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1 .     catharanthine
    ÏàËÆ¶È:76.1%
Helvetica Chimica Acta          1976          59          2437-2442
13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids
Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (¡À)-catharanthine
C21H24N2O2     ÏàËÆ¶È:71.4%
Heterocycles          2002          56          313-330
Synthesis of 2,3-Disubstituted Indoles by Radical Cyclization with Hypophosphorous Acid and Its Application to Total Synthesis of (¡À)-Catharanthine
Matthew T. Reding, Yosuke Kaburagi, Hidetoshi Tokuyama, and Tohru Fukuyama*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     coronaridine
    ÏàËÆ¶È:66.6%
Journal of Natural Products          1988          Vol 51          528
Heyneanine Hydroxyindolenine, A New Indole Alkaloid from Ervatamia coronaria var. plena
Perveen Sharma, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     coronaridine
    ÏàËÆ¶È:66.6%
Helvetica Chimica Acta          1976          59          2437-2442
13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids
Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3-S-ethoxycoronaridine
    ÏàËÆ¶È:66.6%
Academic Journal of Second Military Medical University          2006          27          92-96
Antiaddictive indole alkaloids in Ervatamia yunnanensis and their bioactivity
XUAN Wei-dong, CHEN Hai-sheng, YUAN Zhi-xian, ZHANG Xiao-dong, HUANG Mao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 1
C21H26N2O2     ÏàËÆ¶È:61.9%
Chemical & Pharmaceutical Bulletin          1992          40          2041-2043
Indonesian Medicinal Plants. II. Chemical Structures of Pongapinones A and B, Two New Phenylpropanoids from the Bark of Pongamia pinnata (Papilionaceae)
Isao KITAGAWA,Ru-song ZHANG,Kazuyuki HORI,Katsutoshi TSUCHIYA and Hirotaka SHIBUYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3-hydroxyl coronaridine
    ÏàËÆ¶È:61.9%
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
8 .     catharanthine
    ÏàËÆ¶È:61.9%
Helvetica Chimica Acta          1976          59          2437-2442
13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids
Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     coronaridine
    ÏàËÆ¶È:61.9%
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
10 .     3-R-ethoxycoronaridine
C23H30N2O3     ÏàËÆ¶È:61.9%
Academic Journal of Second Military Medical University          2006          27          92-96
Antiaddictive indole alkaloids in Ervatamia yunnanensis and their bioactivity
XUAN Wei-dong, CHEN Hai-sheng, YUAN Zhi-xian, ZHANG Xiao-dong, HUANG Mao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     heyneanine
    ÏàËÆ¶È:61.9%
Academic Journal of Second Military Medical University          2006          27          92-96
Antiaddictive indole alkaloids in Ervatamia yunnanensis and their bioactivity
XUAN Wei-dong, CHEN Hai-sheng, YUAN Zhi-xian, ZHANG Xiao-dong, HUANG Mao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (-)-3R-Methoxycoronaridine
    ÏàËÆ¶È:59.0%
Phytochemistry          1994          37          1729-1735
Indole alkaloids and terpenoids fromTabernaemontana markgrafiana
Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-(2-oxopropyl)coronaridine
    ÏàËÆ¶È:58.3%
Chemical & Pharmaceutical Bulletin          1992          40          2041-2043
Indonesian Medicinal Plants. II. Chemical Structures of Pongapinones A and B, Two New Phenylpropanoids from the Bark of Pongamia pinnata (Papilionaceae)
Isao KITAGAWA,Ru-song ZHANG,Kazuyuki HORI,Katsutoshi TSUCHIYA and Hirotaka SHIBUYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3-(2-oxopropyl)coronaridine
    ÏàËÆ¶È:58.3%
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
15 .     3-(2-oxopropyl)-coronaridine
    ÏàËÆ¶È:58.3%
Natural Product Sciences          1997          3          42-48
Alkaloids from The Roots of Tabernaemontana Macrocarpa Jack
Husain, Khairana; Said, Ikram M.; Din, Laily B.; Takayama, Hiromitsu; Kitajima, Mariko; Aimi, Norio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     methyl (2¦Â,11¦Â,12¦Â,19¦Á)- 6,7-didehydro-8,21-dioxo-11,21-cycloaspidospermidine-2-carboxylate
C21H20N2O4     ÏàËÆ¶È:57.1%
Helvetica Chimica Acta          2006          Vol. 89          515
Three New Indole Alkaloids from the Leaves of Kopsia officinalis
Hua Zhou, Hong-Ping He, Ning-Chuan Kong, Yue-Hu Wang, Xiang-Dong Liu, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     spiraformin-C
C23H26O6     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          2004          52(10)          1227-1230
New Neolignans from Spiraea formosana
Tian-Shung WU,Chia-Chan HWANG,Ping-Chung KUO,Tsung-Hsiao KUO,Amooru Gangaiah DAMU,and Chung-Ren SU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     11¦Â-(phenylseleno)guaia-4(14),10(15)-dieno-13,6¦Á-lactone
C21H24O2Se     ÏàËÆ¶È:57.1%
Journal of Natural Products          1999          62          22-30
Guaianolides as Immunomodulators. Synthesis and Biological Activities of Dehydrocostus Lactone, Mokko Lactone, Eremanthin, and Their Derivatives
Saori Yuuya, Hisahiro Hagiwara, Toshio Suzuki, Masayoshi Ando, Atsushi Yamada, Kouji Suda, Takao Kataoka, and Kazuo Nagai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     19-Heyneanine
C21H26N2O3     ÏàËÆ¶È:57.1%
Chemistry of Natural Compounds          2008          44          675-678
INDOLE ALKALOIDS FROM Ervatamia flabellformia
Shuang Liang, Haisheng Chen, Li Jin,Weidong Xuan, and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     aristolasicone
    ÏàËÆ¶È:57.1%
Natural Product Research          1993          2          41-48
Structure of Aristoaristone, A New Dimeric Indole Alkaloid from Aristotelia Australasica
J. -C. Quirion; H. -P. Husson; C. Kan; I. R. C. Bick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     compound 5
    ÏàËÆ¶È:57.1%
Natural Product Research          1994          4          189-193
Synthesis of Vinca Alkaloids and Related Compounds. Part LXX1. Ferric Chloride Mediated Coupling Reaction of Rearranged 5-nor-catharanthine with Vindoline
Mih¨¢Ly Bal¨¢zs; Csaba Sz¨¢ntay Jr.; Hedvig Bölcskei; Csaba Sz¨¢ntay
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     coronaridine
    ÏàËÆ¶È:57.1%
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
23 .     19-heyneanine
    ÏàËÆ¶È:57.1%
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
24 .     16-epi-17-¦Á-hydroxy-¡÷(14,15)-kopsinine
C21H24N2O3     ÏàËÆ¶È:57.1%
Journal of Natural Products          1993          Vol 56          2166
Indole Alkaloids from Kopsia teoi
T. Varea, C. Kan, F. Remy, T. Sevenet, J. C. Quirion, H.-P. Husson, H. A. Hadi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     3-oxo-coronaridine
    ÏàËÆ¶È:57.1%
Natural Product Sciences          1997          3          42-48
Alkaloids from The Roots of Tabernaemontana Macrocarpa Jack
Husain, Khairana; Said, Ikram M.; Din, Laily B.; Takayama, Hiromitsu; Kitajima, Mariko; Aimi, Norio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     5,6-Dehydrocoronaridine
    ÏàËÆ¶È:57.1%
Phytochemistry          1994          37          1729-1735
Indole alkaloids and terpenoids fromTabernaemontana markgrafiana
Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     3-epi-¦Â-yohimbine
C21H26N2O3     ÏàËÆ¶È:57.1%
Phytochemistry          1992          31          2031-2034
Alkaloid distribution in Malaysian Uncaria
Toh-Seok Kam, Kee-Huat Lee, Swee-Hock Goh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     sitsirikine
    ÏàËÆ¶È:57.1%
Phytochemistry          1992          31          2507-2511
Indole alkaloids from Aspidosperma pruinosum
Jos¨¦ J. Taveira, Domingos S. Nunes, Luzia Koike, Francisco de A.M. Reis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     3-epi-¦Â-yohimbine
    ÏàËÆ¶È:57.1%
Phytochemistry          1991          30          3441-3444
Dimeric indole alkaloids from Uncaria callophylla
Toh-Seok Kam, Kee-Huat Lee, Swee-Hock Goh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     19-O-Methyl-3,14-dihydroangustoline
C21H23N3O2     ÏàËÆ¶È:57.1%
Phytochemistry Letters          2012          5          316-319
Chromatographic profiling and identification of two new iridoid-indole alkaloids by UPLC¨CMS and HPLC-SPE-NMR analysis of an antimalarial extract from Nauclea pobeguinii
Yong-Jiang Xu, Kenn Foubert, Liene Dhooghe, Filip Lemi¨¨re, Kanyanga Cimanga,Kahunu Mesia, Sandra Apers, Luc Pieters
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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