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12.7,18.5,25.4,31.7,42.5,43,43.4,45.6,46.5,50.3,56.8,111.8,120.3,120.7,120.9,126.6,128.5,133.9,136.4,172,190.8
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1 .     tabernaemontanine
    ÏàËÆ¶È:100%
Acta Botanica Yunnanica          1999          21(2)          260-264
The constituents of Ervatamia divaricata
YU Yang,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     vobasine
    ÏàËÆ¶È:76.1%
China Journal of Chinese Materia Medica          2007          32          1296-1299
Study on chemical constituents in rhigome of Ervatamia hainanensis
LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     vobasine
    ÏàËÆ¶È:76.1%
Phytochemistry          1990          29          3007-3011
Alkaloids from leaves and stem bark of Ervatamia polyneura
Pascale Clivio,Bernard Richard,Hamid A. Hadi,Bruno David,Thierry Sevenet,Monique Zeches,Louisette Le Men-Olivier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     vobasine
    ÏàËÆ¶È:76.1%
Qu¨ªmica Nova          2008          31          20-24
Chemical constituents from Tabernaemontana catharinensis root bark: a brief NMR review of indole alkaloids and in vitro cytotoxicity
Pereira, Paulo S¨¦rgio; França, Suzelei de Castro; Oliveira, Paulo Vinicius Anderson de; Breves, Camila Moniz de Souza; Pereira, Sarazete Izidia Vaz; Sampaio, Suely Vilela; Nomizo, Auro; Dias, Diones Aparecida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     hystrixnine
C21H26N2O2     ÏàËÆ¶È:76.1%
Journal of the Brazilian Chemical Society          2005          16          1331-1335
A New Indole Alkaloid Isolated from Tabernaemontana hystrix Steud (Apocynaceae)
Cecilia Silva Monnerat, Jucimar Jorgeane de Souza, Leda Mathias, Raimundo Braz-Filho and Ivo Jos¨¦ C. Vieira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     16-epivobasine
C21H24O3N2     ÏàËÆ¶È:71.4%
Phytochemistry          1990          29          3007-3011
Alkaloids from leaves and stem bark of Ervatamia polyneura
Pascale Clivio,Bernard Richard,Hamid A. Hadi,Bruno David,Thierry Sevenet,Monique Zeches,Louisette Le Men-Olivier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     vobasine
    ÏàËÆ¶È:71.4%
Journal of Chinese Medicinal Materials          2012          35          226-229
Study on the Alkaloids Constituents from Voacanga africana
MEI Ling, DENG Yun, LI Fu, GUO Da-le, LU Chong-yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     Vincadiffine
    ÏàËÆ¶È:66.6%
Phytochemistry          1994          37          1737-1743
Indole alkaloids fromTabernaemontana glandulosa
Hans Achenbach, Reiner Waibel, Manfred Zwanzger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     16-epiaffinine
    ÏàËÆ¶È:66.6%
Phytochemistry          1984          23          175-178
13C NMR analysis of alkaloids from peschiera fuchsiaefolia
Raquel M. Braga, Hermogenes F. Leit¨¢o Filho, Francisco De A.M. Reist
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     vincadiffine
    ÏàËÆ¶È:63.6%
Heterocycles          1985          23          2505-2508
Pagicerine ¡ª A New Indole Alkaloid from Pagiantha derifera (Pancher et S¨¦bert) Markgraf (Apocynaceae)
Matyse Bert, Genevi¨¨ve Baudouin, François Tillequin, and Michel Koch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     16-epimethuenine
    ÏàËÆ¶È:61.9%
Planta Medica          1984          50          331-334
2-Acylindole Alkaloids from Leaves of Pterotaberna inconspicua
P. Bakana, R. Dommisse, E. Esmans, R. H. Fokkens, L. Pieters, N. M. M. Nibbering and A. J. Vlietinck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     16-epi-affinine
    ÏàËÆ¶È:61.9%
Phytochemistry          1982          21          445-447
Alkaloids of Hunteria zeylanica
C. Lavaud, G. Massiot, J. Vercauteren, L. Le Men-olivier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 29
    ÏàËÆ¶È:61.9%
Heterocycles          1999          51          2227-2254
Effect of C-1, C-2, and C-3 Substituents on the Conformational Equilibrium of Indolo[2,3-a]quinolizidines
Mauri Lounasmaaand Pirjo Hanhinen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     19-Chloro-19,O-seco-diflorlemenine
    ÏàËÆ¶È:59.0%
Phytochemistry          1994          37          1737-1743
Indole alkaloids fromTabernaemontana glandulosa
Hans Achenbach, Reiner Waibel, Manfred Zwanzger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (16R)-16-hydroxy-16,17-dihydrouleine
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1983          Vol 46          206-210
Studies on the Uleine Alkaloids. II. Some Chemical Transformations of Uleine
Robert P. Borris, David C. Lankin, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-08-23 08:16:26
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