| ²é¿´: 642 | »Ø¸´: 3 | ||
| µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû | ||
cuitianzeng½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý¡£¡£¡£
|
|
| 16.24, 17.33, 20.11, 55.05, 55.16, 59.78, 78.80, 79.15, 102.07, 103.56, 124.05, 129.92, 132.31, 132.75, 135.43, 136.74, 152.07, 168.98 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
070300»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
±§Ç¸
ÒѾÓÐ5È˻ظ´
»·¾³285·Ö£¬¹ýÁù¼¶£¬Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Çó²ÄÁϵ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ289·Ö
ÒѾÓÐ11È˻ظ´
»¯Ñ§µ÷¼Á
ÒѾÓÐ9È˻ظ´
303Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
»¯¹¤µ÷¼Á303·Ö£¬¹ýËļ¶
ÒѾÓÐ25È˻ظ´
081200-11408-276ѧ˶Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
298·Ö 070300Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý,ǰ10¸ö¼´¿É
ÒѾÓÐ3È˻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»£¡
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
cuitianzeng
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 30 (СѧÉú)
- ½ð±Ò: 193.8
- É¢½ð: 927
- ºì»¨: 3
- Ìû×Ó: 225
- ÔÚÏß: 350.3Сʱ
- ³æºÅ: 1624600
- ×¢²á: 2012-02-18
- רҵ: ÌìȻҩÎﻯѧ
3Â¥2013-03-03 16:25:42
ÅËÏÜΰ
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 225 (´óѧÉú)
- ½ð±Ò: 3679.1
- ºì»¨: 5
- Ìû×Ó: 708
- ÔÚÏß: 55.3Сʱ
- ³æºÅ: 1114857
- ×¢²á: 2010-10-06
- ÐÔ±ð: GG
- רҵ: Ò©Îï·ÖÎö
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
cuitianzeng: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-03 17:04:19
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
cuitianzeng: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-03 17:04:19
|
²éѯ½á¹û£º¹²²éµ½50¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¡÷7-4-hydroxy-3,5,3',5'-tetramethoxy-7-oxo-8-O-4'-neolignan C18H13O2 ÏàËÆ¶È:61.9% Phytochemistry 1985 24 1051-1055 Neolignans from Virola carinata fruit Sergio H. Cavalcante, Massayoshi Yoshida, Otto R. Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . surinamensin ÏàËÆ¶È:61.1% Journal of Natural Products 1985 Vol 48 830-832 Stereoselective Synthesis of 8.0.4' Neolignans: (¡À)-Surinamensin and (¡À)-Virolin Susana A. Zacchino, H¨¦ctor Badano Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (E)-1-[3',4',5'-Trimethoxyphenyl]-2-[2''-[(para-toluenesulfonyl)oxy]-3''-[(disodium)phosphate]-4''-methoxyphenyl]ethene C25H25Na2O11PS ÏàËÆ¶È:60% Journal of Natural Products 2011 84 1568-1574 Regioselective Synthesis of Water-Soluble Monophosphate Derivatives of Combretastatin A-1 Rajendra P. Tanpure, Benson L. Nguyen, Tracy E. Strecker, Savannah Aguirre, Suman Sharma,David J. Chaplin, Bronwyn G. Siim,Ernest Hamel, John W. Lippert, George R. Pettit,Mary Lynn Trawick, and Kevin G. Pinney Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . erythro-3,4,5-trimethoxy-7-hydroxy-1'(E)-propenyl-3'-methoxy-8.O.4'-neolignan ÏàËÆ¶È:55.5% Journal of Natural Products 1997 60 659-662 In Vitro Evaluation of Antifungal Properties of 8.O.4'-Neolignans Susana Zacchino, Gladis Rodr¨ªguez, Germ¨¢n Pezzenati, and Gabriela Orellana Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 1-(3-Chloro-4-methylphenyl)-3-[(1R)-1-(6-fluoro-1,3-benzothiazol-2-yl)ethyl]imidazolidine-2,4,5-trione C19H13ClFN3O3S ÏàËÆ¶È:52.6% Molecules 2011 16 7565-7582 1, 3-Substituted Imidazolidine-2, 4, 5-triones: Synthesis and Inhibition of Cholinergic Enzymes Vladimir Pejchal, Sarka Stepankova, Zdenka Padelkova, Ales Imramovsky and Josef Jampilek Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 4¦Â,15-epoxymiller-9Z-enolide ÏàËÆ¶È:52.6% Phytochemistry 1987 26 2011-2017 Millerenolides,sesquiterpene lactones from Milleria quinqueflora V. Castro,J. Jakupovic,F. Bohlmann Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . methyl 2-[(2E)-(2-(3,4,5-trimethoxyphenyl)-3-(3-acet-oxy-4-methoxyphenyl))prop-2-enoyl]hydrazinecarboxylate C23H26N2O9 ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry 2010 18 2375-2387 Pyrazolone-fused combretastatins and their precursors: synthesis, cytotoxicity, antitubulin activity and molecular modeling studies Bojan Burja, Tamara Čimbora-Zovko, Sanja Tomić, Tihana Jelušić, Marijan Kočevar, Slovenko Polanc, Maja Osmak Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . N-(2-(4-bromophenyl)-1,4,5,6-tetrahydro-4-(3,4,5-trimethoxyphenyl)-6-oxopyrimidin-5-yl)benzamide C26H24BrN3O5 ÏàËÆ¶È:52.6% Heterocycles 2012 86 411-424 Highly Stereoselective Synthesis of anti-Tetrahydropyrimidine Derivatives under Microwave Heating Qian Wang, An-Xiao Dai, Mian-Shuai Yi, Bo Jiang, Shu-Jiang Tu,* and Guigen Li Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . machilusol A C21H24O5 ÏàËÆ¶È:52.3% Planta Medica 2000 66 403-407 Cytotoxic Neolignans from the Stem Wood of Machilus obovatifolia Ian-Lih Tsai,Jyh-Huey Chen,Chang-Yih Duh,Ih-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound NT1 ÏàËÆ¶È:52.3% Natural Product Communications 2010 5 755-762 Computer-aided Structure Elucidation of Neolignans Mara B. Costantin, Marcelo J. P. Ferreira, Gilberto V. Rodrigues and Vicente P. Emerenciano Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Z-Stilstatin 2 (Z-5) C17H18O6 ÏàËÆ¶È:50% Journal of Natural Products 2009 72 380-388 Antineoplastic Agents. 578. Synthesis of Stilstatins 1 and 2 and Their Water-Soluble Prodrugs George R. Pettit, Andrew Thornhill, Noeleen Melody, and John C. Knight Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . threo-3,4,5-trimethoxy-7-hydroxy-1'-allyl-3',5'-dimethoxy-8.O.4'-neolignan ÏàËÆ¶È:50% Journal of Natural Products 1997 60 659-662 In Vitro Evaluation of Antifungal Properties of 8.O.4'-Neolignans Susana Zacchino, Gladis Rodr¨ªguez, Germ¨¢n Pezzenati, and Gabriela Orellana Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . germacrone C15H22O ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1988 36 2075-2078 Studies on Pharmacologically Active Principles from Indonesian Crude Drugs. II. : Hypothermic Principle from Curcuma xanthorrhiza ROXB. MIKIO YAMAZAKI,YUKIO MAEBAYASHI,NOBUHISA IWASE and YOSHIYUKI KANEKO Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . germacrone C15H22O ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1987 35 53-59 Structures of Sesquiterpenes from Curcuma aromatica SALISB MASANORI KUROYANAGI,AKIRA UENO,KAORU UJIIE and SADAO SATO Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . trans,trans-germacrone ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2008 33 785-788 Sesquiterpenes from stems and leaves of Curcuma wenyujin WANG Lixia, DENG Zhiwei, HUANG Kexin, LIN Wenhan Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Combretastatin A-1 CI8H20O6 ÏàËÆ¶È:50% Journal of Natural Products 1987 Vol 50 119 Isolation, Structure, and Synthesis of Combretastatins A-1 and B-1, Potent New Inhibitors of Microtubule Assembly, Derived from Combretum caffrum George R. Pettit, Sheo Bux Singh, Margaret L. Niven, Ernest Hamel, Jean M. Schmidt Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . crotalarine C18H27NO6 ÏàËÆ¶È:50% Phytochemistry 1993 34 1421-1423 Pyrrolizidine alkaloids from Crotalaria aegyptiaca E. Roeder, T. Sarg, S. El-Dahmy, A.Abdel Ghani Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 3-Methoxy-6-(1-(3,4,5-trimethoxyphenyl)-1H-1,2,3-triazol-5-yl)benzene-1,2-diol C18H19N3O6 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 234-242 Synthesis, biological evaluation and molecular modeling of 1,2,3-triazole analogs of combretastatin A-1 Øyvind W. Akselsen, Kristin Odlo, Jing-Jy Cheng, Giorgio Maccari, Maurizio Botta,Trond Vidar Hansen Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 6 C23H20O8 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1987 35 4162-4168 Studies on the Constituents of the Seeds of Hernandia ovigera L. VI. Isolation and Structural Determination of Three Lignans MARIKO TANOGUCHI,MASAO ARIMOTO,HIDEYUKI SAIKA and HIDEO YAMAGUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 3b' ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 261-265 Intramolecular asymmetric Pummerer reactions as a key step in the synthesis of bicyclic precursors of anthracyclinones Jose Luis Garc¨ªa Ruano, Cristina Garc¨ªa Paredes Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . germacrone ÏàËÆ¶È:50% Phytochemistry 1988 27 3887-3891 Terpenoids from Curcuma heyneana Kurnia Firman,Takeshi Kinoshita,Akiko Itai,Ushio Sankawa Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 4-phenyl-11-phthalimido-2,4,6-triaza-3,5-dioxotetracyclo-[5.4.2.02,6.08,10]tridec-12-ene C24H18N4O4 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2007 44 719-723 Cycloaddition reactions of phthalimide substituted cyclic polyenes with heteroatom dienophiles Stephen S. Templin,Nathaniel J. Wallock,Daniel T. Haworth,William A. Donaldson,Dennis W. Bennett and Tasneem Siddiquee Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound Z isomer 2b C22H21N3O2 ÏàËÆ¶È:50% Indian Journal of Chemistry 2008 47B 1063-1070 A facile synthesis of novel triazabicyclic molecules as potential bicyclic templates for pharmaceutical ligands by the ring opening metathesis-cross metathesis of triazatricyclo[3.2.1.02,⁶]dec-8-ene-3,5-diones Anas,Saithalavi; Sarika,Chechattil; Rajan,Rani; Radhakrishnan,K V Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (E)-1-[(4-Chlorophenyl)imino]-1,3-dihydro-3-methyl-3-(4-methylphenyl)isobenzofuran C22H18ClNO ÏàËÆ¶È:50% Helvetica Chimica Acta 2010 93 1274-1280 Hydriodic Acid-Mediated Cyclization of -Substituted Secondary 2-Ethenylbenzamides: Synthesis of 2-Substituted 2,3-Dihydro-3,3-dimethyl-1H-isoindol-1-ones and 3,3-Disubstituted (E)-1-(Arylimino)-1,3-dihydroisobenzofurans Kazuhiro Kobayashi, Seiki Fujita, Daisuke Nakai, Shogo Fukumoto, Shuhei Fukamachi and Hisatoshi Konishi Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 7-(4-Chlorophenyl)-4-(4-methoxyphenyl)-2-(2-methylprop-1-enyl)-6-nitroquinazoline C25H20ClN3O3 ÏàËÆ¶È:50% Molecules 2010 15 2949-2961 Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines Youssef Kabri, Pierre Verhaeghe, Armand Gellis and Patrice Vanelle Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . germacradienolideisabelin ÏàËÆ¶È:50% Phytochemistry 1981 20 1740-1742 The germacradienolide isabelin from Zexmenia valerii: stereochemistry and conformation of scandenolide and deoxymikanolide Werner Herz, Serengolam V. Govindan Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 2'E-2-(3',7'-Dimethylocta-2',6'-dienyl)-4-hydroxy-1-methoxy-6-methylbenzene C18H26O2 ÏàËÆ¶È:50% Phytochemistry 1981 20 2598-2600 Isoprenoid dihydroquinones from a brown alga, Cystophora sp. Robert J. Capon, Emilio L. Ghisalberti, Phillip R. Jefferies Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . (2'E)-4-acetoxy-2-(3',7'-dimethylocta-2',6'-dienyl)-1-methoxy-6-methylbenzene C20H28O3 ÏàËÆ¶È:50% Phytochemistry 1981 20 2598-2600 Isoprenoid dihydroquinones from a brown alga, Cystophora sp. Robert J. Capon, Emilio L. Ghisalberti, Phillip R. Jefferies Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 2,4-dihydroxy-6-geranylphenyl acetate ÏàËÆ¶È:50% Phytochemistry 1986 25 1617-1619 Dermatotoxic phenolics from glandular trichomes of Phacelia campanularia and P. pedicellata Gary W. Reynolds, Eloy Rodriguez Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . germacrone C15H22O ÏàËÆ¶È:50% Chinese Journal of Natural Medicines 2005 3 280-283 Chemical Studies on the Terpenes from Gorgonian Acanthogorgia vagae Aurivillius(¢ò) ZHANG Wen; GUO Yue-Wei; MOLLO Ernesto; CIMINO Guido Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-03-03 16:23:54
ÅËÏÜΰ
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 225 (´óѧÉú)
- ½ð±Ò: 3679.1
- ºì»¨: 5
- Ìû×Ó: 708
- ÔÚÏß: 55.3Сʱ
- ³æºÅ: 1114857
- ×¢²á: 2010-10-06
- ÐÔ±ð: GG
- רҵ: Ò©Îï·ÖÎö

4Â¥2013-03-03 16:43:42














»Ø¸´´ËÂ¥