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²éѯ½á¹û£º¹²²éµ½13¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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