Microbial transformation of neoandrographolide by Mucor spinosus (AS 3.2450)

Journal of Molecular Catalysis B: Enzymatic

Volumn 68, Issue 1, 2011, Pages 83-88

  Wang, Yixiong ^a   Chen, Lixia ^a   Zhao, Feng ^b   Liu, Zhihui ^a   Li, Jianqiang ^a   Qiu, Feng ^a  

^a SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

^b YANTAI UNIVERSITY   (China)

Author keywords

Microbial transformation; Mucor spinosus; Neoandrographolide; Nitric oxide

Indexed keywords

ACTIVATED MACROPHAGES; INHIBITORY EFFECT; LIPOPOLYSACCHARIDES; MICROBIAL TRANSFORMATION; MUCOR SPINOSUS; NEOANDROGRAPHOLIDE; STRUCTURE-ACTIVITY RELATIONSHIPS;

NITRIC OXIDE;

14 DEOXYANDROGRAPHOLIDE; 17,19 DIHYDROXY 7,13 ENT LABDADIEN 16,15 OLIDE; 17,19 DIHYDROXY 8,13 ENT LABDADIEN 16,15 OLIDE; 19 [(BETA DEXTRO GLUCOPYRANOSYL)OXY] 19 OXO ENT LABDA 8 (17), 13 DIEN 16,15 OLIDE; 3,14 DIDEOXYANDROGRAPHOLIDE; 7 BETA HYDROXY 3,14 DIDEOXYANDROGRAPHOLIDE; 8 (17) 13 ENT LABDADIEN 16,15 OLID 19 OIC ACID; 8 ALPHA,17 BETA EPOXY 3,14 DIDEOXYANDROGRAPHOLIDE; 8 BETA, 17, 19 TRIHYDROXY ENT LABD 13 EN 16, 15 OLIDE; ANDROGRAPHOLIDE; NITRIC OXIDE; PHLOGANTHOLIDE A; UNCLASSIFIED DRUG;

ARTICLE; BIOTRANSFORMATION; MACROPHAGE; MUCOR; NONHUMAN; STRUCTURE ACTIVITY RELATION;

MUCOR SPINOSUS;

EID: 78649334961     PISSN: 13811177     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcatb.2010.09.016     Document Type: Article

References (30)

1. S.K. Mishra, N.S. Sangwan, and R.S. Sangwan Pharmacog. Rev. 1 2007 283 298
2. J. Batkhuu, K. Hattori, F. Takano, S. Fushiya, K.I. Oshiman, and Y. Fujimiya Biol. Pharm. Bull. 25 2002 1169 1174
3. J. Liu, Z.T. Wang, L.L. Ji, and B.X. Ge Mol. Cell. Biochem. 298 2007 49 57
4. J. Liu, Z.T. Wang, and L.L. Ji Am. J. Chin. Med. 35 2007 317 328
5. C. Wiart, K. Kumar, M.Y. Yusof, H. Hamimah, Z.M. Fauzi, and M. Sulaiman Phytother. Res. 19 2004 1069 1070
6. R.E. Kamdem, S. Sang, and C.T. Ho J. Agric. Food Chem. 50 2002 4662 4665
7. A. Kapil, I.B. Koul, S.K. Banerjee, and B.D. Gupta Biochem. Pharmacol. 46 1993 182 185
8. A. Basak, S. Cooper, A.G. Roberge, U.K. Banik, M. Chretien, and N.G. Seidah Biochem. J. 15 1999 107 113
9. W.L. Deng, R.J. Nie, and J.Y. Liu Zhongguoyaoxuezazhi 17 1982 3 6
10. W.L. Deng, J.Y. Liu, and R.J. Nie Zhongguozhongyaozazhi 10 1985 38 42
11. X.J. He, J.K. Li, H. Gao, F. Qiu, K. Hu, X.M. Cui, and X.S. Yao Tetrahedron 59 2003 6603 6607
12. X.J. He, J.K. Li, H. Gao, F. Qiu, K. Hu, X.M. Cui, and X.S. Yao Chem. Pharm. Bull. 51 2003 586 589
13. L. Cui, F. Qiu, and X.S. Yao Drug Metab. Dispos. 33 2005 555 562
14. Z.M. Meng Acta Pharmacol. Sin. 16 1981 571 575
15. Z.M. Zou Zhongcaoyao 8 1978 343 345
16. A. Wendy, and W.A. Loughlin Bioresour. Technol. 9 2000 49 62
17. S. Riva Curr. Opin. Chem. Biol. 5 2001 106 111
18. H. Zhang, F. Qiu, X.S. Yao, and G.X. Qu J. Asian Nat. Prod. Res. 9 2007 311 319
19. H. Zhang, N. Kang, F. Qiu, G.X. Qu, and X.S. Yao Chem. Pharm. Bull. 55 2007 451 454
20. L.X. Chen, F. Qiu, G.X. Qu, and X.S. Yao J. Asian Nat. Prod. Res. 9 2007 463 469
21. T. Matsuda, M. Kuroyanagi, S. Sugiyama, K. Umehara, A. Ueno, and K. Nishi Chem. Pharm. Bull. 42 1994 1216 1225
22. T. Fujita, R. Fujitani, Y. Takeda, Y. Takaishi, and T. Yamada Chem. Pharm. Bull. 32 1984 2117 2125
23. P. Waridel, J.L. Wolfender, J.B. Lachavanne, and K. Hostettmann Phytochemistry 64 2003 1309 1317
24. A.K. Barua, M.K. Chowdhury, S. Biswas, C. Dasgupta, S.K. Banerjee, S.K. Saha, A. Patra, and A.K. Mitra Phytochemistry 24 1985 2037 2039
25. L.X. Chen, H. Wei, F. Qiu, G.X. Qu, and X.S. Yao Helv. Chim. Acta 89 2006 2654 2664
26. V.M. Dirrsch, H. Stuppner, and A.M. Vollmar Planta Med. 64 1998 423 426
27. L.J. Haynes, K. Peach, M.V. Tracey, Modern Methods in Plant Analysis vol. II 1955 Springer-Verlag Berlin 583
28. G.C. Wang, Y.M. Hu, X.Q. Zhang, and W.C. Ye Zhongguoyaokedaxuexuebao 36 2005 405 407
29. L.X. Chen, H.J. Zhu, R. Wang, K.L. Zhou, Y.K. Jing, and F. Qiu J. Nat. Prod. 71 2008 852 855
30. Y.H. Shen, R.T. Li, W.L. Xiao, G. Xu, Z.W. Lin, Q.S. Zhao, and H.D. Sun J. Nat. Prod. 69 2006 319 322