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1 .     Vallesiachotamine
    ÏàËÆ¶È:100%
Archives of Pharmacal Research          2012          35          565-571
In Vitro Antiproliferative Effects of the Indole Alkaloid Vallesiachotamine on Human Melanoma Cells
Paula R. O. Soares,Pollyana Laurindo de Oliveira,Cec¨ªlia M. A. de Oliveira,Lucilia Kato,and L¨ªdia Andreu Guillo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     vallesiachotamine
C21H22N2O3     ÏàËÆ¶È:100%
Phytochemistry          1990          29          3377-3379
17¦Á-O-Methylyohimbine and vallesiachotamine from roots ofAmsonia elliptica
Martina Sauerwein,Koichiro Shimomura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     vallesiachotamine
C21H22N2O3     ÏàËÆ¶È:95.2%
Phytochemistry          1993          33          1117-1119
Alkaloids from Cephaelis dichroa
Pablo N. Solis, Colin W. Wright, Mahabir P. Gupta, J.David Phillipson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     vallesiachotamine
    ÏàËÆ¶È:90.4%
Natural Product Communications          2012          7          731-734
Indole Alkaloids from Vinca major and V. minor Growing in Turkey
Fatemeh Bahadori, G¨¹laçtı Topçu, Mehmet Boğa, Ayla T¨¹rkekul, Ufuk Kolak and Murat Kartal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     (E/Z)-vallesiachotamine
C21H22N2O3     ÏàËÆ¶È:80.9%
Planta Medica          1994          60          561-565
Pharmacological and Phytochemical Studies of Cephaelis axillaris
M. Luisa MartIn ,MahabirP. Gupta, Ana V. Ortiz de Urbina , George A. Karikas, Marina Gordaliza ,Jos¨¦ M. Miguel del Corral. Luis San Roman , Ceferino Sanchez. and Arturo San Feliciano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     dihydrovallesiachotamine
    ÏàËÆ¶È:71.4%
Phytochemistry          1998          48          293-296
Bacterial biotransformation of 3¦Á(S)-Strictosidine to the monoterpenoid indole alkaloid vallesiachotamine
Zhengwu Shen, Wolfgang Eisenreich, Toni M. Kutchan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Naucleaoral B
C20H20N2O3     ÏàËÆ¶È:66.6%
Fitoterapia          2010          81          830-833
Two new cytotoxic isomeric indole alkaloids from the roots of Nauclea orientalis
Jirapast Sichaem, Serm Surapinit, Pongpun Siripong, Suttira Khumkratok, Jonkolnee Jong-aramruang, Santi Tip-pyang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     1-(3-Methyl-4-oxobut-2-enyl)-2-(4-methyl-5-oxopent-3-enyl)-1,2,3,4-tetrahydro-¦Â-carboline
C22H26N2O2     ÏàËÆ¶È:59.0%
European Journal of Organic Chemistry          2012                   1147-1157
Synthesis of the Indolic Pentacyclic Core of Manadomanzamine A Following Biogenetically Based Strategies
Lok-Hang Yan, Philippe Nuhant, Isabelle Sinigaglia, Yann Fromentin, Christian Marazano, Bernard Delpech and Erwan Poupon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     17-epi-ajmalicinine
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1996          59          185-189
Obovamine, a New Indole Alkaloid from Stemmadenia obovata
Alberto Madinaveitia, Matias Reina, Gabriel de la Fuente, and Antonio G. Gonzalez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     corynanthine
C21H25N2O3     ÏàËÆ¶È:57.1%
Planta Medica          2000          66          531-536
Leishmanicidal,Antiplasmodial and Cytotoxic Activity of Indole Alkaloids from Corynanthe pachyceras
Dan Stærk,Else Lemmich,Jette Christensen, Arsalan Kharazmi,Carl Erik Olsen,Jerzy W.Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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