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wushuai2255: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-29 10:54:59
²éѯ½á¹û£º¹²²éµ½944¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     nauclefine
    ÏàËÆ¶È:76.4%
Heterocycles          1998          48          885-891
A New Indole Alkaloid from Sarcocephalus latifolius
Pedro Abreuand Ant¨®nio Pereira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     nauclealine B
C17H16N2O3     ÏàËÆ¶È:70.5%
Journal of Natural Products          2001          64          1001-1005
New Indole Alkaloids from the Bark of Nauclea orientalis
Zhizhen Zhang,Hala N. ElSohly,Melissa R. Jacob, David S. Pasco, Larry A. Walker, and Alice M. Clark
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Nauclealine B
C17H16N2O3     ÏàËÆ¶È:70.5%
Journal of Natural Products          2001          64          1001-1005
New Indole Alkaloids from the Bark of Nauclea orientalis
Zhizhen Zhang,Hala N. ElSohly, Melissa R. Jacob,David S. Pasco, Larry A. Walker, and Alice M. Clark
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     4-[2-(4-dimethylaminophenyl)imidazo[4,5-b]indol-3(4H)-yl]benzene-sulfonamide
C23H21N5O2S     ÏàËÆ¶È:70.5%
Chemical & Pharmaceutical Bulletin          2010          58          375-380
Microwave-Assisted, Solvent-Free and Parallel Synthesis of Some Novel Substituted Imidazoles of Biological Interest
Gyanendra Kumar Sharma and Devender Pathak
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     rutaecarpine
    ÏàËÆ¶È:70.5%
Shoyakugaku Zasshi          1990          44          135-137
A Cytotoxic Principle from Evodia rutaecarpa
ITOKAWA HIDEJI, INAMATSU MUTSUMI, TAKEYA KOICHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     angustine
C20H17N3O     ÏàËÆ¶È:70%
Planta Medica          1992          58          43-48
Indole Alkaloids with in vitro Antiproliferative Activity from the Ammoniacal Extract of Nauclea orientalis
C. A. J. Erde,neier, U. Regenass, T. Rali, and 0. Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     angustine
    ÏàËÆ¶È:70%
Acta Pharmaceutica Sinica          2010          45          747-751
Alkaloids from the leaves of Nauclea officinalis
FAN Long, FAN Chun-lin, WANG Ying, ZHANG Xiao-qi, ZHANG Qing-wen, ZHANG Jun-qing, YE Wen-cai*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 8
C78H60N6O3     ÏàËÆ¶È:68.7%
Journal of Heterocyclic Chemistry          2010          47          1398-1405
Trichloroisocyanuric acid-catalyzed reaction of indoles: An expeditious synthesis of bis-indolyl, tris-indolyl, di(bis-indolyl), tri(bis-indolyl), and tetra(bis-indolyl)methane under solid-state conditions
Hojat Veisi, Reza Gholbedaghi, Javad Malakootikhah, Alireza Sedrpoushan, Behrooz Maleki and Davood Kordestani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     2-[4-(1H-indol-3-yl)methyl-5-hydroxyoxazol-2-yl]acetonitrile
C14H11N3O2     ÏàËÆ¶È:68.7%
Archiv der Pharmazie          2010          343          261-267
Synthesis and Antidepressant Evaluation of Five Novel Heterocyclic Tryptophan-Hybrid Derivatives
Gamal A. Elmegeed, Ayman R. Baiuomy, Mervat M. Abdelhalim and Hanaa Y. Hana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-10-29 08:15:54
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