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1 .     ¦Â-amyrin-n-nonyl ether
C39H68O     ÏàËÆ¶È:82.0%
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
2 .     ¦Â-amyrin 3-margarate
C47H82O2     ÏàËÆ¶È:76.9%
Natural Product Research and Development          1998          10(3)          20-23
TWO NEW TRITERPENE ESTER FROM PRATIA BEGONIFOLIA
Liu Xikui; Chiu Minghua; Li Zhongrong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (3¦Â,11¦Á)-11-hydroxyolean-12-en-3-yl palmitate
C46H80O3     ÏàËÆ¶È:75%
Natural Product Research          2012          26          1869¨C1875
A new triterpene from Barringtonia asiatica
Consolacion Y. Ragasa, Dinah L. Espineli & Chien-Chang Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ¦Â-amyrin 3-palmitate
C46H50O2     ÏàËÆ¶È:74.3%
Natural Product Research and Development          1998          10(3)          20-23
TWO NEW TRITERPENE ESTER FROM PRATIA BEGONIFOLIA
Liu Xikui; Chiu Minghua; Li Zhongrong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     ¦Â-amyrin hexadecanate
    ÏàËÆ¶È:73.1%
Chinese Traditional and Herbal Drugs          2001          32          6-9
Studies on triterpenoids and steroids from Balanophora involucrata
XIA Xin zhong; HAN Hong xing; TU Peng fei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Olean-12-en-3¦Â,16¦Â-diol-3-O-palmitate
    ÏàËÆ¶È:71.7%
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
7 .     oleanol 28-Aldehyde 3-O-¦Â-palmitate
C46H78O3     ÏàËÆ¶È:71.7%
Chemistry of Natural Compounds          2012          48          416-418
A new triterpenoid ester from Lobelia sessilifolia
Jiaming Sun, Xiuli Wang, Hui Zhang and Junshan Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3¦Â-O-(8-Hydroxyoctanoyl)-12-oleanene
C38H64O3     ÏàËÆ¶È:71.7%
Journal of Agricultural and Food Chemistry          2010          58          4945-4950
New Triterpenoids and Other Constituents from a Special Microbial-Fermented Tea¡ªFuzhuan Brick Tea
Tie-Jun Ling, Xiao-Chun Wan, Wei-Wei Ling, Zheng-Zhu Zhang, Tao Xia, Da-Xiang Li and Ru-Yan Hou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3¦Â-palmitate-28-hydroxyl-¦Â-amyrin
    ÏàËÆ¶È:70.7%
Chinese Tladitional Patent Medicine          2012          34          506-508
Chemical constituents from Gentiana farreri Ball. F.
YANG Ai-mei, SUN Jing, HAN Han, SHI Xiao-long, XU Guo-qiang, ZHANG Xiao-ru
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     glut-5-ene-3¦Á-methylbutyrate
C35H58O2     ÏàËÆ¶È:69.2%
Planta Medica          1994          60          594-596
Biologically Active Compounds from the Euphorbiaceae; 2. Two Triterpenoids of Euphorbia cyparissias
Sevil Oks¨¹z. Roberto R. Gil,Heebyung Chai,JohnM. Pezzuto, GeoffreyA. Cordell,and Ayhan Ulubelen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 5a
C30H52O3     ÏàËÆ¶È:69.2%
Phytochemistry          1985          24          2359-2367
Triterpenoids from Mangifera indica
V. Anjaneyulu, K. Harischandra Prasad, K. Ravi, J.D. Connolly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     1¦Â-O-(4-Methoxy cinnamoyl)-15¦Á-hydroxy-¦Â-amyrin
C40H56O4     ÏàËÆ¶È:69.2%
Natural Product Research          2010          24          197-202
Triterpenoids from the stem bark of Rhizophora mucronata
R. M. Rohini; Amit Kumar Das
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-O-oxtylmalonyl-3¦Á,25-dihydroxy-(20S,24R)-epox-ydammarane
C41H70O6     ÏàËÆ¶È:68.2%
Bioorganic & Medicinal Chemistry          2010          18          2964-2975
Papyriferic acid derivatives as reversal agents of multidrug resistance in cancer cells
Juan Xiong, Masatoshi Taniguchi, Yoshiki Kashiwada, Michiko Sekiya, Takashi Yamagishi, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ¦Á,¦Â-amyrin
    ÏàËÆ¶È:68.2%
Natural Product Research and Development          2002          14(3)          1-6
STUDIES ON THE CHEMICAL CONSTITUENTS OF THE FLOWER OF CAMPSIS GRANDIFLORA (THUNB.)K.SCHUM.AND ITS CONTRACEPTIVE EFFECT
ZHAO Qian; LIAO Mao chuan GUO Ji xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3¦Â,24(S),25-trihydroxycycloartane and 3¦Â,24(R),25-trihydroxycycloartane
    ÏàËÆ¶È:68.2%
Zeitschrift f¨¹r Naturforschung C          2004          59          15-18
Chemical Constituents of Euphorbia marschalliana Boiss.
A. R. Jassbi, S. Zamanizadehnajari, and S. Tahara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     1,1-dimethylethyl 6-[(2-cyano-3,12-dioxooleana-1,9(11)-dien-28-oyl)amino]hexylcarbamate
C42H63N3O5     ÏàËÆ¶È:67.5%
Journal of Medicinal Chemistry          2004          47          4923-4932
Design, Synthesis, and Biological Evaluation of Biotin Conjugates of 2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oic Acid for the Isolation of the Protein Targets
Tadashi Honda, Tomasz Janosik, Yukiko Honda, Jie Han, Karen T. Liby, Charlotte R. Williams, Robin D. Couch, Amy C. Anderson, Michael B. Sporn, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     madhucic acid
C38H60O5     ÏàËÆ¶È:66.6%
Helvetica Chimica Acta          2004          Vol. 87          1194
Chemical Constituents from the Fruits of Madhuca latifolia
Bina S. Siddiqui, Shazia Khan, M. Nadeem Kardar, and Huma Aslam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3¦Á-(E)-caffeoyloxyolean-12-en-30-oic acid
C39H54O6     ÏàËÆ¶È:66.6%
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
19 .     3¦Á-(E)-coumaroyloxyolean-12-en-30-oic acid
C39H54O5     ÏàËÆ¶È:66.6%
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
20 .     Cycloartan-3¦Â-(2-methyl butanoate)
    ÏàËÆ¶È:66.6%
Molecules          2000          5          M163
Cycloeucalen-3¦Â-(2-methyl Butanoate). ew Cycloeucalen Isolated from the Espeletiabarclayana Cuatr (Asteraceae)
Tellez Alba ohemi, Torrenegra Ruben, Pedrozo Julio and Mart¨ªnez Astrid
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     4-Butyl-5-N-cyclohexylcarboxamido-4-aza-5¦Á-cholestan-3-one
C37H64N2O2     ÏàËÆ¶È:66.6%
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
22 .     3¦Â-dodecanoyl erythrodiol
C42H72O3     ÏàËÆ¶È:66.6%
Acta Pharmaceutica Sinica          2009          Vol 44          1258−1261
A new erythrodiol triterpene fatty ester from Scorzonera mongolica
WANG Bin; LI Guo-qiang; GUAN Hua-shi; YANG Li-ye; TONG Guo-zhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     compound 1a
C39H51NO5     ÏàËÆ¶È:66.6%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     compound 3a
C40H53NO5     ÏàËÆ¶È:66.6%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     compound 4a
C40H55NO5     ÏàËÆ¶È:66.6%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     ¦Â-amyrin-3-palmitate
C46H80O2     ÏàËÆ¶È:66.6%
Chinese Journal of Natural Medicines          2007          5          259-262
Non-alkaline Constituents From the Leaf of Alstonia scholaris
DU Guo-Shun; CAI Xiang-Hai; SHANG Jian-Hua; LUO Xiao-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     4¦Â-demethyl-24-methylenecy-cloartanyl 3¦Â-p-hydroxy-m-methoxy-trans-cinnamate
C40H58O4     ÏàËÆ¶È:66.6%
Journal of the Indian Chemical Society          1993          70          543-548
Jatrocurin,a New Tetracyclic Triterpene from Jatropha curcas
SUNIL K.TALAPATRA.KABITA MANDAL and BANI TALAPATRA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     compound 1d
C41H62O4     ÏàËÆ¶È:66.6%
Journal of the Indian Chemical Society          1991          68          88-91
Arundinol,A New Triterpene from the Orchid Arundina bambusifolia
P.L.MAJUMDER and SABARI GHOSAL
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     3¦Á-Succinyl-14-taraxeren-28-oic acid
C34H52O6     ÏàËÆ¶È:66.6%
Journal of Asian Natural Products Research          2013          15          515-524
Anti-HIV and NO production inhibition activities of epi-aleuritolic acid derivatives
Jia-Bao Liu, Ying Zhang, Bao-Song Cui, Ying-Li Cao, Shao-Peng Yuan, Ying Guo, Qi Hou & Shuai Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     ¦Á-amyrin hexacosoate
    ÏàËÆ¶È:65.9%
Journal of Chinese Pharmaceutical Sciences          2000          9          131-133
A New Triterpene from Rosemary (Rosmarinus officinalis)
Zhou Qunfang, Xu Zhanhui, Tu Pengfei, Li Gansun and Chen Hongming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     Cholesteryl-9,10-dihydroxystearate
C45H80O4     ÏàËÆ¶È:65.9%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     ¦Â-ÏãÊ÷Ö¬ËØ×Ø¸éËáõ¥
    ÏàËÆ¶È:65.9%
Chinese Traditional and Herbal Drugs          2006          37          338-340
Chemical constituents in Ixeridium gramineum
LIU Jun-xi; WEI Xiao-ning; LU Run-hua; SHI Yan-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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