| ²é¿´: 929 | »Ø¸´: 4 | |||
| µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû | |||
hjw123ʵϰ°æÖ÷
|
[ÇóÖú]
¼±Çó΢Æ×Êý¾Ý¿â²éѯ
|
||
| 140.8,138.9,135.5,131.9,127.2,124.9,99.5,77.5,73.7,70.6,67.1,66.9,61.3,45.4,44.2,33.4,33.2,31.7,31.5,27.9,27.5,24.9,24.1,23.5,20.7,20.6 |
» ²ÂÄãϲ»¶
309·Ö085801Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á£ºÒ»Ö¾Ô¸£ºÄϾ©´óѧ רҵ£º0705 ×Ü·Ö320 £¬±¾¿Æ985£¬ËÄÁù¼¶Òѹý
ÒѾÓÐ3È˻ظ´
»·¾³¹¤³Ì 085701£¬267Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á£º085600²ÄÁÏÓ뻯¹¤£¬¿¼²Ä¿Æ»ù£¬×Ü·Ö319
ÒѾÓÐ21È˻ظ´
311Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
294·Ö080500²ÄÁÏ¿ÆÑ§Ó빤³ÌÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
288Çóµ÷¼Á Ò»Ö¾Ô¸¹þ¹¤´ó ²ÄÁÏÓ뻯¹¤
ÒѾÓÐ19È˻ظ´
288×ÊÔ´Óë»·¾³×¨Ë¶Çóµ÷¼Á£¬²»ÏÞרҵ£¬ÓÐѧÉϾÍÐÐ
ÒѾÓÐ23È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
¼±Çó΢Æ×¿â²éѯ£¡·Ç³£¸Ðл£¡
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
MestReNovaÎÞ·¨½øÐл¯ºÏÎï½á¹¹ÇâÆ×Ô¤²â
ÒѾÓÐ12È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
journal of molecular structureͶ¸åÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
΢Æ×²é½á¹¹£¬ÓÐÆ×ͼ
ÒѾÓÐ3È˻ظ´
¼±Çó΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻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´
lifeliuyan
°æÖ÷
![]()
![]()
![]()
![]()
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hjw123: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-10-15 13:55:55
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hjw123: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-10-15 13:55:55
|
²éѯ½á¹û£º¹²²éµ½265¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . umbellacin F C23H36O6 ÏàËÆ¶È:57.6% Journal of Natural Products 2006 69 338-341 Cytotoxic Xenia Diterpenoids from the Soft Coral Xenia umbellata Ali A. H. El-Gamal, Shang-Kwei Wang, and Chang-Yih Duh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . sclerotiamide C26H29N3O5 ÏàËÆ¶È:57.6% Journal of Natural Products 1996 59 1093-1095 Sclerotiamide: A New Member of the Paraherquamide Class with Potent Antiinsectan Activity from the Sclerotia of Aspergillus sclerotiorum Authrine C. Whyte and James B. Gloer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Notoamide N C26H28ClN3O4 ÏàËÆ¶È:57.6% Organic Letters 2009 Vol.11,No.6 1297-1300 Isolation of Antipodal (-)-Versicolamide B and Notoamides L-N from a Marine-Derived Aspergillus sp. Sachiko Tsukamoto, Tetsuro Kawabata, Hikaru Kato, Thomas J. Greshock,Hiroshi Hirota, Tomihisa Ohta, and Robert M. Williams Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 15 C64H56BF24IrNOP ÏàËÆ¶È:57.6% Heterocycles 2008 76 771-781 Phosphinomethyloxazolines as Efficient Ligands for the Iridium-Catalyzed Enantioselective Hydrogenation of Unfunctionalized Tetrasubstituted Olefins Marcus G. Schrems, Eva Neumann, and Andreas Pfaltz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . sclerotiamide C26H29N3O5 ÏàËÆ¶È:57.6% Chinese Journal of Medicinal Chemistry 2006 16 93-97 Bioactive alkaloids and sterols from a marine fungus 96F197 SONG Shan-shan, WANG Nai-li, GAO Hao, LIU Hong-wei, ZHANG Qing-hua, MICHIO Namikoshi, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (3S,7ar)-6-[2-(2-bromo-6-methoxy-4-methylphenyl)ethyl]-7a-isobutyl-3-isopropyltetrahydropyrrolo[2,1-b]-oxazol-5-one C23H34BrNO3 ÏàËÆ¶È:57.6% The Journal of Organic Chemistry 2004 69 2773-2784 Synthesis of (()-Hamigeran B, (-)-Hamigeran B, and (()-1-epi-Hamigeran B: Use of Bulky Silyl Groups to Protect a Benzylic Carbon-Oxygen Bond from Hydrogenolysis Derrick L. J. Clive and Jian Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 27-hydroxyambrein C30H54O3 ÏàËÆ¶È:56.6% Journal of Natural Products 2007 70 147-153 Chemical Transformation and Biological Activities of Ambrein, a Major Product of Ambergris from Physeter macrocephalus (Sperm Whale) Ya-Ching Shen,Shi-Yie Cheng,Yao-Haur Kuo,Tsong-Long Hwang,Michael Y. Chiang,and Ashraf Taha Khalil Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . kadcoccilactone R C30H46O5 ÏàËÆ¶È:56.6% Tetrahedron 2008 64 11673-11679 Kadcoccilactones K¨CR, triterpenoids from Kadsura coccinea Xue-Mei Gao, Jian-Xin Pu, Wei-Lie Xiao, Sheng-Xiong Huang, Li-Guang Lou, Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . bromophycolide T C27H36Br2O4 ÏàËÆ¶È:55.5% Journal of Natural Products 2010 73 275-278 Bioactive Bromophycolides R−U from the Fijian Red Alga Callophycus serratus An-Shen Lin, E. Paige Stout, Jacques Prudhomme, Karine Le Roch, Craig R. Fairchild, Scott G. Franzblau, William Aalbersberg, Mark E. Hay and Julia Kubanek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (20S,22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â,9¦Á-tetraol C28H46O4 ÏàËÆ¶È:55.5% Chinese Journal of Applied & Environmental Biology 2005 11 67-70 STEROLS FROM ASPERGILLUS OCHRACEUS 43 LI Guoyou; LI Bogang; LIU Guangye & ZHANG Guolin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . carteriosulfonic acid C C34H65NO10S ÏàËÆ¶È:53.8% Journal of Natural Products 2009 72 1651-1656 Carteriosulfonic Acids A-C, GSK-3¦ÂInhibitors from a Carteriospongia sp. Malcolm W. B. McCulloch, Tim S. Bugni, Gisela P. Concepcion, Gary S. Coombs, Mary Kay Harper, Simran Kaur,Gina C. Mangalindan, Misha M. Mutizwa, Charles A. Veltri, David M. Virshup, and Chris M. Ireland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (1S,3Z,7S,8S,11S,12S)-(+)-7,8-epoxyverticill-3-en-12,20-diol 20-acetate C22H36O4 ÏàËÆ¶È:53.8% Phytochemistry 2008 69 2844-2848 Oxygenated verticillene derivatives from Bursera suntui Hugo A. Garc¨ªa-Guti¨¦rrez, Carlos M. Cerda-Garc¨ªa-Rojas, Juan D. Hern¨¢ndez-Hern¨¢ndez,Luisa U. Rom¨¢n-Mar¨ªn, Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (1S,3Z,7S,11S,12S)-(¨C)-Verticilla-3,8(19)-dien-7,12,20-triol 7,20-diacetate C24H38O5 ÏàËÆ¶È:53.8% Phytochemistry 2008 69 2844-2848 Oxygenated verticillene derivatives from Bursera suntui Hugo A. Garc¨ªa-Guti¨¦rrez, Carlos M. Cerda-Garc¨ªa-Rojas, Juan D. Hern¨¢ndez-Hern¨¢ndez,Luisa U. Rom¨¢n-Mar¨ªn, Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . notoamide H C26H29N3O6 ÏàËÆ¶È:53.8% Journal of Natural Products 2008 71(12) 2064-2067 Notoamides F-K, Prenylated Indole Alkaloids Isolated from a Marine-Derived Aspergillus sp. Sachiko Tsukamoto, Hikaru Kato, Masayuki Samizo, Yuka Nojiri, Hiroyuki Onuki, Hiroshi Hirota, and Tomihisa Ohta Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . hanliuine III C26H36O6 ÏàËÆ¶È:53.8% Chinese Chemical Letters 2002 13 432-435 Two New Acyclic Diterpene- ¦Ã-lactones from the Leaves of Salix matsudana Jin Xin WANG, Shang Zhen ZHENG, Tong SHEN, Xu Wei SHEN,Ying LI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . taihangexcisoidesin B C24H34O9 ÏàËÆ¶È:53.8% Chinese Chemical Letters 2009 20 201-203 Two new enf-kaurane diterpenoids from Isodon excisoides Ji Xia Zhang , Yong Xue Wang, Zhi An He, Fu Lin Yan, Han Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . compound 16b C24H36O4 ÏàËÆ¶È:53.8% Steroids 2001 66 623-635 Neighboring group participation. Part 14. The preparation of the four stereoisomers of 16-hydroxymethyl-5¦Á-androstane-3¦Â,17-diol P¨¢l Tapolcs¨¢nyi, J¨¢nos Wölfling, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . ingenol ester 5 ÏàËÆ¶È:53.8% Phytochemistry 1997 45 563-570 Ingenane and lathyrane diterpenes from the latex of Euphorbia canariensis J. Alberto Marco, Juan F. Sanz-Cervera, Alberto Yuste Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (-)-cyclomicro-buxinine C24H37NO2 ÏàËÆ¶È:53.8% Journal of Natural Products 1988 Vol 51 783 Alkaloids from the Leaves of Buxus sempervirens Atta-Ur-Rahman, Dildar Ahmed, M. Iqbal Choudhary, Bilge Sener, Songul Turkoz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . (2E)-3-(3-bromophenyl)-1-((10R,13S)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3(b)-hydroxy-10,13-dimethyl-1H-cyclopenta[a]phenanthren-17(b)-yl) prop-2-en-1-one C28H35BrO2 ÏàËÆ¶È:53.8% Steroids 2011 76 1358-1362 Synthesis and antimicrobial studies of chalconyl pregnenolones Abid H. Banday, M. Iqbal Zargar, Bashir A. Ganaie Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 14-methyl-17-(3-furyl)-14,15-seco-5¦Â-androstane-3¦Â,14¦Á-diol C24H38O3 ÏàËÆ¶È:53.8% Steroids 1996 61 572-582 Digitalis-like compounds: Synthesis and biological evaluation of seco-D and D-homo derivatives Mauro Gobbini, Alessandra Benicchio, Giuseppe Marazzi, Gloria Padoani, Marco Torri, Piero Melloni Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . cyclobuxine D ÏàËÆ¶È:53.8% Chinese Traditional and Herbal Drugs 2006 37 1614-1618 Isolation and identification of two related alkaloids in Huangyangning LIU Jie; HANG Tai-jun; ZHANG Zheng-xing Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . {(2R,5)-5-[(2R)-Benzyloxy-10-(dimethylamino)-decyl]tetrahydrofuran-2-yl}acetonitrile C25H40N2O2 ÏàËÆ¶È:53.8% Pharmazie 2002 57 34-40 Synthesis and biological activity of chiral tetrahydrofuranyl amino acids as building moieties of pamamycin analogues E. Kr¨¹ger-Velthusen - P. J¨¹tten - P.A. Grigoriev - U. Gräfe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . (4E,8E,10E,2S,3R)-2-acetoamino-1,3-diacetoxy-9-methyl-4,8,10-octadecanetriene ÏàËÆ¶È:53.8% Tetrahedron 1994 50 2771-2784 Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus Takenori Natori, Masahiro Morita, Kohji Akimoto, Yasuhiko Koezuka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . JBIR-20 C26H48NO8P ÏàËÆ¶È:53.8% The Journal of Antibiotics 2009 62 159-162 Novel 24-membered macrolides, JBIR-19 and -20 isolated from Metarhizium sp. fE61 Ikuko Kozone, Jun-ya Ueda, Machika Watanabe, Satoru Nogami, Aya Nagai, Shigeki Inaba, Yoshikazu Ohya, Motoki Takagi and Kazuo Shin-ya Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . hanliuin III C26H36O6 ÏàËÆ¶È:53.8% Journal of the Chinese Chemical Society 2002 49 437-441 Studies on Chemical Constituents of Salix matsudana Jin-Xin Wang, Shang-Zhen Zheng*, Li-Ping Sun,Xu-Wei Shen and Ying Li* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . shaliuin I C26H38O5 ÏàËÆ¶È:53.8% Journal of the Chinese Chemical Society 2008 55 401-405 Acyclic Diterpene-¦Ã-lactones and Flavonoid from Salix cheilophila Omitted Tong Shen*, Yong-Qiang Tian,Wu-Xia Liu and Shang-Zhen Zheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . taihangexcisoidesin B C24H34O9 ÏàËÆ¶È:53.8% Journal of Chemical Research 2009 33 35-37 Diterpenoids from Isodon excisoides Zhang, Ji Xia; Wang, Yong Xue; He, Zhi An; Yan, Fu Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . (2'E,4'E,6'E)-6-(1'-carboxyocta-2',4',6'-triene)-11,12-epoxy-9-hydroxydrim-7-ene C23H32O4 ÏàËÆ¶È:53.8% The Journal of Antibiotics 1996 49 505-512 Novel Drimane Sesquiterpene Esters from Aspergillus ustus var. pseudodeflectus with Endothelin Receptor Binding Activity MARTIN A. HAYES, STEPHEN K. WRIGLEY, IAN CHETLAND, ELWOOD E. REYNOLDS, A. MARTYN AINSWORTH, DIDIER V. RENNO, MOHAMMED A. LATIF, XUE-MIN CHENG, DONALD J. HUPE, PETER CHARLTON, ANNETTE M. DOHERTY Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . 5¦Á,18-dihydroxy-10¦Â-methoxy-2¦Á,14¦Â-diacetoxytax¦Á-4(20),11(12)-diene C25H38O7 ÏàËÆ¶È:53.8% Tetrahedron 2012 68 9539-9549 Microbial transformations of taxadienes and the multi-drug resistant tumor reversal activities of the metabolites Xiao Liu, Ridao Chen, Dan Xie, Mei Mei, Jianhua Zou, Xiaoguang Chen, Jungui Dai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . 15¦Â-hydroxy-17-(3-methylphenyl)-18,19,20-trinor-PGF2¦Á isopropyl ester C27H40O5 ÏàËÆ¶È:53.8% Journal of Medicinal Chemistry 1995 38 289-304 Derivatives of 17-Phenyl-18,19,20-trinorprostaglandin F2.alpha. Isopropyl Ester: Potential Antiglaucoma Agents Charlotta Liljebris, Goeran Selen, Bahram Resul, Johan Stjernschantz, Uli Hacksell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . (3R*,4R*)-3-allyl-4-[(1E,4E)-4-ethyl-7-(tetrahydro-2H-pyran-2-yloxy)hepta-1,4-dienyl]-1-tosyl-pyrrolidine C28H41NO4S ÏàËÆ¶È:53.8% Heterocycles 2012 86 171-180 Palladium-CATALYZED TANDEM COUPLING REACTION OF ALKYNE, CONJUGATED DIENE, AND TRIETHYLBORANE Daiki Takushima, Masahiro Fukushima, Hideaki Satomura, Gen Onodera, and Masanari Kimura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . 4-{4-[3-(¦Â-D-glucopyranosyloxy)-5-isopropyl-1H-pyrazol-4-ylmethyl]phenyl}-N-(2-hydroxy-1,1-dimethylethyl)butanamide C27H41N3O8 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2013 21 748-765 Design, synthesis, and structure¨Cactivity relationships of a series of 4-benzyl-5-isopropyl-1H-pyrazol-3-yl ¦Â-d-glycopyranosides substituted with novel hydrophilic groups as highly potent inhibitors of sodium glucose co-transporter 1 (SGLT1) Nobuhiko Fushimi, Hirotaka Teranishi, Kazuo Shimizu, Shigeru Yonekubo, Kohsuke Ohno, Takashi Miyagi, Fumiaki Itoh, Toshihide Shibazaki, Masaki Tomae, Yukiko Ishikawa-Takemura, Takeshi Nakabayashi, Noboru Kamada, Yuji Yamauchi, Susumu Kobayashi, Masayuki I Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . 4-{4-[3-(¦Â-D-glucopyranosyloxy)-5-isopropyl-1H-pyrazol-4-ylmethyl]phenyl}-N-{1,1-dimethyl-2-[2-(dimethylamino)ethylamino]-2-oxoethyl}butanamide C31H49N5O8 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2013 21 748-765 Design, synthesis, and structure¨Cactivity relationships of a series of 4-benzyl-5-isopropyl-1H-pyrazol-3-yl ¦Â-d-glycopyranosides substituted with novel hydrophilic groups as highly potent inhibitors of sodium glucose co-transporter 1 (SGLT1) Nobuhiko Fushimi, Hirotaka Teranishi, Kazuo Shimizu, Shigeru Yonekubo, Kohsuke Ohno, Takashi Miyagi, Fumiaki Itoh, Toshihide Shibazaki, Masaki Tomae, Yukiko Ishikawa-Takemura, Takeshi Nakabayashi, Noboru Kamada, Yuji Yamauchi, Susumu Kobayashi, Masayuki I Structure 13C NMR ̼Æ×Ä£Äâͼ |
5Â¥2013-10-15 09:34:09
lifeliuyan
ʵϰ°æÖ÷
![]()
![]()
![]()
![]()
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
2Â¥2013-10-15 08:09:56
hjw123
°æÖ÷
![]()
![]()
![]()
![]()
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 1283.5
- É¢½ð: 30
- ºì»¨: 2
- Ìû×Ó: 501
- ÔÚÏß: 126.6Сʱ
- ³æºÅ: 733117
- ×¢²á: 2009-03-27
- ÐÔ±ð: GG
- רҵ: ÖÐҩҩЧÎïÖÊ
3Â¥2013-10-15 09:09:38
hjw123
ר¼Ò¹ËÎÊ
![]()
![]()
![]()
![]()
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 1283.5
- É¢½ð: 30
- ºì»¨: 2
- Ìû×Ó: 501
- ÔÚÏß: 126.6Сʱ
- ³æºÅ: 733117
- ×¢²á: 2009-03-27
- ÐÔ±ð: GG
- רҵ: ÖÐҩҩЧÎïÖÊ
4Â¥2013-10-15 09:11:18














»Ø¸´´ËÂ¥