[67]. Monks, D. Scudiero, P. Skehan, R. Shoemake, K. Paull, D. Vistica, C. Hose,
J. Langley, P. Cronise, H. Camplell, L. Mayo, M. Boyd, Feasibility of a high- flux anticancer drug screen use a diverse panel of cultured human tumor cell lines, J. Nalt. Cancer Inst., 1991, 83 (11), 757 – 766.
[68]. F. Hadacek, H. Greger, Testing of antifungal natural products: methodologies, comparability of results and assay choice. Phytochemical Analysis, 2000, 11 (3), 137–147.
[69]. M. Tsubuki, K. Kanai, H. Nagase and T. Honda, Stereocontrolled syntheses of novel styryl lactones, (+)-goniodiol, (+)-goniotriol, (+)-8-acetylgoniotriol, (+)-goniofufurone, (+)-9-deoxygoniopypyrone, (+)-goniopypyrone, and (+)- altholactone from common intermediates and cytotoxicity of their congerers. Tetrahedron, 1999, 55, 2493-2514.
[70]. Y. Ch. Wattanapiromsakul, B. Wangsintaweekul, P. Sangprapan, A. Itharat and N. Keawpradub, Goniothalamin, a cytotoxic compound, isolated from Goniothalamus macrophyllus (Blume) Hook. f. & Thomson var. macrophyllus, Songklanakarin J. Sci. Technol., 2005, 27, 479-487.
[71]. C. Labbe, M. Castillo, J.D. Connolly, Mono and sesquiterpenes from Satureja gilliesil. Phytochemistry, 1993, 3 (2), 441-444.
[72]. B. Szafranek, K. Chrapkowska, M. Pawinska, J. Szafranek, Analysis of leaf surface sesquiterpenes in potato varieties. J. Agric. Food Chem., 2005, 53, 2817-2822.
[73]. D.-W. Ou-Yang, L. Wu, Y.-L. Li, P.-M. Yang, D.-Y. Kong, X.-W. Yang, W.-
D. Zhang, Miscellaneous terpenoid constituents of Abies nephrolepis and their moderate cytotoxic activities. Phytochemistry, 2011, 72, 2197-2204.
[74]. C. Sunardi, K. Padmawinata, L.B.S. Kardono, M. Hanafi, Y. Usuki, Identification of Cytotoxic Alkaloid Phenanthrene Lactams from Stelechocarpus burahol. New Technologies Medicine, 2003, 4 (3), 328-331.
Có thể bạn quan tâm!
-
Dữ Kiện Phổ 13 C-, 1 H-Nmr (125/500 Mhz, Cdcl 3 ) Của Gg14 -
Hoạt Tính Gây Độc Tế Bào Của Các Hợp Chất Từ Cây Giác Đế Đài To Và Giác Đế Cuống Dài -
Nghiên cứu thành phần hóa học và hoạt tính chống ung thư của cây giác đế đài to (goniothalamus macrocalyx ban) và giác đế cuống dài (goniothalamus gracilipes ban) họ na (annonaceae) - 21
Xem toàn bộ 184 trang tài liệu này.
[75]. S.R. Kim, S.H. Hung, S.Y. Kang, K.A. Koo, S. H. Kim, Ch.J. Ma, H.-S. Lee,
M.J. Park, Y.Ch. Kim, Aristolactam BII of Saururus chinensis Attenuates
Glutamate-Induced Neurotoxicity in Rat Cortical Cultures Probably by Inhibiting Nitric Oxide Production. Planta Med. 2004, 70, 391-396.
[76]. I.-L. Tsai, F.-P. Lee, Ch.-Ch. Wu, Ch.-Y. Duh, T. Ishikawa, J.-J. Chen, Y.- Ch. Chen, H. Seki, I.-S. Chen. Planta Med, 2005, 71, 535-542.
[77]. M. Efdi, S. Fujita, T. Inuzuka and M. Koketsu, Chemical studies on
Goniothalamus tapis Miq. Natural Product Research, 2010, 24(7), 657-662. [78]. J.P. Singh, A.K. Singh, A. Singh and R. Ranjan, Chemical constituents of
Artabotrys odoratissimus, Rasyan J. Chem., 2009, 2 (1), 156-158.
[79]. V. Popsavin, B. Sre’co, G. Benedekovi’c, J. Francuz, M. Popsavin, V. Koji’c,
G. Bogdanovi’c, Design, synthesis and antiproliferative activity of styryllactones related to (+)-goniofufurone. Eur.J.Med.Chem., 2010, 45, 2876-2883.
[80]. Y. Fujimoto, Ch. Murasaki, H. Shimada, S. Nishioka, K. Kakinuma, S. Singh,
M. Singh, Y.K. Gupta, and M. Sahai, Annonaceous acetogenins from the seeds of Annona squamosa. Non-adjacent Bis-tetrahydrofuranic acetogenins. Chem. Pharm. Bull., 1994, 42 (6), 1175-1184.
[81]. L. Zeng, Q. Ye, N.H. Oberlies, G. Shi, Z.M. Gu, K. He, and J.L. McLaughlin, Recent advances in Annonaceous acetogenins. Nat. Prod. Rep., 1996, 13, 275-306.
[82]. J.L. Ven, I. Schmitz-Afonso, G. Lewin, O. Laprévote, A. Brunelle, D. Touboul, P. Champy, Comprehensive characterization of Annonaceous acetogenins within a complex extract by HPLC-ESI-LTQ-Orbitrap® using post-column lithium fusion. J. Mass Spectrom., 2012, 47, 1500-1509.
[83]. T.G. McCloud, D.L. Smith, C.-J. Chang and J.M. Cassady, Annonacin, a novel, biologically active polyketide from Annona densicoma. Experientia, 1987, 43, 947-949.
[84]. S.H. Myint, D. Cortes, A. Laurens, R. Hocquemiller, M. Lebceur, A. Cevé, J. Cotte, A.M.Quéro, Solamin, a cytotoxic mono-tetrahydrofuranic -lactone acetogenin from Annona muricata seeds. Phytochemistry, 1991, 30, 3335-
3338.
[85]. C. Gleye, P. Duret, A. Laurens, R. Hocquemiller, and A. Cavé, cis- Monotetrahydrofuran Acetogenins from the Roots of Annona muricata. J. Nat. Prod., 1998, 61, 576-579.
[86]. M.H.Woo, K.Y. Cho, Y. Zhang, L. Zeng, Z.M. Gu, J.L. McLaughlin, Asimilobin and cis- and trans-murisolinones, novel bioactive annonaceous acetogenins from the seeds of Asimina triloba. J. Nat. Prod., 1995, 58, 1533- 1542.
[87]. H. Heymann, Y. Tezuka, T. Kikuchi, and S. Supriyatna, Constituents of Sindora sumatrana MIQ.I. Isolation and NMR Spectral Analysis of Sesquiterpenes from the Dried Pods. Chem. Pharm. Bull., 1994, 42 (1), 138-
146.
[88]. J.-M. Gao, Z.-J. Dong, and J.-K. Liu, A New Ceramide from the Basidiomycete Russula cyanoxantha. Lipids, 2001, 36(2), 175-179.
[89]. E.S.H.E. Ashry, A. Rahman, M.I. Choudhary, S.H. Kandil, A.E. Nemr, T. Gulzar, and A.H. Shobier, Studies on the constituents of the green alga Ulva lactuca. Chemistry of Natural Compounds, 2011, 47(3), 235-238.
[90]. M.-L. Wang, J. Du, P.-Ch. Zhang, R.-Y. Chen, F.-Z. Xie, B. Zhao, D.-Q. Yu.,
Saccopetrins A and B, two novel -lactones from Saccopetalum prolificum. Planta Med, 2002, 68, 719-722.
[91]. N. Panthama, S. Kanokmedhakul, and K. Kanokmedhakul, Polyacetylenes from the Roots of Polyalthia debilis. J. Nat. Prod., 2010, 73, 1366-1369.
[92]. B.N. Chen, G.E. Yang, J.K. Li, H.J. Du, Q.S. Li, and Z.M. Zhang, Cytotoxic constituents from Viscum coloratum. Chemistry of Natural Compounds, 2009, 45, 547-549.
[93]. A.K.Umbetova, Sh.Zh. Esirkegenova, I.M. Chaudri, V.B. Omurkamzinova, and Zh.A. Abilov, Flavonoids of plants from the genus Tamarix. Chemistry of Natural Compounds, 2004, 40 (3), 297-298.
[94]. P.K. Agrawal, Carbon-13 NMR of flavonoids, Elsevier, 1989, 154-162
[95]. G. Lewin, A. Maciuk, S. Thoret, G. Aubert, J. Dubois, and T. Cresteil, Semisynthesis of Natural Flavones Inhibiting Tubulin Polymerization, from Hesperidin. J. Nat. Prod., 2010, 73, 702–706.
[96]. M. Higa, Y. Miyagi, S. Yogi, and K. Hokama, Flavonoid constituents of
Melicope triphylla Merr., Yakugaku zasshi, 1987, 107 (12), 954-958.
[97]. L.Y. Chung, K.F. Yap, S.H. Goh, M.R.Mustafa, Z. Imiyabir, Muscarinic receptor binding activity of polyoxygenated flavones from Melicope subunifoliolata, Phytochemistry, 2008, 69, 1548-1554.
[98]. T.T. Jong, and T.S. Wu, Highly oxygenated flavonoids from Melicope triphylla, Phytochemistry, 1989, 28 (1), 245-246.
[99]. M. Higa, Y. Miyagi, S. Yogi, and K. Hokama, Flavonoid constituents of
Melicope triphylla Merr. II, Yakugaku zasshi, 1990, 110(11), 822-827.
[100]. M. Higa, E. Nakadomari, M. Imamura, K. Ogihara, and T. Suzuka, Isolation of Four New Flavonoids from Melicope triphylla. Chem. Pharm. Bull., 2010, 58(10), 13391342.
[101]. S.P. Moreau, A. Archelas, R. Furstoss, Microbiological Transformations 32: Use of Epoxide Hydrolase Mediated Biohydrolysis as a Way to Enantiopure Epoxides and Vicinal Diols: Application to Substituted Styrene Oxide Derivatives, Tetrahedron, 1996, 52 (13), 4593-4606.
[102]. K.C. Nicolaou, S.A. Snyder, D.A. Longbottom, A.Z. Nalbandian, and X. Huang, New Uses for the Burgess Reagent in Chemical Synthesis: Methods for the Facile and Stereoselective Formation of Sulfamidates, Glycosylamines, and Sulfamides, Chem. Eur. J., 2004, 10, 5581-5606.
[103]. Y. Yang, J. Jiang, L. Quimei, X. Yan, J. Zhao, H. Yuan, Z. Qin, and M. Wang, The Fungicidal Terpenoids and Essential Oil from Litsea cubeba in Tibet. Molecules, 2010, 15, 7075-7082.
[104]. W. Kuriyama, T. Matsumoto, O. Ogata, Y. Ino, K. Aoki, Sh. Tanaka, K. Ishida, T. Kobayashi, N. Sayo, and T. Saito, Catalytic Hydrogenation of Esters. Development of an Efficient Catalyst and Processes for Synthesising
(R)-1,2-Propanediol and 2-(l-Menthoxy)ethanol. Org. ProcessRes. Dev.,
2012, 16, 166−171.
[105]. J. Lee, Y.H. Jeong, D.S. Jang, and E.-K. Seo, Three Terpenes and One Phenolic Compound from Sasa borealis. J. Appl. Biol. Chem., 2007, 50 (1), 13-16.
[106]. L.H. Reddy, P. Couvreur, Squalene : A natural triterpene for use in disease management and therapy. Advanced Drug Delivery Reviews, 2009, 61, 1412- 1426.
[107]. J.W. Gathirwa and T. Maki, Benzylation of Hydroxy Groups with tertiary amine as a base. Tetrahedron, 2012, 68 (1), 370-375.
[108]. T. Getahun, P. Reneela, and A. Dekebo, Isolation and characterization of natural products from Helinus mystachnus (Rhamnaceae). Journal of Chemical and Pharmaceutical Research, 2012, 4 (3), 1756-1762.