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16.0,17.1,17.9,21.5,22.9,23.0,24.4,25.8,25.9,26.2,27.1,28.3,31.2,32.6,35.6,35.7,37.5,37.8,43.8,47.8,47.8,49.4,50.3,80.8,116.4,120.6,123.7,132.5,142.5,145.9,171.2,182.7
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mengbuluo: ½ð±Ò+10 2014-04-18 13:49:23
1 .     (3b)-3-(acetyloxy)lanosta-7,9(11),24-trien-21-oic acid
C32H48O4     ÏàËÆ¶È:100%
Helvetica Chimica Acta          2013          96          2092-2097
Lanostane Triterpenes from Ceriporia lacerate HS-ZJUT-C13A, a Fungal Endophyte of Huperzia serrata
You-Min Ying, Wei-Guang Shan, Li-Wen Zhang, Yan Chen and Zha-Jun Zhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 4a
    ÏàËÆ¶È:81.2%
Journal of Natural Products          1986          Vol 49          1122
Two New Lanostanoids from Ganoderma lucidum
Akio Fujita, Munehisa Arisawa, Manabu Saga, Toshimitsu Hayashi, Naokata Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Dehydroeburicoic acid monoacetate
    ÏàËÆ¶È:78.7%
Phytochemistry          1996          41          1389-1392
Steroids and triterpenoids of Antodia cinnamomea¡ªA fungus parasitic on Cinnamomum micranthum
Shu-Wei Yang, Ya-Ching Shen, Chung-Hsiung Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     31¦Â-acetoxy-5¦Á-lanosta-8,24-dien-21-oic acid
C32H50O4     ÏàËÆ¶È:78.1%
Phytochemistry          1997          46          1143-1146
Steroids of formosan Ganoderma tsugae
Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 4a
    ÏàËÆ¶È:78.1%
Journal of Natural Products          1988          Vol 51          54
Revision of 1H- and 13C-nmr Assignments of Lanostanoids from Ganoderma lucidum by 2D-nmr Studies
Munehisa Arisawa, Akio Fujita, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita, Tohru Kikuchi, Shigetoshi Kadota, Yasuhiro Tezuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Hypocrellol B
C32H50O4     ÏàËÆ¶È:78.1%
Journal of Natural Products          2011          74          2143−2150
Lanostane and Hopane Triterpenes from the Entomopathogenic Fungus Hypocrella sp. BCC 14524
Masahiko Isaka, Panida Chinthanom, Malipan Sappan, Rungtiwa Chanthaket,J. Jennifer Luangsa-ard, Samran Prabpai, and Palangpon Kongsaeree
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     antiquol C acetate
C32H50O2     ÏàËÆ¶È:75%
Journal of Natural Products          2002          65          158-162
Eupha-7,9(11),24-trien-3a-ol (¡°Antiquol C¡±) and Other Triterpenes from Euphorbia antiquorum Latex and Their Inhibitory Effects on Epstein-Barr Virus Activation
Toshihiro Akihisa, E. M. Kithsiri Wijeratne, Harukuni Tokuda, Fumio Enjo, Masakazu Toriumi,Yumiko Kimura, Kazuo Koike, Tamotsu Nikaido, Yasuhiro Tezuka, and Hoyoku Nishino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3¦Â,16¦Á-dihydroxylanosta-7,9(11),24-trien-21-oic acid
    ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin          1996          44          847-849
Isolation of Inhibitors of TPA-Induced Mouse Ear Edema from Hoelen, Poria cocos
Haruo NUKAYA,Hirokazu YAMASHIRO,Hirotatsu FUKAZAWA,Hitoshi ISHIDA and Kuniro TSUJI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3¦Â-acetoxy-¦Â-amyrin
    ÏàËÆ¶È:75%
China Journal of Chinese Materia Medica          2006          31          131-133
Chemical constituents from roots of Ficus hirta
LI Chun, BU Pengbin, YUE Dangkun, SUN Youfu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ganodermanondiol
C30H48O3     ÏàËÆ¶È:75%
Journal of Natural Products          1986          Vol 49          1122
Two New Lanostanoids from Ganoderma lucidum
Akio Fujita, Munehisa Arisawa, Manabu Saga, Toshimitsu Hayashi, Naokata Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ganodermanondiol
    ÏàËÆ¶È:75%
Journal of Natural Products          1988          Vol 51          54
Revision of 1H- and 13C-nmr Assignments of Lanostanoids from Ganoderma lucidum by 2D-nmr Studies
Munehisa Arisawa, Akio Fujita, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita, Tohru Kikuchi, Shigetoshi Kadota, Yasuhiro Tezuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ganodermanondiol
C30H48O3     ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2005          36          502-504
ËÉɼÁéÖ¥µÄ»¯Ñ§³É·ÖÑо¿
ÆÕÇí»Ý,³Âºç,³ÂÈôÜ¿
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ganoderm anondiol
C30H48O3     ÏàËÆ¶È:75%
Lishizhen Medicine and Materia Medica Research          2009          20          1771-1773
Chemical Constituents from Fruiting Bodies of Ganoderma lucidum.
CHEN Man; ZHANG Mi; ZHANG Han-qing; SUN Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 1a
C39H51NO5     ÏàËÆ¶È:74.2%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     fomitopsic acid B,21-(carboxyacetoxy)lanosta-7,9(11),24-trien-3-one
C32H48O3     ÏàËÆ¶È:72.7%
Phytochemistry          1999          52          1621-1627
Steroids from the fungus Fomitopsis pinicola
Joachim Rosecke, Wilfried A. Konig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     methyl 3¦Á-acetyloxylanosta-8,24-dien-21-oate
    ÏàËÆ¶È:72.7%
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
17 .     Ganoderiol A triacetate
C36H56O7     ÏàËÆ¶È:72.2%
Molecules          2007          12          2038-2046
Two Novel Lanostane Triterpenoids from Ganoderma Sinense
Yin Qiao, Xian-min Zhang and Ming-hua Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     inonotsulide C
C30H46O3     ÏàËÆ¶È:71.8%
Helvetica Chimica Acta          2007          Vol. 90          2047
Three New Lanostane Triterpenoids from Inonotus obliquus
Sayaka Taji, Takeshi Yamada, Yasuko In, Shun-ichi Wada, Yoshihide Usami, Kazuo Sakuma, and Reiko Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     daldinialanone
C30H46O2     ÏàËÆ¶È:71.8%
Journal of Natural Products          2002          65          1869-1874
Chemical Constituents of the Ascomycete Daldinia concentrica
Dang Ngoc Quang, Toshihiro Hashimoto, Masami Tanaka, Manuela Baumgartner, Marc Stadler,and Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     compound 3
    ÏàËÆ¶È:71.8%
Journal of Natural Products          1998          61          485-487
Mediation of the Cytotoxicity of Lanostanoids and Steroids of Ganoderma tsugae through Apoptosis and Cell Cycle
Kim-Hong Gan, Yih-Fen Fann, Shu-Hui Hsu, Kou-Wha Kuo, and Chun-Nan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     ¦Â-Amyrin Acetate
C32H52O2     ÏàËÆ¶È:71.8%
Chemistry of Natural Compounds          2007          43          497-498
CHEMICAL CONSTITUENTS OF STEM BARK FROM Periploca sepium
Yang-Min Ma, Qi-Hua Shi, and Yang Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     ganodermanontriol
C30H48O4     ÏàËÆ¶È:71.8%
Journal of Chinese Pharmaceutical Sciences          1993          2          91-96
Studies on the Triterpenoid Constituents of the Spores from Ganoderma lucidum Karst
Ruo-Yun Chen De-Quan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     ganodermanontriol
C30H48O4     ÏàËÆ¶È:71.8%
Acta Pharmaceutica Sinica          1991          26          267-273
STUDIES ON THE TRITERPENOID CONSTITUENTS OF THE SPORES FROM GANODERMA LUCIDUM KARST
RY Chen and DQ Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     ganoderic acid SZ
C30H44O3     ÏàËÆ¶È:71.8%
Natural Product Research          2005          19          461-465
Ganoderic acid Sz, a new lanostanoid from the mushroom Ganoderma lucidum
Canjun Li; Jianhua Yin; Fujiang Guo; Decheng Zhang; Hao H. Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     3¦Á-acetyloxylanosta-8,24-diene-21-oic acid
    ÏàËÆ¶È:71.8%
Natural Product Research          2007          21          401-405
A new triterpenic alcohol from Fomitopsis pinicola
Assya Petrova; Simeon Popov; Melania Gjosheva; Vassya Bankova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     ¦Â-amyrin acetate
    ÏàËÆ¶È:71.8%
China Journal of Chinese Materia Medica          2008          33          405-408
Studies on phenolic compounds from Stellera chamaejasme
FENG Bao, GONG Xiaojie, SHI Liying, JIAN Ge, PEI Yue-hu, WANG Yong-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     ¦Â-amyrin acetate
    ÏàËÆ¶È:71.8%
China Journal of Chinese Materia Medica          2006          31          1798-1800
Studises on chemical constituents of Balanophora spicata
DAI Zhong, WANG Feng, WANG Gangli, LIN Ruichao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     3¦Á-acetoxylanosta-8,24-dien-21-oic acid
    ÏàËÆ¶È:71.8%
Phytochemistry          1999          52          1621-1627
Steroids from the fungus Fomitopsis pinicola
Joachim Rosecke, Wilfried A. Konig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     agnosterone, lanosta-7,9(11),24-trien-3-one
    ÏàËÆ¶È:71.8%
Phytochemistry          1999          52          1621-1627
Steroids from the fungus Fomitopsis pinicola
Joachim Rosecke, Wilfried A. Konig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     tsugaric acid A
C32H50O4     ÏàËÆ¶È:71.8%
Phytochemistry          1997          46          1143-1146
Steroids of formosan Ganoderma tsugae
Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     3¦Á-hydroxy-5¦Á-lanosta-8,24-dien-21-oic acid
C32H50O4     ÏàËÆ¶È:71.8%
Phytochemistry          1997          46          1143-1146
Steroids of formosan Ganoderma tsugae
Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     3-oxo-5¦Á-lanosta-8,24-dien-21-oic acid
    ÏàËÆ¶È:71.8%
Phytochemistry          1997          46          1143-1146
Steroids of formosan Ganoderma tsugae
Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     ganodelmanontriol
C30H48O4     ÏàËÆ¶È:71.8%
Journal of Natural Products          1986          Vol 49          1122
Two New Lanostanoids from Ganoderma lucidum
Akio Fujita, Munehisa Arisawa, Manabu Saga, Toshimitsu Hayashi, Naokata Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     ganodermatriol triacetate
    ÏàËÆ¶È:71.8%
Journal of Natural Products          1988          Vol 51          54
Revision of 1H- and 13C-nmr Assignments of Lanostanoids from Ganoderma lucidum by 2D-nmr Studies
Munehisa Arisawa, Akio Fujita, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita, Tohru Kikuchi, Shigetoshi Kadota, Yasuhiro Tezuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     ganodermanontriol
    ÏàËÆ¶È:71.8%
Journal of Natural Products          1988          Vol 51          54
Revision of 1H- and 13C-nmr Assignments of Lanostanoids from Ganoderma lucidum by 2D-nmr Studies
Munehisa Arisawa, Akio Fujita, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita, Tohru Kikuchi, Shigetoshi Kadota, Yasuhiro Tezuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     compound 5a
    ÏàËÆ¶È:71.8%
Journal of Natural Products          1988          Vol 51          54
Revision of 1H- and 13C-nmr Assignments of Lanostanoids from Ganoderma lucidum by 2D-nmr Studies
Munehisa Arisawa, Akio Fujita, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita, Tohru Kikuchi, Shigetoshi Kadota, Yasuhiro Tezuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     3¦Á-acetyloxylanosta-8,24-dien-21-oic acid
    ÏàËÆ¶È:71.8%
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
38 .     ¦Â-amyrin acetate
    ÏàËÆ¶È:71.8%
Korean Journal of Pharmacognosy          2007          38(1)          76-83
Triterpenoids and Flavonoids Isolated from the Leaves of Alnus firma
Yu, Young-Beob; Nakamura, Norio; Miyashiro, Hirotsugu; Hattori, Masao; Park, Jong-Cheol
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     Hypocrellol G
C32H48O5     ÏàËÆ¶È:71.8%
Journal of Natural Products          2011          74          2143−2150
Lanostane and Hopane Triterpenes from the Entomopathogenic Fungus Hypocrella sp. BCC 14524
Masahiko Isaka, Panida Chinthanom, Malipan Sappan, Rungtiwa Chanthaket,J. Jennifer Luangsa-ard, Samran Prabpai, and Palangpon Kongsaeree
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     ¦Â-amyrin acetate
C32H52O20     ÏàËÆ¶È:71.8%
Chinese Traditional and Herbal Drugs          2008          39          182-184
Ò»Ö¦»Æ»¨»¯Ñ§³É·ÖµÄÑо¿
ѦÏþϼ;ÖÙºÆ;Ò¦ÇìÇ¿
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     ganodermanontriol
    ÏàËÆ¶È:71.8%
Chinese Traditional and Herbal Drugs          2007          38          1610-1612
Chemical constituents from fruiting bodies of Ganoderma tsugae (¢ò)
LIU Chao; PU Qiong-hui; WANG Hong-qing; CHEN Ruo-yun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     ganodermanontriol
    ÏàËÆ¶È:71.8%
Chinese Traditional and Herbal Drugs          2005          36          1601-1603
Chemical constituents from fruiting bodies of Ganoderma lucidum
ZHANG Xiao-qi; YIN Zhi-qi; YE Wen-cai; ZHAO Shou-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     dehydroeburiconic acid
C31H48O3     ÏàËÆ¶È:71.8%
Chinese Traditional and Herbal Drugs          2005          36          811-814
Chemical constituents of Fomes officinalis (¢ñ)
WU Xia; YANG Jun-shan; DONG Yue-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     ¦Â-amyrin acetate
C32H52O2     ÏàËÆ¶È:71.8%
Chinese Journal of Natural Medicines          2007          5          31-34
Chemical Constituents of Corydalis saxicola
WANG Qi-Zhi; LIANG Jing-Yu; YUAN Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     ¦Â-amyrin acetate
    ÏàËÆ¶È:71.8%
Chinese Journal of Natural Medicines          2010          8          183-185
Chemical Constituents from Euphorbia ebracteolata
DENG Bin; MU Shu-Zhen; HAO Xiao-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     pulcherryl acetate
    ÏàËÆ¶È:71.8%
Chinese Pharmaceutical Journal          2010          45          727-732
Antitumor Triterpenes from Scorzonera mongolica Maxim
WANG Bin, YANG Li-ye, LI Guo-qiang, GUAN Hua-shi, TONG Guo-zhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     ¦Â-amyrin acetate
    ÏàËÆ¶È:71.8%
Journal of Shenyang Pharmaceutical University          2006          23          10-12
Triterpenes from the fruits of Cucurbita pepo cv. Dayangua
GE Shan, WANG Da-cheng, XIANG Hua, ZHU Wan-ju, DENG Xu-ming, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     ¦Â-amyrin acetate
    ÏàËÆ¶È:71.8%
Journal of China Pharmaceutical University          2003          34          377-379
Stuides on the Chemical Constituents of Euphorbia ebracteolata
FU Guang-Miao; YU Bo-Yang; ZHU Dan-Ni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     24¦Á-acetoxy-3-oxoreissant-5-en-25-ol
    ÏàËÆ¶È:71.8%
Journal of the Chemical Society, Perkin Transactions 1          1989                   2259-2267
Studies on terpenoids and steroids. Part 19. Structures of three novel 19(10¡ú9)abeo-8¦Á,9¦Â,10¦Á-euphane triterpenoids from Reissantia indica(Celastraceae)
Chandra B. Gamlath, A. A. Leslie Gunatilaka and Suganthini Subramaniam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     ¦Â-amyrin acetate
C32H52O2     ÏàËÆ¶È:71.8%
Natural Product Research and Development          2008          20          280-282
Chemical Constituents of Twig Bank from Periploca sepium
MA Yang-min;SHI Qing-hua; KONG Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     ¦Â-amyrin acetate
    ÏàËÆ¶È:71.8%
Natural Product Research and Development          2006          18          74-75
Chemical Constituents of Balanophora japonica Makino
RUAN Han-li; ZHANG Yong-hui; PI Hui-fang; ZHAO Wei; WU Ji-zhou £¨
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     ¦Â-amyrin acetate
C32H52O2     ÏàËÆ¶È:71.8%
Natural Product Research and Development          2003          15          483-486
CHEMICAL CONSTITUENTS FROM EUPHORBIA WALLICHII
WANG Huan;ZHANG Xiao-feng; PAN Li; YANG Shu-min; MA Yun-bao; LUO Xiao-dong *
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     (10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-((2R,5R,6S)-5,6,7-trihydroxy-6-methylheptan-2-yl)-4,5,6,10,12,13,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
C30H48O4     ÏàËÆ¶È:71.8%
Journal of Natural Products          2011          74          2332-2337
Semisynthesis and Biological Evaluation of Ganodermanontriol and Its Stereoisomeric Triols
Erin M. Kennedy, Steven J. P¡¯Pool, Jiahua Jiang, Daniel Sliva, and Robert E. Minto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     ganodermanontriol
C30H48O4     ÏàËÆ¶È:71.8%
Agricultural and Biological Chemistry          1986          50          2887-2890
Ganoderiol A and B, New Triterpenoids from the Fungus Ganoderma lucidum (Reishi)
Hiroji SATO, Tsuyoshi NISHITOBA, Sachiko SHIRASU, Kyoko ODA, Sadao SAKAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     3¦Â-acetoxy-17¦Â-hydroxy-28-norolean-12-ene
C31H50O3     ÏàËÆ¶È:71.8%
Phytotherapy Research          2008          22          1303-1306
Triterpenoids and a sterol from the stem-bark of Styrax japonica and their protein tyrosine phosphatase 1B inhibitory activities
Joo-Hee Kwon, Min-Jung Chang, Hyo-Won Seo, Jeong-Hun Lee, Byung-Sun Min, MinKyun Na, Jin Cheol Kim, Mi Hee Woo, Jae Sue Choi, Hyeong Kyu Lee and KiHwan Bae
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     ¦Â-amyrin acetate
    ÏàËÆ¶È:71.8%
Indian Journal of Chemistry Section B          1994          33B          302-304
Chemical constituents of Artemisia roxburghiana Bess
Yu Li, Yangping Shi & Yohua Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     ¦Â-amyrin acetate
    ÏàËÆ¶È:71.8%
The Chinese Pharmaceutical Journal          2000          52          195-201
Chemical Constituents from the Leaves of Formosan Ficus septica
²ÌÑÌÁ¦(Ian-Lih Tsai), ê?ÖÇ»Ý(Jyh-Huey Chen), ¶Å²ýÒæ(Chang-Yih Duh), ê?Òæ•N(Ih-Sheng Chen)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     compound 19
    ÏàËÆ¶È:71.8%
Journal of the American Chemical Society          1981          103          2075-2080
Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara
Shujiro Seo, Yutaka Tomita, Kazuo Tori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     ¦Á-amyrol acetate
    ÏàËÆ¶È:71.8%
Chinese Journal of Applied & Environmental Biology          2010          16          197-201
Chemical Study on Sambucus adnata Wall
CHEN Xiaozhen; LI Guoyou; WU Xiaoqing; HUANG Qingchun & ZHANG Guolin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     ¦Â-amyrin acetate
    ÏàËÆ¶È:71.8%
Chinese Traditional and Herbal Drugs          2012          43          1263-1266
Chemical constituents from stem barks of Daphne giraldii
LIAO Shi-yu; JIANG Jian-qin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     ¦Â-ÏãÊ÷Ö¬´¼ÒÒËáõ¥
C32H52O2     ÏàËÆ¶È:71.8%
Natural Product Research and Development          2012          24          1206-1209
Chemical Constituents from Blumea megacephala
ZHONG Lin-jing; LIN Xiao-yan; HUANG Ming-yu; HUANG Xiu-wang; ZHANG Yong-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     (22R)-hydroxylanosta-7,9(11),24-trien-3-one
    ÏàËÆ¶È:71.8%
Natural Product Research          2013          27          486-490
Cytotoxic constituents from the fungus Daldinia concentrica (Xylariaceae)
Dang Ngoc Quang, Duong Minh Lam, Nguyen Thi Hong Hanh & Do Duc Que
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
63 .     ¦Â-ÏãÊ÷Ö¬´¼ÒÒËáõ¥
C32H52O2     ÏàËÆ¶È:71.8%
Journal of Tropical and Subtropical Botany          2009          17          160-163
Chemical Constituents of Periploca forrestii Schltr .
GANG, Xiuhai, ZHOU, Xin, CHEN, Huaguo, GONG, Xiaojian, ZHANG, Jianxin, WANG, Daoping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
64 .     ¦Â-amyrin acetate
C32H52O2     ÏàËÆ¶È:71.8%
Journal of Tropical and Subtropical Botany          2012          20          529-532
Chemical Constituents from Stems of Artocarpus nitidus subsp.1ingnanensis
TI Hui-hui, LIU Mei-fang, LIN Li-dong, WEI Xiao-yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
65 .     D:C-Frirdomadeir-7-en-3¦Â-yl acetate
    ÏàËÆ¶È:71.8%
Helvetica Chimica Acta          1991          74          1329-1338
Madeiranes, a New Class of Pentacyclic Triterpenes: D-Friedo-madeir-14-en-3¦Â-ol and -3-one, D:C-Friedomadeir-7-en-3¦Â-ol and -3-one
Maria-Jos¨¦ Umbelino Ferreira, Ana M. Lobo, Caroline A. O'Mahoney, David J. Williams and Hugo Wyler
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
66 .     ¦Â-amyrin acetate
    ÏàËÆ¶È:71.8%
Lishizhen Medicine and Materia Medica Research          2013          24          786-787
Study on Chemical Constituents of Codonopsis thalictrifolia Wall£® var£® mollis ( Chipp) L£®T£®Shen
JING Jing, ZHANG Ji-fa, LI Hui, HUANG Shuai, SHAN Lian-hai, ZHOU Xian-li*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
67 .     compound 2
    ÏàËÆ¶È:71.8%
Magnetic Resonance in Chemistry          1997          35          643-646
Assignment of Carbon-13 and Proton Nuclear Magnetic Resonance Spectra of Madeirane Triterpenes
Jos¨¦ R. Ascenso and Maria Jos¨¦ U. Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
68 .     compound 5a
    ÏàËÆ¶È:70.5%
Journal of Natural Products          1986          Vol 49          1122
Two New Lanostanoids from Ganoderma lucidum
Akio Fujita, Munehisa Arisawa, Manabu Saga, Toshimitsu Hayashi, Naokata Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
69 .     compound 3a
C40H53NO5     ÏàËÆ¶È:69.4%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
70 .     compound 11
    ÏàËÆ¶È:69.4%
Journal of the Chinese Chemical Society          1991          38          71-76
Studies on the Constituents of Ganoderma lucidum
½ªºêÕÜ(Hung-Cheh Chiang);ÖìÊÀ²ý(Shih-Chang Chu)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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