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Smiling920гæ (³õÈëÎÄ̳)
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[ÇóÖú]
άÆÕÇóÖú£¬Ð»Ð»£¡ ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (126 MHz, DMSO) ¦Ä 7.53, 17.37, 48.79, 67.26, 67.33, 94.21, 95.00, 96.43, 101.71, 103.84, 116.08, 117.93, 123.68, 125.44, 126.50, 136.99, 145.57, 148.06, 159.50, 161.87, 164.77, 184.54. |
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Smiling920: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллภ2015-03-25 20:27:19
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Smiling920: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллภ2015-03-25 20:27:19
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1 . (E)-3-(3,4-dihydroxybenzylidene)-5,7-dihydroxy-6,8-dimethylchroman-4-one C18H16O6 ÏàËÆ¶È:68.1% Chemistry of Natural Compounds 2015 51 54−56 Two New Homoisoflavanones from the Rhizome of Polygonatum odoratum Yan-Yun Che, Yong Qian, Yi Wu, Wei-Qu, Jing-Yu Liang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 1 C17H14O7 ÏàËÆ¶È:59.0% Phytochemistry 1991 30 713-714 Homoisoflavanones and other constituents from Muscari racemosum Irena Materov, V¨¢clav Suchy, Duan Uhr¨ªn, Karel Ubik, Zuzana Granaiov¨¢, Boris Bobovnicky Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (E)-3-(3,4-dihydroxybenzylidene)-5,7-dihydroxy-8-methoxy-6-methylchroman-4-one C18H16O7 ÏàËÆ¶È:59.0% Chemistry of Natural Compounds 2015 51 54−56 Two New Homoisoflavanones from the Rhizome of Polygonatum odoratum Yan-Yun Che, Yong Qian, Yi Wu, Wei-Qu, Jing-Yu Liang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . kaempferol 4 -O-¦Á-L-rhamnopyranoside ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2008 56(9) 1253-1258 Microbial Metabolism of Biologically Active Secondary Metabolites from Nerium oleander L. Amany IBRAHIM,Sherief Ibrahim KHALIFA,Ishrak KHAFAGI,Diaa Tohamy YOUSSEF,Shabana KHAN,Mostafa MESBAH,and Ikhlas KHAN Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . quercetin 3'-xyloside ÏàËÆ¶È:50% Phytochemistry 1998 49 1997-2000 Myricetin 3-rhamnosyl(1¡ú6)galactoside from Nympha¨¦a xmarliacea Torgils Fossen, Nils Åge Frøystein, Øyvind M. Andersen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (E)-5,7-dihydroxy-6,8-dimethyl-3-(4'-hydroxybenzylidene)chroman-4-one C18H16O5 ÏàËÆ¶È:50% Journal of Natural Products 2010 73 548-552 Homoisoflavonoids from the Fibrous Roots of Polygonatum odoratum with Glucose Uptake-Stimulatory Activity in 3T3-L1 Adipocytes Hong Zhang, Fan Yang, Jin Qi, Xiao-Chen Song, Zheng-Fang Hu, Dan-Ni Zhu and Bo-Yang Yu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . heteroartonin A C26H28O7 ÏàËÆ¶È:50% Phytochemistry 1995 40 1279-1282 Prenylflavonoids of Artocarpus heterophyllus Mei-Ing Chung, Chai-Ming Lu, Pao-Lin Huang, Chun-Nan Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 4-morpholino-6-phenyl-2-(pyridin-2-yl)pyridine-3-carbonitrile C21H18N4O ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2010 47 691-696 Facile synthesis of 2,6-diaryl-4-secondary aminonicotinonitriles and highly substituted unsymmetrical 2,2'-bipyridines Sidhanath V. Bhosale, Umesh D. Patil, Mohan B. Kalyankar, Santosh V. Nalage, Vijay S. Patil and Kamlesh R. Desale Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . afzelin C21H20O10 ÏàËÆ¶È:50% Chinese Journal of Pharmaceuticals 2009 40 662-704 Study on Chemical Constituents of Urena lobata L.I.Flavonoid Constituents JIA Lu, JING Lin-lin, ZHOU Sheng-an, A You-mei, KONG De-yun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . trifluoromethanesulfonic acid 4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-1-butenyl)phenyl] propyl}-2-methylphenyl ester ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2013 21 1823-1833 A series of nonsecosteroidal vitamin D receptor agonists for osteoporosis therapy Hirotaka Kashiwagi, Yoshiyuki Ono, Masateru Ohta, Susumu Itoh, Fumihiko Ichikawa, Suguru Harada, Satoshi Takeda, Nobuo Sekiguchi, Masaki Ishigai, Tadakatsu Takahashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . N-(3-Chloro-4-fluorophenyl)-6-methoxy-7-(2-(2-(2-nitro-1H-imidazol-1-yl)ethoxy)ethoxy)quinazolin-4-amine ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2014 22 6796-6805 Identification of novel 4-anilinoquinazoline derivatives as potent EGFR inhibitors both under normoxia and hypoxia Weiyan Cheng, Youting Yuan, Ni Qiu, Peng Peng, Rong Sheng, Yongzhou Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . talaroxanthenone C20H20O4 ÏàËÆ¶È:50% Marine Biotechnology 2015 17 110−119 Acetylcholinesterase Inhibitors from a Marine Fungus Talaromyces sp. Strain LF458 Bin Wu & Birgit Ohlendorf & Vanessa Oesker & Jutta Wiese & Susann Malien & Rolf Schmaljohann & Johannes F. Imhoff Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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