New alkaloids from the seeds of Strychnos nux-vomica

Tetrahedron

Volumn 68, Issue 16, 2012, Pages 3288-3294

  Zhao, Nan ^a,b   Li, Li ^a   Liu, Jun Hong ^a,b   Zhuang, Peng Yu ^a   Yu, Shi Shan ^a   Ma, Shuang Gang ^a   Qu, Jing ^a   Chen, Nai Hong ^a   Wu, Li Jun ^b  

^a PEKING UNION MEDICAL COLLEGE   (China)

^b SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

Author keywords

ECD calculation; Indolomonoterpenic alkaloid; Neuroprotective activity; Structural elucidation; Strychnos nux vomica

Indexed keywords

10 HYDROXYL ICAJINE; 11 HYDROXYL ICAJINE; 5 HYDROXYL VOMICINE; 5 OXOBRUCINE; 5 OXOPSEUDOSTRYCHNINE; ALKALOID; DIPYRONE; ISOPSEUDOSTRYCHNINE; NEUROPROTECTIVE AGENT; STRYVOMICINE; STRYVOMITINE; UNCLASSIFIED DRUG;

ARTICLE; BIOSYNTHESIS; CELL STRAIN; CIRCULAR DICHROISM; DRUG ISOLATION; DRUG STRUCTURE; MASS SPECTROMETRY; NEUROPROTECTION; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PLANT SEED; PRIORITY JOURNAL; STEREOCHEMISTRY; STRYCHNOS NUX VOMICA;

STRYCHNOS; STRYCHNOS NUX-VOMICA;

EID: 84862778021     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.03.006     Document Type: Article

References (20)

1. ChPC Chinese Pharmacopoeia Vol. 1 2010 Chemical Industry Beijing p 47
2. N.G. Bisset, and J.D. Phillipson Lloydia 39 1976 263 325
3. H.C.B. Kemal, G.B. Norman, and J.H. Peter Phytochemistry 18 1979 512 514
4. W. Klyne, R.J. Swan, B.W. Bycroft, and H. Schmid Helv. Chim. Acta 49 1966 833 841
5. N.G. Bisset, J. Bosly, B.C. Das, and G. Spiteller Phytochemistry 14 1975 1411 1414
6. M.J. Frisch, G.W. Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G.A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H.P. Hratchian, A.F. Izmaylov, J. Bloino, G. Zheng, J.L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J.J.A. Montgomery, J.E. Peralta, F. Ogliaro, M. Bearpark, J.J. Heyd, E. Brothers, K.N. Kudin, V.N. Staroverov, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J.C. Burant, S.S. Iyengar, J. Tomasi, M. Cossi, N. Rega, N.J. Millam, M. Klene, J.E. Knox, J.B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R.E. Stratmann, O. Yazyev, A.J. Austin, R. Cammi, C. Pomelli, J.W. Ochterski, R.L. Martin, K. Morokuma, V.G. Zakrzewski, G.A. Voth, P. Salvador, J.J. Dannenberg, S. Dapprich, A.D. Daniels, Ö. Farkas, J.B. Foresman, J.V. Ortiz, J. Cioslowski, and D.J. Fox Gaussian 09; Revision B. 01 2009 Gaussian Wallingford, CT
7. N. Berova, L. Di Bari, and G. Pescitelli Chem. Soc. Rev. 36 2007 914 931
8. W. Klyne, and J. Buckingham Atlas of Stereochemistry Absolute Configurations of Organic Molecules 1974 Chapman and Hall London pp 150-151
9. R. Verpoorte, P.J. Hylands, and N.G. Bisset Org. Magn. Reson. 9 1977 567 571
10. M. Miwako, N. Masato, K. Daisuke, and S. Yoshihiro J. Am. Chem. Soc. 125 2003 9801 9807
11. J.E. Michael, L.D. Rosa, L.K. Kai, and C.V. Peter Org. Lett. 16 2000 2479 2481
12. B.A. Moscowitz, K. Mislow, M.A.W. Glass, and C. Djerassi J. Am. Chem. Soc. 84 1962 1945 1955
13. N.G. Bisset, B.C. Das, and J. Parello Tetrahedron 29 1973 4137 4148
14. B. Nina, N. Kji, and W.W. Robert Circular Dichroism: Principles and Applications 2nd ed. 2000 Wiley-VCH New York, NY pp 262-279
15. R. Verpoorte, T.A. Beek, R.L.M. Riegman, P.J. Hylands, and M.G. Bisset Org. Magn. Reson. 22 1984 345 348
16. Z.N. Ji, and G.Q. Liu Acta Pharmacol. Sin. 22 2001 459 462
17. C. Sandra, A.S. Medhat, R.J. Christopher, C.C. Diana, A. Buzulagu, and I. Yoshitaka Nat. Struct. Mol. Biol. 14 2007 1157 1164
18. M.S. Shearman Methods Enzymol. 309 1999 716 723
19. T. Mosmman J. Immunol. Methods 65 1983 55 63
20. S.G. Ma, W.Z. Tang, Y.X. Liu, Y.C. Hu, S.S. Yu, Y. Zhang, X.G. Chen, J. Qu, J.H. Ren, Y.B. Liu, S. Xu, J. Liu, Y.Y. Liu, Y. Li, H.N. Lv, and X.F. Wu Phytochemistry 72 2011 115 125