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dwblsj
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| 13C NMR (101 MHz, CDCl3) ¦Ä 12.81, 15.18, 22.84, 29.13, 56.07, 73.32, 85.75, 106.64, 107.83, 126.02, 127.78, 128.34, 128.34, 128.90, 128.90, 130.02, 135.63, 142.02, 162.77, 162.94, 168.74, 193.02 |
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ר¼Ò¾Ñé: +726 - PhEPI: 3
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dwblsj: ½ð±Ò+8, ¡ïÓаïÖú 2013-06-25 17:45:56
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dwblsj: ½ð±Ò+8, ¡ïÓаïÖú 2013-06-25 17:45:56
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°´´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 12.81, 15.18, 22.84, 29.13, 56.07, 73.32, 85.75, 106.64, 107.83, 126.02, 127.78, 128.34, 128.34, 128.90, 128.90, 130.02, 135.63, 142.02, 162.77, 162.94, 168.74, 193.02 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½263¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 2',4'-Dihydroxy-3'-(2-hydroxybenzyl)-6'-methoxychalcone ÏàËÆ¶È:63.6% Archives of Pharmacal Research 2006 29 497-502 Cytotoxic C-benzylated chalcone and other constituents of Ellipeiopsis cherrevensis Lalita Wirasathien, Thitima Pengsuparp, Masataka Moriyasu, Kazuko Kawanishi and Rutt Suttisri Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 6-Benzyloxy-7-methoxy-2-methyl-N-(2-(thiophen-2-yl)ethyl)quinoline-3-carboxamide C25H24O3N2S ÏàËÆ¶È:60.8% Molecules 2012 17 5497-5507 Quinoline-3-carboxamide Derivatives as Potential Cholesteryl Ester Transfer Protein Inhibitors Wen-Yan Li, Xu-Qiong Xiong, Dong-Mei Zhao, Yu-Fang Shi, Zhi-Heng Yang, Chao Yu, Pei-Wei Fan, Mao-Sheng Cheng and Jing-Kang Shen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (2S)-5-methoxy-6'',6''-dimethyl-4'',5''-dihydrocyclopropa[4'',5'']furano[2'',3'':7,8]flavanone C21H20O4 ÏàËÆ¶È:59.0% Phytochemistry 2012 78 135-146 Distinct chemotypes of Tephrosia vogelii and implications for their use in pest control and soil enrichment Philip C. Stevenson, Geoffrey C. Kite, Gwilym P. Lewis, F¨¦lix Forest, Stephen P. Nyirenda,Steven R. Belmain, Gudeta W. Sileshi, Nigel C. Veitch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . flavokawin B C17H16O4 ÏàËÆ¶È:59.0% Phytochemistry 1981 20 2503-2506 Phenolic compounds from the rhizomes of Alpinia speciosa Hideji Itokawa, Makoto Morita, Susumu Mihashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 1,6-Diphenyl-N,N'-dioctyl-3:4,9:10-perylenetetracarboxydiimide C52H52N2O4 ÏàËÆ¶È:59.0% European Journal of Organic Chemistry 2012 2367-2374 Diaryl-Substituted Perylene Bis(imides): Synthesis, Separation, Characterization and Comparison of Electrochemical and Optical Properties of 1,7- and 1,6-Regioisomer Somnath Dey, Alexander Efimov and Helge Lemmetyinen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 2',4'-dihydroxy-6'-methoxy-3'-methylchalcone C17H16O4 ÏàËÆ¶È:59.0% Zeitschrift f¨¹r Naturforschung C 2004 59 86-92 Prolyl Endopeptidase Inhibitors from Syzygium samarangense (Blume) Merr. & L. M. Perry E. C.Amor, I. M. Villaseñor, A. Yasin, and M. I. Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . stercurensin C17H16O4 ÏàËÆ¶È:59.0% Phytotherapy Research 2005 19 246-251 Antihyperglycaemic flavonoids from Syzygium samarangense (Blume) Merr. and Perry Ma. Hanshella C. Resurreccion-Magno, Irene M. Villaseñor, Nobuyuki Harada and Kenji Monde Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3-[4-(benzyloxy)phenyl]-1-(2-hydroxy-4,6-dimethoxyphenyl)-prop-2-en-1-one ÏàËÆ¶È:59.0% Journal of Medicinal Chemistry 2007 50 3921-3927 First Total Synthesis of Protoapigenone and Its Analogues as Potent Cytotoxic Agents An-Shen Lin, Kyoko Nakagawa-Goto, Fang-Rong Chang, Donglei Yu, Susan L. Morris-Natschke, Chin-Chung Wu, Shu-Li Chen, Yang-Chang Wu, and Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 2'-hydroxy-4',6'-dimethoxy-3'-methylchalcone C18H18O4 ÏàËÆ¶È:59.0% Pharmaceutical Biology 2007 45 777-783 Cytotoxic C-Methylated Chalcones from Syzygium samarangense. Evangeline C. Amor, Irene M. Villaseñor, Rowena Antemano, Zeebah Perveen, Gisela P. Concepcion, M.I. Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 2',4'-dihydroxy-6'-methoxy-3'-methylchalcone C17H16O4 ÏàËÆ¶È:59.0% Pharmaceutical Biology 2007 45 777-783 Cytotoxic C-Methylated Chalcones from Syzygium samarangense. Evangeline C. Amor, Irene M. Villaseñor, Rowena Antemano, Zeebah Perveen, Gisela P. Concepcion, M.I. Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (+)-tephropurpurin C24H24O7 ÏàËÆ¶È:58.3% Journal of Natural Products 1997 60 869-873 Activity-Guided Isolation of Constituents of Tephrosia purpurea with the Potential to Induce the Phase II Enzyme, Quinone Reductase Leng Chee Chang, Clarissa Gerhäuser, Lynda Song, Norman R. Farnsworth, John M. Pezzuto, and A. Douglas Kinghorn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Isorubraine C25H26O4 ÏàËÆ¶È:56.5% Bioorganic & Medicinal Chemistry Letters 2009 19 2728-2730 Two novel monoterpene¨Cchalcone conjugates isolated from the seeds of Alpinia katsumadai Shu-Zhen Hua, Jian-Guang Luo, Xiao-Bing Wang, Jun-Song Wang, Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 5 C27H24O5 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 2003 51(3) 330-332 Two Novel Ravenelones from the Edible Mushroom Pulveroboletus ravenelii Dang Ngoc QUANG,Toshihiro HASHIMOTO, Makiko NUKADA,Isao YAMAMOTO,Masami TANAKA, Shigeru TAKAOKA,and Yoshinori ASAKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . obovatachalcone ÏàËÆ¶È:54.5% Phytochemistry 2000 55 799-804 C-prenylflavonoids from roots of Tephrosia tunicata C¨¦sar C. Andrei, Dalva T. Ferreira, Milton Faccione, Luiz Alberto B. de Moraes, Mario G. de Carvalho, Raimundo Braz-Filho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . Pongachalcone I ÏàËÆ¶È:54.5% Molecules 2007 12 1420-1429 An Efficient and Rapid Synthetic Route to Biologically Interesting Pyranochalcone Natural Products Yong R. Lee, Xue Wang and Likai Xia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . Methyl 1-[((2S)-1-4-[(benzyloxy)carbonyl]benzyl-5-oxotetrahydro-1H-pyrrol-2-yl)methyl]-1H-imidazole-4-carboxylate C18H19N3O5 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2011 19 2888-2902 Synthesis, in silico docking experiments of new 2-pyrrolidinone derivatives and study of their anti-inflammatory activity Panagiota Moutevelis-Minakakis , Eleni Papavassilopoulou,George Michas, Kalliopi Georgikopoulou,Maria-Eleni Ragoussi, Niki Neophytou ,Panagiotis Zoumpoulakis , Thomas Mavromoustakos ,Dimitra Hadjipavlou-Litina Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (Z)-4-(2-((4-Methoxybenzyl)amino)-4-oxo-1H-imidazol-5(4H)-ylidene)-2-phenyl-4,5,6,7-tetrahydropyrrolo[2,3-c]azepin-8(1H)-one C25H23N5O3 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2012 20 1475-1481 Synthesis and evaluation of debromohymenialdisine-derived Chk2 inhibitors Rahman Shah Zaib Saleem,Theresa A. Lansdell,Jetze J. Tepe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . ethyl 4-hydroxy-2,6-diphenyl-5-(phenylsulfanyl)-1,2,5,6-tetrahydro-3-pyridine-carboxylate C26H25NO3S ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 2010 58 602-610 A Facile Synthesis and Discovery of Highly Functionalized Tetrahydro-pyridines and Pyridines as Antimycobacterial Agents Suresh Kumar Raju, Michael Rajesh Stephen, Perumal Subbu, Banerjee Debjani, Yogeeswari Perumal and Sriram Dharmarajan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . ethyl 5-[(4-chlorophenyl)sulfanyl]-4-hydroxy-2,6-diphenyl-1,2,5,6-tetrahydro-3-pyridinecarboxylate C26H24ClNO3S ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 2010 58 602-610 A Facile Synthesis and Discovery of Highly Functionalized Tetrahydro-pyridines and Pyridines as Antimycobacterial Agents Suresh Kumar Raju, Michael Rajesh Stephen, Perumal Subbu, Banerjee Debjani, Yogeeswari Perumal and Sriram Dharmarajan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . ethyl 4-hydroxy-5-[(4-methylphenyl)sulfanyl]-2,6-diphenyl-1,2,5,6-tetrahydro-3-pyridinecarboxylate C27H27NO3S ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 2010 58 602-610 A Facile Synthesis and Discovery of Highly Functionalized Tetrahydro-pyridines and Pyridines as Antimycobacterial Agents Suresh Kumar Raju, Michael Rajesh Stephen, Perumal Subbu, Banerjee Debjani, Yogeeswari Perumal and Sriram Dharmarajan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . ethyl 4-hydroxy-2,6-diphenyl-5-(phenylsulfanyl)-3-pyridinecarboxylate C26H21NO3S ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 2010 58 602-610 A Facile Synthesis and Discovery of Highly Functionalized Tetrahydro-pyridines and Pyridines as Antimycobacterial Agents Suresh Kumar Raju, Michael Rajesh Stephen, Perumal Subbu, Banerjee Debjani, Yogeeswari Perumal and Sriram Dharmarajan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . methyl 5-{[(2-ethylanilino)carbony]amino}-1,3-diphenyl-1H-4-pyrazolecarboxylate C26H24N4O3 ÏàËÆ¶È:54.5% Journal of Heterocyclic Chemistry 2000 37 1247-1252 A convenient synthesis of pyrazolo[3,4-d]pyrimidine-4,6-dione and pyrazolo[4,3-d]pyrimidine-5,7-dione derivatives M. El Haddad, M. Soukri, S. Lazar, A. Bennamara, G. Guillaumet and M. Akssira Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 5-(2-fluoroethyl) 3-(4-methoxybenzyl) 2,4-diethyl-6-phenylpyridine-3,5-dicarboxylate C27H28NO5F ÏàËÆ¶È:54.5% Heterocycles 2008 75 339-356 Synthesis of in vivo Metabolites of the New Adenosine A3 Receptor PET-Radiotracer [18F]FE@SUPPY Karem Shanab, Wolfgang Wadsak, Leonhard-Key Mien, Markus Mitterhauser, Wolfgang Holzer, Victoria Polster, Helmut Viernstein, and Helmut Spreitzer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . (3S,5S)-5-benzyl-3-(6-(benzyloxy)-7-hydroxybenzo[d][1,3]dioxol-4-yl)morpholin-2-on C25H23NO6 ÏàËÆ¶È:54.5% Heterocycles 2008 76 747-757 A Simple Chiral Template for the Synthesis of Fuctionalized ¦Á-Arylglycine Derivatives Hiyoku Nakata, Takahiro Imai, Satoshi Yokoshima, and Tohru Fukuyama Structure 13C NMR ̼Æ×Ä£Äâͼ |

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