| ²é¿´: 313 | »Ø¸´: 4 | ||||
yangjh9988Òø³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ2È˲ÎÓë
|
|
΢Æ×ÇóÖú 43.35,67.38,99.99,109.51,110.87,114.17,116.38,118.78,119.91,121.69,128.56,128.70,135.08,137.95,140.20,147.78,148.44,162.74,206.88 ÈܼÁ:±ûͪ ÏàËÆ¶È£º´óÓÚµÈÓÚ50% ·Ç³£¸Ðл£¡ |
» ²ÂÄãϲ»¶
302·ÖÇóµ÷¼Á Ò»Ö¾Ô¸°²»Õ´óѧ085601
ÒѾÓÐ5È˻ظ´
²ÄÁÏÓ뻯¹¤371Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
313Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϹ¤³Ì302·ÖÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©
ÒѾÓÐ4È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ8È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ6È˻ظ´
Çó
ÒѾÓÐ4È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´

audreygc
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 236 (´óѧÉú)
- ½ð±Ò: 5115.1
- ºì»¨: 5
- Ìû×Ó: 519
- ÔÚÏß: 131Сʱ
- ³æºÅ: 1978000
- ×¢²á: 2012-09-05
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯ½á¹û£º¹²²éµ½5¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . N-trans-feruloyloctopamine ÏàËÆ¶È:52.6% Phytochemistry 2005 66 2468-2473 Characterization of cross-linked hydroxycinnamic acid amides isolated from potato common scab lesions Russell R. King , Larry A. Calhoun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 16,19-epoxy-¡÷14-vincanol C19H20N2O ÏàËÆ¶È:52.6% Phytochemistry 2012 83 116-124 Alkaloids from Melodinus yunnanensis Xiang-Hai Cai, Yan Li, Ya-Ping Liu, Xiao-Ning Li, Mei-Fen Bao, Xiao-Dong Luo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . N-·´Ê½°¢Îºõ£»ùÀÒ°· ÏàËÆ¶È:52.6% China Journal of Chinese Materia Medica 2013 38 1004-1007 Chemical constituents from Litsea greenmaniana JIANG Ming, LIN Sheng, GUO Qing-lan, JIANG Zhi-bo, WANG Su-juan, YANG Yong-chun, LIN Peng-cheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (E)-1,5-Bis(4-hydroxy-3-methoxyphenyl)pent-4-ene-1,3-dione C19H18O6 ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry 2013 21 5510-5517 Synthesis and tubulin-binding properties of non-symmetrical click C5-curcuminoids Antonio Caldarelli, Eleonora Penucchini, Diego Caprioglio, Armando A. Genazzani, Alberto Minassi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Compound 26b C24H22N3O5 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2010 20 3930-3935 A rapid synthesis of lavendustin-mimetic small molecules by click fragment assembly Jieun Yoon, Jae-Sang Ryu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
» ±¾ÌûÒÑ»ñµÃµÄºì»¨£¨×îÐÂ10¶ä£©
2Â¥2014-04-29 15:34:04
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yangjh9988: ½ð±Ò+12, ¡ï¡ï¡ïºÜÓаïÖú 2014-04-29 16:28:31
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yangjh9988: ½ð±Ò+12, ¡ï¡ï¡ïºÜÓаïÖú 2014-04-29 16:28:31
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½349¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . palmarumycin JC2 C20H14O5 ÏàËÆ¶È:75% Phytochemistry 2004 65 2387-2390 Deoxypreussomerins from Jatropha curcas: are they also plant metabolites? N. Ravindranath, M. Ravinder Reddy, G. Mahender, R. Ramu, K. Ravi Kumar,Biswanath Das Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . palmarumycin BG1 C20H14O5 ÏàËÆ¶È:65% Chinese Traditional and Herbal Drugs 2013 44 2208-2212 Chemical constituents from stems of Ficus auriculata SHAO Tai-ming, SONG Xiao-ping, CHEN Guang-ying, HAN Chang-ri, ZHENG Cai-juan, YAO Guo-gui Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2-(Benzyloxy)-6-(4-(trifluoromethyl)phenyl)pyridine C19H14F3NO ÏàËÆ¶È:63.1% Tetrahedron 2012 68 1351-1358 Palladium-catalyzed Suzuki¨CMiyaura cross-coupling reaction of potassium 2-pyridyl trifluoroborate with aryl (heteroaryl) halides Wei Ren, Jingya Li, Dapeng Zou, Yangjie Wu, Yusheng Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-(2-methoxyphenylamino)-6-(3-acetamidophenyl)pyrazine C19H18N4O2 ÏàËÆ¶È:63.1% Journal of Medicinal Chemistry 2006 49 407-416 Novel Inhibitors of B-RAF Based on a Disubstituted Pyrazine Scaffold. Generation of a Nanomolar Lead Ion Niculescu-Duvaz, Esteban Roman, Steven R. Whittaker, Frank Friedlos, Ruth Kirk, Ian J. Scanlon, Lawrence C. Davies, Dan Niculescu-Duvaz, Richard Marais, and Caroline J. Springer Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-(3-chloro-4-fluorobenzylamino)-6-(3-acetamidophenyl)pyrazine C19H16ClFN4O ÏàËÆ¶È:63.1% Journal of Medicinal Chemistry 2006 49 407-416 Novel Inhibitors of B-RAF Based on a Disubstituted Pyrazine Scaffold. Generation of a Nanomolar Lead Ion Niculescu-Duvaz, Esteban Roman, Steven R. Whittaker, Frank Friedlos, Ruth Kirk, Ian J. Scanlon, Lawrence C. Davies, Dan Niculescu-Duvaz, Richard Marais, and Caroline J. Springer Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . palmarumycin CP1 C20H12O4 ÏàËÆ¶È:63.1% European Journal of Organic Chemistry 1994 1994 1093-1097 Biologically Active Metabolites from Fungi, 4. Palmarumycins CP1¨CCP4 from Coniothyrium palmarum: Isolation, Structure Elucidation, and Biological Activity Karsten Krohn, Andreas Michel, Ulrich Flörke, Hans-J¨¹rgen Aust, Siegfried Draeger and Barbara Schulz Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3,3'-[Methylenebis(4,1-phenylenenitrilo)]bis[1,3-dihydro]-2H-indol-2-one ÏàËÆ¶È:60% Molecules 2006 11 59-63 Synthesis of Some New bis-Schiff Bases of Isatin and 5-Fluoroisatin in a Water Suspension Medium A. A. Jarrahpour and D. Khalili Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-(2'-benzothia-zolyl)-2,3-dihydro-2-(4-methylphenyl)-4(1H)-quinazolinone C22H17N3OS ÏàËÆ¶È:60% Journal of Heterocyclic Chemistry 2008 45 1629-1632 Synthesis of a novel class of 3-(2'-benzothiazolyl)-2,3-dihydroquinazolin-4(1H)-ones under solvent-free and catalyst-free conditions Ahmad Shaabani,Abbas Rahmati and Jafar Moghimirad Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 1-(3-Fluorophenyl)-5-[(4-methylbenzyl)amino]-3-(N-methylpyrrol-3-yl)-1H-pyrazole C22H21FN4 ÏàËÆ¶È:60% European Journal of Organic Chemistry 2012 967-974 Highly Regioselective One-Pot, Three-Component Synthesis of 1-Aryl-3,4-Substituted/Annulated-5-(Cycloamino)/(Alkylamino)pyrazoles from ¦Â-Oxodithioesters Ganesh C. Nandi, Maya S. Singh, Hiriyakkanavar Ila and Hiriyakkanavar Junjappa Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (Z)-1-benzyl-3-(2-methoxyphenylimino)indolin-2-one C22H18N2O2 ÏàËÆ¶È:60% Tetrahedron 2012 68 3649-3653 Facile and highly diastereoselective synthesis of 3-aminooxindoles via AgOAc-catalyzed vinylogous Mannich reaction Yu-Hua Shi, Zheng Wang, Ying Shi, Wei-Ping Deng Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-(3,4-methylenedioxyphenylamino)-6-(3-acetamidophenyl)pyrazine C19H16N4O3 ÏàËÆ¶È:60% Journal of Medicinal Chemistry 2006 49 407-416 Novel Inhibitors of B-RAF Based on a Disubstituted Pyrazine Scaffold. Generation of a Nanomolar Lead Ion Niculescu-Duvaz, Esteban Roman, Steven R. Whittaker, Frank Friedlos, Ruth Kirk, Ian J. Scanlon, Lawrence C. Davies, Dan Niculescu-Duvaz, Richard Marais, and Caroline J. Springer Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . spiropreussione A C19H12O5 ÏàËÆ¶È:57.8% Journal of Natural Products 2009 72 1712-1715 Spirobisnaphthalene Analogues from the Endophytic Fungus Preussia sp. Xiaomei Chen, Qiyuan Shi, Geng Lin, Shunxing Guo, and Junshan Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3,14-DIHYDRORUTECARPINE C18H15N3O ÏàËÆ¶È:57.8% Chemistry of Natural Compounds 1997 33 221-267 QUINAZOLINE ALKALOIDS IN NATURE A. L. D'yakonov and M. V. Telezhenetskaya Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . N-((1H-Indol-5-yl)methyl)-2,3-dihydroxybenzamide C16H14N2O3 ÏàËÆ¶È:57.8% Bioorganic & Medicinal Chemistry 2011 19 4935-4952 Design of HIV-1 integrase inhibitors targeting the catalytic domain as well as its interaction with LEDGF/p75: A scaffold hopping approach using salicylate and catechol groups Xing Fan, Feng-Hua Zhang, Rasha I. Al-Safi, Li-Fan Zeng, Yumna Shabaik, Bikash Debnath, Tino W. Sanchez, Srinivas Odde, Nouri Neamati, Ya-Qiu Long Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 4-[2-(4-dimethylaminophenyl)imidazo[4,5-b]indol-3(4H)-yl]benzene-sulfonamide C23H21N5O2S ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 2010 58 375-380 Microwave-Assisted, Solvent-Free and Parallel Synthesis of Some Novel Substituted Imidazoles of Biological Interest Gyanendra Kumar Sharma and Devender Pathak Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3-(2'-benzothiazolyl)-2,3-dihydro-2-(phenyl)-quinazolin-4(1H)-one C21H15N3OS ÏàËÆ¶È:57.8% Journal of Heterocyclic Chemistry 2008 45 1629-1632 Synthesis of a novel class of 3-(2'-benzothiazolyl)-2,3-dihydroquinazolin-4(1H)-ones under solvent-free and catalyst-free conditions Ahmad Shaabani,Abbas Rahmati and Jafar Moghimirad Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3-(2'-benzothiazolyl)-2,3-dihydro-2-(4-bromophenyl)-quinazolin-4(1H)-one C21H14BrN3OS ÏàËÆ¶È:57.8% Journal of Heterocyclic Chemistry 2008 45 1629-1632 Synthesis of a novel class of 3-(2'-benzothiazolyl)-2,3-dihydroquinazolin-4(1H)-ones under solvent-free and catalyst-free conditions Ahmad Shaabani,Abbas Rahmati and Jafar Moghimirad Structure 13C NMR ̼Æ×Ä£Äâ |

3Â¥2014-04-29 15:35:24
yangjh9988
Òø³æ (ÕýʽдÊÖ)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 995.7
- Ìû×Ó: 342
- ÔÚÏß: 69.4Сʱ
- ³æºÅ: 170951
- ×¢²á: 2006-01-18
- רҵ: ÌìÈ»Óлú»¯Ñ§

4Â¥2014-04-29 15:35:30
yangjh9988
Òø³æ (ÕýʽдÊÖ)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 995.7
- Ìû×Ó: 342
- ÔÚÏß: 69.4Сʱ
- ³æºÅ: 170951
- ×¢²á: 2006-01-18
- רҵ: ÌìÈ»Óлú»¯Ñ§

5Â¥2014-04-29 16:29:15














»Ø¸´´ËÂ¥
yangjh9988