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34.12,36.04,37.71,39.10,39.48,47.17,48.84,50.74,54.46,58.49,67.90,77.34,78.00,107.01,123.14,131.88,135.16,137.26,149.52,156.09,178.83
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2
16.36,18.82,19.13,21.36,21.87,22.01,28.6,28.7,29.7,30.00,31.62,33.24,34.12,36.04,37.71,39.10,39.48,47.17,48.84,50.74,54.46,58.49,67.90,77.34,78.00,107.01,123.14,131.88,135.16,137.26,149.52,156.09,178.83   
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1 .     sulphurenic acid
C31H50O4     ÏàËÆ¶È:75.7%
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

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

2 .     tumulosic acid
    ÏàËÆ¶È:72.7%
Chemical & Pharmaceutical Bulletin          2008          56(10)          1459-1462
13CCytotoxic and Anti-oxidant Activities of Lanostane-Type Triterpenes Isolated from Poria cocos
Liang ZHOU,Yaochun ZHANG,Leslie Adell GAPTER,Hui LING,Rajesh AGARWAL,and Ka-yun NG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

3 .     versisponicacid D
C33H52O5     ÏàËÆ¶È:72.7%
Chemical & Pharmaceutical Bulletin          2000          48(10)          1418-1421
Five Lanostane Triterpenoids and Three Saponins from the Fruit Body of Laetiporus versisporus
Kazuko YOSHIKAWA,Kenji MATSUNOTO,Chie MINE,Shinya BANDO,and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

4 .     sulphurenic acid
    ÏàËÆ¶È:72.7%
Chemical & Pharmaceutical Bulletin          2000          48(10)          1418-1421
Five Lanostane Triterpenoids and Three Saponins from the Fruit Body of Laetiporus versisporus
Kazuko YOSHIKAWA,Kenji MATSUNOTO,Chie MINE,Shinya BANDO,and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

5 .     Eburicoic acid
C31H50O3     ÏàËÆ¶È:72.7%
Chemistry of Natural Compounds          2000          36          72-75
LOW-MOLECULAR-WEIGHT MUSHROOM METABOLITES.V. EBURICOIC ACID FROM Polyporus ailanthus
L. S. Kamaiov, M. A. Agzamova,S. F. Aripova, and M. I. lsaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

6 .     tumulosic acid
    ÏàËÆ¶È:72.7%
Journal of Asian Natural Products Research          2008          10          640-646
Poriacosones A and B: two new lanostane triterpenoids from Poria cocos
Yan Zheng and Xiu-Wei Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

7 .     eburicoic acid
C31H50O3     ÏàËÆ¶È:72.7%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

8 .     eburicoic acid
C31H50O3     ÏàËÆ¶È:72.7%
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

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

9 .     laetiposide E
C36H58O8     ÏàËÆ¶È:69.4%
Chemical & Pharmaceutical Bulletin          2000          48(10)          1418-1421
Five Lanostane Triterpenoids and Three Saponins from the Fruit Body of Laetiporus versisporus
Kazuko YOSHIKAWA,Kenji MATSUNOTO,Chie MINE,Shinya BANDO,and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

10 .     compound 3a
    ÏàËÆ¶È:66.6%
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

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

11 .     compound 4a
C40H55NO5     ÏàËÆ¶È:66.6%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

12 .     procerursenyl acetate
    ÏàËÆ¶È:66.6%
Indian Journal of Chemistry          2009          48B          443-446
Phytochemical investigation of Calotropis procera Ait roots
Alam,Perwez; Ali,Mohd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

13 .     laetiposide G
C37H60O9     ÏàËÆ¶È:64.8%
Chemical & Pharmaceutical Bulletin          2000          48(10)          1418-1421
Five Lanostane Triterpenoids and Three Saponins from the Fruit Body of Laetiporus versisporus
Kazuko YOSHIKAWA,Kenji MATSUNOTO,Chie MINE,Shinya BANDO,and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

14 .     laetiposide A
    ÏàËÆ¶È:64.8%
Chemical & Pharmaceutical Bulletin          2000          48(10)          1418-1421
Five Lanostane Triterpenoids and Three Saponins from the Fruit Body of Laetiporus versisporus
Kazuko YOSHIKAWA,Kenji MATSUNOTO,Chie MINE,Shinya BANDO,and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

15 .     tsugaric acid C
C32H50O5     ÏàËÆ¶È:64.8%
Journal of Natural Products          2000          63          514-516
New Lanostanoids of Ganoderma tsugae
Huey-Jen Su,Yih-Fen Fann,Mei-Ing Chung, Shen-Jeu Won, and Chun-Nan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

16 .     laetiposide A
C37H60O9     ÏàËÆ¶È:64.8%
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

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

17 .     (R)-4-[3¦Â-hydroxy-28-norlup-20(29)-en-17¦Â-yl]-2-methy-lene-c-butyrolactone
C34H52O3     ÏàËÆ¶È:64.7%
Bioorganic & Medicinal Chemistry          2010          18          2549-2558
Synthesis and biological evaluation of antitumor-active ¦Ã-butyrolactone substituted betulin derivatives
Ren¨¦ Csuk, Alexander Barthel, Stefan Schwarz, Harish Kommera, Reinhard Paschke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

18 .     pachymic acid
    ÏàËÆ¶È:63.6%
Chemical & Pharmaceutical Bulletin          2008          56(10)          1459-1462
13CCytotoxic and Anti-oxidant Activities of Lanostane-Type Triterpenes Isolated from Poria cocos
Liang ZHOU,Yaochun ZHANG,Leslie Adell GAPTER,Hui LING,Rajesh AGARWAL,and Ka-yun NG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

19 .     fomefficinic acid C
C31H50O4     ÏàËÆ¶È:63.6%
Chemical & Pharmaceutical Bulletin          2004          52(11)          1375-1377
New Lanostane-Type Triterpenes from Fomes officinalis
Xia WU, JunShan YANG,Liang ZHOU, and YueSheng DONG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

20 .     versisponicacid A
C30H48O5     ÏàËÆ¶È:63.6%
Chemical & Pharmaceutical Bulletin          2000          48(10)          1418-1421
Five Lanostane Triterpenoids and Three Saponins from the Fruit Body of Laetiporus versisporus
Kazuko YOSHIKAWA,Kenji MATSUNOTO,Chie MINE,Shinya BANDO,and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

21 .     quadrangularate D
C32H50O4     ÏàËÆ¶È:63.6%
Chemical & Pharmaceutical Bulletin          2000          48(4)          496-504
Methyl Quadrangularates A-D and Related Triterpenes from Combretum quadrangulare
Arjun Hari BANSKOTA,Yasuhiro TEZUKA,Kim Qui TRAN,Ken TANAKA, Ikuo SAIKI and Shigetoshi KADOTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

22 .     24-methylenelanost-8-ene-3b,15a,21-triol
C31H52O3     ÏàËÆ¶È:63.6%
Planta Medica          2006          72          199-203
New Lanostanes and Naphthoquinones Isolated from Antrodia salmonea and their Antioxidative Burst Activity in Human Leukocytes
Chien-Chang Shen,Yuh-Chiang Shen,Yea-Hwey Wang,Lie-Chwen Lin,Ming-Jaw Don,Kuo-Tong Liou,Wen-Yen Wang,Yu-Chang Hou,Tun-Tschu Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

23 .     16¦Á-hydroxy-3,4-secolanosta-4(28),7,9(11),24(31)-tetraene-3,21-dioic acid-3-ethyl ester
C33H50O5     ÏàËÆ¶È:63.6%
Helvetica Chimica Acta          2009          92          660-667
Two New Triterpenes from the Surface Layer of Poria cocos
Chun-Hua Yang, Shi-Fang Zhang, Wen-Ying Liu, Zun-Jian Zhang, Jing-Han Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

24 .     pachymic acid
    ÏàËÆ¶È:63.6%
Journal of Asian Natural Products Research          2008          10          289-292
Two new lanostane triterpenoids from Poria cocos
Yan Zheng and Xiu-Wei Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

25 .     poricoic acid A
    ÏàËÆ¶È:63.6%
Phytochemistry          1995          39          1165-1169
Triterpenes from the surface layer of Poria cocos
Takaaki Tai, Tetsuro Shingu, Tohru Kikuchi, Yasuhiro Tezuka, Akira Akahori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

26 .     poricoic acid AM
C32H48O5     ÏàËÆ¶È:63.6%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

27 .     compound 2
C33H52O5     ÏàËÆ¶È:63.6%
Phytochemistry          1992          31          2548-2549
A lanostane triterpenoid from Poria cocos
Tetsuro Shingu, Takaaki Tai, Akira Akahori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

28 .     poricoic acid A
C31H46O5     ÏàËÆ¶È:63.6%
Phytochemistry          1991          30          2796-2797
Triterpenoids from Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

29 .     Methyl quadrangularate D
C32H50O4     ÏàËÆ¶È:63.6%
Bioorganic & Medicinal Chemistry Letters          1998          8          3519-3524
Cytotoxic cycloartane-type triterpenes from Combretum quadrangulare
Arjun H. Banskota, Yasuhiro Tezuka, Le Kim Phung, Kim Qui Tran, Ikuo Saiki, Yoshihisa Miwa, Tooru Taga, Shigetoshi Kadota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

30 .     versisponic acid D
C33H52O5     ÏàËÆ¶È:63.6%
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

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

31 .     betulinic acid
C30H48O3     ÏàËÆ¶È:63.6%
Journal of Shenyang Pharmaceutical University          2006          23          760-763
Chemical constituents of Chaenomeles speciosa (Sweet.) Nakai
YIN Kai, GAO Hui-yuan, LI Xing-nuo, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

32 .     cucurbita-5,23(E)-diene-3¦Â,7¦Â,25,29-tetraol
C30H50O4     ÏàËÆ¶È:63.6%
Bioorganic & Medicinal Chemistry          2009          17          6942-6951
New potent P-glycoprotein modulators with the cucurbitane scaffold and their synergistic interaction with doxorubicin on resistant cancer cells
C¨¢tia Ramalhete, Joseph Moln¨¢r, Silva Mulhovo, Virg¨ªlio E. Ros¨¢rio, Maria-Jos¨¦ U. Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

33 .     25-methoxycucurbita-5,23(E)-diene-3¦Â,7¦Â,29-triol
C31H52O4     ÏàËÆ¶È:63.6%
Bioorganic & Medicinal Chemistry          2009          17          6942-6951
New potent P-glycoprotein modulators with the cucurbitane scaffold and their synergistic interaction with doxorubicin on resistant cancer cells
C¨¢tia Ramalhete, Joseph Moln¨¢r, Silva Mulhovo, Virg¨ªlio E. Ros¨¢rio, Maria-Jos¨¦ U. Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

34 .     (R)-4-[3¦Â-methoxy-28-norlup-20(29)-en-17¦Â-yl]-2-methylene-c-butyrolactone
C35H54O3     ÏàËÆ¶È:62.8%
Bioorganic & Medicinal Chemistry          2010          18          2549-2558
Synthesis and biological evaluation of antitumor-active ¦Ã-butyrolactone substituted betulin derivatives
Ren¨¦ Csuk, Alexander Barthel, Stefan Schwarz, Harish Kommera, Reinhard Paschke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

35 .     fomitoside J
C37H60O8     ÏàËÆ¶È:62.1%
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

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

36 .     (R)-4-[3¦Â-tert-butyloxy-28-norlup-20(29)-en-17¦Â-yl]-2-methylene-c-butyrolactone
C38H60O3     ÏàËÆ¶È:61.1%
Bioorganic & Medicinal Chemistry          2010          18          2549-2558
Synthesis and biological evaluation of antitumor-active ¦Ã-butyrolactone substituted betulin derivatives
Ren¨¦ Csuk, Alexander Barthel, Stefan Schwarz, Harish Kommera, Reinhard Paschke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

37 .     hispidol B 25-methyl ether
C31H54O4     ÏàËÆ¶È:60.6%
Chemical & Pharmaceutical Bulletin          2008          56(6)          839-842
Terpenoids and Coumarins Isolated from the Fruits of Poncirus trifoliata
Guang-Hua XU,Jeong-Ah KIM,So-Young KIM,b Jae-Chun RYU,Young-Soo KIM,d Sang-Hun JUNG,Mi-Kyeong KIM,and Seung-Ho LEE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

38 .     3¦Â-methoxy-24-methylenelanost- 9(11)-en-25-ol
C32H54O2     ÏàËÆ¶È:60.6%
Chemical & Pharmaceutical Bulletin          2007          55(6)          908-911
Lanostane-Type Triterpenoids from Diospyros discolor
Chiy-Rong CHEN,Chao-Wen CHENG,Min-Hsiung PAN,Yun-Wen LIAO,Chih-Ying TZENG,and Chi-I CHANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

39 .     fomefficinic acid A
C31H48O3     ÏàËÆ¶È:60.6%
Chemical & Pharmaceutical Bulletin          2004          52(11)          1375-1377
New Lanostane-Type Triterpenes from Fomes officinalis
Xia WU, JunShan YANG,Liang ZHOU, and YueSheng DONG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

40 .     fomefficinic acid D
C31H48O4     ÏàËÆ¶È:60.6%
Chemical & Pharmaceutical Bulletin          2004          52(11)          1375-1377
New Lanostane-Type Triterpenes from Fomes officinalis
Xia WU, JunShan YANG,Liang ZHOU, and YueSheng DONG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

41 .     saponaceoic acid II
C30H48O4     ÏàËÆ¶È:60.6%
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

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

42 .     1-O-acetyl-23-deoxojessic acid
C33H53O5     ÏàËÆ¶È:60.6%
Chemical & Pharmaceutical Bulletin          2000          48(4)          496-504
Methyl Quadrangularates A-D and Related Triterpenes from Combretum quadrangulare
Arjun Hari BANSKOTA,Yasuhiro TEZUKA,Kim Qui TRAN,Ken TANAKA, Ikuo SAIKI and Shigetoshi KADOTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

43 .     quadrangularate P
C32H52O5     ÏàËÆ¶È:60.6%
Chemical & Pharmaceutical Bulletin          2000          48(4)          496-504
Methyl Quadrangularates A-D and Related Triterpenes from Combretum quadrangulare
Arjun Hari BANSKOTA,Yasuhiro TEZUKA,Kim Qui TRAN,Ken TANAKA, Ikuo SAIKI and Shigetoshi KADOTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

44 .     8¦Á-hydroxyfernan-25,7¦Â-olide
C30H48O3     ÏàËÆ¶È:60.6%
Phytochemistry          2001          58          363-367
Triterpenoids from Adiantum caudatum
Keiko Tsuzuki, Ayumi Ôhashi, Yôko Arai, Kazuo Masuda, Akihito Takano, Kenji Shiojima, Hiroyuki Ageta, Shao-Qing Cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

45 .     3¦Â-acetoxy-7¦Â-methoxycucurbita- 5,23(E)-dien-25-ol
C33H54O4     ÏàËÆ¶È:60.6%
Journal of Natural Products          2008          71(8)          1327-1330
Cucurbitane-Type Triterpenoids from the Stems of Momordica charantia
Chi-I Chang, Chiy-Rong Chen, Yun-Wen Liao, Hsueh-Ling Cheng, Yo-Chia Chen, and Chang-Hung Chou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

46 .     integracide B
    ÏàËÆ¶È:60.6%
Journal of Natural Products          2003          66          1338-1344
Chemistry and Structure-Activity Relationship of HIV-1 Integrase Inhibitor Integracide B and Related Natural Products
Sheo B. Singh,John G. Ondeyka, William A. Schleif, Peter Felock,and Daria J. Hazuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     15¦Á-hydroxydehydrotumulosic acid
C31H48O5     ÏàËÆ¶È:60.6%
Journal of Natural Products          2007          70          948-953
Triterpene Acids from Poria cocos and Their Anti-Tumor-Promoting Effects
Toshihiro Akihisa,Yuji Nakamura, Harukuni Tokuda, Emiko Uchiyama, Takashi Suzuki,Yumiko Kimura,Kazuo Uchikura, and Hoyoku Nishin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     3¦Â,23¦Â-dimethoxy-5¦Á-lanosta-24(241)-ene
C32H54O2     ÏàËÆ¶È:60.6%
Journal of Natural Products          2002          65          79-81
Lanostanoids of Amentotaxus formosana
Huey-Jen Su, Shiow-Hwa Day, Sheng-Zehn Yang,Michael Y.Chiang,and Chun-Nan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

49 .     lup-28-al-20(29)-en-3¦Â-ol
C30H48O2     ÏàËÆ¶È:60.6%
Journal of Natural Products          2002          65          645-648
Differentiation- and Apoptosis-Inducing Activities by Pentacyclic Triterpenes on a Mouse Melanoma Cell Line
Keishi Hata, Kazuyuki Hori, and Saori Takahashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

50 .     25,26,27-trisno¦Á-3¦Â-methoxy-lanost-9(11)-en-24-oic acid
C28H46O3     ÏàËÆ¶È:60.6%
Journal of Natural Products          2000          63          1055-1057
Four New Trisnorlanostene-Type Triterpenoids from the Stem Bark of Pinus luchuensis
Shun-ich Wada and Reiko Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

51 .     compound 1a
    ÏàËÆ¶È:60.6%
Journal of Natural Products          2000          63          99-103
Bioactive Steroids from the Whole Herb of Euphorbia chamaesyce
Reiko Tanaka,Kazuaki Kasubuchi, Shunji Kita, Harukuni Tokuda, Hoyoku Nishino, and Shunyo Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

52 .     compound 5
    ÏàËÆ¶È:60.6%
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

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53 .     goreishisduremethylester
C31H48O4     ÏàËÆ¶È:60.6%
Planta Medica          1991          57          468-470
Triterpensaponine aus der chinesischen Droge,,Daxueteng" (Caulis Sargentodoxae) Triterpene Saponins from the Chinese Drug "Daxueteng"(Caulis Sargentodoxae)
EloirPaulo Schenkel, Wolfgang Werner und Karl Ernst Schulte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

54 .     betulinic acid
C30H48O3     ÏàËÆ¶È:60.6%
Acta Botanica Yunnanica          2008          30(4)          515-518
A New Polyisoprenylated Benzoylphloroglucinol Derivative from Hypericum henryi subsp1 uraloides ( Guttiferae)
GUO Na,CHEN Xuan-Qin, ZHAO Qin-Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

55 .     24-methylenecholest-5-ene-3¦Â,16¦Â-diol-3-O-¦Á-L-fucopyranoside
C34H56O6     ÏàËÆ¶È:60.6%
Chemical & Pharmaceutical Bulletin          1990          38          2400-2403
Marine Sterols. XVII. : Polyhydroxysterols of the Soft Corals of the Andaman and Nicobar Coasts. : (2). Isolation and Structures of Three 16¦Â-Hydroxy Steroidal Glycosides from an Alcyonium sp. Soft Coral
Masaru KOBAYASHI,Fuyuko KANDA,Srinivasa Rao DAMARLA,Desaraju Venkata RAO and Chaganti Bheemasankara RAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

56 .     24-methylenecholest-5-ene-3¦Â,7¦Â,16¦Â-triol-3-O-¦Á-L-fucopyranoside
C34H56O7     ÏàËÆ¶È:60.6%
Chemical & Pharmaceutical Bulletin          1990          38          2400-2403
Marine Sterols. XVII. : Polyhydroxysterols of the Soft Corals of the Andaman and Nicobar Coasts. : (2). Isolation and Structures of Three 16¦Â-Hydroxy Steroidal Glycosides from an Alcyonium sp. Soft Coral
Masaru KOBAYASHI,Fuyuko KANDA,Srinivasa Rao DAMARLA,Desaraju Venkata RAO and Chaganti Bheemasankara RAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

57 .     acetate
C33H5204     ÏàËÆ¶È:60.6%
Chemistry of Natural Compounds          2000          36          72-75
LOW-MOLECULAR-WEIGHT MUSHROOM METABOLITES.V. EBURICOIC ACID FROM Polyporus ailanthus
L. S. Kamaiov, M. A. Agzamova,S. F. Aripova, and M. I. lsaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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58 .     3,4-secolanosta-4(28),7,9(11),24(31)-tetraene-3,21-dioic acid-3-ethyl ester
C33H50O4     ÏàËÆ¶È:60.6%
Helvetica Chimica Acta          2009          92          660-667
Two New Triterpenes from the Surface Layer of Poria cocos
Chun-Hua Yang, Shi-Fang Zhang, Wen-Ying Liu, Zun-Jian Zhang, Jing-Han Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

59 .     betulinic acid
C30H48O3     ÏàËÆ¶È:60.6%
Acta Botanica Sinica          2002          44          354-358
Triterpenoids from the Dai Medicinal Plant Winchia calophylla
ZHU Wei-Ming, SHEN Yue-Mao, HONG Xin, ZUO Guo-Ying, YANG Xiao-Sheng, HAO Xiao-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

60 .     saikogenin Q
    ÏàËÆ¶È:60.6%
Acta Pharmaceutica Sinica          1995          30          435-439
ISOLATION AND IDENTIFICATION OF SAIKOGENIN Q AND SAIKOSAPONIN Q FROM BUPLEUM SMITHII WOLFF VAR PARVIFOLIUM SHAN ET Y LI
HS Luo; YY; zhao; LB Ma; YZ Jin; JR Peng and RY Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4Â¥2012-05-22 14:07:13
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1 .     senkirkin
C19H27NO6     ÏàËÆ¶È:52.3%
Planta Medica          1986          52          484-486
Pyrrolizidin-Alkaloide aus Emilia sonchifolia
Pyrrolizidine Alkaloids from Emilia sonchifolia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     acorientine
C20H27NO3     ÏàËÆ¶È:52.3%
Chemistry of Natural Compounds          2000          36          419-477
HETISANE-TYPE DITERPENOID ALKALOIDS
I. A. Bessonova and Sh. A. Saidkhodzhaeva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     senkirkine
    ÏàËÆ¶È:52.3%
Journal of Natural Products          1988          Vol 51          690
Macrocyclic Pyrrolizidine Alkaloids from Senecio anonymus. Separation of a Complex Alkaloid Extract Using Droplet Counter-Current Chromatography
Leon H. Zalkow, Clarita F. Asibal, Jan A. Glinski, Sandra J. Bonetti, Leslie T. Gelbaum, Donald VanDerveer, Garth Powis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     acorientine
C20H27NO3     ÏàËÆ¶È:52.3%
Phytochemistry          1996          41          957-961
Diterpenoid alkaloids from Aconitum orientale
Ayhan Ulubelen, Ali H. Meriçli, Filiz Meriçli, Funda Yilmaz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     compound 35
    ÏàËÆ¶È:52.3%
Journal of Heterocyclic Chemistry          2000          37          245-251
Synthesis of vinca alkaloids and related compounds part 94. Epimerization of compounds with aspidospermane and D-secoaspidospermane skeleton
György Kalaus, Lajos Szab¨®, J¨¢nos Éles, Csaba Sz¨¢ntay, Imre Juh¨¢sz, IstvÁn Greiner, J¨¢nos Brlik and M¨¢ria Kajt¨¢r-Peredy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     senkirkine
    ÏàËÆ¶È:52.3%
Phytochemistry          1982          21          439-443
13C NMR spectroscopy of Pyrrolizidine alkaloids
Russell J. Molyneux, James N. Roitman, Mabry Benson, Robert E. Lundin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

7 .     senkirkine
    ÏàËÆ¶È:52.3%
Chinese Traditional and Herbal Drugs          1996          27          203-205
Isolation and Identification of Pyrrolizidine Alkaloids From Amber Groundsel(Senecio ambraceus)
Liu Ke and Roeder E
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

8 .     senkirkine
    ÏàËÆ¶È:52.3%
Journal of China Pharmaceutical University          2008          39          20-22
A new biflavonoid from Senecio argunensis Turcz.
LI Ning; ZHANG Chao-feng; ZHANG Mian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     compound 5
    ÏàËÆ¶È:52.3%
Tetrahedron          1986          42          215-221
A new class of tricyclic diterpenes from eremophila georgii diels (myoporaceae)
P.G. Forster, E.L. Ghisalberti, P.R. Jefferies, B.W. Skelton, A.H. White
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     stephabenine
C27H29NO7     ÏàËÆ¶È:52%
Chemical & Pharmaceutical Bulletin          1983          31          2574-2577
Alkaloids from the Fruits of Stephania japonica MIERS. I. Structure of Stephabenine : A New Hasubanan Ester-Ketal Alkaloid
SACHIKO KONDO,MATAO MATSUI and YASUO WATANABE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     stephabenine
    ÏàËÆ¶È:52%
Journal of Natural Products          1985          Vol 48          746-750
Alkaloids from the Fruits of Stephania japonica 2. Structures of Oxostephabenine and N, O-Dimethyloxostephine
Yumi Yamamura, Matao Matsui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     28-acetoxy-15¦Á-hydroxymansumbinone
C24H3604     ÏàËÆ¶È:50%
Phytochemistry          2002          59          399-403
Two octanordammarane triterpenes from Commiphora kua
Aman Dekebo, Ermias Dagne, Lars K. Hansen, Odd R. Gautun, Arne J. Aasen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

13 .     14-Hydroxygelsecrotonidine
C22H24N2O6     ÏàËÆ¶È:50%
Tetrahedron          2008          64          7690-7694
Four novel gelsedine-type oxindole alkaloids from Gelsemium elegans
Yousuke Yamada, Mariko Kitajima, Noriyuki Kogure, Hiromitsu Takayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-05-22 14:01:04
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3Â¥2012-05-22 14:04:56
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