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1 .     Abibalsamin B
C41H60O5     ÏàËÆ¶È:68.2%
Organic Letters          2012          14          1504-1507
Abibalsamins A and B, Two New Tetraterpenoids from Abies balsamea Oleoresin
Serge Lavoie, Jean Legault, Charles Gauthier, Vakhtang Mshvildadze,Sylvain Mercier, and Andr e Pichette
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     Abiestetrane A
C40H58O4     ÏàËÆ¶È:67.5%
Tetrahedron          2012          68          7763-7767
Abiestetranes A and B, two unique tetraterpenes from Abies fabri
Yong-Li Li, Shou-De Zhang, Hui-Zi Jin, Jun-Mian Tian, Yun-Heng Shen, Xian-Wen Yang, Hong-Lin Li, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Abiestetrane B
C40H58O4     ÏàËÆ¶È:67.5%
Tetrahedron          2012          68          7763-7767
Abiestetranes A and B, two unique tetraterpenes from Abies fabri
Yong-Li Li, Shou-De Zhang, Hui-Zi Jin, Jun-Mian Tian, Yun-Heng Shen, Xian-Wen Yang, Hong-Lin Li, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     Abibalsamin A
C40H58O5     ÏàËÆ¶È:62.5%
Organic Letters          2012          14          1504-1507
Abibalsamins A and B, Two New Tetraterpenoids from Abies balsamea Oleoresin
Serge Lavoie, Jean Legault, Charles Gauthier, Vakhtang Mshvildadze,Sylvain Mercier, and Andr e Pichette
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     bismagdalenic acid
C40H60O4     ÏàËÆ¶È:62.5%
Tetrahedron          1997          53          2005-2012
The isolation of novel diterpenoids, including a C40 bis-diterpenoid, from the Brazilian plant Vellozia magdalenae (Velloziaceae)
Angelo C. Pinto, Moacir G. Pizzolatti, Rosângela de A. Epifanio, Walter Frankmölle, William Fenical
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     tirucalla-7,24-dien-3 -yl 2'E,4'Edecadienoate
C40H64O2     ÏàËÆ¶È:60%
Journal of Natural Products          2009          72          1258-1264
Diterpenoids and Triterpenoids from Euphorbia retusa
Hamada Haba, Catherine Lavaud, Abdulmagid Alabdul Magid, and Mohammed Benkhaled
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     ¦Â-amyrin-n-nonyl ether
C39H68O     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2010          58          1093-1095
Two New Aristolochic Acid Derivatives from the Roots of Aristolochia fangchi and Their Cytotoxicities
Yu Cai and Tian-Ge Cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     Taraxast-20(30)-ene-3¦Â,16¦Â-diol-3-O-palmitate
     ÏàËÆ¶È:60%
Pharmazie          2006          61          70-73
Triterpenoids from Pyrethrum tatsienense
Yang Ai-Mei, Liu Xia, Lu Run-Hua and Shi Yan-Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     Avenestergenin B-1
C38H55NO6     ÏàËÆ¶È:60%
Journal of the Chemical Society, Perkin Transactions 1          1986                   1905-1915
The isolation of avenacins A-1, A-2, B-1, and B-2, chemical defences against cereal ¡®take-all¡¯ disease. Structure of their ¡®aglycones¡¯, the avenestergenins, and their anhydro dimers
Michael J. Begley, Leslie Crombie, W. Mary L. Crombie and Donald A. Whiting
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     2-((R)-[3¦Â-acetoxy-28-norlup-20(29)-en-17¦Â-yl]hydroxymethyl)-c-butyrolactone
C36H54O4     ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry          2010          18          1344-1355
Synthesis and biological evaluation of antitumour-active betulin derivatives
Ren¨¦ Csuk, Alexander Barthel, Ralph Kluge, Dieter Ströhl, Harish Kommera, Reinhard Paschke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     njaoamine D
C40H56N4O     ÏàËÆ¶È:60%
Tetrahedron          2007          63          2432-2438
Njaoamines A¨CF, new cytotoxic polycyclic alkaloids from the haplosclerid sponge Reniera sp.
Fernando Reyes, Rogelio Fern¨¢ndez, Carlos Urda, Andr¨¦s Francesch, Santiago Bueno, Carlos de Eguilior, Carmen Cuevas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     bismagdalenic acid dimethyl ester
C42H62O4     ÏàËÆ¶È:59.5%
Tetrahedron          1997          53          2005-2012
The isolation of novel diterpenoids, including a C40 bis-diterpenoid, from the Brazilian plant Vellozia magdalenae (Velloziaceae)
Angelo C. Pinto, Moacir G. Pizzolatti, Rosângela de A. Epifanio, Walter Frankmölle, William Fenical
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     Lobophytone R
C41H64O8     ÏàËÆ¶È:58.5%
Marine drugs          2010          8          2837-2848
Lobophytones O¨CT,New Biscembranoids and Cembranoid from Soft Coral Lobophytum pauciflorum
Pengcheng Yan,Zhiwei Deng,Leen van Ofwegen,Peter Proksch and Wenhan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     Dibenzyl (3¦Â,3'¦Â)-3,3'-[Hexane-1,6-diylbis(1H-1,2,3-triazole-1,4-diylmethanediyloxy)]bisolean-12-en-28-oate
     ÏàËÆ¶È:58.5%
Chemistry & Biodiversity          2010          7          690-697
Synthesis of Oleanolic Acid Dimers as Inhibitors of Glycogen Phosphorylase
Keguang Cheng, Jun Liu, Hongbin Sun and Juan Xie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (20R)-20,25-epoxy-dammaran-3¦Â,6¦Á,12¦Â-triol-3,6-di-(3',3'-dimethyl) succinate
C42H68O10     ÏàËÆ¶È:58.5%
Bioorganic & Medicinal Chemistry          2009          17          3003-3010
Synthesis of dammarane-type triterpene derivatives and their ability to inhibit HIV and HCV proteases
Ying Wei, Chao-Mei Ma, Masao Hattori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     4-(2'-(1H-benzoazol-3-yl)ethyl)-5-Ncyclohexylcarboxamido-4-aza-5¦Â-cholestan-3-one
C43H65N3O2     ÏàËÆ¶È:58.1%
Steroids          2008          73          1270-1276
Synthesis of 4-azasteroids by an intramolecular Ugi reaction
Fernando Alonso, Sof¨ªa L. Acebedo, Andrea C. Bruttomesso, Javier A. Ram¨ªrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     (3b,20R)-20- hydroxylanost-25-en-3-yl palmitate
C46H82O3     ÏàËÆ¶È:57.5%
Helvetica Chimica Acta          2006          Vol. 89          558
Terpenoids from Eupatorium fortunei TURCZ
Hai-Xia Jiang, Ya Li, Jing Pan, and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     3¦Â-[(2E,4E)-5-oxo-decadienoyloxy]-olean-12-ene
C40H62O3     ÏàËÆ¶È:57.5%
Chemical & Pharmaceutical Bulletin          2006          54(6)          920-921
Pentacyclic Triterpenoids from Leaves of Excoecaria agallocha
Jian-Hua ZOU,Jungui DAI,Xiaoguang CHEN,and Jing-Quan YUAN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     3¦Á-(E)-caffeoyloxyolean-12-en-30-oic acid
C39H54O6     ÏàËÆ¶È:57.5%
Journal of Natural Products          2008          71(5)          789-792
Oleanane-Type Triterpenes from the Flowers and Roots of Saussurea muliensis
Chun-Mei Liu, He-Xiang Wang, Shi-Lei Wei, and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     cis-securinegin
C40H60O4     ÏàËÆ¶È:57.5%
Journal of Natural Products          1998          61          96-98
Dammarane Triterpenes from the Leaves of Securinega melanthesoides
Barbara Sch¨¹ tz, Jimmy Orjala, Otto Sticher, and Topul Rali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     cis-hydroxycinnamoyl ester of amyrin
C39H56O3     ÏàËÆ¶È:57.5%
Journal of Natural Products          1997          60          1150-1151
Triterpene Esters from Australian Acacia
Marina Ali, Andrew Heaton, and David Leach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     12-O-acetyl-3¦Á,12¦Â,17¦Á,20(S),24(R)-pentahydroxydammar-25-en-3-yl hydrogen propanedioate
C35H56O9     ÏàËÆ¶È:57.5%
Planta Medica          1997          63          347-351
New Dammaranes, Esterified with Malonic Acid, from Leaves of Betula pendula
U. Hilpisch, R. Hartmann, and K.-W. Glombitza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     dammarenediol II 3-O-p-coumarate
C39H58O4     ÏàËÆ¶È:57.5%
Chemical & Pharmaceutical Bulletin          1996          44          1033-1038
Chemical Evaluation of Betula Species in Japan. II. Constituents of Betula platyphylla var. japonica
Hiroyuki FUCHINO,Soh KONISHI,Tetsuya SATOH,Akiko YAGI,Kohei SAITSU,Tatsuya TATSUMI and Nobutoshi TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     3¦Â,28-diacetoxy-30-cyclohexylaminolup-20(29)-ene
     ÏàËÆ¶È:57.5%
Chemistry of Natural Compounds          2005          41          692-700
SYNTHESIS OF 30-AMINO DERIVATIVES OF LUPANE TRITERPENOIDS
N. V. Uzenkova, N. I. Petrenko, M. M. Shakirov,E. E. Shul'ts, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     3,28-di-O-acetyl-30-N-(pentadodecylamino)-lup-20(29)-ene
C49H85NO4     ÏàËÆ¶È:57.5%
Chemistry of Natural Compounds          2004          40          571-573
SYNTHESIS OF 30-AMINO DERIVATIVES OF 3,28-DI-O-ACETYLBETULIN
O. B. Flekhter, I. E. Smirnova, F. Z. Galin,G. V. Giniyatullina E. V. Tret'yakova,and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-10-22 12:22:32
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