| ²é¿´: 380 | »Ø¸´: 1 | |||
ltx0744624½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×Êý¾ÝÇóÖú
|
|
13C-NMR ÈܼÁë®´ú¼×´¼ 18.7,19.1,29.8,58.1,68.4,71.9,72.0,78.1,78.4,115.0,115.3,118.9,122.6,126.8,128.1,129.8,130.0,131.3,131.8,136.7,139.7,140.6,155.9,157.0 |
» ²ÂÄãϲ»¶
268·Ö085602»¯Ñ§¹¤³Ìµ÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁÏר˶322
ÒѾÓÐ14È˻ظ´
288Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
085404£¬285·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
083200 ³õÊÔ305·Ö Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
085400 328·Ö Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Çó»úеר˶297µÚ¶þÅúµ÷¼Á
ÒѾÓÐ4È˻ظ´
332£¬085601Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
367Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
һ־Ը³¶«´óѧ071000ÉúÎïѧѧ˶³õÊÔ·ÖÊý276Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×Êý¾ÝÇóÖú¡ª¡ªÈý¸ö»¯ºÏÎï лл£¡
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬¸ø30J
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
±ÏÒµ¼±ÐèÊý¾Ý£¬Î¢Æ×ÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý ÖØ½±
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾ÝÇóÖú ¼±±ÏÒµ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
¼±ÇóÇóÖú΢Æ×Êý¾Ý¼ìË÷CÆ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
ltx0744624(¶¹¸ç´ú·¢): ½ð±Ò+20, лл 2013-09-21 11:27:43
ltx0744624(¶¹¸ç´ú·¢): ½ð±Ò+20, лл 2013-09-21 11:27:43
|
²éѯ½á¹û£º¹²²éµ½51¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2-[3-(benzyloxy)phenyl]-1,1-bis(4-hydroxyphenyl)-1-butene C29H26O3 ÏàËÆ¶È:64% Bioorganic & Medicinal Chemistry 2013 21 311-320 Ridaifen B, a tamoxifen derivative, directly binds to Grb10 interacting GYF protein 2 Senko Tsukuda, Tomoe Kusayanagi, Eri Umeda, Chihiro Watanabe, Yu-ta Tosaki, Shinji Kamisuki, Toshifumi Takeuchi, Yoichi Takakusagi, Isamu Shiina, Fumio Sugawara Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (Z)-N-(4-(1',2'-bis(4'',4'''-(benzyloxy) phenyl) but-1'-enyl)phenyl)isobutyramide ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2013 21 4120-4131 Synthesis and biological evaluation of novel tamoxifen analogues Michael S. Christodoulou, Nikolas Fokialakis, Daniele Passarella, A¨ªda Nelly Garc¨ªa-Arg¨¢ez, Ornella Maria Gia, Ingemar Pongratz, Lisa Dalla Via, Serkos A. Haroutounian Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . butyrolactone I ÏàËÆ¶È:58.3% Phytotherapy Research 2012 26 1872-1877 New Antifungal Compounds from Aspergillus terreus Isolated from Desert Soil Amani S. Awaad, Al-Jaber A. Nabilah and Mohamed E. Zain Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (Z)-N-(4-(1',2'-bis(4'',4'''-(benzyloxy) phenyl)but-1'-enyl)phenyl) propionamide ÏàËÆ¶È:56% Bioorganic & Medicinal Chemistry 2013 21 4120-4131 Synthesis and biological evaluation of novel tamoxifen analogues Michael S. Christodoulou, Nikolas Fokialakis, Daniele Passarella, A¨ªda Nelly Garc¨ªa-Arg¨¢ez, Ornella Maria Gia, Ingemar Pongratz, Lisa Dalla Via, Serkos A. Haroutounian Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 13,17-Epoxy-16-hydroxy macrolactin A C24H34O6 ÏàËÆ¶È:54.1% Journal of Natural Products 2011 74 2582-2587 Cyclic Ether-Containing Macrolactins, Antimicrobial 24-Membered Isomeric Macrolactones from a Marine Bacillus sp. M. A. Mojid Mondol, Fakir Shahidullah Tareq, Ji Hye Kim, Min ah Lee, Hyi-Seung Lee, Yeon-Ju Lee, Jong Seok Lee, and Hee Jae Shin Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 4-(2-benzyloxyphenylmethyl)-5-methyl-1H-pyrazol-3-yl ¦Â-D-glucopyranoside C24H28N2O7 ÏàËÆ¶È:54.1% Bioorganic & Medicinal Chemistry 2012 20 6598-6612 Structure¨Cactivity relationship studies of 4-benzyl-1H-pyrazol-3-yl ¦Â-d-glucopyranoside derivatives as potent and selective sodium glucose co-transporter 1 (SGLT1) inhibitors with therapeutic activity on postprandial hyperglycemia Nobuhiko Fushimi, Hideki Fujikura, Hiroaki Shiohara, Hirotaka Teranishi, Kazuo Shimizu, Shigeru Yonekubo, Kohsuke Ohno, Takashi Miyagi, Fumiaki Itoh, Toshihide Shibazaki, Masaki Tomae, Yukiko Ishikawa-Takemura, Takeshi Nakabayashi, Noboru Kamada, Tomonaga Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 4-(2-benzyloxyphenylmethyl)-5-ethyl-1H-pyrazol-3-yl ¦Â-D-glucopyranoside C25H30N2O7 ÏàËÆ¶È:54.1% Bioorganic & Medicinal Chemistry 2012 20 6598-6612 Structure¨Cactivity relationship studies of 4-benzyl-1H-pyrazol-3-yl ¦Â-d-glucopyranoside derivatives as potent and selective sodium glucose co-transporter 1 (SGLT1) inhibitors with therapeutic activity on postprandial hyperglycemia Nobuhiko Fushimi, Hideki Fujikura, Hiroaki Shiohara, Hirotaka Teranishi, Kazuo Shimizu, Shigeru Yonekubo, Kohsuke Ohno, Takashi Miyagi, Fumiaki Itoh, Toshihide Shibazaki, Masaki Tomae, Yukiko Ishikawa-Takemura, Takeshi Nakabayashi, Noboru Kamada, Tomonaga Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 4-(2-benzyloxyphenylmethyl)-5-tert-butyl-1H-pyrazol-3-yl ¦Â-D-glucopyranoside C27H34N2O7 ÏàËÆ¶È:54.1% Bioorganic & Medicinal Chemistry 2012 20 6598-6612 Structure¨Cactivity relationship studies of 4-benzyl-1H-pyrazol-3-yl ¦Â-d-glucopyranoside derivatives as potent and selective sodium glucose co-transporter 1 (SGLT1) inhibitors with therapeutic activity on postprandial hyperglycemia Nobuhiko Fushimi, Hideki Fujikura, Hiroaki Shiohara, Hirotaka Teranishi, Kazuo Shimizu, Shigeru Yonekubo, Kohsuke Ohno, Takashi Miyagi, Fumiaki Itoh, Toshihide Shibazaki, Masaki Tomae, Yukiko Ishikawa-Takemura, Takeshi Nakabayashi, Noboru Kamada, Tomonaga Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . gentchroman,N-methyl iodide salt C32H42INO4 ÏàËÆ¶È:54.1% Journal of Medicinal Chemistry 1994 37 696-700 An X-ray Crystallographic Study of the Nonsteroidal Contraceptive Agent Centchroman Suprabhat Ray, Amita Tandon, Indra Dwivedy, Scott R. Wilson, James P. O'Neil, John A. Katzenellenbogen Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-(3-[3-(2-methoxyethoxymethoxy)-phenyl]-acryloyl)-4(S)-phenyloxazolidin-2-one C22H23O6N ÏàËÆ¶È:54.1% The Journal of Peptide Research 2005 65 105-112 Syntheses of optically pure, conformationally constrained, and highly hydrophobic unusual amino acids: 2-amino-3, 3-diarylpropionic acids J. Lin, S. Liao and V.J. Hruby Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-(3-[3-(2-methoxyethoxymethoxy)-phenyl]-acryloyl)-4(R)-phenyloxazolidin-2-one C22H23O6N ÏàËÆ¶È:54.1% The Journal of Peptide Research 2005 65 105-112 Syntheses of optically pure, conformationally constrained, and highly hydrophobic unusual amino acids: 2-amino-3, 3-diarylpropionic acids J. Lin, S. Liao and V.J. Hruby Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (E)-3-(4'-(1'',2''-bis(4''',4''''-(benzyloxy) phenyl)but-1''-enyl)phenyl)-1,1-dimethylurea ÏàËÆ¶È:54.1% Bioorganic & Medicinal Chemistry 2013 21 4120-4131 Synthesis and biological evaluation of novel tamoxifen analogues Michael S. Christodoulou, Nikolas Fokialakis, Daniele Passarella, A¨ªda Nelly Garc¨ªa-Arg¨¢ez, Ornella Maria Gia, Ingemar Pongratz, Lisa Dalla Via, Serkos A. Haroutounian Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (Z)-3-(4'-(1'',2''-bis(4''',4''''-(benzyloxy)phenyl)but-1''-enyl)phenyl)-1,1-dimethylurea ÏàËÆ¶È:54.1% Bioorganic & Medicinal Chemistry 2013 21 4120-4131 Synthesis and biological evaluation of novel tamoxifen analogues Michael S. Christodoulou, Nikolas Fokialakis, Daniele Passarella, A¨ªda Nelly Garc¨ªa-Arg¨¢ez, Ornella Maria Gia, Ingemar Pongratz, Lisa Dalla Via, Serkos A. Haroutounian Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (Z)-3-(4'-(1'',2''-bis(4''',4''''-(benzyloxy)phenyl)but-1''-enyl)phenyl)-1,1-diethylurea ÏàËÆ¶È:54.1% Bioorganic & Medicinal Chemistry 2013 21 4120-4131 Synthesis and biological evaluation of novel tamoxifen analogues Michael S. Christodoulou, Nikolas Fokialakis, Daniele Passarella, A¨ªda Nelly Garc¨ªa-Arg¨¢ez, Ornella Maria Gia, Ingemar Pongratz, Lisa Dalla Via, Serkos A. Haroutounian Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (E)-N-(4-(1',2'-bis(4'',4'''-hydroxyphenyl)-but-1'-enyl) phenyl)isobutyramide C26H27NO3 ÏàËÆ¶È:54.1% Bioorganic & Medicinal Chemistry 2013 21 4120-4131 Synthesis and biological evaluation of novel tamoxifen analogues Michael S. Christodoulou, Nikolas Fokialakis, Daniele Passarella, A¨ªda Nelly Garc¨ªa-Arg¨¢ez, Ornella Maria Gia, Ingemar Pongratz, Lisa Dalla Via, Serkos A. Haroutounian Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 5 ÏàËÆ¶È:52% Phytochemistry 1987 26 1805-1810 Three phenylpropanoid glycosides from Mussatia Carlos Jimenez,Mary Carmen Villaverde,Ricardo Riguera,Luis Castedo,Frank R. Stermitz Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . cytochalasin Z12 C28H35NO5 ÏàËÆ¶È:50% Journal of Natural Products 2008 71(7) 1127-1132 Novel Open-Chain Cytochalsins from the Marine-Derived Fungus Spicaria elegans Rui Liu, Zhenjian Lin, Tianjiao Zhu, Yuchun Fang, Qianqun Gu, and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . lysidiside F C25H30O11 ÏàËÆ¶È:50% Planta Medica 2007 73 163-166 Resveratrol/Phloroglucinol Glycosides from the Roots of Lysidice rhodostegia Song Gao, Jing Liu, Guang-Miao Fu, You-Cai Hu, Shi-Shan Yu,Li-Hua Fan, De-Quan Yu, Jing Qu Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 4-O-[¦Â-D-glucopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl]phenylethylcinnamamide C31H29NO12 ÏàËÆ¶È:50% Planta Medica 2009 75 1591-1596 Chemical Constituents of Dracocephalum forrestii Su-Mei Li, Xian-Wen Yang, Yong-Li Li, Yun-Heng Shen, Lin Feng, Yue-HuWang, Hua-Wu Zeng, Xiao-Hua Liu,Chang-Sheng Zhang, Chun-Lin Long,Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3-carboxy-6,7-dihydroxy-1-(3 ',4 '-dihydroxyphenyl)-naphthalene-9,5''-O-shikimic acid ester ÏàËÆ¶È:50% Phytochemistry 1999 52 1647-1650 Lignans from the liverworts Lepidozia incurvata, Chiloscyphus polyanthos and Jungermannia exsertifolia ssp. cordifolia Frank Cullmann, Andreas Schmidt, Frank Schuld, Matthias L. Trennheuser, Hans Becker Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-09-12 22:45:28













»Ø¸´´ËÂ¥