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17.220,20.359,22.453,22.561,25.935,26.413,34.031,35.402,38.637,38.916,39.194,39.472,39.750,40.028,40.305,46.350,48.531,46.531,115.802,123.555,133.527,137.310,142.962,148.704,196.475,215.398
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tongge: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-11-26 13:13:50
1 .     11-hydroxy-12-methoxyabieta-8,11,13-triene-3,7-dione
    ÏàËÆ¶È:61.5%
Journal of Shenyang Pharmaceutical University          2009          26          956-961
Isolation and identification of chemical constituents from Taxus cuspidta Sibe. et Zucc.
LI Ya-nan, WANG Wen-ze, WU Li-jun, WANG Ji-wen, GAO Hui-yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (-)-agelasine D
C26H41N5O     ÏàËÆ¶È:57.6%
Bioorganic & Medicinal Chemistry          2010          18          1297-1311
From anti-fouling to biofilm inhibition: New cytotoxic secondary metabolites from two Indonesian Agelas sponges
Triana Hertiani, RuAngelie Edrada-Ebel, Sofia Ortlepp, Rob W.M. van Soest, Nicole J. de Voogd, Victor Wray, Ute Hentschel, Svetlana Kozytska, Werner E.G. M¨¹ller, Peter Proksch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     compound 3
C28H40O4     ÏàËÆ¶È:57.1%
Phytochemistry          1985          24          1047-1050
Tetraprenyltoluquinols from the brown alga Cystoseira jabukae
Vincenzo Amico, Francesca Cunsolo, Mario Piattelli, Giuseppe Ruberto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     Macrocarpoic acid B
C30H46O4     ÏàËÆ¶È:56.6%
Natural Product Communications          2006          1          1073-1078
Triterpenes from Maytenus macrocarpa and Evaluation ofTheir Anti-HIV Activity
Sonia Piacente, Lourdes Campaner Dos Santos, Naheed Mahmood and Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     Sumaresinolic acid
C30H48O4     ÏàËÆ¶È:56.6%
Natural Product Communications          2009          4          1323-1326
Triterpenes from Warszewiczia coccinea (Rubiaceae) asInhibitors of Acetylcholinesterase
Angela I. Calder¨®n, Johayra Simithy, Giuliana Quaggio, Alex Espinosa,Jose Luis L¨®pez-P¨¦rez and Mahabir P. Gupta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     ÆÑ¹«Ó¢çÞ´¼
    ÏàËÆ¶È:55.5%
Journal of Shenyang Pharmaceutical University          2008          25          623-626
Chemical constituents of the stems and leaves of Calophyllum inophyllum
LIU Dan, LI Zhan-lin, LI Yan-zhi, HUA Hui-ming, LIU Ming-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     2¦Á-Hydroxyurs-12-en-28-oic acid
C30H48O3     ÏàËÆ¶È:55.1%
Journal of Natural Products          2009          72          1414-1418
Synthesis of 3-Deoxypentacyclic Triterpene Derivatives as Inhibitors of Glycogen Phosphorylase
Pu Zhang,Jia Hao,Jun Liu,Qian Lu, Huaming Sheng, Luyong Zhang, and Hongbin Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     3-oxo-20S-hydroxytaraxastane
C30H52O2     ÏàËÆ¶È:55.1%
Fitoterapia          2001          72          709-711
Triterpenes from the resin of Protium heptaphyllum
G.S. Susunaga, A.C. Siania, M.G. Pizzolatti,R.A. Yunes, F. Delle Monache
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     11¦Â-hydroxydihydrocedrelone
C26H32O6     ÏàËÆ¶È:53.8%
Journal of Natural Products          2000          63          947-951
Tetranortriterpenoids from Walsura yunnanensis
Xiao-Dong Luo, Shao-Hua Wu, Yun-Bao Ma, and Da-Gang Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     Isopseudolarifuroic acid B
C26H40O3     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry Letters          2001          11          3119-3122
Two Novel Cytotoxic and Antimicrobial Triterpenoids from Pseudolarix kaempferi
Sheng-Ping Yang, Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     agelasine-D
C26H39N5     ÏàËÆ¶È:53.8%
Bulletin of the Chemical Society of Japan          1986          59          2495-2504
Structures of Agelasines, Diterpenes Having a 9-Methyladeninium Chromophore Isolated from the Okinawan Marine Sponge Agelas nakamurai Hoshino
Houming Wu, Hideshi Nakamura, Jun¡¯ichi Kobayashi, Masaki Kobayashi, Yasushi Ohizumi, Yoshimasa Hirata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     amphidinolide T4
C25H42O5     ÏàËÆ¶È:53.8%
The Journal of Organic Chemistry          2001          66          134-142
Amphidinolides T2, T3, and T4, New 19-Membered Macrolides from the Dinoflagellate Amphidinium sp. and the Biosynthesis of Amphidinolide T1
Jun'ichi Kobayashi, Takaaki Kubota, Tetsuya Endo, and Masashi Tsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 19
    ÏàËÆ¶È:53.8%
Journal of Agricultural and Food Chemistry          2008          56          2985-2988
Preparation and Phytotoxicity of Novel Kaurane Diterpene Amides with Potential Use as Herbicides
Maria Am¨¦lia Diamantino Boaventura, Rondinelle Gomes Pereira, Luiza B. de Oliveira Freitas, Leandro Alves dos Reis and Henriete da Silva Vieira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     floridenol
C25H42O     ÏàËÆ¶È:53.8%
Journal of the American Chemical Society          1981          103          7009-7011
Unusual sesterterpenoids from the secretion of Ceroplastes floridensis (Coccidae), an orchard pest. Application of the allylic benzoate method for determination of absolute configuration
Yoko Naya, Kazuo Yoshihara, Takashi Iwashita, Hajime Komura, Koji Nakanishi, Yasuo Hata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     foliasalaci B1
C30H50O2     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2008          56(7)          915-920
Hnew Triterpene Constituents, Foliasalacins A1¡ªA4, B1¡ªB3, and C, from the Leaves of Salacia chinensis
Masayuki YOSHIKAWA,Yi ZHANG, Tao WANG, Seikou NAKAMURA, and Hisashi MATSUDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     22¦Â,29-dihyroxy-12-oleanen-3-one
C30H48O3,     ÏàËÆ¶È:53.3%
Journal of Natural Products          2008          71(11)          1829-1832
Triterpenoids and Aromatics from Derris laxiflora
Hsi-Lin Chiu, Jyh-Horng Wu, Yu-Tang Tung, Tzong-Huei Lee, Shin-Chang Chien, and Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     3-O-acetyldaturadiol
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          1379-1384
Activity of Triterpenoid Glycosides from the Root Bark of Mussaenda macrophylla against Two Oral Pathogens
Nam-Cheol Kim, Anne E. Desjardins, Christine D. Wu, and A. Douglas Kinghorn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     29-hydroxy-3-oxo-olean-12-en-28-oic acid
C30H46O4     ÏàËÆ¶È:53.3%
Phytochemistry          2000          53          805-810
Triterpenoids from Tripterygium wilfordii
Hongquan Duan, Yoshihisa Takaishi, Hiroshi Momota, Yasukazu Ohmoto, Takao Taki, Yongfeng Jia , Duan Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     methylsumaresinolate
    ÏàËÆ¶È:53.3%
Phytochemistry          1994          37          1517-1575
13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features
Shashi B. Mahato, Asish P. Kundu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     methyl-3-episumaresinolate
    ÏàËÆ¶È:53.3%
Phytochemistry          1994          37          1517-1575
13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features
Shashi B. Mahato, Asish P. Kundu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     21-oxo-3,4-seco-olean-4(23)-12-dien-3-oic acid
C30H46O3     ÏàËÆ¶È:53.3%
Phytochemistry          1991          30          1221-1223
Seco ring-A triterpene acids from the resin of Dacryodes normandii
Ian C. Parsons, Alexander I. Gray, Peter G. Waterman, Catherine Lavaud, Georges Massiot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     ÐܹûËá(ursolic acid)
    ÏàËÆ¶È:53.3%
Chinese Traditional and Herbal Drugs          2011          42(5)          841-843
Chemical constituents in root of Actinidia chinensis
CHEN Xiao-xiao, YANG Shang-jun, BAI Shao-yan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     sumresinolic
C30H48O4     ÏàËÆ¶È:53.3%
Natural Product Research and Development          2009          21          242-245
Study on Chemical Constituents of Uncaria rhynchophylla
DENG Mei-cai; JIAO Wei; DONG Wei-wei; YANG Chun-bin; LU Run-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     hongdoushan C
C27H42O6     ÏàËÆ¶È:51.8%
Journal of Natural Products          2002          65          1700-1702
Three New C-14 Oxygenated Taxanes from the Wood of Taxus yunnanensis
Arjun H. Banskota, Tepy Usia, Yasuhiro Tezuka, Kyoji Kouda, Nhan Trung Nguyen, and Shigetoshi Kadota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     3-(11'-Carboxy-3',7',15'-trimethylhexadecyl)-4,5-dihydroxybenzoic acid
C31H44O6     ÏàËÆ¶È:51.8%
Phytochemistry Letters          2009          2          119-112
Caldensinic acid, a prenylated benzoic acid from Piper caldense
Giovana C. Freitas, Rodrigo O. Saga Kitamura, João Henrique G. Lago, Maria Claudia M. Young, Elsie F. Guimarães, Massuo J. Kato
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     ent-methylisoozate dimer
C42H64O4     ÏàËÆ¶È:51.8%
Phytochemistry          1999          51          813-817
Labdane dimers from Xylopia aromatica
Dirceu Martins, Lidilhone Hamerski, Sandra A.V. Alvarenga, Nidia F. Roque
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     urs-12(13)-en-3-on-28-oic acid
    ÏàËÆ¶È:51.8%
Acta Scientiarum Naturalium Universitatis Sunyatseni          1996          35(S2)          40-44
Studies on the Chemical Constituents of the Lu Lu Tong(2)
Lai Zuoqi, Dong Yong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     oleanolic acid
    ÏàËÆ¶È:51.7%
Chinese Traditional and Herbal Drugs          2011          42          230-233
Chemical constituents of Limonium sinense
LIU Xing-kuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     methyl 3-epi-sumaresinolate
C31H50O4     ÏàËÆ¶È:51.6%
Journal of Natural Products          1992          Vol 55          963
Triterpenes from Miconia stenostachya
Wilfred R. Chan, Veronica Sheppard, Kathleen A. Medford, Winston F. Tinto, William F. Reynolds, Stewart McLean
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     oleanolic aldehyde acetate
    ÏàËÆ¶È:51.6%
Korean Journal of Pharmacognosy          2010          41          97-102
Inhibition of IL-6 Production in TNF- Stimulated MG-63 by the Triterpenoids Isolated from Aucuba japonica
Jin, Qinglong; Jin, Hong-Guang; Shin, Ji-Eun; Choi, Eun-Jin; Woo, Eun-Rhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     oleanolic aldehyde acetate
    ÏàËÆ¶È:51.6%
Korean Journal of Pharmacognosy          2010          41          97-102
Inhibition of IL-6 Production in TNF-¦Á Stimulated MG-63 by the Triterpenoids Isolated from Aucuba japonica
Qinglong Jin, Hong-Guang Jin, Ji Eun Shin, Eun Jin Choi and Eun-Rhan Woo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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