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1 .     3¦Â-hydroxytirucallic acid
C30H48O3     ÏàËÆ¶È:93.3%
Zeitschrift f¨¹r Naturforschung C          2003          58          505-516
Immunomodulatory Triterpenoids from the Oleogum Resin of Boswellia carterii Birdwood
F. A. Badria, B. R. Mikhaeil, G. T. Maatooq, and M. M. A. Amer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3¦Á-ôÇ»ù¸ÊËì-8,24-¶þÏ©-21-Ëá
    ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2011          42          1293-1296
Chemical constituents from frankincense
WANG, Feng, HUA, Hui-ming, WANG, Shu-mei, LIANG, Sheng-wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3¦Â-hydroxy-lanosra-8,24-dien-21-al
    ÏàËÆ¶È:90%
Planta Medica          1984          50          197-198
3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus
Kirsti Kahlos, R. Hiltunen and M. v. Schantz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     trametenolic acid B
    ÏàËÆ¶È:90%
Phytochemistry          1999          52          1621-1627
Steroids from the fungus Fomitopsis pinicola
Joachim Rosecke, Wilfried A. Konig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3¦Â-hydroxylanosta-8,24-dien-oic acid
    ÏàËÆ¶È:90%
Chinese Traditional and Herbal Drugs          2007          38          20-23
Chemical constituents of Stenoloma chusanum
REN Bing-ru; XIA Bing; LI Wei-lin; WU Ju-lan; ZHANG Han-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3¦Â-ôÇ»ùÑòëçÞ-8,24-¶þÏ©-21-ôÈËá
    ÏàËÆ¶È:90%
Chinese Journal of Medicinal Chemistry          2003          13          34-37
Isolation and identification of the chemical constituent of Hemerocallis fulva(L.)L.
YANG Zhong-duo, LI Yuan-chao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     trametenolicacid
    ÏàËÆ¶È:90%
Natural Product Research and Development          2010          22          433-436
Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus
ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     trametenolic acid
    ÏàËÆ¶È:90%
Lishizhen Medicine and Materia Medica Research          2006          17          1178-1181
Chemical Constituents of Inonotus obliquus
ZHAO Fen-qin, PIAO Hui-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     methyl trametenolate
    ÏàËÆ¶È:87.0%
Planta Medica          1984          50          197-198
3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus
Kirsti Kahlos, R. Hiltunen and M. v. Schantz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
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²éѯ½á¹û£º¹²²éµ½11593¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     3¦Â-hydroxytirucallic acid
C30H48O3     ÏàËÆ¶È:96.6%
Zeitschrift f¨¹r Naturforschung C          2003          58          505-516
Immunomodulatory Triterpenoids from the Oleogum Resin of Boswellia carterii Birdwood
F. A. Badria, B. R. Mikhaeil, G. T. Maatooq, and M. M. A. Amer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3¦Á-ôÇ»ù¸ÊËì-8,24-¶þÏ©-21-Ëá
    ÏàËÆ¶È:96.6%
Chinese Traditional and Herbal Drugs          2011          42          1293-1296
Chemical constituents from frankincense
WANG, Feng, HUA, Hui-ming, WANG, Shu-mei, LIANG, Sheng-wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3¦Â-hydroxylanosta-8,24-dien-oic acid
    ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2007          38          20-23
Chemical constituents of Stenoloma chusanum
REN Bing-ru; XIA Bing; LI Wei-lin; WU Ju-lan; ZHANG Han-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     trametenolicacid
    ÏàËÆ¶È:93.3%
Natural Product Research and Development          2010          22          433-436
Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus
ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     trametenolic acid
    ÏàËÆ¶È:93.3%
Lishizhen Medicine and Materia Medica Research          2006          17          1178-1181
Chemical Constituents of Inonotus obliquus
ZHAO Fen-qin, PIAO Hui-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     methyl trametenolate
    ÏàËÆ¶È:90.3%
Planta Medica          1984          50          197-198
3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus
Kirsti Kahlos, R. Hiltunen and M. v. Schantz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Â-hydroxy-lanosra-8,24-dien-21-al
    ÏàËÆ¶È:90%
Planta Medica          1984          50          197-198
3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus
Kirsti Kahlos, R. Hiltunen and M. v. Schantz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     trametenolic acid B
    ÏàËÆ¶È:90%
Phytochemistry          1999          52          1621-1627
Steroids from the fungus Fomitopsis pinicola
Joachim Rosecke, Wilfried A. Konig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3¦Â-ôÇ»ùÑòëçÞ-8,24-¶þÏ©-21-ôÈËá
    ÏàËÆ¶È:90%
Chinese Journal of Medicinal Chemistry          2003          13          34-37
Isolation and identification of the chemical constituent of Hemerocallis fulva(L.)L.
YANG Zhong-duo, LI Yuan-chao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     trematenolic acid
    ÏàËÆ¶È:86.6%
Chemical & Pharmaceutical Bulletin          2002          50(12)          1603-1606
New Triterpenoids from Tricholoma saponaceum
Kazuko YOSHIKAWA,Mina KUROBOSHI, Shigenobu ARIHARA,Naoko MIURA, Noriyuki TUJIMURA,and Kenji SAKAMOTO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     trametenolic acid
    ÏàËÆ¶È:86.6%
Journal of Natural Products          2005          68          69-73
Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2
Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     trametenolic acid
    ÏàËÆ¶È:86.6%
Journal of Natural Products          1999          62          543-545
New Lanostanoid Glycosides from the Fruit Body of Laetiporus versisporus
Kazuko Yoshikawa, Kenji Matsumoto, and Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     trametenolic acid
    ÏàËÆ¶È:86.6%
Planta Medica          1984          50          197-198
3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus
Kirsti Kahlos, R. Hiltunen and M. v. Schantz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     trametenolic acid B
    ÏàËÆ¶È:86.6%
Phytochemistry          1996          41          1041-1046
Antimicrobial steroids from the fungus Fomitopsis pinicola
Anne Caroline Keller, Marc P. Maillard, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     trametenolic acid
C30H48O3     ÏàËÆ¶È:86.6%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     3¦Â-dihydroxy-lanosta-8,24-diene-21-acid
    ÏàËÆ¶È:86.6%
Chinese Traditional and Herbal Drugs          2001          32          4-6
Studies on chemical constituents of Fuscoporia obliqua
HE Jian; FENG Xiao zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     inotodiol
    ÏàËÆ¶È:86.6%
Chinese Traditional and Herbal Drugs          2001          32          4-6
Studies on chemical constituents of Fuscoporia obliqua
HE Jian; FENG Xiao zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     trametenolicacid
    ÏàËÆ¶È:86.6%
Natural Product Research and Development          2010          22          433-436
Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus
ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     compound 1
C31H50O3     ÏàËÆ¶È:83.8%
Chinese Journal of Chemistry          2001          19          702-704
A Novel Lanostanoid Lactone From the Alga Hypnea cerricornis
Xiao-Hua Xu, Xiao Chen, Jian-Hua Lu, Guang-Min Yao, Yan-Ming Li and Long-Mei Zeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     astrapteridiol
C30H50O3     ÏàËÆ¶È:83.3%
Journal of Natural Products          2008          71(12)          2077-2079
Lanostane-Type Triterpenes from the Mushroom Astraeus pteridis with Antituberculosis Activity
Rita Stanikunaite, Mohamed M. Radwan, James M. Trappe, Frank Fronczek, and Samir A. Ross
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     euphol
    ÏàËÆ¶È:83.3%
China Journal of Chinese Materia Medica          2005          30          1162-1165
Studies on chemical constitutes of green alga Chaetomorpha basiretorsa and their bioactivity
Shi Dayong, HAN Lijun, SUN Jie, YANG Yongchun, SHI Jiangong, FAN Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     15-deacetoxy-7,11-dihydroperenniporiol
    ÏàËÆ¶È:83.3%
Phytochemistry          1984          23          2885-2888
Two perenniporiol derivatives, lanostane-type triterpenoids, from the cultured mycelia of Perenniporia ochroleuca
Chieko Ino, Masao Hirotani, Tsutomu Furuya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     3¦Â-hydroxy-lanosta-8,24-diene-21-al
    ÏàËÆ¶È:83.3%
Chinese Traditional and Herbal Drugs          2001          32          4-6
Studies on chemical constituents of Fuscoporia obliqua
HE Jian; FENG Xiao zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     3¦Â-21-dihydroxy-lanosta-8,24-diene
    ÏàËÆ¶È:83.3%
Chinese Traditional and Herbal Drugs          2001          32          4-6
Studies on chemical constituents of Fuscoporia obliqua
HE Jian; FENG Xiao zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     Inoterpene D
C30H50O3     ÏàËÆ¶È:83.3%
Tetrahedron          2009          65          2443-2450
Absolute stereostructures of inoterpenes A¨CF from sclerotia of Inonotus obliquus
Seikou Nakamura, Junko Iwami, Hisashi Matsuda, Shuichi Mizuno, Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     21-hydroxylanosterol
C30H50O2     ÏàËÆ¶È:83.3%
Indian Journal of Chemistry          1987          26B          722-724
21-Hydroxylanosterol,a New Lanostane Derivative from Stem Bark of Uvariastrum zenkeri Engl. & Diels
ILIAS MUHAMMAD & CHOUDHUPY M HASAN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     compound 2a
C39H53NO5     ÏàËÆ¶È:82.8%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
3Â¥2013-08-02 10:08:32
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