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1 .     (20S,24R)3¦Â,20,21¦Â,25-tetrahydroxy-21,24-cyclodammarane
C30H52O4     ÏàËÆ¶È:70%
Chinese Chemical Letters          2011          22          1461-1464
Two new dammarane-type sapogenins from Gynostemma pentaphyllum
Xia Li,Jia Qing Cao,Lin Shi,Yu Qing Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Abiesatrine I
C31H54O3     ÏàËÆ¶È:67.7%
Organic & Biomolecular Chemistry          2010          8          2609-2616
Abiesatrines A¨CJ: anti-inflammatory and antitumor triterpenoids from Abies georgei Orr
Xian-Wen Yang, Su-Mei Li, Liang Wu, Yong-Li Li, Lin Feng, Yun-Heng Shen, Jun-Mian Tian, Jian Tang, Ning Wang, Yonghong Liu and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     sodwanone E
    ÏàËÆ¶È:66.6%
Journal of Natural Products          1997          60          700-703
Sodwanones K, L, and M; New Triterpenes from the Marine Sponge Axinella weltneri
Amira Rudi, Maurice Aknin, Emile M. Gaydou, and Yoel Kashman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Aglaiabbreviatin D
C30H48O2     ÏàËÆ¶È:66.6%
Journal of Natural Products          2010          73          2042-2046
Triterpenoids from Aglaia abbreviata and Their Cytotoxic Activities
Feng Zhang, Jun-Song Wang, Yu-Cheng Gu, and Ling-Yi Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 7
    ÏàËÆ¶È:66.6%
Magnetic Resonance in Chemistry          1988          26          581-590
13C NMR assignment of dammarane triterpenes and dendropanoxide: Application of 2D long-range 13C[BOND]1H correlation spectra
Motoo Tori, Reiko Matsuda, Masakazu Sono and Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Neoabiestrine H
C30H52O4     ÏàËÆ¶È:66.6%
Phytochemistry          2012          81          159-164
Cytotoxic triterpenoids from Abies recurvata
Yong-Li Li, Yan-Xia Gao, Xian-Wen Yang, Hui-Zi Jin, Ji Ye, Luke Simmons, Ning Wang, Andre Steinmetz, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Â-acetoxyl-isofouquierol
C32H54O4     ÏàËÆ¶È:65.6%
Chinese Journal of Natural Medicines          2010          8          414-418
Triterpenoids from the Fruits of Forsythia suspensa
XUE Jiao; XIE Li; LIU Bao-Rui; YU Li-Xia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 12
    ÏàËÆ¶È:65.6%
Magnetic Resonance in Chemistry          1988          26          581-590
13C NMR assignment of dammarane triterpenes and dendropanoxide: Application of 2D long-range 13C[BOND]1H correlation spectra
Motoo Tori, Reiko Matsuda, Masakazu Sono and Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     leucastrin A
C31H54O2     ÏàËÆ¶È:64.5%
Chemical & Pharmaceutical Bulletin          2006          54          1370-1379
Studies on Nepalese Crude Drugs. XXIX. Chemical Constituents of Dronapuspi, the Whole Herb of Leucas cephalotes SPRENG.
Yukinori Miyaichi, Akiko Segawa and Tsuyoshi Tomimori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Combretanone E
C31H50O3     ÏàËÆ¶È:64.5%
Journal of Natural Products          2011          74          249-255
Cycloartane Triterpenes Isolated from Combretum quadrangulare in a Screening Program for Death-Receptor Expression Enhancing Activity
Kazufumi Toume, Takafumi Nakazawa, Takashi Ohtsuki, Midori A. Arai, Takashi Koyano, Thaworn Kowithayakorn, and Masami Ishibashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Neoabiestrine I
C31H54O4     ÏàËÆ¶È:64.5%
Phytochemistry          2012          81          159-164
Cytotoxic triterpenoids from Abies recurvata
Yong-Li Li, Yan-Xia Gao, Xian-Wen Yang, Hui-Zi Jin, Ji Ye, Luke Simmons, Ning Wang, Andre Steinmetz, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     genipatriol
C30H50O3     ÏàËÆ¶È:63.3%
Journal of Natural Products          2003          66          398-400
Genipatriol, a New Cycloartane Triterpene from Genipa spruceana
Chowdhury Faiz Hossain, Melissa R. Jacob, Alice M. Clark, Larry A. Walker, and Dale G. Nagle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (23E)-23-dehydro-25-hydroxysunpollenol
C30H52O3     ÏàËÆ¶È:63.3%
Journal of Natural Products          2003          66          1476-1479
Sunpollenol and Five Other Rearranged 3,4-seco-Tirucallane-Type Triterpenoids from Sunflower Pollen and Their Inhibitory Effects on Epstein-Barr Virus Activation
Motohiko Ukiya, Toshihiro Akihisa, Harukuni Tokuda, Kazuo Koike,Yumiko Kimura,Takeshi Asano,Shigeyasu Motohashi,Tamotsu Nikaido, and Hoyoku Nishino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     sodwanone M
C30H50O5     ÏàËÆ¶È:63.3%
Journal of Natural Products          1997          60          700-703
Sodwanones K, L, and M; New Triterpenes from the Marine Sponge Axinella weltneri
Amira Rudi, Maurice Aknin, Emile M. Gaydou, and Yoel Kashman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Cyclosieversigenin
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          1992          28          603-607
TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS XLIV. STRUCTURE OF CYCLOCARPOSIDES A AND C
B. A. Imomnazarov and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Cyclosieversigenin
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          1992          28          461-463
TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS XLIII. CYCLOARALOSIDE B FROM Astragalus amarus
M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Cyclosieversigenin
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          1991          27          457-459
TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS XXXIX. CYCLOARALOSIDE D FROM Astragalus amarus
M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     20S-dammarane-23-ene-3¦Â,20,25-triol
    ÏàËÆ¶È:63.3%
Journal of Asian Natural Products Research          2008          10          33-37
Dammarane triterpenes from Ligustrum lucidum
XIAO-HUA XU, NIAN-YUN YANG, SHI-HUI QIAN, NING XIE and JING-AO DUAN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     fern-7-en-3¦Á-ol
    ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          1999          47          543-547
Fern Constituents : Six New Triterpenoid Alcohols from Adiantum capillus-veneris
Takahisa NAKANE,Yoko ARAI,Kazuo MASUDA,Yuh ISHIZAKI,Hiroyuki AGETA and Kenji SHIOJIMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     3¦Á-hydroxytirucalla-7,24(25)-dien-6-oxo-21,16-olide
C30H44O4     ÏàËÆ¶È:63.3%
Journal of Natural Products          2010          73          693-697
Sterols and Terpenoids from Melia azedarach
Qin-Gang Tan, Xiao-Ning Li, Hao Chen, Tao Feng, Xiang-Hai Cai and Xiao-Dong Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     3-epibetulinate
    ÏàËÆ¶È:63.3%
Journal of Natural Products          1984          Vol 47          673-676
Isoprenoids from the Leaves of Quercus suber
Pietro Monaco, Lucio Previtera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     sodwanone E
C30H50O5     ÏàËÆ¶È:63.3%
Journal of Natural Products          1994          Vol 57          1416
Sodwanones A-F, New Triterpenoids from the Marine Sponge Axinella weltneri
Amira Rudi, Yoel Kashman, Yehuda Benayahu, Michael Schleyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     lup-20(29)-en-3-on-28-ol
    ÏàËÆ¶È:63.3%
Acta Pharmaceutica Sinica          2005          Vol 40          935-939
Chemical constituents from the mangrove plant Ceriops tagal
ZHANG Yan; DENG Zhi-wei; GAO Tian-xiang; FU Hong-zheng; LIN Wen-han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     compound 348
    ÏàËÆ¶È:63.3%
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
25 .     8,26-cyclo-urs-21-en-3¦Â,20¦Â-diol
C30H48O2     ÏàËÆ¶È:63.3%
Zeitschrift f¨¹r Naturforschung B          2008          63b          1335-1338
Pentacyclic Triterpenes and Other Constituents from Ficus cordata (Moraceae)
Herve M. P. Poumale, Rodrigue T. Kengap, Jean Claude Tchouankeu,Felix Keumedjio, Hartmut Laatsch, and Bonaventure T. Ngadjui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     Mesendanin R
C30H52O3     ÏàËÆ¶È:63.3%
Helvetica Chimica Acta          2012          95          286-300
Triterpenoids from Melia toosendan
Shi-Hui Dong, Xiu-Feng He, Lei Dong, Yan Wu, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     Elaeocarpucin F
C30H48O5     ÏàËÆ¶È:63.3%
Journal of Natural Products          2012          75          444−452
Isolation, Structure Elucidation, and Biological Evaluation of 16,23-Epoxycucurbitacin Constituents from Eleaocarpus chinensis
Li Pan, Yeonjoong Yong,Ye Deng, Daniel D. Lantvit, Tran Ngoc Ninh, Heebyung Chai,Esperanza J. Carcache de Blanco, Djaja D. Soejarto, Steven M. Swanson, and A. Douglas Kinghorn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     cycloastragenol
    ÏàËÆ¶È:63.3%
Phytochemistry          1990          29          3271-3274
Cycloartane triterpene glycosides from EgyptianAstragalus species
Nadia A. El-Sebakhy,Fathalla M. Harraz,Rokia M. Abdallah,Aya M. Asaad,F. Orsini,F. Pelizzoni,G. Sello,L. Verotta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     Isofouquierone
    ÏàËÆ¶È:63.3%
Phytochemistry          1985          24          2925-2928
Dammarane Triterpenes from the stem bark of Commiphora Dalzielii
Peter G. Waterman, Stephen Ampofo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     Isofouquierol
    ÏàËÆ¶È:63.3%
Chinese Journal of Natural Medicines          2010          8          414-418
Triterpenoids from the Fruits of Forsythia suspensa
XUE Jiao; XIE Li; LIU Bao-Rui; YU Li-Xia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     20R,24S-Epoxy-17-epi-cycloartan- 3¦Â,6¦Á,25-triol-16-one
C30H48O5     ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          2010          46          407-411
Triterpene glycosides from Astragalus and their genins. LXXXVII. Chemical transformation of cycloartanes. IX. Partial synthesis of cycloasalgenin
I. M. Isaev, D. A. Iskenderov and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     (20S)-dammar-23-ene-3¦Â,20,25-triol
    ÏàËÆ¶È:63.3%
Chemistry & Biodiversity          2013          10          96-128
Chemical Constituents and Biological Activities of Plants from the Genus Ligustrum
Bei-Bei Gao, Gai-Mei She and Dong-Mei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     3¦Á-hydroxytirucalla-7,24(25)-dien-6-oxo-21,16-olide
    ÏàËÆ¶È:63.3%
Natural Product Sciences          2013          19          342-346
A New Apotirucallane-type Triterpenoid from the Fruit of Melia azedarach
Jin, Qinghao;Lee, Chul;Lee, Jin Woo;Lee, Moon-Soon;Lee, Mi Kyeong;Hwang, Bang Yeon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     compound 5
    ÏàËÆ¶È:63.3%
Magnetic Resonance in Chemistry          1988          26          581-590
13C NMR assignment of dammarane triterpenes and dendropanoxide: Application of 2D long-range 13C[BOND]1H correlation spectra
Motoo Tori, Reiko Matsuda, Masakazu Sono and Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     Lupeportlandol
C30H50O     ÏàËÆ¶È:63.3%
Journal of the Brazilian Chemical Society          2004          15          742-747
Isoprenoid Compounds from Euphorbia portlandica. X-ray Structure of Lupeportlandol, a New Lupane Triterpene
Ana M. Madureira, Maria Teresa Duarte, Maria F¨¢tima M. Piedade Jos¨¦ R. Ascenso and Maria-Jos¨¦ U. Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     lithocarpic acid D
C30H50O4     ÏàËÆ¶È:63.3%
Journal of Natural Products          2014          77          1910-1920
Lithocarpic Acids A¨CN, 3,4-seco-Cycloartane Derivatives from the Cupules of Lithocarpus polystachyus
Hongmin Wang, Ruonan Ning, Yu Shen, Zhenhua Chen, Jinlong Li, Rujun Zhang, Ying Leng, and Weimin Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     Kuguacin V
C30H48O5     ÏàËÆ¶È:63.3%
Planta Medica          2015          81          327−332
The Antigluconeogenic Activity of Cucurbitacins from Momordica charantia
Jian-Chao Chen1, Clara Bik-San Lau2,3, Judy Yuet-Wa Chan2,3, Kwok-Pui Fung2,3, Ping-Chung Leung2,3, Jie-Qing Liu1,Lin Zhou1, Ming-Jin Xie4, Ming-Hua Qiu1
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     cycloasgenin B
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          2004          40          303-357
Triterpenoids from Astragalus Plants
R. P. Mamedova, M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     3¦Â-acetoxy-25-hydroxydammara-20,23-diene
    ÏàËÆ¶È:62.5%
Planta Medica          2003          69          258-264
New Dihydrobenzofurans and Triterpenoids from Roots of Microglossa pyrifolia
homas J.Schmidt,Meike R.Hildebrand,G¨¹nter Willuhn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     cyclosieversigenin 6-Monoacetate
    ÏàËÆ¶È:62.5%
Chemistry of Natural Compounds          2008          44          732-737
TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXVIII. CHEMICAL TRANSFORMATION OF CYCLOARTANES.VI. PARTIAL SYNTHESIS OF CYCLOADSURGENINa
I. M. Isaev, D. A. Iskenderov, and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     nepehinol acetate
    ÏàËÆ¶È:62.5%
Acta Pharmaceutica Sinica          1992          27          445-451
TRITERPENE CONSTITUENTS FROM EUPHORBIA NEMTOCYPHA HAND-MAZZ
D Cao; YL Su; JS Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     (22S)-6-O-acetyl-21¦ÂH-hopane-3¦Â,6¦Â,22,29-tetrol
C32H54O5     ÏàËÆ¶È:62.5%
Natural Product Research          2004          18          379-385
(22S)-6-O-acetyl-21¦ÂH-hopane-3¦Â,6¦Â,22,29-tetrol from Oakmoss (Evrnia prunastri)
Bjart Frode Lutnaes; Torger Bruun; Helge Kjøsen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     6-Monoacetate
C34H54O7     ÏàËÆ¶È:62.5%
Chemistry of Natural Compounds          2010          46          407-411
Triterpene glycosides from Astragalus and their genins. LXXXVII. Chemical transformation of cycloartanes. IX. Partial synthesis of cycloasalgenin
I. M. Isaev, D. A. Iskenderov and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     3¦Â-acetoxy-25-hydroxydammara-20,23-diene
C32H52O3     ÏàËÆ¶È:62.5%
Journal of Tropical and Subtropical Botany          2014          22          413-418
Phenolic Derivatives and Steroids from Eupatorium adenophorum Spreng
REN Hui, ZHANG Mei, ZHOU Zhong-yu, TAN Jian-wen, WAN Fang-hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     compound 4
    ÏàËÆ¶È:62.5%
Natural Medicines          1997          51          358-360
Studies on the Constituents of Astragalus membranaceus II. : Structure of Triterpenoidal Glycoside, Huangqiyenin D, from its Leaves
Kuang Haixue,Zhang Ning, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     (3¦Â)-9,18-dihydroxyolean-12-en-3-yl acetate
C32H52O4     ÏàËÆ¶È:62.5%
Helvetica Chimica Acta          2013          96          533-537
Two New Pentacyclic Triterpenes from Abelmoschus esculentus
Yonghui Zhou, Xin Jia, Jinmin Shi, Yinpeng Xu, Linlin Jing and Lu Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     3-O-¦Â-D-(2'-OAc)-xylopyranosyl-6-O-¦Â-D-xylopyranosyl-3¦Â,6¦Á,16¦Â,24(R),25-pentahydroxycycloartane
C42H70O14     ÏàËÆ¶È:62.5%
Chemistry of Natural Compounds          2014          50          1012-1015
Cycloartane Glycosides from Euphorbia boissierana
L. N. Gvazava, V. S. Kikoladze
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     3-O-¦Â-D-(2'-OAc)-xylopyranosyl-6-O-¦Â-D-glucopyranosyl-3¦Â,6¦Á,16¦Â,24(R),25-pentahydroxycycloartane
C43H72O15     ÏàËÆ¶È:62.5%
Chemistry of Natural Compounds          2014          50          1012-1015
Cycloartane Glycosides from Euphorbia boissierana
L. N. Gvazava, V. S. Kikoladze
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     foliasalaci A1
C31H54O2     ÏàËÆ¶È:61.2%
Chemical & Pharmaceutical Bulletin          2008          56(7)          915-920
Hnew Triterpene Constituents, Foliasalacins A1¡ªA4, B1¡ªB3, and C, from the Leaves of Salacia chinensis
Masayuki YOSHIKAWA,Yi ZHANG, Tao WANG, Seikou NAKAMURA, and Hisashi MATSUDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     foliasalaci A2
C31H54O2     ÏàËÆ¶È:61.2%
Chemical & Pharmaceutical Bulletin          2008          56(7)          915-920
Hnew Triterpene Constituents, Foliasalacins A1¡ªA4, B1¡ªB3, and C, from the Leaves of Salacia chinensis
Masayuki YOSHIKAWA,Yi ZHANG, Tao WANG, Seikou NAKAMURA, and Hisashi MATSUDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     igniaren D
C31H52O2     ÏàËÆ¶È:61.2%
Planta Medica          2009          75          1602-1607
Lanostanes from Phellinus igniarius and Their iNOS Inhibitory Activities
Guei-JaneWang, Tung-Hu Tsai, Tun-Tschu Chang, Cheng-Jen Chou, Lie-Chwen Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     lanost-25-en-3¦Â-ol acetyl derivative
    ÏàËÆ¶È:61.2%
Planta Medica          1999          65          478-479
A New Lanostane-Type Triterpenoid from Chamaesyce prostrata
Susana Rojas, Martha Maclas, Perla Castañeda,Robert Bye, Edelmira Linares, and Rachel Mata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     24-methylene-lanosta-8-en-2¦Â,3¦Â,21-triol
C31H52O3     ÏàËÆ¶È:61.2%
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
54 .     methyl senexdiolate
    ÏàËÆ¶È:61.2%
Journal of Natural Products          1993          Vol 56          2170
The Absolute Stereochemistry of Senexdiolic Acid at C-22
Antonio G. Gonz¨¢lez, Teresa Siverio Exp¨®sito, Jaime Bermejo Barrera, Ana Garc¨ªa Castellano, Francisco J. Toledo Marante
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     isomotiol(fern-8-en-3¦Â-ol) acetate
    ÏàËÆ¶È:61.2%
Korean Journal of Pharmacognosy          1985          16(3)          155-159
Studies on the Terpenoid constituents of Euphorbia supina Rafin
Chung, Bo-Sup; Kim, Ha-Gyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     leucastrin A 3,20-ditrimethylsilyl ether derivative
C37H61OSi2     ÏàËÆ¶È:61.2%
Chemical & Pharmaceutical Bulletin          2006          54          1370-1379
Studies on Nepalese Crude Drugs. XXIX. Chemical Constituents of Dronapuspi, the Whole Herb of Leucas cephalotes SPRENG.
Yukinori Miyaichi, Akiko Segawa and Tsuyoshi Tomimori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     (20S,22R,25R)-5¦Á-spirostane-2¦Á,3¦Â,6¦Â-triol triacetate
    ÏàËÆ¶È:61.2%
Phytochemistry          1988          27          2943-2945
Steroid sapogenins from Nothoscordum gramineum var. philippianum and Tristagma uniflorum
M.C. Brunengo,O.L. Tombesi,D. Doller,E.G. Gros
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