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1 .     À×¹«ÌÙÄÚõ¥¼×
    ÏàËÆ¶È:88.8%
Journal of China Pharmaceutical University          1991          22          175-176
Studies on Chemical Constituents from the Stems of Tripterygium Hypoglaucum ¢ò
Ding Li; Zhang Zhengxing; An Dengkui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Wilforlide A
    ÏàËÆ¶È:82.7%
Chinese Pharmaceutical Journal          2009          44          1375-1377
Studies on Chemical Constituents of the Euonymus alatus(Thunb.) Sieb.¢ò
ZHOU Xin, LIU Yun, GONG Xiao-jian, ZHAO Chao, CHEN Hua-guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ursolic acid
C30H46O3     ÏàËÆ¶È:79.1%
Chemical & Pharmaceutical Bulletin          1993          41          1238-1243
Two New 2-Arylbenzofuran Derivatives from Hypoglycemic Activity-Bearing Fractions of Morus insignis
Purusotam BASNET,Shigetoshi KADOTA,Satoshi TERASHIMA,Mineo SHIMIZU and Tsuneo NAMBA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ursolic acid
C30H48O3     ÏàËÆ¶È:79.1%
Chemical & Pharmaceutical Bulletin          1985          33          5355-5357
Studies on Bioactive Substances in Crude Drugs Used for Arthritic Diseases in Traditional Chinese Medicine. III. Isolation and Identification of Anti-inflammatory and Analgesic Principles from the Whole Herb of Pyrola rotundifolia L.
TAKUO KOSUGE,MASAMI YOKOTA,KIYOSHI SUGIYAMA,TAKAKI MURE,HIROYO YAMAZAWA and TOSUKE YAMAMOTO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     ursolic acid
C30H48O3     ÏàËÆ¶È:76.9%
Korean Journal of Pharmacognosy          2004          35(2)          116-121
Phytochemical Constituents of Synurus excelsus
Nam, Jung-Hwan; Choi, Sang-Zin; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     wilforlide B
    ÏàËÆ¶È:72.4%
Planta Medica          2013          79          797-805
Simultaneous Quantification of 18 Bioactive Constituents in Tripterygium wilfordii Using Liquid Chromatography-Electrospray Ionization-Mass Spectrometry
Zeng, Feng; Wang, Wei; Guan, Shuhong; Cheng, Chunru; Yang, Min; Avula, Bharathi; Khan, Ikhlas A.; Guo, De-an:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     À×¹«ÌÙÄÚõ¥ÒÒ
    ÏàËÆ¶È:72.4%
Journal of Plant Resources and Environment          1992          1          50-53
À¥Ã÷ɽº£Ìľ¥Öл¯ºÏÎïµÄ·ÖÀë¼°Æä¿¹Ñ×»îÐÔ
¶¡Àè, ÕÅÕýÐÐ, Ðì¼á, Õźìϲ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 6i
    ÏàËÆ¶È:70.3%
Australian Journal of Chemistry          1981          34          1451-1465
Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols
JM Coxon and JR Gibson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ¦Á-amyrin
    ÏàËÆ¶È:69.2%
Journal of China Pharmaceutical University          2008          39          279-281
Chemical constituents of Japanese herb Sonchus oleraceus
BAI Yu-hua; YU Hui; CHANG Nai-dan; Masayoshi Ando
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     5¦Â-Cholestane-3¦Á,5,6¦Á-triol
    ÏàËÆ¶È:68%
Steroids          2007          72          95-104
4,5-Epoxycholestane-3,6-diols: Templates for generating the full set of eight cholestane-3,5,6-triol stereoisomers in multigram scales, but not for a cholestane-3,4,6-triol
Kejun Zhao, Yongfeng Wang, Li Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     homodestruxin B
    ÏàËÆ¶È:68%
Phytochemistry          1991          30          2311-2316
HPLC purification of destruxins produced by Alternaria brassicae in culture and leaves of Brassica napus
L. Buchwaldt, J.S. Jensen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Cholest-4-en-3,6-dione
    ÏàËÆ¶È:68%
Steroids          1998          63          76-79
Steroidal 5-en-3-ones, intermediates of the transformation of steroidal 5-en-3¦Â-ols to steroidal 4-en-3,6-diones oxidized by pyridinium dichromate and pyridinium chlorochromate
Sheng-Hui Li, Tong-Shuang Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ¦Á-amyrin
    ÏàËÆ¶È:67.8%
Chinese Journal of Medicinal Chemistry          2010          20          520-523
Chemical constituents of radix Marsdeniae sinensis
HU Hu, i WU Yi-xuan, HE Xiang-jiu*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     6¦Â-Methoxy-3¦Á,5-cyclo-5¦Á-23,24-bisnorcholan-22-ol
    ÏàËÆ¶È:66.6%
Steroids          2005          70          551-562
Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Alexey V. Antonchick, Andrey P. Antonchick, Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     cholest-4-ene-3,6-dione
C27H42O2     ÏàËÆ¶È:66.6%
Steroids          2005          70          907-912
Synthesis and antifungal activity of oxygenated cholesterol derivatives
Jean Michel Brunel, C¨¦line Loncle, Nicolas Vidal, Michel Dherbomez, Yves Letourneux
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     4¦Â-Chloro-5¦Á-cholestane-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:66.6%
Steroids          2007          72          95-104
4,5-Epoxycholestane-3,6-diols: Templates for generating the full set of eight cholestane-3,5,6-triol stereoisomers in multigram scales, but not for a cholestane-3,4,6-triol
Kejun Zhao, Yongfeng Wang, Li Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     cholest-4-ene-3,6-dione
    ÏàËÆ¶È:66.6%
Chinese Journal of Natural Medicines          2008          6          348-353
Chemical Constituents of Marine Sponge Biemna fortis Topsent
HUANG Xiao-Chun; LIU Hai-Li; GUO Yue-Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ursolic acid
    ÏàËÆ¶È:66.6%
Archives of Pharmacal Research          2002          25          280-284
Phytochemical constituents from the fruits ofAcanthopanax sessiliflorus
Sanghyun Lee, Bak-Kwang Kim, Seon Haeng Cho and Kuk Hyun Shin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     ¦Á-amyrin
    ÏàËÆ¶È:66.6%
Archives of Pharmacal Research          2003          26          902-905
Constituents from the non-polar fraction of Artemisia apiacea
Sanghyun Lee, Kyoung Soon Kim, Sang Hee Shim, You Mie Park and Bak-Kwang Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     ¦Á-amyrin
    ÏàËÆ¶È:66.6%
Chinese Pharmaceutical Journal          2008          43          900-902
Studies on Chemical Constituents of Acetyl Acetate Extracted Fraction from Veratrum dahuricum
NIE Li-yue TANG Jian~LI Hui-liang JIN Hui-zi ZHANG Wei-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     ursolic acid
    ÏàËÆ¶È:66.6%
Chinese Pharmaceutical Journal          2009          44          1287-1290
Studies on Chemical Constituents from Rhaponticum carthamoides (Willd.) Iljin
HUANG Min-fang, LI Ning, NI Hui, JIA Xiao-guang*, LI Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     ursolic acid
    ÏàËÆ¶È:66.6%
Modern Chinese Medicine          2006          8(6)          18-20
Studies on the Chemical Constituents of Ledum palustre L.
Qiu Guihua, Zuo Wenjian, Wang Jinhui, L i Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     uvaol
    ÏàËÆ¶È:66.6%
Modern Chinese Medicine          2011          13(1)          23-25
Isolation and Identification of Chemical Constituents from RosmarinusOfficinalis L1
WANG Hui, , GAO Hui-yuan, ZHANG Zhen-qiu, WULi-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     cholest-4-en-3,6-dione
    ÏàËÆ¶È:66.6%
Indian Journal of Chemistry Section B          2012          51B          1027-1031
Studies on the reaction of N-bromo-succinimide in dimethylsulphoxide: Part X ¡ª Action on cholest-4-en-3,6-dione
Pradhan, B P; Debnath, Utpal; Pradhan, Nagendra Narayan; Ghosh, Pranab
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     3¦Â-OH,¦Á-amirina
    ÏàËÆ¶È:66.6%
Qu¨ªmica Nova          2008          31          744-750
Chemical constituents and antiedematogenic activity of Peltodon radicans (Lamiaceae)
Costa, Habdel Nasser Rocha da; Santos, Maria Cristina dos; Alcantara, Antônio Flavio de Carvalho; Silva, Marilda Conceição; França, Roberta Cabral; Pil¨®-Veloso, Dorila
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     26,27-dinor-4,4-dimethyl-cholesta-8,14-dien-3-ol
    ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2011          42          15-17
Chemical constituents in root bark of Torricellia angulata var. intermedia (¢ó)
ZHANG Jin-wen, GUO Jie-ru, TANG Fei, ZHANG Xiao-qiong, TU Nian, WANG Yan-yan, ZHANG Yong-hui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     5¦Á-Cholestan-4¦Â-ol
C27H48O     ÏàËÆ¶È:66.6%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     compound 6h
    ÏàËÆ¶È:66.6%
Australian Journal of Chemistry          1981          34          1451-1465
Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols
JM Coxon and JR Gibson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     rubifolic acid
    ÏàËÆ¶È:65.5%
China Journal of Chinese Materia Medica          2009          34          2761-2764
Chemical constituents of Galium verum
ZHAO Chunchao, SHAO Jianhua, CAO Dandan, ZHANG Yuwei LIXian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     triptocallic acid A
C30H48O4     ÏàËÆ¶È:65.5%
Phytochemistry          1997          45          293-296
A diterpenoid and triterpenes from tissue cultures of Tripterygium wilfordii
Kimiko Nakano, Yoshiko Oose, Yuuko Masuda, Hikari Kamada, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     urslic acid
C30H48O3     ÏàËÆ¶È:65.5%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2003          42(2)          52-55
The Chemical Constituents of Heliicteres angustifolia Linn.
GUO Xin-dong, AN Lin-kin, XI Di, MA Lin, GU Lian-quan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     Ursolic Acid
    ÏàËÆ¶È:65.5%
Journal of Agricultural and Food Chemistry          2002          50          607-609
New Prenylated Benzoic Acid and Other Constituents from Almond Hulls (Prunus amygdalus Batsch)
Shengmin Sang, Karen Lapsley, Robert T. Rosen, and Chi-Tang Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     Ursolic Acid
    ÏàËÆ¶È:65.5%
Journal of Agricultural and Food Chemistry          2002          50          607-609
New Prenylated Benzoic Acid and Other Constituents from Almond Hulls (Prunus amygdalus Batsch)
Shengmin Sang, Karen Lapsley, Robert T. Rosen, and Chi-Tang Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     ursolic acid
C30H48O3     ÏàËÆ¶È:65.5%
Chinese Traditional and Herbal Drugs          2012          43          55-59
Chemical constituents from flowers of Incarvillea younghusbandii
WU Juan; ZHOU Xian-li; ZHOU Xiao-li;
Domyallbesttohaveahappylife.
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