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[ÇóÖú] ÇóÖú΢Æ×Êý¾ÝÒ»¸ö GA-19

GA-19 MEOD
12,28,28.5,32.5,34.1,42.4,43.3,53.9,56.1,56.3,67.3,105.9,112.3,113.6,114.2,129.9
,132.4,156.5,157.6,202.7
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1 .     3-methoxy-16-methylene-13¦Á-estra-1,3,5(10)-trien-17¦Â-ol
C20H26O2     ÏàËÆ¶È:60%
Steroids          2003          68          451-458
Stereoselective halogenation of the 16-hydroxymethyl-3-methoxy-13¦Á-estra-1,3,5(10)-trien-17-ols and their solvolytic investigation
J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, P¨¦ter Forg¨®, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     3-methoxy-19-norpregna-1,3,5(10),20-tetraene
C21H28O     ÏàËÆ¶È:57.1%
Journal of Natural Products          1999          62          1538-1541
Four New Steroids from Two Octocorals
Yasuhiko Tomono, Hiroshi Hirota, Yukimitsu Imahara, and Nobuhiro Fusetani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     1,2,10-trimethoxyaporphin
     ÏàËÆ¶È:55%
Journal of Natural Products          1987          Vol 50          297
The 13C-Nmr Spectra of 1,2,10-Trioxygenated Aporphines
Bruce K. Cassels, Andr¨¦ Cav¨¦, Michel Leboeuf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     Diazoketone
     ÏàËÆ¶È:55%
Tetrahedron Letters          2005          46          4569-4572
Ring fragmentation processes resulting from acid catalysed diazo ketone cyclisations
Oliver E. Hutt, Lewis N. Mander, Anthony C. Willis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     11-Methoxy-6-methyl-6,7,8,9,14,15-hexahydro-5Hdibenzo[c,g]azacycloundecene hydrochloride
C20H26ClNO     ÏàËÆ¶È:55%
Archiv der Pharmazie          2010          343          207-214
Ring Expansions of Tetrahydroprotoberberines and Related Dibenzo[c,g]azecines Modulate the Dopamine Receptor Subtype Affinity and Selectivity
Maria Schulze, Oliver Siol, Werner Meise, Jochen Lehmann and Christoph Enzensperger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     ervachinine E
C20H24N2O2     ÏàËÆ¶È:55%
Chinese Journal of Natural Medicines          2012          10          226-229
A new monoterpenoid indole alkaloid from Ervatamia chinensis
Ling-Li GUO, Yu ZHANG, Hong-Ping HE, Yan LI, Jian-Ping YU, Xiao-Jiang HAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     compound 6
     ÏàËÆ¶È:54.5%
Steroids          1994          59          305-309
Synthesis of new 16-spirosteroids
Lutz F. Tietze, J¨¢nos Wölfling, Gyula Schneider, Mathias Noltemeyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-isocyanate-17-acetylgona-1,3,5(10),13(17)-tetraene
C19H25NO2     ÏàËÆ¶È:52.3%
Steroids          2006          71          459-468
Efficient synthesis of C-11 functionalized steroids
Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     1-[2-(3-Chlorpropyl-5-methoxy)-phenyl]-6,7-dimethoxy-3,4-dihydroisochinolin-hydrochlorid
C21H25Cl2NO3     ÏàËÆ¶È:52.3%
Pharmazie          1999          54          658-666
Synthese von Isochino[1,2-a][2]benzazepinen und biochemische Testung isomerer Homoberbine und verwandter Papaverin-Derivate auf Hemmung der Phosphodiesterasen
W. Meise - O. Onusseit - M. Clemens
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     N-(4-amino-2,6-diisopropylphenyl)-N'-{[4-(3-methoxyphenyl)-1-pyridin-4-ylpiperidin-4-yl]methyl} urea dihydrochloride
C31H41N5O2     ÏàËÆ¶È:52.3%
Bioorganic & Medicinal Chemistry          2009          17          4636-4646
Synthesis and structure¨Cactivity relationships of N-(4-amino-2,6-diisopropylphenyl)-N¡¯-(1,4-diarylpiperidine-4-yl)methylureas as anti-hyperlipidemic agents
Shigehiro Asano, Hitoshi Ban, Koichi Kino, Katsuhisa Ioriya, Masami Muraoka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     6-hexyl-6-methyl-5,6-dihydro-9-phenanthridinylmethyl Ether
C21H27NO     ÏàËÆ¶È:52.3%
European Journal of Organic Chemistry          2010                   4719-4731
AuI-Catalyzed Direct Hydroamination/Hydroarylation and Double Hydroamination of Terminal Alkynes
Nitin T. Patil, Pediredla G. V. V. Lakshmi and Vipender Singh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     stephalonganine B
C19H23NO4     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2006          Vol. 89          1105
New Stephaoxocane Alkaloids from Stephania longa
Hua Zhang and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 6
C20H26N2O2     ÏàËÆ¶È:50%
Helvetica Chimica Acta          1999          Vol. 82          170
A New Rearrangement in Iboga Alkaloids
Alberto Madinaveitia, Gabriel de la Fuente, and Antonio Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     belladine
C19H25NO3     ÏàËÆ¶È:50%
Phytochemistry          2005          66          373-382
Alkaloids from Nerine filifolia
Jerald J. Nair, William E. Campbell, Reto Brun, Francesc Viladomat,Carles Codina, Jaume Bastida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     9-O-demethyl-7-methyllycorenine
C18H23NO4     ÏàËÆ¶È:50%
Journal of Natural Products          2007          70          1458-1461
Benzylphenethylamine Alkaloids from Hosta plantaginea with Inhibitory Activity against Tobacco Mosaic Virus and Acetylcholinesterase
Yue-Hu Wang,Zhong-Kai Zhang,Fu-Mei Yang, Qian-Yun Sun, Hong-Ping He, Ying-Tong Di,Shu-Zhen Mu,Yang Lu, Ying Chang, Qi-Tai Zheng, Ming Ding, Jia-Hong Dong, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     diketone
C15H20O3     ÏàËÆ¶È:50%
Journal of Natural Products          2000          63          1557-1559
Sesquiterpenes from the Basidiomycete Omphalotus illudens
Trevor C. McMorris, Ricardo Lira, Peter K. Gantzel, Michael J. Kelner, and Robin Dawe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     (+)-trans-3'-bromo-4'-benzoyloxy-3',4'-dihydroseselin
     ÏàËÆ¶È:50%
Journal of Natural Products          1998          61          982-986
Synthesis and Cytotoxic Activity of Pyranocoumarins of the Seselin and Xanthyletin Series
Prokopios Magiatis, Eleni Melliou, Alexios-Leandros Skaltsounis, Sofia Mitaku, St¨¦phane L¨¦once, Pierre Renard, Alain Pierr¨¦, and Ghanem Atassi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     cossonidine
C20H27NO2     ÏàËÆ¶È:50%
Journal of Natural Products          1996          59          145-147
The Structure of Cossonidine: A Novel Diterpenoid Alkaloid
Matias Reina, Jose A. Gav¨ªn, Alberto Madinaveitia, Rafael D. Acosta, and Gabriel de la Fuente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     gardnerine
     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1978          26          3444-3449
Gardneria Alkaloids. XII. Carbon Magnetic Resonance Spectra of Gardneria Alkaloids. A Study on the Configuration of the Side Chain Double Bonds of Indole Alkaloids
NORIO AIMI,KEIICHI YAMAGUCHI,SHINICHIRO SAKAI,JOJU HAGINIWA and AKINORI KUBO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     compound 11
     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          1988          24          241-246
1H and 13C NMR SPECTRA OF BIOLOGICALLY ACTIVE COMPOUNDS.III. DIASTEREOMERS OF (¡À)-7-THIA- AND 13-THIA-16-ARYLOXY ANALOGS OF II-DEOXYPROSTAGLANDINS OF THE E l SERIES
L. M. Khalluov, A. A. Panasenko E. V. Vasil'eva, N. A. Danilova,Ya. L. Vel'der, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     metabolite-F
     ÏàËÆ¶È:50%
Steroids          2002          67          907-915
On the structures of hydroxylated metabolites of estradiol 17-sulfate by rat liver microsomes
Yoshimi Itoh, Noriko Matsuda, Keiko Matsuura, Kazuhiro Watanabe, Kaori Takanashi, Shinji Itoh, Hidetoshi Takagi, Itsuo Yoshizawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     16¦Â-chloromethyl-3-methoxy-13¦Á-estra-1,3,5(10)-trien-17¦Á-ol
     ÏàËÆ¶È:50%
Steroids          2003          68          451-458
Stereoselective halogenation of the 16-hydroxymethyl-3-methoxy-13¦Á-estra-1,3,5(10)-trien-17-ols and their solvolytic investigation
J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, P¨¦ter Forg¨®, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     16¦Â-iodomethyl-3-methoxy-13¦Á-estra-1,3,5(10)-trien-17¦Á-ol
C20H27IO2     ÏàËÆ¶È:50%
Steroids          2003          68          451-458
Stereoselective halogenation of the 16-hydroxymethyl-3-methoxy-13¦Á-estra-1,3,5(10)-trien-17-ols and their solvolytic investigation
J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, P¨¦ter Forg¨®, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     3-Methoxy-7¦Á-methylestra-1,3,5(10),15-tetraen-17-one
     ÏàËÆ¶È:50%
Steroids          2004          69          495-499
The synthesis of functionalized 13,14-seco-steroids via Grob fragmentation
Vladimir A. Khripach, Vladimir N. Zhabinskii, Galina P. Fando, Alla I. Kuchto, Alexander S. Lyakhov, Alla A. Govorova, Marinus B. Groen, Jaap van der Louw, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-carboethoxy-17acetylgona-1,3,5(10),13(17)-tetraene
C23H28O4     ÏàËÆ¶È:50%
Steroids          2006          71          459-468
Efficient synthesis of C-11 functionalized steroids
Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-amino-17-acetylgona-1,3,5(10),13(17)-tetraene
C20H25NO2     ÏàËÆ¶È:50%
Steroids          2006          71          459-468
Efficient synthesis of C-11 functionalized steroids
Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     methyldactyloidin
     ÏàËÆ¶È:50%
Natural Product Research          1998          12          91-95
Dactyloidin, a New Diaryl Nonanoid from Myristica Dactyloides
H. M. T. B. Herath; A. M. A. Priyadarshani; Joanne Jamie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     methyldactyloidin
     ÏàËÆ¶È:50%
Natural Product Research          1999          14          141-146
Demethyldactyloidin and Other Constituents in Myristica Ceylanica
H. M. T. B. Herath; Wimal Padmasiri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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