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12.98, 22.29, 24.74, 28.98, 29,02, 29.16, 29.31, 31.63, 33.70, 39.50, 50.95, 53.36, 103.48, 114.43, 114.88, 115.47, 127.59, 129.86, 131.99, 157.38, 191.42
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zxw_ll

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3Â¥: Originally posted by yuxuanyuhong at 2014-03-13 08:56:41
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1 .     (E)-5-(4-(hexadecyloxy)styryl)benzene-1,3-diol
    ÏàËÆ¶È:59.0%
Bioorganic & Medicinal Chemistry          2011          19          5321-5333
Chemical modifications of resveratrol for improved protein kinase C alpha activity
Joydip Das, Satyabrata Pany, Anjoy Majhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     tert-Butyl (5S)-3-(1-Hydroxydecylidene)-2,4-dioxo-5-[4-(prop-2-en-1-yloxy)benzyl]pyrrolidine-1-carboxylate
    ÏàËÆ¶È:56%
Chemistry & Biodiversity          2010          7          2830-2845
Structure¨CActivity Relationships of Precursors and Analogs of Natural 3-Enoyl-tetramic Acids
Bertram Barnickel, Frances Bayliffe, Randi Diestel, Karl Kempf, Sabine Laschat, Steffen Pachali, Florenz Sasse, Andrea Schlenk and Rainer Schobert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     (2'S)-1-O-(9-Oxo-10(E),12(E)-octadecadienoyl) glycerol
C21H36O5     ÏàËÆ¶È:54.5%
Bulletin of the Korean Chemical Society          2010          31          2051-2053
Anti-melanogenic Fatty Acid Derivatives from the Tuber-barks of Colocasia antiquorum var. esculenta
Ki Hyun Kim, Eunjung Moon, Sun Yeou Kim, Kang Ro Lee*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     N-{3-[3,17¦Â-dihydroxy-estra-1,3,5 (10)-trien-16¦Â-yl]-propyl}-2-(ammonium hydrochloride)-acetamide
C23H34N2O3     ÏàËÆ¶È:52.1%
Steroids          2001          66          821-831
Chemical synthesis of 16¦Â-propylaminoacyl derivatives of estradiol and their inhibitory potency on type 1 17¦Â-hydroxysteroid dehydrogenase and binding affinity on steroid receptors
Martin R. Tremblay, Sheng-Xiang Lin, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     N-{3-[3,17¦Â-dihydroxy-estra-1,3,5 (10)-trien-16¦Â-yl]-propyl}-2-(S)-(1-hydroxycarbonylpropan-3-yl)-2-(ammoniumhydrochloride)-acetamide
C26H38N2O5     ÏàËÆ¶È:50%
Steroids          2001          66          821-831
Chemical synthesis of 16¦Â-propylaminoacyl derivatives of estradiol and their inhibitory potency on type 1 17¦Â-hydroxysteroid dehydrogenase and binding affinity on steroid receptors
Martin R. Tremblay, Sheng-Xiang Lin, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     N-{3-[3,17¦Â-dihydroxy-estra-1,3,5 (10)-trien-16¦Â-yl]-propyl}-2-(S)-(1-hydroxymethyl)-2-(ammonium hydrochloride)-acetamide
C24H36N2O4     ÏàËÆ¶È:50%
Steroids          2001          66          821-831
Chemical synthesis of 16¦Â-propylaminoacyl derivatives of estradiol and their inhibitory potency on type 1 17¦Â-hydroxysteroid dehydrogenase and binding affinity on steroid receptors
Martin R. Tremblay, Sheng-Xiang Lin, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     16¦Â-(aminopropyl)-E2
C21H31NO2     ÏàËÆ¶È:50%
Steroids          2001          66          821-831
Chemical synthesis of 16¦Â-propylaminoacyl derivatives of estradiol and their inhibitory potency on type 1 17¦Â-hydroxysteroid dehydrogenase and binding affinity on steroid receptors
Martin R. Tremblay, Sheng-Xiang Lin, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     compound 4f
C23H31N3O2     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          498-503
Synthesis and antibacterial activity study of a novel class of cationic anthraquinone analogs
Jianjun Zhang, Nathan Redman, Anthony Phillip Litke, Jia Zeng, Jixun Zhan, Ka Yee Chan,Cheng-Wei Tom Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     compound 4g
C27H39N3O2     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          498-503
Synthesis and antibacterial activity study of a novel class of cationic anthraquinone analogs
Jianjun Zhang, Nathan Redman, Anthony Phillip Litke, Jia Zeng, Jixun Zhan, Ka Yee Chan,Cheng-Wei Tom Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     Sodium 2-{4'-methoxy-6-[(2-oxocyclopentyl)methyl]-biphenyl-3-yl}propanoate
C22H23NaO4     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          3299-3311
Synthesis and biological evaluation of loxoprofen derivatives
Naoki Yamakawa ,Shintaro Suemasu, Masaaki Matoyama , Ken-ichiro Tanaka, Takashi Katsu ,Keishi Miyata , Yoshinari Okamoto , Masami Otsuka , Tohru Mizushima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     compound 1
    ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2003          51          1439-1440
Constituents of Hypericum laricifolium and Their Cyclooxygenase (COX) Enzyme Activities
Hesham Rushdey El-Seedi, Therese Ringbom, Kurt Torssell and Lars Bohlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     methyl [1¦Á,2¦Á(Z),3¦Á,4¦Á]-7-[3-[(hexylamino)methyl)-7-oxabicyclo[2.2.1]hept-2-yl]-5-heptenoate
    ÏàËÆ¶È:50%
Journal of Medicinal Chemistry          1990          33          2465-2476
7-Oxabicyclo[2.2.1]heptyl carboxylic acids as thromboxane A2 antagonists: aza .omega.-chain analogs
Masami Nakane, Joyce A. Reid, Wen Ching Han, Jagabandhu Das, Vu Chi Truc, Martin F. Haslanger, Dianne Garber, Don N. Harris, Anders Hedberg,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     (E)-5-(4-(octyloxy)styryl)benzene-1,3-diol
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          5321-5333
Chemical modifications of resveratrol for improved protein kinase C alpha activity
Joydip Das, Satyabrata Pany, Anjoy Majhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2014-03-12 22:45:51
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

yuxuanyuhong

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ÎÄÏ׽ܳö¹±Ï×ÎÄÏ׽ܳö¹±Ï×

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2Â¥: Originally posted by zxw_ll at 2014-03-12 22:45:51
²éѯ½á¹û£º¹²²éµ½13¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
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1 .     (E)-5-(4-(hexadecyloxy)styryl)benzene-1,3-diol
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