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2Â¥: Originally posted by СÂü1211 at 2012-04-02 13:22:51:
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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

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




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

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




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

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




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

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




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

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




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

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




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

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




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

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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

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




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

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




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

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




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

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




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

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




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

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




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

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




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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1 .     19¦Â-28-Epoxy-18¦Á-oieanan-3-one
    ÏàËÆ¶È:73.3%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




2 .     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

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




3 .     »·°¢¶ûÍ¢-23Z-Ï©-3¦Â,25-¶þ´¼£¨cycloart-23Z-ene-3¦Â,25-diol)
C30H50O2     ÏàËÆ¶È:72.4%
Chinese Traditional and Herbal Drugs          2011          42(4)          664-667
Chemical constituents of Dracocephalum heterophyllum and antibacterial activity
REN Ai-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




4 .     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

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




5 .     3¦Á,21¦Â-dihydroxy-olean-12-ene
    ÏàËÆ¶È:70%
Phytochemistry          2008          69          1057-1064
21¦Â-Hydroxy-oleanane-type triterpenes from Hippocratea excelsa
David C¨¢ceres-Castillo, Gonzalo J. Mena-Rej¨®n,Roberto Cedillo-Rivera, Leovigildo Quijano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




6 .     ¦Á-boswellic acid
    ÏàËÆ¶È:70%
Phytochemistry          2003                   537-541
A lupane triterpene from frankincense (Boswellia sp., Burseraceae)
G¨¦rald Culioli, Carole Mathe, Paul Archier, Cathy Vieillescazes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




7 .     ¦Â-boswellic acid
    ÏàËÆ¶È:70%
Phytochemistry          2003                   537-541
A lupane triterpene from frankincense (Boswellia sp., Burseraceae)
G¨¦rald Culioli, Carole Mathe, Paul Archier, Cathy Vieillescazes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




8 .     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

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




9 .     siaresinolic 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

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




10 .     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

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




11 .     subprogenin A
    ÏàËÆ¶È:70%
Chemical & Pharmaceutical Bulletin          1991          39          1908-1910
FOUR NEW AND TWELVE KNOWN SAPOGENOLS FROM SOPHORAE SUBPROSTRATE RADIX
Takashi TAKESHITA,Kei YOKOYAMA,Ding YI,Junei KINJO and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




12 .     Abrisapogenol F
    ÏàËÆ¶È:70%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




13 .     pinicolic acid B, 3,16-dioxolanosta-8,24-dien-21-oic acid
    ÏàËÆ¶È:70%
Phytochemistry          1999          52          1621-1627
Steroids from the fungus Fomitopsis pinicola
Joachim Rosecke, Wilfried A. Konig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




14 .     Soyasapogenol E
    ÏàËÆ¶È:70%
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

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




15 .     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

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




16 .     soyasapogenol E
    ÏàËÆ¶È:70%
Journal of Natural Products          1991          Vol 54          830
Constituents of Leguminous Plants, XIII. New Triterpenoid Saponins from Wistaria brachybotrys
Takao Konoshima, Mutsuo Kozuka, Mitsumasa Haruna, Kazuo Ito
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




17 .     subprogenin A
    ÏàËÆ¶È:70%
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

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




18 .     Soyasapogenol E
    ÏàËÆ¶È:70%
Korean Journal of Pharmacognosy          2008          39(3)          186-193
Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols
Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




19 .     bayogenin
    ÏàËÆ¶È:70%
Planta Medica          1995          61          246-249
New Triterpenoid Saponins, Asterbatanoside D and E, from Aster batangensis
hao, Yu; Zhou, Bing-Nan; Ma, Kan; Wu, Hou-Ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




20 .     2,3-seco-19¦Â,28-Epoxy-28-oxo-18¦Á-olean-2,3-dioic Acid
C30H46O6     ÏàËÆ¶È:70%
Chemistry of Natural Compounds          2010          46          393-396
Effective synthesis of 2,3-seco-2,3-dicarboxyplatanic acid
O. B. Kazakova, E. F. Khusnutdinova, O. S. Kukovinets, T. I. Zvereva and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




21 .     ³£´ºÌÙÔíÜÕÔª
C30H48O4     ÏàËÆ¶È:70%
Journal of China Pharmaceutical University          2003          34          222-224
Chemical Constituents from the Root of Polygala fallax Hemsl.
ZHU Dan-Ni; LI Li; ZHU Yao-Jun; YAN Yong-Qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




22 .     ¦Á-Boswellic acid
C30H48O3     ÏàËÆ¶È:70%
Natural Product Communications          2008          3          21-26
Boswellic Acids with Acetylcholinesterase InhibitoryProperties from Frankincense
Masahiro Ota and Peter J. Houghton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




23 .     3-oxo-22¦Á-hydroxy-olean-12-en-28-oic acid
C30H46O4     ÏàËÆ¶È:70%
Natural Product Communications          2012          7          13-14
Constituents of Kenyan Gardenia volkensii
Esther W. Kinuthia, Moses K. Langat*, Elizabeth M. Mwangi and Peter K Cheplogoi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




24 .     3¦Á-hydroxyolean-12-dien-23,28-dioic acid
    ÏàËÆ¶È:68.9%
Acta Pharmaceutica Sinica          2004          Vol 39          354-358
Structures of four new triterpenoid saponins from the leaves of Oplopanax elatus Nakai
WANG Guang-shu; YANG Xiao-hong; XU Jing-da
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




25 .     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

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




26 .     17,24-epoxy-20¦Á,25-dihydroxy-21-norbaccharan-3-one
C29H48O4     ÏàËÆ¶È:68.9%
Journal of Natural Products          2010          73          1873-1878
Isolation and Characterization of Minor Analogues of Silvestrol and Other Constituents from a Large-Scale Re-collection of Aglaia foveolata
Li Pan, Leonardus B. S. Kardono, Soedarsono Riswan, Heebyung Chai, Esperanza J. Carcache de Blanco, Caroline M. Pannell, Djaja Doel Soejarto, Thomas G. McCloud, David J. Newman, and A. Douglas Kinghorn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




27 .     3-oxoberenjenol
    ÏàËÆ¶È:67.7%
Journal of Natural Products          2007          70          835-838
Constituents of Oxandra cf. xylopioides with Anti-inflammatory Activity
Benjamin Rojano, Edwin P¨¦rez,Bruno Figad¨¨re,Marie Th¨¦r¨¨se Martin, Mar¨ªa C. Recio,Rosa Giner,Jos¨¦ L. R¨ªos, Guillermo Schinella,and Jairo S¨¢ez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




28 .     3-oxoolean-12-en-30-oic acid methyl ester
C31H47O3     ÏàËÆ¶È:67.7%
Chemistry of Natural Compounds          2009          45          519-521
BECKMANN REARRANGEMENT OF 11-DEOXO-GLYCYRRHETICACID 3-KETOXIME
L. R. Mikhailova, M. V. Khudobko,L. A. Baltina, Jr., and L. A. Baltina
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




29 .     3-oxcolean-12-en-28-oic acid
    ÏàËÆ¶È:67.7%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




30 .     compound 1b
    ÏàËÆ¶È:67.7%
Natural Product Research          1994          5          233-240
Two new Triterpenoid Saponins, Asterbatanoside F and G, from Aster batangensis
Yu Shao; Bing-Nan Zhou; Long-Ze Lin; Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7Â¥2012-04-02 15:57:58
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Chemistry & Biodiversity          2008          Vol. 5          751
New Pentacyclic Triterpenes from Gypsophila oldhamiana and Their Biological Evaluation as Glycogen Phosphorylase Inhibitors
Jian-Guang Luo, Jun Liu, and Ling-Yi Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




2 .     3-Keto,16¦Á-hydroxy,24-noroleanolic acid
    ÏàËÆ¶È:75.8%
Bioorganic & Medicinal Chemistry          2008          16          2912-2920
New triterpenoid saponins with strong ¦Á-glucosidase inhibitory activity from the roots of Gypsophila oldhamiana
Jian-Guang Luo, Li Ma, Ling-Yi Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




3 .     compound 5
C27H40O4     ÏàËÆ¶È:71.4%
Phytochemistry          1990          29          919-922
Dammarane triterpenes of Salvia hierosolymitana
Samuel Pedreros,Benjamin Rodr¨ªguez,Mar¨ªa C. De La Torre,Maurizio Bruno,Giuseppe Savona,Aurea Perales,Maria R. Torres
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




4 .     Methyl(20R)-20-(4-methyl-3-pentenyl)-3-oxo-pregnan-1-en-21-oate
C28H42O3     ÏàËÆ¶È:71.4%
Steroids          2010          75          1153-1163
Synthesis and antitumor evaluation of methyl spongoate analogs
Cheng-Shi Jiang, Cai-Guo Huang, Bo Feng, Jia Li, Jing-Xu Gong, Tibor Kurt¨¢n, Yue-Wei Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




5 .     Soyasapogenol E
    ÏàËÆ¶È:70%
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

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




6 .     camelliagenone
C30H48O4     ÏàËÆ¶È:70%
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

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




7 .     3-oxoolean-12-en-30-oic acid methyl ester
C31H47O3     ÏàËÆ¶È:67.7%
Chemistry of Natural Compounds          2009          45          519-521
BECKMANN REARRANGEMENT OF 11-DEOXO-GLYCYRRHETICACID 3-KETOXIME
L. R. Mikhailova, M. V. Khudobko,L. A. Baltina, Jr., and L. A. Baltina
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




8 .     3-Oxo-16¦Â-hydroxy-olean-12-en-28-al
C30H46O3     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          2007          55(4)          577-579
A Novel Benzofuran Derivative, a New Olean-Type Triterpene and Other Constituents from Ligularia odontomanes
Dong Qing FEI, Gang WU, Chun Mei LIU, and Kun GAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




9 .     22¦Â-hydroxy-12-oleanen-3-one
C30H48O2     ÏàËÆ¶È:66.6%
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

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




10 .     29-hydroxy-12-oleanene-3,22-dione
C30H46O3     ÏàËÆ¶È:66.6%
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

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




11 .     23-Hydroxylongispinogenin
    ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




12 .     Abrisapogenol F
    ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




13 .     soyasapogenol E
    ÏàËÆ¶È:66.6%
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

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




14 .     gypsogenic acid
    ÏàËÆ¶È:66.6%
Archives of Pharmacal Research          1985          8          133-137
Phytochemical study on Melandrium firmum
Won Sick Woo, Jae Sue Choi and Hye Soon Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




15 .     3-oxo-22¦Á-hydroxy-olean-12-en-28-oic acid
C30H46O4     ÏàËÆ¶È:66.6%
Natural Product Communications          2012          7          13-14
Constituents of Kenyan Gardenia volkensii
Esther W. Kinuthia, Moses K. Langat*, Elizabeth M. Mwangi and Peter K Cheplogoi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




16 .     acinospesigenin-A
C32H50O6     ÏàËÆ¶È:65.6%
Journal of Natural Products          2003          66          1121-1123
Acinospesigenin-A, -B, and -C: Three New Triterpenoids from Phytolacca acinosa
Summon Koul, T. K. Razdan,and C. S. Andotra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




17 .     19a-hydroxy-3-oxo-24-norolean-12-en-28-oic acid
C29H44O4     ÏàËÆ¶È:65.5%
Helvetica Chimica Acta          2006          Vol. 89          1971
Three New 24-Noroleanane Triterpenoids from Quercus aliena var. acuteserrata
Hua-Dong Chen, Sheng-Ping Yang, Shang-Gao Liao, Chuan-Rui Zhang, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




18 .     2a,19a-dihydroxy-3-oxo-24-norolean-12-en-28-oic acid
C29H44O5     ÏàËÆ¶È:65.5%
Helvetica Chimica Acta          2006          Vol. 89          1971
Three New 24-Noroleanane Triterpenoids from Quercus aliena var. acuteserrata
Hua-Dong Chen, Sheng-Ping Yang, Shang-Gao Liao, Chuan-Rui Zhang, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




19 .     24-nor-2¦Á,3¦Â-dihydroxyolean-4(23),12-ene (4)
C29H46O2     ÏàËÆ¶È:65.5%
Planta Medica          2006          72          643-649
New Polyhydroxylated Triterpenes and Anti-Inflammatory Activity of Salvia hierosolymitana
A. De Felice,A. Bader,A. Leone,S. Sosa,R. Della Loggia,A. Tubaro,N. De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




20 .     17¦Â-hydroxy-3,16-dioxo-28-norolean-12-ene
C29H44O3     ÏàËÆ¶È:65.5%
Planta Medica          2003          69          258-264
New Dihydrobenzofurans and Triterpenoids from Roots of Microglossa pyrifolia
homas J.Schmidt,Meike R.Hildebrand,G¨¹nter Willuhn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




21 .     3-keto,16¦Á-hydroxyl,24-noroleanolic acid
    ÏàËÆ¶È:65.5%
Phytochemistry          1998          48          529-536
Triterpenoid saponins and sapogenins from Vaccaria segetalis
Zhonghua Jia, Kazuo Koike, Momoe Kudo, Hongyu Li, Tamotsu Nikaido
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




22 .     aglycone of dianchinenoside A
    ÏàËÆ¶È:65.5%
Journal of Natural Products          1993          Vol 56          1065
Dianchinenosides A and B, Two New Saponins from Dianthus chinensis
Hong-yu Li, Kazuo Koike, Taichi Ohmoto, Keiji Ikeda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




23 .     (5R,8R,9R,10S,14S,17R,18R)-28-norolean-12-en-3,11,16-trione
C29H42O3     ÏàËÆ¶È:65.5%
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

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




24 .     3-N-1-[N(3-[4-Aminobutyl])-1,3-diaminopropane]-7,22-dihydroxy-23,24-bisnor-5¦Á-cholane trihydrochloride
C29H55N3O2     ÏàËÆ¶È:65.5%
Bioorganic & Medicinal Chemistry          2000          8          2059-2065
Synthesis and antimicrobial activity of squalamine analogue
Hong-Seok Kim, Bo-Seung Choi, Kyung-Chan Kwon, Sang-Ok Lee, Hyun Jung Kwak, Cheol Hae Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




25 .     (22E,24S)-3¦Á,5-cyclo-stigmast-22-en-6-one
    ÏàËÆ¶È:65.5%
Steroids          2012          77          91-99
Brassinosteroids and analogs as neuroprotectors: Synthesis and structure¨Cactivity relationships
Jihane Ismaili, Martin Boisvert, Fanny Longpr¨¦, Julie Carange, C¨¦line Le Gall, Maria-Grazia Martinoli, Benoit Daoust
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




26 .     ¦Â-sitosterol-3-O-stearate
    ÏàËÆ¶È:65.5%
Natural Product Research and Development          1996          8(1)          5-9
THE CONSTITUENTS FROM THE RHIZOMA OF ALTSMA ORIENTALIS (SAM) JUZEP.
Cai Lining; Wang Hongshu; Cao Hongxing; Zhang Ruyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




27 .     21¦Â,28-dihydroxy-3-oxo-olean-12,20(30)-diene
C29H44O3     ÏàËÆ¶È:65.5%
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

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




28 .     3-oxohederagenin
    ÏàËÆ¶È:64.5%
Journal of Natural Products          1999          62          445-448
Triterpenoid Saponins of Acanthopanax nipponicus Leaves
Masazumi Miyakoshi, Katsuya Shirasuna, Yasuaki Hirai, Kazushi Shingu, Susumu Isoda, Junzo Shoji, Yoshiteru Ida, and Torao Shimizu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




29 .     pisonolic acid
C31H48O5     ÏàËÆ¶È:64.5%
Journal of Natural Products          2011          74          976-982
Antitubercular Chromones and Flavonoids from Pisonia aculeata
Ming-Chun Wu, Chien-Fang Peng, Ih-Sheng Chen, and Ian-Lih Tsai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




30 .     remangilone B
C28H38O3     ÏàËÆ¶È:64.2%
Journal of Natural Products          1999          62          471-476
Remangilones A-C, New Cytotoxic Triterpenes from Physena madagascariensis
Yonghong Deng, Tian-Yi Jiang, Shijie Sheng, Manoelson Tianasoa-Ramamonjy, and John K. Snyder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8Â¥2012-04-02 16:03:54
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