| ²é¿´: 143 | »Ø¸´: 1 | ||
lucia808Ìú³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý
|
|
CNMR(ë®´úÂÈ·Â)£º 184.9£¬178.4£¬167.8£¬160.6£¬157.1£¬137.2£¬132.8£¬132.3£¬130.9£¬128.9£¬109.6£¬107.5£¬96.9£¬65.6£¬58.6£¬56.7£¬48.9£¬32.9£¬30.6£¬22.8£¬19.2£¬13.7 |
» ²ÂÄãϲ»¶
085602µ÷¼Á ³õÊÔ×Ü·Ö335
ÒѾÓÐ7È˻ظ´
»¯Ñ§357·Ö£¬¿¼Ñе÷¼Á
ÒѾÓÐ7È˻ظ´
278Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
085400µç×ÓÐÅÏ¢319Çóµ÷¼Á£¨½ÓÊÜ¿çרҵµ÷¼Á£©
ÒѾÓÐ6È˻ظ´
323Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸±±¾©2£¬²ÄÁÏÓ뻯¹¤308Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
26¿¼Ñе÷¼Á0710 0860
ÒѾÓÐ13È˻ظ´
296²ÄÁÏר˶Çóµ÷¼Á
ÒѾÓÐ22È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ12È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý¿â
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý ÖØ½±
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý~
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
wm0629
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 341 (´óѧÉú)
- ½ð±Ò: 6381.8
- ºì»¨: 3
- Ìû×Ó: 1962
- ÔÚÏß: 77.9Сʱ
- ³æºÅ: 2217415
- ×¢²á: 2013-01-01
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©ÅÚÖÆ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lucia808: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-04-27 18:52:21
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lucia808: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-04-27 18:52:21
|
²éѯ½á¹û£º¹²²éµ½22¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 14-methoxyxestoquinone C21H16O5 ÏàËÆ¶È:54.5% Journal of Medicinal Chemistry 1995 38 4503-4507 Topoisomerase II-Mediated DNA Cleavage by Adocia- and Xestoquinones from the Philippine Sponge Xestospongia sp. Gisela P. Concepcion, Tommaso A. Foderaro, Glenn S. Eldredge, Emil Lobkovsky, Jon Clardy, Louis R. Barrows, Chris M. Ireland Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 5-(3''-benzoyloxypropyl)-7-methoxy-2-(3', 4'-methylenedioxyphenyl)-benzofuran C26H22O6 ÏàËÆ¶È:54.1% Phytochemistry 2003 63 939-943 Benzofurans and another constituent from seeds of Styrax officinalis Yurdanur Yayla Akgul, Huseyin Anil Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . cyclotryprostatin A C22H25N3O5 ÏàËÆ¶È:50% Chemistry of Natural Compounds 2004 40 615-617 FUMITREMORGINS FROM THE MARINE ISOLATE OF THE FUNGUS Aspergillus fumigatus Sh. Sh. Afiyatullov, A. I. Kalinovskii, M. V. Pivkin,P. S. Dmitrenok, and T. A. Kuznetsova Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . scutequinone C21H22O4 ÏàËÆ¶È:50% Chinese Chemical Letters 1996 7 441-442 A NEW DITERPENOID FROM COLEUS SCUTELLARIOIDES QING MU HONGJIE ZHANG,CHAO MING LI AND HAN DONG SUN Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 12-Heptanoyl-11-methoxy-3-methyl-¦Â-carboline C20H24N2O2 ÏàËÆ¶È:50% Molecules 2008 13 1584-1598 A Simple, Rapid and Mild One Pot Synthesis of Benzene Ring Acylated and Demethylated Analogues of Harmine under Solvent-free Conditions Sabira Begum, Syed N. Ali, Farhat Farhat, Syed I. Hassan and Bina S. Siddiqui Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-{1-[(4-Chlorophenyl)carbonyl]-5-methoxy-2-methyl-1H-indol-3-yl}acetic acid 1-(1,2-dicarba-closo-dodecaboranyl)methyl ester ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 3242-3248 Synthesis and evaluation of carbaborane derivatives of indomethacin as cyclooxygenase inhibitors Matthias Scholz,Anna L. Blobaum, Lawrence J. Marnett , Evamarie Hey-Hawkins Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 6a C23H29NO2 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2007 44 909-914 A facile synthesis of 1-alkyl-5-arylalkoxy-6-methoxy-3,4-dihydroisoquinolines Heong-Seup Yim,Ho-Kyun Kim,Jeum-Jong Kim,Deok-Heon Kweon,Yong-Jin Yoon,Sang-Gyeong Lee and Jung-Ho Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 12-Nonanoyl-11-methoxy-3-methyl-5,6-dihydro-¦Â-carboline C22H30N2O2 ÏàËÆ¶È:50% Molecules 2010 15 68-82 An Efficient, Mild and Solvent-Free Synthesis of Benzene Ring Acylated Harmalines Sabira Begum, Farhat Zubair, Syed Nawazish Ali and Bina Shaheen Siddiqui Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 4a C30H33ClN2O5 ÏàËÆ¶È:50% Tetrahedron Letters 2001 42 7751-7754 Benzaldehyde-derived chloroformates and their application towards the synthesis of methoxyfenozide-N-[(acyloxy)benzyloxy]carbonyl derivatives Mark J Mulvihill, Duyan V Nguyen, Brian MacDougall, Blanca Martinez-Teipel, Rhoda Joseph, James Gallagher, Damian Weaver, Arkady Gusev, KiHo Chung, William Mathis Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Py-2T C52H64Si2S2 ÏàËÆ¶È:50% Zeitschrift f¨¹r Naturforschung B 2004 59 1332-1336 Selective Substitution of Hex2SiFCl for the Preparation of Polymers with Two Different Alternate p-Electron Systems Linked by Hex2Si Units J. Ohshita, K. Kawashima, A. Iwata, H. Tang, M. Higashi, and A. Kunai Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (4S,5R,6R)-4-(Hydroxymethyl)-2-phenyl-6-(tetradec-1-enyl)-5,6-dihydro-4H-1,3-oxazin-5-ol C25H39NO3 ÏàËÆ¶È:50% European Journal of Organic Chemistry 2012 2614-2620 Total Syntheses of D-xylo- and D-arabino-Phytosphingosine Based on the Syntheses of Chiral 1,3-Oxazines Yu Mu, Tian Jin, Gun-Woo Kim, Jin-Seok Kim, Sung-Soo Kim, Yong-Shou Tian, Chang-Young Oh and Won-Hun Ham Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 1-(3,5-di-tert-butyl-4-hydroxyphenyl)-2-(2-(butylami-no)-5,6-dimethyl-1H-benzo[d]imidazol-1-yl)ethanone C29H41N3O2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 1918-1924 Selective benzimidazole inhibitors of the antigen receptor-mediated NF-¦ÊB activation pathway Karl J. Okolotowicz, Ranxin Shi, Xueying Zheng, Mary MacDonald, John C. Reed, John R. Cashman Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . cyclotryprostatin A C22H25N3O5 ÏàËÆ¶È:50% Tetrahedron 1997 53 59-72 Novel mammalian cell cycle inhibitors, cyclotroprostatins A-D, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase Cheng-Bin Cui, Hideaki Kakeya, Hiroyuki Osada Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . nepethalate B C38H58O8 ÏàËÆ¶È:50% Helvetica Chimica Acta 2011 94 2106-2110 Nepethalates A and B: Two New Phthalate Derivatives from Nepeta clarkei (pages 2106¨C2110) Javid Hussain, Najeeb Ur Rehman, Hidayat Hussain, Liaqat Ali, Ahmed Al-Harrasi and Viqar Uddin Ahmad Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 2-bromo-N-[2-(butylselanyl)-3-nitrobenzyl]-4-methylaniline C18H21N2O2SeBr ÏàËÆ¶È:50% European Journal of Organic Chemistry 2011 5485-5497 Synthesis and Glutathione Peroxidase-Like Activities of Isoselenazolines Vijay P. Singh, Harkesh B. Singh and Ray J. Butcher Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ethyl 5-(tert-butylthiocarbonylmethyl)-1-(2,4-dimethoxyphenyl)-3-phenyl-1H-pyrrole-2-carboxylate C27H31NO5S ÏàËÆ¶È:50% European Journal of Organic Chemistry 2010 191-200 A New Method for the Synthesis of Multisubstituted Pyrroles of Biological Interest by Double Nucleophilic Addition to ,¦Â-Unsaturated Imines Atsushi Takahashi, Shiho Kawai, Iwao Hachiya and Makoto Shimizu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 5-butoxyflavone C19H18O3 ÏàËÆ¶È:50% Journal of Medicinal Chemistry 1995 38 4937-4943 Synthesis and Biological Evaluation of Substituted Flavones as Gastroprotective Agents Jeffrey J. Ares, Pamela E. Outt, Jared L. Randall, Peter D. Murray, Pamela S. Weisshaar, Linda M. O'Brien, Beth L. Ems, Sunil V. Kakodkar, Gary R. Kelm, Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (1S,2E,4R,7Z,11E)-2,7,11-cembratriene-4-O-methyl-4-ol-6-one C21H34O2 ÏàËÆ¶È:50% Planta Medica 2011 77 467-476 Bioactive Natural, Biocatalytic, and Semisynthetic Tobacco Cembranoids Hany N. Baraka, Mohammad A. Khanfar, John C. Williams, Emad M. El-Giar, Khalid A. El Sayed Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Cyclotryprostatin A ÏàËÆ¶È:50% Journal of Agricultural and Food Chemistry 2012 60 3424-3431 Metabolites from Aspergillus fumigatus, an Endophytic Fungus Associated with Melia azedarach, and Their Antifungal, Antifeedant, and Toxic Activities Xiao-Jun Li, Qiang Zhang, An-Ling Zhang, and Jin-Ming Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 5-(Cyclohexylmethoxy)-3-(((4-hydroxybenzyl)(2-hydroxyethyl)amino)methyl)-4H-chromen-4-one C26H31NO5 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 5757-5762 Novel interleukin-5 inhibitors based on hydroxyethylaminomethyl-4H-chromen-4-one scaffold Cheonik Joo, Eeda Venkateswararao, Ki-Cheul Lee, Vinay K. Sharma, Min-Sik Kyung, Youngsoo Kim, Sang-Hun Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 3-(((4-Chlorobenzyl)(2-hydroxyethyl)amino)methyl)-5-(cyclohexylmethoxy)-4H-chromen-4-one C26H30ClNO4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 5757-5762 Novel interleukin-5 inhibitors based on hydroxyethylaminomethyl-4H-chromen-4-one scaffold Cheonik Joo, Eeda Venkateswararao, Ki-Cheul Lee, Vinay K. Sharma, Min-Sik Kyung, Youngsoo Kim, Sang-Hun Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 5-Methoxy-2-[N-(2-benzamidoethyl)-N-ethylamino]tetralin hydrochloride C22H28N2O2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1999 7 1111-1121 Structural analogues of 5-OMe-BPAT: synthesis and interactions with dopamine D2, D3, and serotonin 5-HT1A receptors Evert J. Homan, Esther Kroodsma, Swier Copinga, Lena Unelius, Nina Mohell, Håkan V. Wikström, Cor J. Grol Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-04-27 17:30:20














»Ø¸´´ËÂ¥