Bioactive phenolics and terpenoids from Manglietia insignis

Fitoterapia

Volumn 84, Issue 1, 2013, Pages 58-63

  Shang, Shan Zhai ^a,c   Kong, Ling Mei ^a,c   Yang, Li Ping ^a   Jiang, Jing ^b   Huang, Jin ^b   Zhang, Hai Bo ^a   Shi, Yi Ming ^a,c   Zhao, Wei ^a   Li, Hong Lin ^b   Luo, Huai Rong ^a   Li, Yan ^a   Xiao, Wei Lie ^a   Sun, Han Dong ^a  

^a KUNMING INSTITUTE OF BOTANY   (China)

^b EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^c UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Bioactivity; Magnoliaceae; Manglietia insignis; Neolignan; Sesquiterpene

Indexed keywords

MANGLIETIA INSIGNIS EXTRACT; MANINSIGIN A; MANINSIGIN B; MANINSIGIN C; MANINSIGIN D; NEOLIGNAN; PHENOL DERIVATIVE; PLANT EXTRACT; SESQUITERPENE DERIVATIVE; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG ISOLATION; DRUG SCREENING; DRUG STRUCTURE; HUMAN; HUMAN CELL; MANGLIETIA INSIGNIS; MEDICINAL PLANT; NERVE FIBER GROWTH; NONHUMAN; PLANT LEAF; PLANT STEM; PRIORITY JOURNAL;

ANIMALS; CELL LINE, TUMOR; HUMANS; MAGNOLIACEAE; MODELS, MOLECULAR; NEURONS; PHENOLS; PLANT LEAVES; PLANT STEMS; RATS; TERPENES;

EID: 84873347747     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2012.10.010     Document Type: Article

References (29)

1. Jiangsu New Medical College Chinese drug dictionary 1977 Shanghai Science and Technology Publishing Shanghai 1628
2. K. Watanabe Pharmacology of Magnolia bark with special reference to gastrointestinal functions Gendai Toyo Igaku 7 1986 54 59
3. U.J. Youn, Q.C. Chen, W.Y. Jin, I.S. Lee, H.J. Kim, and J.P. Lee Cytotoxic lignans from the stem bark of Magnolia officinalis J Nat Prod 70 2007 1687 1689
4. C.C. Shen, C.L. Ni, Y.C. Shen, Y.L. Huang, C.H. Kuo, and T.S. Wu Phenolic constituents from the stem bark of Magnolia officinalis J Nat Prod 72 2009 168 171
5. K.Y. Jung, D.S. Kim, S.R. Oh, S.H. Park, I.S. Lee, and J.J. Lee Magnone A and B, novel anti-PAF tetrahydrofuran lignans from the flower buds of Magnolia fargesii J Nat Prod 61 1998 808 811
6. T. Konoshima, M. Kozuka, H. Tokuda, H. Nishino, A. Iwashima, and M. Haruna Studies on inhibitors of skin tumor promotion, IX. neolignans from Magnolia officinalis J Nat Prod 54 1991 816 822
7. R. Graziose, T. Rathinasabapathy, C. Lategan, A. Poulev, P.J. Smith, and M. Grace Antiplasmodial activity of aporphine alkaloids and sesquiterpene lactones from Liriodendron tulipifera L J Ethnopharmacol 133 2011 26 30
8. K.Y. He, S.Q. Zhang, X.C. Li, Y.S. Fan, and X.Y. Jin Chemical composition and free radicals restraining activity of extracts from three Manglietia species leaves J For Res 18 2007 193 198
9. J.M. Chen, W.Z. Song, and X.J. Zhou Studies of the medicinal plants of the Magnoliaceae VIII. Studies on the major effective constituents of Manglietia insignis Zhongyao Tongbao 10 1985 370 371
10. R.P. Zhang, H.J. Zhang, Z.W. Lin, Y.L. Zhen, and H.D. Sun Diterpenoids from Isodon adenoloma Phytochemistry 31 1992 4237 4240
11. L.J. Reed, and H. Muench A simple method of estimating fifty per cent endpoints Am J Hyg 27 1938 493 497
12. M. Inoue, H. Zhai, H. Sakazaki, H. Furuyama, Y. Fukuyama, and M. Hirama TMC-95A, a reversible proteasome inhibitor, induces neurite outgrowth in PC12 cells Bioorg Med Chem Lett 14 2004 663 665
13. A. Pradines, M. Magazin, P. Schiltz, G. Le Fur, D. Caput, and P. Ferrara Evidence for nerve growth factor-potentiating activities of the nonpeptidic compound SR 57746A in PC12 Cells J Neurochem 64 1995 1954 1964
14. Gietz R. Daniel, and R.A. Woods Transformation of yeast by lithium acetate/single-stranded carrier DNA/polyethylene glycol method G. Christine, R.F. Gerald, Methods in enzymology 2002 Academic Press 87
15. Z. Lin, H. Shen, J. Huang, S. Chen, L. Chen, and J. Chen Butyl 4-(butyryloxy)benzoate functions as a new selective estrogen receptor [beta] agonist and induces GLUT4 expression in CHO-K1 cells J Steroid Biochem Mol Biol 110 2008 150 156
16. Yeast Protocols Handbook Clontech Laboratories, Inc. 2009 A Takara Bio Company
17. S. Yahara, T. Nishiyori, A. Kohda, and T. Nohara Isolation and characterization of phenolic compounds from Magnoliae Cortex produced in China Chem Pharm Bull 39 1991 2024 2036
18. X.M. Deng, Y.X. Cheng, J. Zhou, N.H. Tan, and Z.T. Ding Magnoquinone and neolignans from Magnolia rostrata Acta Bot Yunnanica 23 2001 121 125
19. M.S.M. Yuen, F. Xue, T.C.W. Mak, and H.N.C. Wong On the absolute structure of optically active neolignans containing a dihydrobenzo[b]furan skeleton Tetrahedron 54 1998 12429 12444
20. Y.C. Li, and Y.H. Kuo Four new compounds, ficusal, ficusesquilignan A, B, and ficusolide diacetate from the heartwood of Ficus microcarpa Chem Pharm Bull 48 2000 1862 1865
21. M. Miyamura, T. Nohara, T. Tomimatsu, and I. Nishiokat Seven aromatic compounds from bark of Cinnamomum cassia Phytochemistry 22 1983 215 218
22. N. Kumar, B. Ravindranath, and T.R. Seshadri Terpenoids of Pterocarpus santalinus heartwood Phytochemistry 13 1974 633 636
23. S. Yamauchi, T. Ina, T. Kirikihira, and T. Masuda Synthesis and antioxidant activity of oxygenated furofuran lignans Biosci Biotechnol Biochem 68 2004 183 192
24. Y. Katayama, and T. Fukuzumi Formation of new acetal linkages in the metabolism of syringaresinol structure of lignin by Coriolus versicolor FEMS Microbiol Lett 58 1989 247 253
25. X.Q. Jin, D.M. Xu, Y.J. Xu, D.B. Cui, Z.Y. Tian, and Y. Lu The structure identification of zhepiresionol Acta Pharm Sin 28 1993 212 215
26. H. Achenbach, M. Stöcker, and M.A. Constenla Flavonoid and other constituents of Bauhinia manca Phytochemistry 27 1988 1835 1841
27. Y. Fukuyama, Y. Otoshi, K. Miyoshi, K. Nakamura, M. Kodama, and M. Nagasawa Neurotrophic sesquiterpene-neolignans from Magnolia obovata: structure and neurotrophic activity Tetrahedron 48 1992 377 392
28. Parks DJ, Blanchard SG, Bledsoe RK, Chandra G, Consler TG, Kliewer S, et al. Bile acids: nature lignands for an orphan nuclear receptor. Science 1999;284:1365-8.
29. E.J. Sohn, C.S. Kim, Y.S. Kim, D.H. Jung, D.S. Jang, and Y.M. Lee Effects of magnolol (5,5′-diallyl-2,2′-dihydroxybiphenyl) on diabetic nephropathy in type 2 diabetic Goto-Kakizaki rats Life Sci 80 2007 468 475