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1 .     22¦Â-hydroxy-12-oleanen-3-one
C30H48O2     ÏàËÆ¶È:76.6%
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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2 .     Abrisapogenol F
    ÏàËÆ¶È:76.6%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     29-hydroxy-12-oleanene-3,22-dione
C30H46O3     ÏàËÆ¶È:73.3%
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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4 .     abrisapogenol F
C30H48O2     ÏàËÆ¶È:73.3%
Chemical & Pharmaceutical Bulletin          1989          37          846-848
NEW TRITERPENOID SAPOGENOLS FROM ABRUS CANTONIENSIS (I)
Takashi TAKESHITA,Shuichi HAMADA and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     Machaeric acid
C30H46O4     ÏàËÆ¶È:73.3%
Chemistry of Natural Compounds          2007          43          214-215
CHEMICAL RESEARCH OF Caragana microphylla Seeds
Yan Huo, Cheng Guo, Shan Lu,Qiao-Yan Zhang, and Lu-Ping Qin
Structure     13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Soyasapogenol E
    ÏàËÆ¶È:73.3%
Phytochemistry          1998          49          709-717
Bioactive polar triterpenoids from Melilotus messanensis
Francisco A. Mac¨ªas, Ana M. Simonet, Juan Carlos G. Galindo, Pedro C. Pacheco, Jose A. S¨¢nchez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     camelliagenone
C30H48O4     ÏàËÆ¶È:73.3%
Chemical & Pharmaceutical Bulletin          2011          59(6)          778-782
New Triterpenes from Barringtonia asiatica
Consolacion Yasaña RAGASA, Dinah Lorenzana ESPINELI, and Chien-Chang SHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     regelin D
C31H48O4     ÏàËÆ¶È:70.9%
Acta Pharmaceutica Sinica          1989          Vol 24          75-79
STUDIES ON NEW TRITERPENOIDS OF TRIPTERYGIUM REGELII
GM Pang; CJ Zhao; H Hori and S Inayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     3-Oxo-12-en-28-(2'-nitro-vinyl)-olean
C31H47NO3     ÏàËÆ¶È:70.9%
Journal of Asian Natural Products Research          2012          14          355-363
Synthesis and biological evaluation of oleanolic acid derivatives as antitumor agents
Lei Chen,Jian-Bo Wu,Fan Lei,Shan Qian,Li Hai and Yong Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




10 .     olean-18-en-3-one
    ÏàËÆ¶È:70%
Chemical & Pharmaceutical Bulletin          2002          50(9)          1273-1275
Fern Constituents: Triterpenoids from Adiantum capillus-veneris
Takahisa NAKANE,Yoshiko MAEDA, Hideharu EBIHARA,Yoko ARAI,Kazuo MASUDA,Akihito TAKANO, Hiroyuki AGETA,Kenji SHIOJIMA,Shao-Qing CAI,and Osama Bashir ABDEL-HALIM
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




11 .     sumaresinolic acid
    ÏàËÆ¶È:70%
Journal of Natural Products          2006          69(5)          807-810
Triterpenoids from the Resin of Styrax tonkinensis and Their Antiproliferative and Differentiation Effects in Human Leukemia HL-60 Cells
Feng Wang, Huiming Hua, Yuehu Pei, Duo Chen, and Yongkui Jing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




12 .     19¦Á-hydroxyoleanonic acid
C30H46O4     ÏàËÆ¶È:70%
Journal of Natural Products          2006          69          1092-1094
Triterpenes from Natural and Transformed Roots of Plocama pendula
Braulio M. Fraga, Carmen E. Daz, and Nayra Quintana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     22¦Â-Hydroxyoleanonic Acid
    ÏàËÆ¶È:70%
Chemistry of Natural Compounds          2006          42          442-444
OPTIMIZATION OF LANTADENES ISOLATION AND PREPARATION OF 22b-HYDROXYOLEANONIC ACID
Manu Sharma and P. D. Sharma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




14 .     ¦Â-amyrone
    ÏàËÆ¶È:70%
Acta Botanica Sinica          2001          43          426-430
The Chemical Constituents of Amoora yunnanensis
LUO Xiao-Dong, WU Shao-Hua, MA Yun-Bao, WU Da-Gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




15 .     3-oxo-19¦Á-hydroxyurs-12-en-28-oic acid
    ÏàËÆ¶È:70%
China Journal of Chinese Materia Medica          2005          30          1833-1836
Triterpenes from root of Rhaponticum uniflorum
ZHANG Yonghong, ZHANG Jiangang, XIE Jieming, CHEN Gelin, CHENG Dongliang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     cycloartenol
    ÏàËÆ¶È:70%
China Journal of Chinese Materia Medica          2003          28          1040-1042
Studies on Chemical Constituents in of Ervatamia hainanensis
TAN Xingqi, CHEN Haisheng, XU Congli, LIU Runhui, XUAN Weidong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




17 .     soyasapogenol E
    ÏàËÆ¶È:70%
Journal of Natural Products          1988          Vol 51          335
Melilotigenin, a New Sapogenin from Melilotus officinalis
Sam Sik Kang, Won Sick Woo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




18 .     3-oxo-19¦Á-hydorxyurs-12-en-28-oic acid
C30H46O4     ÏàËÆ¶È:70%
Phytochemistry          1992          31          1317-1320
Pomolic acid derivatives from the rootof Sanguisorba officinalis
Cheng, D. and Cao, X.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




19 .     21-oxo-3,4-seco-olean-4(23)-12-dien-3-oic acid
C30H46O3     ÏàËÆ¶È:70%
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

--------------------------------------------------------------------------------




20 .     ¦Â-amyrenone
C30H48O     ÏàËÆ¶È:70%
Chinese Journal of Natural Medicines          2010          8          270-273
Chemical Constituents from the Roots of Dysoxylum densiflorum
LI Chang-Song; YU Hong-Wei; LI Guo-You; ZHANG Guo-Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




21 .     ¦Â-amyrone
    ÏàËÆ¶È:70%
Chinese Journal of Natural Medicines          2010          8          244-246
A New Benzoic Acid Derivative from Eclipta prostrata
SUN Zhi-Hua; ZHANG Chao-Feng; ZHANG Mian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     Cycloartenol
C26H34O11     ÏàËÆ¶È:70%
Chemistry of Natural Compounds          2010          46          459-461
Chemical investigation of Ervatamia yunnanensis
Jing-Ling Du, Yong-Sheng Jin, Li-Ming Qiao, Li Jin and Hai-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     3¦Â,4¦Á,14¦Á,20R,24R-4,14-¶þ¼×»ùÂó½Ç
    ÏàËÆ¶È:70%
Journal of China Pharmaceutical University          1997          28          271-274
Sterols from Sedum sarmentosum
He Aimin; Hao Hongyan; Wang Mingshi; Zhang Decheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     2¦Á-Hydroxyurs-12-en-28-oic acid
C30H48O3     ÏàËÆ¶È:68.9%
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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25 .     3¦Á,22¦Â-dihydroxyolean-12-ene
C30H50O2     ÏàËÆ¶È:68.9%
Natural Product Research          2002          16          415-418
Alysinol - A New Triterpene from Alysicarpus Monolifer
Naheed Riaz; Itrat Anis; Pir Muhammad Khan; Raza Shah; Abdul Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     compound 3
    ÏàËÆ¶È:68.9%
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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27 .     (5R,8R,9R,10S,14S,17R,18R)-28-norolean-12-en-3,11,16-trione
C29H42O3     ÏàËÆ¶È:68.9%
Phytochemistry          2011          72          1804-1813
Triterpenes and neolignans from the roots of Nannoglottis carpesioides
Cai-Bin Xue, Duo-Wu Chai, Xiao-Jie Jin, Yu-Rong Bi, Xiao-Jun Yao, Wang-Suo Wu, Ying Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     Conicasterol H
C29H48O3     ÏàËÆ¶È:68.9%
Steroids          2012          77          484-495
4-Methylenesterols from Theonella swinhoei sponge are natural pregnane-X-receptor agonists and farnesoid-X-receptor antagonists that modulate innate immunity
Simona De Marino ,Raffaella Ummarino,Maria Valeria D¡¯Auria,Maria Giovanna Chini ,Giuseppe Bifulco,Claudio D¡¯Amore ,Barbara Renga, Andrea Mencarelli,Sylvain Petek ,Stefano Fiorucci,Angela Zampella
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     mzikonone
C28H38O5     ÏàËÆ¶È:68.9%
Phytochemistry          1988          27          2353-2355
A new limonoid from Turraea robusta
Mohamed S. Rajab,Michael D. Bentley,Ahmed Hassanali,Andrew Chapya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     21¦Â,28-dihydroxy-3-oxo-olean-12,20(30)-diene
C29H44O3     ÏàËÆ¶È:68.9%
Tetrahedron          2001          57          8413-8424
Immunosuppressive terpenoids from extracts of Tripterygium wilfordii
Hongquan Duan, Yoshihisa Takaishi, Hiroshi Momota, Yasukazu Ohmoto, Takao Taki, Motoo Tori, Shigeru Takaoka, Yongfeng Jia, Duan Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5Â¥2012-04-02 15:38:01
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