Park, and C.R. Wolf Cancer Res. 67 2007 9248
14. S.L. Hwang, P.H. Shih, and G.C. Yen J. Agric. Food Chem. 60 2012 877
15. M. Iriti, and E.M. Varoni Nutrients 5 2013 2564
16. X.D. Dai, C.E. Qiu, B. Dai, and D.A. Yang Chin. J. Ethnomed. Ethnopharm. 20 9 2009 9
17. Wang, M. Z. Beijing: Chinese Peking Union Medical College; 2007.
18. L. Chen, X.D. Zhang, Y. Jiao, S.J. Fu, and R.B. Huang Chin. J. Exp. Trad. Med. Form 18 2012 254
19. J. Jian, S.J. Zhang, L. Qiu, J.C. Huang, and R.B. Huang Chin. Hosp. Pharm. J. 30 2010 1734
20. R.R. Rao, A.K. Tiwari, P.P. Reddy, K.S. Babu, G. Suresh, A.Z. Ali, K. Madhusudana, S.B. Agawane, P. Badrinarayan, G.N. Sastry, and J.M. Rao Med. Chem. Res. 21 2012 760
21. Y.R. Lee, and D.H. Kim Synthesis 4 2006 603
22. Y.R. Lee, X. Wang, and L.K. Xia Molecules 12 2007 1420
23. A.F. Magalhaes, A.M.G.A. Tozzi, B.H.L.N. Sales, and E.G. Magalhaes Phytochemistry 42 1996 1459
24. L.C. Chang, C. Gerhauser, L. Song, N.R. Farnsworth, J.M. Pezzuto, and A.D. Kinghorn J. Nat. Prod. 60 1997 869
25. E.V. Rao, and N.R. Raju Phytochemistry 18 1979 1581
26. Y.R. Lee Jr., and A.T.M. Morehead Tetrahedron 51 1995 4909
27. T. Tanaka, M. Iinuma, K. Yuki, Y. Fujii, and M. Mizuo Phytochemistry 31 1992 993
28. K. Mei, S.L. Zhang, S.T. He, P. Li, M. Jin, F. Xue, G.S. Luo, H.Y. Zhang, L.R. Song, W.H. Duan, and W. Wang Tetrahedron Lett. 49 2008 2681
29. Cao, L.; Si, J. Y. Faming Zhuanli Shenqing 2012 CN 102462727 A 20120523.
30. S.C. Gupta, and S.K. Mukerjee Indian J. Chem. 11 1973 1263
31. I. Azizul, and A.J. Rafiqul Bangladesh Acad. Sci. 12 1998 1
32. A.L. Tokes, G. Litkei, K. Gulacsi, S. Antus, E.B. Gacs, C. Szantay, and L.L. Darko Tetrahedron 55 1999 9283
33. C.C. Andrei, D.T. Ferreira, M. Faccione, L.A.B. Moraes, M.G. Carvalho, and R. Braz-Filho Phytochemistry 55 2002 799
34. L. Ji, Y.L. Yuan, L.P. Luo, Z. Chen, X.Q. Ma, Z.J. Ma, and L. Cheng Steroids 77 2012 441
35. L.Y. Yu, F.X. Zhang, Z.J. Hu, H. Ding, H.F. Tang, Z.J. Ma, and X.F. Zhao Fitoterapia 93 2014 115
36. G.M. Morris, R. Huey, W. Lindstrom, M.F. Sanner, R.K. Belew, D.S. Goodsell, and A.J. Olson J. Comput. Chem. 30 2009 2785
37. K.A. Nolan, J.R. Doncaster, M.S. Dunstan, K.A. Scott, A.D. Frenkel, D. Siegel, D. Ross, J. Barnes, C. Levy, D. Leys, R.C. Whitehead, I.J. Stratford, and R.A. Bryce J. Med. Chem. 52 2009 7142