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ѯ½á¹û£º¹²²éµ½5399¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Methoxyvermistatin C19H18O7 ÏàËÆ¶È:90% Helvetica Chimica Acta 2007 Vol. 90 1925 Structural and Biological Properties of Vermistatin and Two New Vermistatin Derivatives Isolated from the Marine-Mangrove Endophytic Fungus Guignardia sp. No. 4382 Xue-Kui Xia, Hua-Rong Huang, Zhi-Gang She, Ji-Wen Cai, Liu Lan, Jian-Ye Zhang, Li-Wu Fu, L. L. P. Vrijmoed, and Yong-Cheng Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 7-oxoglaucine C20H17NO5 ÏàËÆ¶È:70% Chemistry of Natural Compounds 1996 32 737-858 ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES" Chapter 2, continued R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2-(4,6-dimethoxy-2-hydroxyphenyl)-5-(E)-propenylbenzofuran ÏàËÆ¶È:70% Phytochemistry 1987 26 2041-2043 Ramosissin and other methoxylated nor-neolignans from Krameria ramosissima Hans Achenbach,Johann Grob,Xorge A. Dominguez,Julia Verde Star,Fernando Salgado Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . vermistatin ÏàËÆ¶È:70% Heterocycles 2005 65 2771-2776 New Vermistatin Derivatives Isolated from Penicillium simplicissimum Shin-ichirou Komai, Tomoo Hosoe, Takeshi Itabashi, Koohei Nozawa, Takashi Yaguchi, Kazutaka Fukushima, and Ken-ichi Kawai* Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . oxoglaucine ÏàËÆ¶È:70% Phytochemistry 1980 19 995-997 13C NMR analysis of some oxoaporphine alkaloids Anita J. Marsaioli, Aderbal F. Magalhães, Edmundo A. R¨²veda, Francisco de A. M. Reis Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1,4-Diacetoxy-2-acetyl-5,6,8-trimethoxynaphthalene C19H20O8 ÏàËÆ¶È:70% Journal of the Chemical Society, Perkin Transactions 1 1991 2743-2748 Naphthopyranquinones. Confirmation of the structures of the ventiloquinones E, G and J by synthesis Charles B. de Koning, Robin G. F. Giles and Ivan R. Green Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . fijiensin C18H16O6 ÏàËÆ¶È:70% Experientia 1990 46 982-984 Fijiensin, the first phytotoxin fromMycosphaerella fijiensis, the causative agent of Black Sigatoka disease R. K. Upadhyay, G. A. Strobel, S. J. Coval and J. Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . vermistatin C18H16O6 ÏàËÆ¶È:70% The Journal of Antibiotics 1986 39 1598-1601 3-N-METHYLPAROMOMYCIN I PRODUCED BY A STREPTOMYCES S. RENGARAJU, S. NARAYANAN, P. L. GANJU, M. A. AMIN, M. R. S. IYENGAR, SHUICHI GOMI, JIRO ITCH, SHINJI MIYADOH, TAKASHI SHOMURA, MASAJI SEZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . N2-(tert-butyl)-7-methoxy-N3-[2-(1,3,4-oxadiazol-2-yl)phenyl]benzofuran-2,3-diamine C21H22N4O3 ÏàËÆ¶È:70% Helvetica Chimica Acta 2012 95 788-794 One-Pot Four-Component Synthesis of N2-Alkyl-N3-[2-(1,3,4-oxadiazol-2-yl)aryl]benzofuran-2,3-diamines (pages 788¨C794) Mehdi Adib, Ehsan Sheikhi, Morteza Karimzadeh, Hamid Reza Bijanzadeh and Massoud Amanlou Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 4-(2,4-dimethoxyphenyl)-5-phenylthieno[3,2-b]pyridin-7(4H)-one C21H17NO3S ÏàËÆ¶È:70% Tetrahedron 2013 69 3167-3181 Efficient synthesis of novel thieno[3,2-b]-, [2,3-c]- and [3,2-c]pyridones by Sonogashira coupling of bromothiophenes with terminal alkynes and subsequent intramolecular C¨CN bond-forming reaction Viktor O. Iaroshenko, Sajid Ali, Tariq Mahmood Babar, Muhammad S.A. Abbasi, Vyacheslav Ya Sosnovskikh, Alexander Villinger, Andrey Tolmachev, Peter Langer Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-(3-(4-(3-(2-Chlorophenyl)ureido)phenyl)isoxazole-5-carboxamido)-3-methylbutanoic acid ÏàËÆ¶È:70% European Journal of Medicinal Chemistry 2012 54 324-342 Synthesis and biological evaluation of isoxazole, oxazole, and oxadiazole containing heteroaryl analogs of biaryl ureas as DGAT1 inhibitors Ravindra D. Jadhav, Kishorkumar S. Kadam, Shivaji Kandre, Tandra Guha, M. Mahesh Kumar Reddy, Manoja K. Brahma, Nitin J. Deshmukh, Amol Dixit, Lalit Doshi, Nisha Potdar, Arno A. Enose, Ram A. Vishwakarma, H. Sivaramakrishnan, Shaila Srinivasan, Kumar V.S. Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-(3-(4-(3-(3-Chlorophenyl)ureido)phenyl)isoxazole-5-carboxamido)-3-methylbutanoic acid ÏàËÆ¶È:70% European Journal of Medicinal Chemistry 2012 54 324-342 Synthesis and biological evaluation of isoxazole, oxazole, and oxadiazole containing heteroaryl analogs of biaryl ureas as DGAT1 inhibitors Ravindra D. Jadhav, Kishorkumar S. Kadam, Shivaji Kandre, Tandra Guha, M. Mahesh Kumar Reddy, Manoja K. Brahma, Nitin J. Deshmukh, Amol Dixit, Lalit Doshi, Nisha Potdar, Arno A. Enose, Ram A. Vishwakarma, H. Sivaramakrishnan, Shaila Srinivasan, Kumar V.S. Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 2-(3-(4-(3-(4-Methoxyphenyl)ureido)phenyl)isoxazole-5-carboxamido)-3-methylbutanoic acid ÏàËÆ¶È:70% European Journal of Medicinal Chemistry 2012 54 324-342 Synthesis and biological evaluation of isoxazole, oxazole, and oxadiazole containing heteroaryl analogs of biaryl ureas as DGAT1 inhibitors Ravindra D. Jadhav, Kishorkumar S. Kadam, Shivaji Kandre, Tandra Guha, M. Mahesh Kumar Reddy, Manoja K. Brahma, Nitin J. Deshmukh, Amol Dixit, Lalit Doshi, Nisha Potdar, Arno A. Enose, Ram A. Vishwakarma, H. Sivaramakrishnan, Shaila Srinivasan, Kumar V.S. Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-Methyl-2-(3-(4-(3-(2-(trifluoromethyl)phenyl)ureido)phenyl) isoxazole-5-carboxamido)butanoic acid ÏàËÆ¶È:70% European Journal of Medicinal Chemistry 2012 54 324-342 Synthesis and biological evaluation of isoxazole, oxazole, and oxadiazole containing heteroaryl analogs of biaryl ureas as DGAT1 inhibitors Ravindra D. Jadhav, Kishorkumar S. Kadam, Shivaji Kandre, Tandra Guha, M. Mahesh Kumar Reddy, Manoja K. Brahma, Nitin J. Deshmukh, Amol Dixit, Lalit Doshi, Nisha Potdar, Arno A. Enose, Ram A. Vishwakarma, H. Sivaramakrishnan, Shaila Srinivasan, Kumar V.S. Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 1-benzyl-3-butylaminocarbonyl-6,7-dimethoxyisoquinoline C23H26N2O3 ÏàËÆ¶È:66.6% Heterocycles 2006 68 993-1006 A Convenient Synthesis of Papaverine Analogs via Photocyclization of N-Acyl-¦Á-dehydroarylalaninamide Derivatives Hideki Hoshina, Kei Maekawa, Kaori Kobayashi, Tetsutaro Igarashi, and Tadamitsu Sakurai* Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3-butylaminocarbonyl-1-(4-chlorobenzyl)-6,7-dimethoxyisoquinoline C23H25N2O3Cl ÏàËÆ¶È:66.6% Heterocycles 2006 68 993-1006 A Convenient Synthesis of Papaverine Analogs via Photocyclization of N-Acyl-¦Á-dehydroarylalaninamide Derivatives Hideki Hoshina, Kei Maekawa, Kaori Kobayashi, Tetsutaro Igarashi, and Tadamitsu Sakurai* Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 2-(3-(4-(3-(2-Fluoro-5-methylphenyl)ureido)phenyl)isoxazole-5-carboxamido)-3-methylbutanoic acid ÏàËÆ¶È:66.6% European Journal of Medicinal Chemistry 2012 54 324-342 Synthesis and biological evaluation of isoxazole, oxazole, and oxadiazole containing heteroaryl analogs of biaryl ureas as DGAT1 inhibitors Ravindra D. Jadhav, Kishorkumar S. Kadam, Shivaji Kandre, Tandra Guha, M. Mahesh Kumar Reddy, Manoja K. Brahma, Nitin J. Deshmukh, Amol Dixit, Lalit Doshi, Nisha Potdar, Arno A. Enose, Ram A. Vishwakarma, H. Sivaramakrishnan, Shaila Srinivasan, Kumar V.S. Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 2-(3-(4-(3-(4-Fluoro-2-methylphenyl)ureido)phenyl)isoxazole-5-carboxamido)-3-methylbutanoic acid ÏàËÆ¶È:66.6% European Journal of Medicinal Chemistry 2012 54 324-342 Synthesis and biological evaluation of isoxazole, oxazole, and oxadiazole containing heteroaryl analogs of biaryl ureas as DGAT1 inhibitors Ravindra D. Jadhav, Kishorkumar S. Kadam, Shivaji Kandre, Tandra Guha, M. Mahesh Kumar Reddy, Manoja K. Brahma, Nitin J. Deshmukh, Amol Dixit, Lalit Doshi, Nisha Potdar, Arno A. Enose, Ram A. Vishwakarma, H. Sivaramakrishnan, Shaila Srinivasan, Kumar V.S. Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Hydroxyvermistatin C18H16O7 ÏàËÆ¶È:65% Helvetica Chimica Acta 2007 Vol. 90 1925 Structural and Biological Properties of Vermistatin and Two New Vermistatin Derivatives Isolated from the Marine-Mangrove Endophytic Fungus Guignardia sp. No. 4382 Xue-Kui Xia, Hua-Rong Huang, Zhi-Gang She, Ji-Wen Cai, Liu Lan, Jian-Ye Zhang, Li-Wu Fu, L. L. P. Vrijmoed, and Yong-Cheng Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3,5-diacetyltambulin C22H20O9 ÏàËÆ¶È:65% Journal of Natural Products 1999 62 833-837 Chemical Constituents and Biological Activities of the Fruit of Zanthoxylum integrifoliolum Ih-Sheng Chen, Tzu-Li Chen, Ya-Ling Chang, Che-Ming Teng, and Wei-Yu Lin Structure 13C NMR ̼Æ×Ä£Äâͼ |
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