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zengjundeyo: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-09 14:36:45
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zengjundeyo: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-09 14:36:45
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²éѯ½á¹û£º¹²²éµ½114¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |
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