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1 .     ganoderiol B
C30H48O2     ÏàËÆ¶È:93.5%
Journal of Chinese Pharmaceutical Sciences          1997          6          291-791
Triterpenoids from the Fruiting Body of Ganoderma lucidum
Fang-Sheng Wang, Hui Cai, Jun-Shan Yang, Yu-Mei Zhang and Ying-Ju Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ganoderiol B
C30H48O2     ÏàËÆ¶È:93.5%
Acta Pharmaceutica Sinica          1996          31          200-204
STUDIES ON THE TRITERPENOID CONSTITUENTS FROM THE FRUITING BODY OF GANODERMA LUCIDUM (FR.)KARST.
FS Wang; H Cai; JS Yang; YM Zhang and YJ Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ganodermadiol
C30H48O2     ÏàËÆ¶È:93.5%
Journal of Natural Products          1986          Vol 49          621
Three New Lanostanoids from Ganoderma lucidum
Munehisa Arisawa, Akio Fujita, Manabu Saga, Hideki Fukumura, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ganodermadiol
    ÏàËÆ¶È:93.5%
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
5 .     5¦Á-lanosta-7,9(11),24-trien-3¦Â,26-diol
    ÏàËÆ¶È:93.5%
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
6 .     Ganoderiol B
    ÏàËÆ¶È:93.5%
Lishizhen Medicine and Materia Medica Research          2008          19          2776-2777
Studies on the Chemical Constituents and Cytotoxicity from the Fruiting Body of Ganoderma lucidum
MAN Su-li; GAO Wen-yuan; YAN Lu-lu; ZHANG Xuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     ganoderiol B
C30H48O2     ÏàËÆ¶È:93.5%
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
8 .     Ganodermadiol
    ÏàËÆ¶È:93.5%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ganoderiol B
C30H48O2     ÏàËÆ¶È:93.5%
Mycosystema          2015          34          124−130
Compounds from the fruiting bodies of Phellinus baumii and their inhibition to tumor cell proliferation
FENG Na WU Na, YANG Yan ZHANG Jing-Song TANG Qing-Jiu SHAO Qian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3¦Â, 21-dihydroxylanosta- 7,9(11)-diene
    ÏàËÆ¶È:83.8%
Planta Medica          1986          52          495-496
3¦Â,22-Dihydroxylanosta-7,9(11),24-triene: A New, Minor Compound from Inonotus obliquus
Kirsti Kahlos and R. Hiltunen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     lucidumol B
    ÏàËÆ¶È:83.8%
Chemical & Pharmaceutical Bulletin          1998          46          1607-1612
Triterpenes from the Spores of Ganoderma lucidum and Their Inhibitory Activity against HIV-1 Protease
Byung-Sun MIN,Norio NAKAMURA,Hirotsugu MIYASHIRO,Ki-Whan BAE and Masao HATTORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     23-Hydroxyganoderic Acid S
C30H48O5     ÏàËÆ¶È:83.8%
Journal of Natural Products          2010          73          897-900
Antiplasmodial Lanostanes from the Ganoderma lucidum Mushroom
Michael Adams, Marco Christen, Inken Plitzko, Stefanie Zimmermann, Reto Brun, Marcel Kaiser and Matthias Hamburger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound I
    ÏàËÆ¶È:83.8%
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
14 .     ganodermatriol
    ÏàËÆ¶È:83.8%
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
15 .     ganoderiol
C30H50O4     ÏàËÆ¶È:83.8%
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
16 .     ganodermatriol
C30H48O3     ÏàËÆ¶È:83.8%
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
17 .     ¦Ã-lanostadienol
    ÏàËÆ¶È:83.8%
Organic Magnetic Resonance          1974          6          603-611
Carbon-13 NMR spectra of some tetra-and pentacyclic triterpenoids
S. A. Knight
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     dihydroagnosterol
    ÏàËÆ¶È:83.8%
Magnetic Resonance in Chemistry          1989          27          1012-1024
1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol
Gary T. Emmons, William K. Wilson and George J. Schroepfer Jr
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Lucidumol B
    ÏàËÆ¶È:83.8%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Ganoderiol A
    ÏàËÆ¶È:83.8%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     ganoderiol A
C30H50O4     ÏàËÆ¶È:80.6%
Journal of Chinese Pharmaceutical Sciences          1997          6          291-791
Triterpenoids from the Fruiting Body of Ganoderma lucidum
Fang-Sheng Wang, Hui Cai, Jun-Shan Yang, Yu-Mei Zhang and Ying-Ju Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     ganoderiol A
C30H50O4     ÏàËÆ¶È:80.6%
Acta Pharmaceutica Sinica          1996          31          200-204
STUDIES ON THE TRITERPENOID CONSTITUENTS FROM THE FRUITING BODY OF GANODERMA LUCIDUM (FR.)KARST.
FS Wang; H Cai; JS Yang; YM Zhang and YJ Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     Ganodermatriol
    ÏàËÆ¶È:80.6%
Journal of Natural Medicines          2009          63          304-310
Metabolism and pharmacokinetics in rats of ganoderiol F, a highly cytotoxic and antitumor triterpene from Ganoderma lucidum
Qun Zhang, Feng Zuo, Norio Nakamura, Chao-Mei Ma and Masao Hattori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     ganoderiol A
    ÏàËÆ¶È:80.6%
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
25 .     epoxyganoderiol C
C30H48O3     ÏàËÆ¶È:80.6%
Agricultural and Biological Chemistry          1988          52          211-216
Novel Triterpenoids and a Steroid from the Fungus Ganoderma lucidum
Tsuyoshi NISHITOBA, Hiroji SATO, Kyoko ODA, Sadao SAKAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     agnosterol
    ÏàËÆ¶È:80.6%
Magnetic Resonance in Chemistry          1989          27          1012-1024
1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol
Gary T. Emmons, William K. Wilson and George J. Schroepfer Jr
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     Epoxyganoderiol C
    ÏàËÆ¶È:80.6%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     inonotsutriol C
C30H48O3     ÏàËÆ¶È:77.4%
Helvetica Chimica Acta          2008          Vol. 91          1513
Three New Lanostane Triterpenoids, Inonotsutriols A, B, and C, from Inonotus obliquus
Sayaka Taji, Takeshi Yamada, and Reiko Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     lucialdehyde A
C30H46O2     ÏàËÆ¶È:77.4%
Chemical & Pharmaceutical Bulletin          2002          50(6)          837-840
New Triterpene Aldehydes, Lucialdehydes A¡ªC, from Ganoderma lucidum and Their Cytotoxicity against Murine and Human Tumor Cells
Jiang-Jing GAO,Byung-Sun MIN,Eun-Mi AHN,Norio NAKAMURA,Hyeong-Kyu LEE,and Masao HATTORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     5¦Á-lanosta-7,9(11),24-triene-3¦Â-hydroxy-26-al
C30H46O2     ÏàËÆ¶È:77.4%
Journal of Natural Products          2002          65          417-421
New Lanostanoids from the Fungus Ganoderma concinna
Antonio G. Gonz¨¢lez,Francisco Le¨®n, Augusto Rivera, Juan I. Padr¨®n, Javier Gonz¨¢lez-Plata,Juan C. Zuluaga,Jos¨¦ Quintana, Francisco Est¨¦vez, and Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     3¦Â,22-dihydroxylanosta-7,9(11),24-triene
    ÏàËÆ¶È:77.4%
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
32 .     ganodermatriol
C30H48O3     ÏàËÆ¶È:77.4%
Journal of Chinese Pharmaceutical Sciences          1997          6          291-791
Triterpenoids from the Fruiting Body of Ganoderma lucidum
Fang-Sheng Wang, Hui Cai, Jun-Shan Yang, Yu-Mei Zhang and Ying-Ju Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     ganodermatriol
C30H48O3     ÏàËÆ¶È:77.4%
Acta Pharmaceutica Sinica          1996          31          200-204
STUDIES ON THE TRITERPENOID CONSTITUENTS FROM THE FRUITING BODY OF GANODERMA LUCIDUM (FR.)KARST.
FS Wang; H Cai; JS Yang; YM Zhang and YJ Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     24-methylenelanosta-7,9(11)dien-3¦Â-ol
    ÏàËÆ¶È:77.4%
Phytochemistry          1998          49          2053-2056
24-methylene tetracyclic triterpenes from Polyalthia lancilimba
Y. P. Lue, Q. Mu, H. L. Zheng, C. M. Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     24-methylene-lanosta-7,9(11)dien-3¦Â-ol
C31H50O     ÏàËÆ¶È:77.4%
Journal of Natural Products          1987          Vol 50          762
Chemistry in the Annonaceae, XXIII. 24-Methylene-lanosta-7,9(11)-dien-3¦Â-ol from Artabotrys odorotissimus Stem Bark
Choudhury M. Hasan, Shaheen Shahnaz, Ilias Muhammad, Alexander I. Gray, Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     compound 20
    ÏàËÆ¶È:77.4%
Magnetic Resonance in Chemistry          1989          27          258-262
Epoxidation-induced shifts in the carbon-13 NMR spectra of steroids: Lanostane derivatives
Jacek Martynow and Zdzisław Paryzek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     compound 20
    ÏàËÆ¶È:77.4%
Magnetic Resonance in Chemistry          1989          27          258-262
Epoxidation-induced shifts in the carbon-13 NMR spectra of steroids: Lanostane derivatives
Jacek Martynow and Zdzisław Paryzek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     5¦Á-Lanosta-7,9(11),24-triene-3¦Â-hydroxy-26-al
    ÏàËÆ¶È:77.4%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     Lucialdehyde A
    ÏàËÆ¶È:77.4%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     Lanosta-7,9(11)-dien-3¦Â-acetyloxy-24,26-dihydroxy-25-methoxy
C33H54O5     ÏàËÆ¶È:75.7%
Phytochemistry          2015          110          133−139
Lanostanoids with acetylcholinesterase inhibitory activity from the mushroom Haddowia longipes
Shuang-Shuang Zhang, Qing-Yun Ma, Sheng-Zhuo Huang, Hao-Fu Dai, Zhi-Kai Guo, Zhi-Fang Yu, You-Xing Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     24Z-ethylidenelanost-8-en-3¦Â-ol
C31H54O     ÏàËÆ¶È:75%
Phytochemistry          1994          37          201-203
Lanostane triterpenes from the bark of Neolitsea sericea
Mahesh C. Sharma, Tatsuro Ohira, Mitsuyoshi Yatagai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     Lanosta-7,9(11)-dien-3¦Â-acetyloxy-24,25,26-trihydroxy
C32H52O5     ÏàËÆ¶È:75%
Phytochemistry          2015          110          133−139
Lanostanoids with acetylcholinesterase inhibitory activity from the mushroom Haddowia longipes
Shuang-Shuang Zhang, Qing-Yun Ma, Sheng-Zhuo Huang, Hao-Fu Dai, Zhi-Kai Guo, Zhi-Fang Yu, You-Xing Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     3¦Â,22-dihydroxylanosta-7,9(11), 24- triene
C30H48O2     ÏàËÆ¶È:74.1%
Planta Medica          1986          52          495-496
3¦Â,22-Dihydroxylanosta-7,9(11),24-triene: A New, Minor Compound from Inonotus obliquus
Kirsti Kahlos and R. Hiltunen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     lanosta-7,9(11),24-trien-3¦Â,21-diol
    ÏàËÆ¶È:74.1%
Phytochemistry          1999          52          1621-1627
Steroids from the fungus Fomitopsis pinicola
Joachim Rosecke, Wilfried A. Konig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     ganodermenonol
C30H46O2     ÏàËÆ¶È:74.1%
Journal of Natural Products          1986          Vol 49          621
Three New Lanostanoids from Ganoderma lucidum
Munehisa Arisawa, Akio Fujita, Manabu Saga, Hideki Fukumura, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     ganodermenonol
    ÏàËÆ¶È:74.1%
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
47 .     lanost-8(9)-en-3¦Â-ol
    ÏàËÆ¶È:74.1%
Canadian Journal of Chemistry          1977          55          2813-2828
The semiempirical derivation of 13C nuclear magnetic resonance chemical shifts. Hydrocarbons, alcohols, amines, ketones, and olefins
Helmut Beierbeck, John K. Saunders, John W. Apsimon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     ganodercochlearin C
C31H50O3     ÏàËÆ¶È:74.1%
Journal of Natural Products          2014          77          737-743
Hepatoprotective Effects of Triterpenoids from Ganoderma cochlear
Xing-Rong Peng, Jie-Qing Liu, Cui-Fang Wang, Xu-Yang Li, Yi Shu, Lin Zhou, and Ming-Hua Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     3¦Â-hydroxy-5¦Á-lanost-8-ene
    ÏàËÆ¶È:74.1%
Magnetic Resonance in Chemistry          1989          27          258-262
Epoxidation-induced shifts in the carbon-13 NMR spectra of steroids: Lanostane derivatives
Jacek Martynow and Zdzisław Paryzek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     dihydrolanosterol
    ÏàËÆ¶È:74.1%
Magnetic Resonance in Chemistry          1989          27          1012-1024
1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol
Gary T. Emmons, William K. Wilson and George J. Schroepfer Jr
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     compound 1
    ÏàËÆ¶È:74.1%
Magnetic Resonance in Chemistry          1989          27          258-262
Epoxidation-induced shifts in the carbon-13 NMR spectra of steroids: Lanostane derivatives
Jacek Martynow and Zdzisław Paryzek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     Ganodermenonol
    ÏàËÆ¶È:74.1%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     (24E)-24-ethyl-29-nor-5¦Á-lanosta-7,9(11),24(241)-trien-3¦Â-yl acetate
C26H38O2     ÏàËÆ¶È:71.8%
Chemical & Pharmaceutical Bulletin          1996          44          1202-1207
Eight Novel Sterols from the Roots of Bryonia dioica JACQ.
Toshihiro AKIHISA,Yumiko KIMURA,Wilhelmus C. M. C. KOKKE,Takashi ITOH and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     Lanosta-7,9(11),24E-trien-3¦Â-acetyloxy-26,27-dihydroxy
C32H50O4     ÏàËÆ¶È:71.8%
Phytochemistry          2015          110          133−139
Lanostanoids with acetylcholinesterase inhibitory activity from the mushroom Haddowia longipes
Shuang-Shuang Zhang, Qing-Yun Ma, Sheng-Zhuo Huang, Hao-Fu Dai, Zhi-Kai Guo, Zhi-Fang Yu, You-Xing Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     compound 9b
    ÏàËÆ¶È:71.8%
Magnetic Resonance in Chemistry          1989          27          1012-1024
1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol
Gary T. Emmons, William K. Wilson and George J. Schroepfer Jr
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     tirucalla-7,23,25-trien-3¦Â-ol
C30H48O     ÏàËÆ¶È:70.9%
Journal of Natural Products          2001          64          159-163
New Tirucallane-Type Triterpenes from Dysoxylum variabile
Hongmei Liu, Jörg Heilmann, Topul Rali, and Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     compound 5
    ÏàËÆ¶È:70.9%
Journal of Natural Products          1998          61          1491-1496
Phycomysterols and Other Sterols from the Fungus Phycomyces blakesleeanus
Alejandro F. Barrero, J. Enrique Oltra, Juan A. Poyatos, David Jim¨¦nez, and Eulalia Oliver
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     3-episapelin A
    ÏàËÆ¶È:70.9%
Chemical & Pharmaceutical Bulletin          1992          40          1053-1055
Cytotoxic Quassinoids and Tirucallane-Type Triterpenes from the Woods of Eurycoma longifolia
Hideji ITOKAWA,Etsuko KISHI,Hiroshi MORITA and Koichi TAKEYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     adianenone
C30H48O     ÏàËÆ¶È:70.9%
Chemistry of Natural Compounds          2007          43          563-566
CHEMICAL CONSTITUENTS FROM THE ROOTS OF Polygonum bistorta
Xiao-Bai Sun, Pei-Hua Zhao, Yang-Jun Xu,Li-Mei Sun, Mei-Ai Cao, and Cheng-Shan Yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     taiwaniatriol
C31H54O4     ÏàËÆ¶È:70.9%
Acta Botanica Sinica          2004          46          1002-1008
Terpenoids and Phenols from Taiwania flousiana
XIANG Ying, YANG Sheng-Ping, ZHAN Zha-Jun, YUE Jian-Min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     simiarenone
    ÏàËÆ¶È:70.9%
China Journal of Chinese Materia Medica          2009          34          183-185
Studies on chemical constituents from roots of Polygonum amplexicaule
REN Hengchun, WAN Dingrong, ZOU Zhongmei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     ganodermatriol triacetate
C36H54O6     ÏàËÆ¶È:70.9%
Journal of Natural Products          1986          Vol 49          621
Three New Lanostanoids from Ganoderma lucidum
Munehisa Arisawa, Akio Fujita, Manabu Saga, Hideki Fukumura, Toshimitsu Hayashi, Mineo Shimizu, Naokata Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
63 .     ganodermatriol triacetate
    ÏàËÆ¶È:70.9%
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
64 .     compound 9
    ÏàËÆ¶È:70.9%
Journal of Natural Products          1989          Vol 52          595
13C-NMR Correlation of Stereochemistry in Lanostanoid Triterpenes
Lee-Juian Lin, Ming-Shi Shiao, Kuan Rong Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
65 .     ganodermanontriol
C30H48O4     ÏàËÆ¶È:70.9%
Natural Product Sciences          2009          15          173-179
Steroids and Triterpenoid from the Fruit Bodies of Ganoderma lucidum and Their Cytotoxic Activity
Lee, Joon-Seok; Lee, Mi-Kyoung; Hung, Tran-Manh; Lee, Ik-Soo; Min, Byung-Sun; Bae, Ki-Hwan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
66 .     Dehydroeburicoic acid
C31H48O3     ÏàËÆ¶È:70.9%
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
67 .     ganodermic acid Jb
C30H46O4     ÏàËÆ¶È:70.9%
Phytochemistry          1988          27          873-875
Triterpenes in Ganoderma lucidum
Ming-Shi Shiao,Lee-Juian Lin,Sheau-Farn Yeh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
68 .     24-methyl-ene-24(25)-dihydrolanosterol
    ÏàËÆ¶È:70.9%
Phytochemistry          1990          29          2513-2520
Effect on ergosterol biosynthesis of a fungicide,SSF-109,in Botrytis cinerea
Noboru Shirane,Akira Murabayashi,Michio Masuko,Atsuko Uomori,Yohko Yoshimura,Shujiro Seo,Kiyohisa Uchida,Ken'ichi Takeda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
69 .     compound II
    ÏàËÆ¶È:70.9%
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
70 .     ganodermanontriol
    ÏàËÆ¶È:70.9%
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
71 .     eburicol
    ÏàËÆ¶È:70.9%
Chinese Pharmaceutical Journal          2009          44          418-421
Studies on Chemical Constituents in Forsythia suspensa (Thunb.) Vahl
FENG Wei-sheng, LI Ke-ke, ZHENG Xiao-ke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
72 .     3¦Â-hydroxy-4,4,14¦Á-trimethyl-5¦Á-pregna-7,9(11)-diene-20S-carboxylic acid
C25H38O3     ÏàËÆ¶È:70.9%
Journal of the Chemical Society, Perkin Transactions 1          1984                   1219-1221
New metabolic products of Verticillium lecanii. Part 2. 3¦Â,12¦Â,-Dihydroxy-4,4,14¦Á-trimethyl-5¦Á-pregna-7,9(11)-diene-20S-carboxylic acid and 4,4,14¦Á-trimethyl-3-oxo-5¦Á-pregna-7,9(11)-diene-20S-carboxylic acid
John Frederick Grove
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
73 .     24-methylene-24(25)-dihydrolanosterol
    ÏàËÆ¶È:70.9%
Natural Product Research and Development          2009          21          424-427
Chemical Constituents from the Endophytic Fungus Rhizoctonia sp. J5 of Antiaris toxicaria
QUE Dong-mei; DAI Hao-fu; HUANG Gui-xiu; DAI Wen-jun; MEI Wen-li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
74 .     ganodermanontriol
C30H48O4     ÏàËÆ¶È:70.9%
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
75 .     ergosta-5,23-dien-3¦Â-ol,acetate
    ÏàËÆ¶È:70.9%
China Journal of Chinese Materia Medica          2014          39          1034-1039
Chemical constituents from Ganoderma philippii
YANG Shuang, MA Qing-yun, NG Sheng-zhuo, DAI Hao-fu, GUO Zhi-kai, YU Zhi-fang, ZHAO You-xing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
76 .     3-episapeline A
    ÏàËÆ¶È:70.9%
Chinese Traditional and Herbal Drugs          2014          45          755-759
Chemical constituents from Toona ciliata var. henryi and their anti-inflammatory activities
ZHANG Feng, CEN Juan, LI Qin, WANG Hai-yan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
77 .     euphorbol
    ÏàËÆ¶È:70.9%
Chinese Journal of Oceanology and Limnology          2011          29          63-67
Chemical constituents of marine algal-derived endophytic fungus Exophiala oligosperma EN-21*
LI Fang, LI Ke, LI Xiaoming, WANG Bingui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
78 .     lanostenol
    ÏàËÆ¶È:70.9%
Organic Magnetic Resonance          1974          6          603-611
Carbon-13 NMR spectra of some tetra-and pentacyclic triterpenoids
S. A. Knight
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
79 .     ÁéÖ¥Ëá Z
    ÏàËÆ¶È:70.9%
Journal of Tropical and Subtropical Botany          1999          7          248-251
Õ­Ò¶Ïʱ°»¨µÄ»¯Ñ§³É·ÖÑо¿
Áõ½¨Ïé, ÎâÊç¾ý, κТÒå, ÑîÈÊÖÞ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
80 .     (3S,24R)-tirucall-7-ene-3,24,25-triol
C30H52O3     ÏàËÆ¶È:70.9%
Helvetica Chimica Acta          2014          97          1526-1530
Tirucallane-Type Triterpenoids from Celastrus stylosus Wall.
Wei-Guang Shan, Zai-Lin Gao, You-Min Ying, Jia-Gui Xiang, Fa-Song Wang and Zha-Jun Zhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
81 .     (22R)-3¦Â-hydroxy-24-methyl-lanosta-7,9,24(25)-trien-26,22-olide
C31H46O3     ÏàËÆ¶È:70.9%
Phytochemistry          2014          108          171-176
Terpenoids with alpha-glucosidase inhibitory activity from the submerged culture of Inonotus obliquus
You-Min Ying, Lin-Yan Zhang, Xia Zhang, Hai-Bo Bai, Dong-E Liang, Lie-Feng Ma, Wei-Guang Shan, Zha-Jun Zhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
82 .     Lucidadiol
    ÏàËÆ¶È:70.9%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
83 .     Ganodermatriol
    ÏàËÆ¶È:70.9%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
84 .     Ganodermic acid Jb
    ÏàËÆ¶È:70.9%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
85 .     3¦Á-acetoxy-6¦Â,25-dihydroxy-20(S),24(S)-epoxydammarane
C32H52O4     ÏàËÆ¶È:68.7%
Phytochemistry          1997          46          1139-1141
Dammarane-type triterpenes from Cordia spinescens
Norio Nakamura, Shiho Kojima, Yasmina Aura Lim, Meselhy R. Meselhy, Masao Hattori, Mahabir P. Gupta, Mireya Correa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
86 .     compound 8b
    ÏàËÆ¶È:68.7%
Magnetic Resonance in Chemistry          1989          27          1012-1024
1H and 13C NMR assignments for lanostan-3¦Â-ol derivatives: Revised assignments for lanosterol
Gary T. Emmons, William K. Wilson and George J. Schroepfer Jr
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
87 .     Ficutirucin D
C32H52O4     ÏàËÆ¶È:68.7%
Chemical & Pharmaceutical Bulletin          2015          63          237−243
Tirucallane-Type Triterpenoids from the Fruit of Ficus carica and Their Cytotoxic Activity
Lin Jing, Yang-Mei Zhang, Jian-Guang Luo, Ling-Yi Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
88 .     inonotsulide C
C30H46O3     ÏàËÆ¶È:67.7%
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
89 .     antiquol C
C30H48O     ÏàËÆ¶È:67.7%
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
90 .     euphorbol
C31H52O     ÏàËÆ¶È:67.7%
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
91 .     eupha-7,24-diene-3¦Â,22¦Â-diol
C30H50O2     ÏàËÆ¶È:67.7%
Journal of Natural Products          1999          62          1003-1005
Four New Triterpenes from the Heartwood of Melaleuca leucadendron
Ching-Kuo Lee and Ming-Huey Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
92 .     lucidadiol
C30H48O3     ÏàËÆ¶È:67.7%
Journal of Natural Products          1999          62          1700-1701
Lanostanoid Triterpenes from Ganoderma lucidum
Antonio G. Gonz¨¢lez, Francisco Le¨®n, Augusto Rivera, Claudia M. Muñ oz, and Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
93 .     swertenol
    ÏàËÆ¶È:67.7%
Chemical & Pharmaceutical Bulletin          1995          43          1634-1639
Composite Constituents : Forty-Two Triterpenoids Including Eight Novel Compounds Isolated from Picris hieracioides subsp. Japonica
Kenji SHIOJIMA,Kazuo MASUDA,Hideki SUZUKI,Tokuhide LIN,Yuko OOISHI and Hiroyuki AGETA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
94 .     compound 3b
    ÏàËÆ¶È:67.7%
Chemical & Pharmaceutical Bulletin          1994          42          694-697
Isolation and Characterization of Immunosuppressive Components of Three Mushrooms, Pisolithus tinctorius, Microporus flabelliformis and Lenzites betulina
Haruhiro FUJIMOTO,Megumi NAKAYAMA,Yuji NAKAYAMA and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
95 .     3¦Â,25-dihydroxytirucalla-7,23(24)-dien
    ÏàËÆ¶È:67.7%
Chinese Chemical Letters          2006          17          195-197
New Triterpenes from Siyekucai (Ixeris chinensis)
Shu Jun ZHANG, Jin Lan WANG, Qi Gang DENG, Masayoshi ANDO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
96 .     ganodermanontriol
C30H48O4     ÏàËÆ¶È:67.7%
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
97 .     ganodermanontriol
C30H48O4     ÏàËÆ¶È:67.7%
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
98 .     butyrospermol
    ÏàËÆ¶È:67.7%
China Journal of Chinese Materia Medica          2009          34          867-870
Chemical constituents from roots of Phlamis umbrosa
LIU Pu, DENG Ruixue, DUAN Hongquan, YIN Wei ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
99 .     22,23-epoxy-tirucalla-7-ene-3¦Â,24,25-triol
C30H50O4     ÏàËÆ¶È:67.7%
Phytochemistry          2000          54          801-805
Tirucallane triterpenoids from Dysoxylum hainanense
Xiao-Dong Luo, Shao-Hua Wu, Yun-Bao Ma, Da-Gang Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
100 .     ganodermanondiol
C30H48O3     ÏàËÆ¶È:67.7%
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
101 .     ganodelmanontriol
C30H48O4     ÏàËÆ¶È:67.7%
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
102 .     ganodermanondiol
    ÏàËÆ¶È:67.7%
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
103 .     ganodermanontriol
    ÏàËÆ¶È:67.7%
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
104 .     Eburicol
    ÏàËÆ¶È:67.7%
Phytochemistry          1996          41          1301-1308
Sterol analysis of DMI-resistant and -sensitive strains of Venturia inaequalis
Noboru Shirane, Hideyuki Takenaka, Kazuo Ueda, Yutaka Hashimoto, Kenji Katoh, Hideo Ishii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
105 .     compound 3
    ÏàËÆ¶È:67.7%
Phytochemistry          1994          36          417-419
A tetracyclic triterpenoid from Garuga pinnata
G. Venkatraman, P. S. Thombare, B. K. Sabata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
106 .     swertenol
    ÏàËÆ¶È:67.7%
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
107 .     compound 394
    ÏàËÆ¶È:67.7%
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
108 .     compound 2
    ÏàËÆ¶È:67.7%
Phytochemistry          1993          32          161-163
Euphane triterpenoid from Garuga pinnata
G. Venkatraman, P.S. Thombare, B.K. Sabata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
109 .     compound 2
    ÏàËÆ¶È:67.7%
Phytochemistry          1991          30          3822-3823
A dammarane fromStevia salicifolia
Rachel Mata, Vero¡änica Rodri¡äguez, Rogelio Pereda-Miranda, Robert Bye, Edelmira Linares
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
110 .     Hypocrellol A
C30H48O3     ÏàËÆ¶È:67.7%
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
111 .     olibanumol J
C30H52O3     ÏàËÆ¶È:67.7%
Chemical & Pharmaceutical Bulletin          2009          57          957-964
Absolute Stereostructures of Olibanumols A, B, C, H, I, and J from Olibanum, Gum-Resin of Boswellia carterii, and Inhibitors of Nitric Oxide Production in Lipopolysaccharide-Activated Mouse Peritoneal Macrophages
Masayuki Yoshikawa, Toshio Morikawa, Hideo Oominami and Hisashi Matsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
112 .     inonotsudiol A
C30H48O2     ÏàËÆ¶È:67.7%
Phytochemistry          2010          71          1774-1779
An unusual lanostane-type triterpenoid, spiroinonotsuoxodiol, and other triterpenoids from Inonotus obliquus
Noriko Handa, Takeshi Yamada, Reiko Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
113 .     euphol
    ÏàËÆ¶È:67.7%
Chinese Traditional and Herbal Drugs          2010          41          877-881
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Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
114 .     tirucallol
    ÏàËÆ¶È:67.7%
Chinese Traditional and Herbal Drugs          2008          39          1779-1781
Optimization of purification of Panax notoginseng extract for injection
CHU Yang; SONG Hong-tao; LI Dan; YAN Lu; LIU Dan; CHEN Da-wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
115 .     ganodermanontriol
    ÏàËÆ¶È:67.7%
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
116 .     ganodermanondiol
C30H48O3     ÏàËÆ¶È:67.7%
Chinese Traditional and Herbal Drugs          2005          36          502-504
ËÉɼÁéÖ¥µÄ»¯Ñ§³É·ÖÑо¿
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Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
117 .     Inoterpene A
C30H52O3     ÏàËÆ¶È:67.7%
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
118 .     Inoterpene B
C30H52O3     ÏàËÆ¶È:67.7%
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
119 .     22,23;24,25-diepoxy-3¦Â-hydroxy-7-tirucallene
C30H48O3     ÏàËÆ¶È:67.7%
Planta Medica          2011          77          1844-1847
Cytotoxic Triterpenoids from Azadirachta indica
Chen, JinXiong; Chen, JianChao; Sun, Yun; Yan, YuXin; Kong, LingMei; Li, Yan; Qiu, MingHua:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
120 .     (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:67.7%
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