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1 .     pseudolaric acid B-¦Â-D-glucoside
C29H38O13     ÏàËÆ¶È:70%
Journal of Natural Products          1995          Vol 58          57-67
Antifungal Evaluation of Pseudolaric Acid B, a Major Constituent of Pseudolarix kaempferi
Erguang Li, Alice M. Clark, Charles D. Hufford
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     PAB-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:70%
Journal of Separation Science          2009          32          309-313
Preparative isolation of pseudolaric acids A and B, and their glucosides from the root bark of Pseudolarix kaempferi using high-speed counter-current chromatography
Quan-Bin Han, Lina Wong, Fanny Lai, Nian-Yun Yang, Jing-Zheng Song, Chun-Feng Qiao and Hong-Xi Xu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     2',3'-dihydroxy-1'-propoxypseudolarate B
C26H34O10     ÏàËÆ¶È:66.6%
Journal of Natural Products          2002          65          1041-1044
Five New Diterpenoids from Pseudolarix kaempferi
Sheng-Ping Yang, Yan Wu, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     6'-O-acetylpseudolaric acid B O-¦Â-D-glucopyranoside
C31H40O14     ÏàËÆ¶È:64.5%
Journal of Natural Products          2002          65          1041-1044
Five New Diterpenoids from Pseudolarix kaempferi
Sheng-Ping Yang, Yan Wu, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3-(2-chlorobenzyl)androsta-3,5-dien-17-yl acetate
    ÏàËÆ¶È:63.3%
Russian Journal of Organic Chemistry          2008          44          785-790
noaccess785-790
Pd-catalyzed alkylation of halogen-substituted steroids with organozinc compounds
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     N-((tert-butylcarbamoyl)methyl)-N-benzyl-3¦Â-hydroxyandrost-5-en-17¦Â-carboxamide
C33H48N2O3     ÏàËÆ¶È:60%
Steroids          2010          75          659-664
Synthesis and preliminary biological screening of sterol analogues as new antifungal agents against plant pathogens
Fernando Alonso, Adriana M. Cirigliano, Gabriela M. Cabrera, Javier A. Ram¨ªrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     N-((tert-butylcarbamoyl)methyl)-N-(4-chlorophenyl)-3¦Â-hydroxyandrost-5-en-17¦Â-carboxamide
C32H45ClN2O3     ÏàËÆ¶È:60%
Steroids          2010          75          659-664
Synthesis and preliminary biological screening of sterol analogues as new antifungal agents against plant pathogens
Fernando Alonso, Adriana M. Cirigliano, Gabriela M. Cabrera, Javier A. Ram¨ªrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     N-((tert-butylcarbamoyl)methyl)-N-phenyl-3¦Â-hydroxyandrost-5-en-17¦Â-carboxamide
C32H46N2O3     ÏàËÆ¶È:60%
Steroids          2010          75          659-664
Synthesis and preliminary biological screening of sterol analogues as new antifungal agents against plant pathogens
Fernando Alonso, Adriana M. Cirigliano, Gabriela M. Cabrera, Javier A. Ram¨ªrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     6,12,13,14,21,22-triepoxycytochalasin B
C29H37NO8     ÏàËÆ¶È:60%
Magnetic Resonance in Chemistry          2008          46          650-659
Synthesis, complete 1H and 13C NMR assignment and crystal structure of novel epoxide derivatives of cytochalasin B (pages 650¨C659)
Pieter S. Steyn, Jaco C. Breytenbach, Jeanne H. Botha, Manuel A. Fernandes and Philippus L. Wessels
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     N-{2-[3-(2,3-Dimethylphenylaminosulfonyl)phenylamino-carbonyl]ethyl}-(Z)-9-octadecenoic acid amide
C35H53N3O4S     ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry          2000          8          1991-2006
Design, synthesis and early structure¨Cactivity relationship of farnesyltransferase inhibitors which mimic both the peptidic and the prenylic substrate
Martin Schlitzer, Markus Böhm, Isabel Sattler, Hans-Martin Dahse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3-(4-methylbenzyl)androsta-3,5-dien-17-yl acetate
    ÏàËÆ¶È:60%
Russian Journal of Organic Chemistry          2008          44          785-790
noaccess785-790
Pd-catalyzed alkylation of halogen-substituted steroids with organozinc compounds
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (N-(3-Methoxyquinolinyl-2-carbonyl)-D-Ser-Pip-Gly-Sar-NMe-Val)2(serine hydroxyl) dilactone
C62H80N12O16     ÏàËÆ¶È:58.0%
Bioorganic & Medicinal Chemistry          1998          6          85-102
Synthesis of key sandramycin analogs: systematic examination of the intercalation chromophore
Dale L. Boger, Jyun-Hung Chen, Kurt W. Saionz, Qing Jin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     euphorbia factor L7b
C33H40O9     ÏàËÆ¶È:58.0%
Bioorganic & Medicinal Chemistry          2009          17          4786-4792
Lathyrane diterpenes from Euphorbia lathyris as modulators of multidrug resistance and their crystal structures
Wei Jiao, Weiwei Dong, Zhefeng Li, Meicai Deng, Runhua Lu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 7
    ÏàËÆ¶È:56.6%
Journal of Natural Products          1999          62          949-953
18, 20-Hemiacetal-type and Other Withanolides from Dunalia brachyacantha
Gloria L. Silva, Gerardo Burton, and Juan C. Oberti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     physachenolide B
    ÏàËÆ¶È:56.6%
Planta Medica          2004          70          59-64
18-Acetoxywithanolides from Physalis chenopodifolia
Emma Maldonado,Fernando R. Torres, Mahinda Mart¨ªnez,Ana L. P¨¦rez-Castorena
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     N-((tertbutylcarbamoyl)methyl)-N-phenyl-3¦Â-hydroxypregn-5-ene-20-carboxamide
C34H50N2O3     ÏàËÆ¶È:56.6%
Steroids          2010          75          659-664
Synthesis and preliminary biological screening of sterol analogues as new antifungal agents against plant pathogens
Fernando Alonso, Adriana M. Cirigliano, Gabriela M. Cabrera, Javier A. Ram¨ªrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     16-(4-nitro-benzylidene)-3¦Â-morpholino-5¦Á-androstan-17¦Â-yl acetate
C32H44N2O5     ÏàËÆ¶È:56.6%
Steroids          2011          76          709-723
Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents
Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     16-(4-chloro-benzylidene)-3¦Â-piperidino-5¦Á-androstan-17¦Â-yl acetate
C33H46ClNO2     ÏàËÆ¶È:56.6%
Steroids          2011          76          709-723
Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents
Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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