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ÑîÀûÇí: ½ð±Ò+20, ¡ïÓаïÖú 2013-04-23 18:09:35
1 .     daedalol A
C31H48O4     ÏàËÆ¶È:80.6%
Bioorganic & Medicinal Chemistry          2011          19          6581-6586
Daedalols A¨CC, fungal-derived BACE1 inhibitors
Analia Sorribas, Jorge I. Jim¨¦nez, Wesley Y. Yoshida, Philip G. Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3¦Á-hhydroxy-24-methylene-23-oxolanost-8-en-26-carboxylic acid
C31H48O4     ÏàËÆ¶È:74.1%
Fitoterapia          2009          80          263-266
Antibacterial triterpenes from the threatened wood-decay fungus Fomitopsis rosea
Milena Popova, Boryana Trusheva, Melania Gyosheva, Iva Tsvetkova, Vassya Bankova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     fomitopsin A
C34H50O8     ÏàËÆ¶È:70.9%
Phytochemistry          2005          66          1656-1661
Lanostane triterpenoids from the inedible mushroom Fomitopsis spraguei
Dang Ngoc Quang, Yuuki Arakawa, Toshihiro Hashimoto, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     24-methylenecycloartanol
    ÏàËÆ¶È:68.9%
Chinese Traditional and Herbal Drugs          2005          36          669-671
ÌÙ¿à²Î»¯Ñ§³É·ÖÑо¿(¢ò)
ÕÅÁÕ,ÐìÀöÕä,ÑîÊÀÁÖ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (3¦Á,18¦Â,20¦Â)-3-methoxyamino-11-oxo-olean-12-en-29-oicacid hydrochloride
    ÏàËÆ¶È:67.7%
Bioorganic & Medicinal Chemistry          2010          18          7522-7541
Synthesis of novel 3-amino and 29-hydroxamic acid derivatives of glycyrrhetinic acid as selective 11¦Â-hydroxysteroid dehydrogenase 2 inhibitors
Christian Stanetty, Laszlo Czollner, Iris Koller, Priti Shah, Rawindra Gaware, Thierry Da Cunha, Alex Odermatt, Ulrich Jordis, Paul Kosma, Dirk Claßen-Houben
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (24S)-ergostane-6-acetate-3¦Â,5¦Á,6¦Â,25-tetraol
C30H52O5     ÏàËÆ¶È:66.6%
Marine Drugs          2012          10          1422-1432
Polyoxygenated Sterols from the South China Sea Soft Coral Sinularia sp.
Rui Li, Chang-Lun Shao, Xin Qi, Xiu-Bao Li, Jing Li, Ling-Ling Sun and Chang-Yun Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Neoabiestrine H
C30H52O4     ÏàËÆ¶È:66.6%
Phytochemistry          2012          81          159-164
Cytotoxic triterpenoids from Abies recurvata
Yong-Li Li, Yan-Xia Gao, Xian-Wen Yang, Hui-Zi Jin, Ji Ye, Luke Simmons, Ning Wang, Andre Steinmetz, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Neoabiestrine I
C31H54O4     ÏàËÆ¶È:64.5%
Phytochemistry          2012          81          159-164
Cytotoxic triterpenoids from Abies recurvata
Yong-Li Li, Yan-Xia Gao, Xian-Wen Yang, Hui-Zi Jin, Ji Ye, Luke Simmons, Ning Wang, Andre Steinmetz, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Euphonerin A
C31H52O3     ÏàËÆ¶È:64.5%
Planta medica          2012          78          1370-1377
Cycloartane Triterpenes and Ingol Diterpenes Isolated from Euphorbia neriifolia in a Screening Program for Death-Receptor Expression-Enhancing Activity
Toume, Kazufumi; Nakazawa, Takafumi; Hoque, Tahmina; Ohtsuki, Takashi; Arai, Midori A.; Koyano, Takashi; Kowithayakorn, Thaworn; Ishibashi, Masami:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Euphonerin C
C31H52O3     ÏàËÆ¶È:64.5%
Planta medica          2012          78          1370-1377
Cycloartane Triterpenes and Ingol Diterpenes Isolated from Euphorbia neriifolia in a Screening Program for Death-Receptor Expression-Enhancing Activity
Toume, Kazufumi; Nakazawa, Takafumi; Hoque, Tahmina; Ohtsuki, Takashi; Arai, Midori A.; Koyano, Takashi; Kowithayakorn, Thaworn; Ishibashi, Masami:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     serrulatin E
C30H50O6     ÏàËÆ¶È:63.3%
Helvetica Chimica Acta          2008          Vol. 91          665
Triterpenoids from the Edible Leaves of Photinia serrulata
Ya-Ling Song, Yue-Hu Wang, Qing Lu, Hui-Jun Qiao, and Yong-Xian Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     methyl 3¦Â,23(R)-dihydroxy-29-no¦Á-lanosta-8,24-dien-28-oate 3-sulfate
C30H47O7S     ÏàËÆ¶È:63.3%
Journal of Natural Products          2000          63          210-216
New Triterpenoid Sulfates from the Red Alga Tricleocarpa fragilis1
F. David Horgen, Bryan Sakamoto, and Paul J. Scheuer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     oleanolic acid
    ÏàËÆ¶È:63.3%
Natural Product Sciences          2005          11          13-15
Phytochemical Investigation of the Leaves of Flaveria trinervia
Umadevi, S.; Mohanta, G.P.; Balakrishna, K.; Manavalan, R.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Caloncobic acid A
C30H46O4     ÏàËÆ¶È:63.3%
Journal of Natural Products          2012          75          599-604
Cycloartane and Friedelane Triterpenoids from the Leaves of Caloncoba glauca and Their Evaluation for Inhibition of 11¦Â-Hydroxysteroid Dehydrogenases
James D. Simo Mpetga, Yu Shen, Pierre Tane, Shi-Fei Li, Hong-Ping He, Hippolyte K. Wabo, Mathieu Tene, Ying Leng, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Artabotryol D
C30H50O4     ÏàËÆ¶È:63.3%
Helvetica Chimica Acta          2010          93          1925-1932
Artabotryols A ¨C E, New Lanostane Triterpenes from the Seeds of Artabotrys odoratissimus
Chitrasen Gupta, Subedar Prasad, Mahendra Sahai, Teigo Asai, Noriyuki Hara and Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     sapinmusaponin B
C42H72O14     ÏàËÆ¶È:63.3%
Journal of Agricultural and Food Chemistry          2005          53          4722-4727
New Dammarane-Type Saponins from the Galls of Sapindus mukorossi
Yao-Haur Kuo, Hui-Chi Huang, Li-Ming Yang Kuo, Ya-Wen Hsu, Kuo-Hsiung Lee, Fang-Rong Chang, and Yang-Chang Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     20(R),24(S)-epoxy-6¦Á,16¦Â,25-trihydroxycycloartan-3-one
C30H48O5     ÏàËÆ¶È:63.3%
Phytochemistry          2013          88          99-104
Microbial transformation of cycloastragenol
Melis Kuban, Gaye Öngen, Ikhlas A. Khan, Erdal Bedir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (22R)-cycloart-23-ene-3¦Â,22¦Á,25-triol
    ÏàËÆ¶È:63.3%
Bioorganic & Medicinal Chemistry          2006          14          938-943
Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure¨Cactivity relationship
Mahmud Tareq Hassan Khan, Sher Bahadar Khan, Arjumand Ather
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     cycloart-20-ene-3¦Â,25-diol
C30H48O     ÏàËÆ¶È:63.3%
Bioorganic & Medicinal Chemistry          2006          14          938-943
Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure¨Cactivity relationship
Mahmud Tareq Hassan Khan, Sher Bahadar Khan, Arjumand Ather
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     cycloart-25-ene-3¦Â,(22R)22-diol
C30H50O2     ÏàËÆ¶È:63.3%
Bioorganic & Medicinal Chemistry          2006          14          938-943
Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure¨Cactivity relationship
Mahmud Tareq Hassan Khan, Sher Bahadar Khan, Arjumand Ather
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     24¦Î,25-dimethyl-cholest-5-ene-2¦Â,3¦Á-diol disodium sulfate
C29H48O8S2Na2     ÏàËÆ¶È:62.0%
Natural Product Research          2007          21          953-958
A new cytotoxic cholesterol sulfate from marine sponge Halichondria rugosa
Hong-Jun Zhang; Jing-Bo Sun; Hou-Wen Lin; Zeng-Lei Wang; Hua Tang; Ping Cheng; Wan-Sheng Chen; Yang-Hua Yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     olean-12-en-2¦Á,3¦Â-diol
    ÏàËÆ¶È:62.0%
Fitoterapia          2001          72          585-587
Triterpenes from Licania licaniaeflora
Alessandra Braca, Chandra Sortino, Jeannette Mendez, Ivano Morelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     crustulinol
C30H50O6     ÏàËÆ¶È:62.0%
Tetrahedron letters          1983          24          1635-1638
Fungal metabolites XIII: New cytotoxic triterpene from Hebeloma species (basidiomycetes)
M. De Bernardi, G. Fronza, M.P. Gianotti, G. Mellerio, G. Vidari, P. Vita-Finzi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     donellanic acid A
C29H42O4     ÏàËÆ¶È:62.0%
Tetrahedron          2012          68          4621-4627
Donellanic acids A¨CC: new cyclopropanic oleanane derivatives from Donella ubanguiensis (Sapotaceae)
Aurelie V.B. Djoumessi, Louis P. Sandjo, Johannes C. Liermann, Dieter Schollmeyer, Victor Kuete, Vincent Rincheval, Abegaz M. Berhanu, Samuel O. Yeboah, Pascal Wafo, Bonaventure T. Ngadjui, Till Opatz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Á-triol
    ÏàËÆ¶È:62.0%
Chinese Journal of Applied & Environmental Biology          2009          15          615-620
Chemical Constituents from Polygonum perfoliatum
LI Hongfang; MA Qingyun; LIU Yuqing; QIAN Jinfu; ZHOU Jun & ZHAO Youxing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     fasciospongine A
    ÏàËÆ¶È:60%
Journal of Natural Products          2009          72          319-323
Bioactive Sulfated Sesterterpene Alkaloids and Sesterterpene Sulfates from the Marine Sponge Fasciospongia sp.
Guangmin Yao, Tamara P. Kondratyuk, Ghee T. Tan, John M. Pezzuto,and Leng Chee Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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