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fengxue01

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heroqe

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1 .     3,14-dihydrodecussine
    ÏàËƶÈ:100%
Journal of Natural Products          1981          Vol 44          415-421
Some New Decussine-Type Alkaloids From Strychnos decussata, Strychnos dale and Strychnos elaecocarpa
Wenche N. A. Rolfsen, Ajibola A. Olaniyi, Robert Verpoorte, Lars Bohlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     akagerine
C20H24N2O2     ÏàËƶÈ:70%
Phytochemistry          2001          57          653-659
Main glucosidase conversion products of the gluco-alkaloids dolichantoside and palicoside
Viviane Brandt, Monique Tits, Jacques Penelle, Michel Fr¨¦d¨¦rich, Luc Angenot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     3-Bromo-4,4',5-trimethoxy-4'-O-tert-butyldiphenylsilyl-E-isomer
    ÏàËƶÈ:61.9%
Journal of Natural Products          2005          68          1450-1458
Antineoplastic Agents. 509. Synthesis of Fluorcombstatin Phosphate and Related 3-Halostilbenes
George R. Pettit, Mathew D. Minardi, Heidi J. Rosenberg, Ernest Hamel, Michael C. Bibby, Sandie W. Martin, M. Katherine Jung, Robin K. Pettit, Timothy J. Cuthbertson, and Jean-Charles Chapuis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     ¦Á-yohimbine
C21H27N2O3     ÏàËƶÈ:61.9%
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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5 .     ¦Á-yohimbine
C21H26N203     ÏàËƶÈ:61.9%
Chemistry of Natural Compounds          1996          32          386-512
ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES CHAPTER , continued
R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Suitankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     7,8-dimethoxy-3',4'-methylenedioxyflavone
C18H14O6     ÏàËƶÈ:60%
Chemical & Pharmaceutical Bulletin          2002          50(9)          1271-1272
Two New 5-Deoxyflavones from Albizia odoratissima
Yerra KOTESWARA RAO,Mopur VIJAYA BHASKAR REDDY,Chunduri VENKATA RAO, Duvvuru GUNASEKAR,a Alan BLOND, Cristelle CAUX,and Bernard BODO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     multicaulin
C20H22O     ÏàËƶÈ:60%
Journal of Natural Products          1997          60          1275-1280
Norditerpenoids and Diterpenoids from Salvia multicaulis with Antituberculous Activity
Ayhan Ulubelen, G¨¹laçt¨¬ Topcu, and Candan Bozok Johansson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     borrerine
    ÏàËƶÈ:60%
Journal of Natural Products          1985          Vol 48          120-123
RMN du Carbone 13 des Alcaloïdes du Type Borr¨¦rine-Borr¨¦v¨¦rine-Isoborr¨¦v¨¦rine
F. Tillequin, M. Koch, A. Rabaron
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     2-(4-(2,3,4-Tetrahydro-1H-pyrido[3,4-b]indol-1-yl)butyl)isoindoline 1,3-dione
C23H23N3O2     ÏàËƶÈ:60%
Journal of Natural Products          2011          74          1972-1979
Antimalarial ¦Â-Carbolines from the New Zealand Ascidian Pseudodistoma opacum
Susanna T. S. Chan, A. Norrie Pearce, Michael J. Page, Marcel Kaiser, and Brent R. Copp
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (3R,12bS)-methyl (3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl)acetate
C20H26O2N2     ÏàËƶÈ:60%
Heterocycles          2010          81          1791-1798
Formal Syntheses of Dihydrocorynantheine and Isorhynchophylline via Proline Catalyzed Mannich-Michael Reaction
Kazuhiro Nagata, Hitomi Ishikawa, Ayako Tanaka, Michiko Miyazaki, Takuya Kanemitsu, and Takashi Itoh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Magnoflorine
    ÏàËƶÈ:60%
Archives of Pharmacal Research          2008          31          1405-1412
Inhibitory activities of the alkaloids from Coptidis Rhizoma against aldose reductase
Hyun Ah Jung, Na Young Yoon, Hyun Ju Bae, Byung-Sun Min and Jae Sue Choi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     N-(3-(1H-imidazol-2-yl)propyl)-2-(4-(2-(7-chloroquinolin-4-ylamino)ethyl)piperazin-1-yl)-2-oxoacetamide
C23H28ClN7O2     ÏàËƶÈ:60%
Bioorganic & Medicinal Chemistry          2009          17          6451-6462
Synthesis of oxalamide and triazine derivatives as a novel class of hybrid 4-aminoquinoline with potent antiplasmodial activity
Naresh Sunduru, Moni Sharma, Kumkum Srivastava, S. Rajakumar, S.K. Puri, J.K. Saxena, Prem M.S. Chauhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     3-Iodo-4,4',5-trimethoxy-3'-O-tert-butyldiphenylsilyl-E-stilbene
C33H35IO4Si     ÏàËƶÈ:59.0%
Journal of Natural Products          2012          75          385−393
Antineoplastic Agents. 548. Synthesis of Iodo- and Diiodocombstatin Phosphate Prodrugs
George R. Pettit, Heidi J. Rosenberg, Rachel Dixon, John C. Knight, Ernest Hamel,Jean-Charles Chapuis, Robin K. Pettit,Fiona Hogan, Brandy Sumner, Kenneth B. Ain,and Brindi Trickey-Platt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     5-Methoxy-2-{N-[2-(2-hydroxy-5-iodo)benzamidoethyl]-N-n-propylamino}tetralin hydrochloride
C23H29N2O3I     ÏàËƶÈ:59.0%
Bioorganic & Medicinal Chemistry          1998          6          2111-2126
2-Aminotetralin-derived substituted benzamides with mixed dopamine D2, D3, and serotonin 5-HT1A receptor binding properties: A novel class of potential atypical antipsychotic agents
Evert J. Homan, Swier Copinga, Lotta Elfström, Trees van der Veen, Jan-Pieter Hallema, Nina Mohell, Lena Unelius, Rolf Johansson, Håkan V. Wikström, Cor J. Grol
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     16-epi-isositsirikin
    ÏàËƶÈ:57.1%
Planta Medica          1982          46          88-90
Alkaloide in Tabernaemontana-Arten, XVI [1] 1 2-Methoxy-17,18-dehydro-vincamine and 1 6-epi-Isositsirikine, Alkaloids from Tabernaemontana psorocarpa
H. Achenbach, C. Renner und I. AddaeMensah
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     3-isorauniticine
    ÏàËƶÈ:57.1%
Planta Medica          1981          41          406-418
13C NMR Data of 3-Isoajmalicine and 19-Epiajmalicine
Raimo Uusvuori and Mauri Lounasmaa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     compound 13
C21H26N2O2     ÏàËƶÈ:57.1%
Phytochemistry          1999          51          839-844
Alkaloids from the stem-bark of Alstonia macrophylla
Toh-Seok Kam, Ing-Ho Iek, Yeun-Mun Choo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     ¦Á-yohimbine
    ÏàËƶÈ:57.1%
Journal of Natural Products          1983          Vol 46          708-722
Aspidosperma de Guyane: Alcaloïdes des Graines de Aspidosperma oblongum
G. M. T. Robert, A. Ahond, C. Poupat, P. Potier, H. Jacquemin, S. K. Kan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     (-)-tetrahydroalstonine
    ÏàËƶÈ:57.1%
Journal of Natural Products          1985          Vol 48          273-278
Partial Synthesis via Indole Alkaloids: A New Hexacyclic Derivative of (-)-Tetrahydroalstonine
Bernhard Mompon, Thierry Vassal, Philippe Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     (+)-vincadine
    ÏàËƶÈ:57.1%
Helvetica Chimica Acta          1976          59          2711-2723
13C-NMR. Spectroscopy of Naturally Occuring Substances. XLII. Conformational analysis of quebrachamine-like indole alkaloids and related substances
Ernest Wenkert, Edward W. Hagaman, Nicole Kunesch, Nai-yi Wang and B¨¦la Zsadon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     16¦Â-carbomethoxy-15,20¦Â-dihydrocleavamine
C21H24O2N     ÏàËƶÈ:57.1%
Helvetica Chimica Acta          1976          59          2711-2723
13C-NMR. Spectroscopy of Naturally Occuring Substances. XLII. Conformational analysis of quebrachamine-like indole alkaloids and related substances
Ernest Wenkert, Edward W. Hagaman, Nicole Kunesch, Nai-yi Wang and B¨¦la Zsadon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     yohimbine
    ÏàËƶÈ:57.1%
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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23 .     3-benzoyl-5-ethoxycarbonyl-1-phenyl-6-methyl-4-(3-nitro-phenyl)-3,4-dihydropyrimidin-2(1H)-one
C27H23N3O6     ÏàËƶÈ:57.1%
Journal of Heterocyclic Chemistry          2001          38          1051-1054
Investigation the chemical reactivity of positions N-3, C-5 and C6-methyl group in biginelli type compounds and synthesis of new dihydropyrimidine derivatives
Y. R. Mirzaei, H. Azamat and H. Namazi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     11-Hydroxypalmatine
C21H22NO5I     ÏàËƶÈ:57.1%
Journal of Asian Natural products Research          2010          12          99-105
Anti-hyperglycemic effect of 11-hydroxypalmatine, a palmatine derivative from Stephania glabra tubers
Deepak Kumar Semwal; Usha Rawat; Ravindra Semwal; Randhir Singh; Gur Jas Preet Singh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     5-(4-chlorophenyl)-N-(3-(4-(2,3-dichlorophenyl)piperazin-1-yl)propyl)-1,2-dimethyl-1H-pyrrole-3-carboxamide
    ÏàËƶÈ:57.1%
Bioorganic & Medicinal Chemistry          2010          18          6156-6169
Further optimization of novel pyrrole 3-carboxamides for targeting serotonin 5-HT2A, 5-HT2C, and the serotonin transporter as a potential antidepressant
Suk Youn Kang, Eun-Jung Park, Woo-Kyu Park, Hyun Jung Kim, Gildon Choi, Myung Eun Jung, Hee Jeong Seo, Min Ju Kim, Ae Nim Pae, Jeongmin Kim, Jinhwa Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     tetrahydroalstonine
    ÏàËƶÈ:57.1%
Natural Product Research and Development          2007          19          235-239
Indole Alkaloids from Rauwolfia vomitoria
LI Lin;HE Hong-ping; ZHOU Hua; HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     ¦Á-yohimbine
    ÏàËƶÈ:57.1%
Natural Product Research and Development          2007          19          235-239
Indole Alkaloids from Rauwolfia vomitoria
LI Lin;HE Hong-ping; ZHOU Hua; HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     Segoline A
    ÏàËƶÈ:56.5%
Tetrahedron Letters          2001          42          2669-2671
A new alkaloid from the purple Indian Ocean tunicate Eudistoma bituminis
Isabelle Viracaoundin, Robert Faure, Emile Marcel Gaydou, Maurice Aknin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     (4R,19S)-coleon A
    ÏàËƶÈ:55%
Phytochemistry          2006          67          1818-1825
Insect-antifeedant and antibacterial activity of diterpenoids from species of Plectranthus
Julia Wellsow, Ren¨¦e J. Grayer, Nigel C. Veitch, Tetsuo Kokubun, Roberto Lelli, Geoffrey C. Kite, Monique S.J. Simmonds
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     compound 2b
    ÏàËƶÈ:55%
Phytochemistry          2004          65          2101-2105
Lignans from the roots of Echinops giganteus
Mathieu Tene, Pierre Tane, Beiban L. Sondengam, Joseph D. Connolly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4Â¥2012-04-06 11:17:58
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