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| 13C NMR (MeOD) ¦Ä 28.9, 35.1, 40.8, 51.7, 66.9, 73.3, 102.3, 108.9, 116.0, 116.3, 131.0, 131.5, 137.8, 157.2, 159.9, 209.5 |
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hotony: ½ð±Ò+10 2015-05-02 21:45:44
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hotony: ½ð±Ò+10 2015-05-02 21:45:44
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²éѯ½á¹û£º¹²²éµ½32¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2,6-bis[4-(hex-5-enyloxy)phenylmethyloxymethyl]-4-methoxypyridine C34H43NO5 ÏàËÆ¶È:68.7% European Journal of Organic Chemistry 2010 4932-4940 27- to 39-Membered Pyridine Macrocycles Ulrich L¨¹ning, Ellen Mak, Melanie Zindler, Britta Hartkopf and Rainer Herges Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Dehydrocoelenterazine-acetone adduct ÏàËÆ¶È:64.7% Bioorganic & Medicinal Chemistry Letters 1993 3 2647-2652 Symplectoteuthis bioluminescence (1) Structure and binding form of chromophore in photoprotein of a luminous squid Hiroyuki Takahashi, Minoru Isobe Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (S)-4-((S)-1-((4-methoxybenzyl)oxy)pent-4-en-1-yl)-2,2-dimethyl-1,3-dioxan-5-one C19H28O5 ÏàËÆ¶È:64.7% Chemistry-A European Journal 2012 18 14250-14254 Synthesis of the Originally Proposed Structure of Palmerolide C (pages 14250¨C14254) Dr. Gordon J. Florence and Joanna Wlochal Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (2R,3S,4S)-2,3-trans-3,4-cis-7,4'-dimethoxy-3,4-flavandiol C17H18O5 ÏàËÆ¶È:62.5% Phytochemistry 2007 68 1277-1284 Flavonoids and isoflavonoids from Gynerium sagittatum Angelyne Benavides, Carla Bassarello, Paola Montoro, Wagner Vilegas, Sonia Piacente, Cosimo Pizza Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 4-[4-(¦Â-D-glucopyranosyloxy)phenyl]-2-butanone ÏàËÆ¶È:62.5% Phytochemistry 2007 68 487-492 Biotransformation of raspberry ketone and zingerone by cultured cells of Phytolacca americana Kei Shimoda, Toshio Harada, Hatsuyuki Hamada, Nobuyoshi Nakajima,Hiroki Hamada Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 4-[(3S)-3-hydroxybutyl]phenyl-¦Â-D-glucopyranoside ÏàËÆ¶È:62.5% Phytochemistry 2007 68 487-492 Biotransformation of raspberry ketone and zingerone by cultured cells of Phytolacca americana Kei Shimoda, Toshio Harada, Hatsuyuki Hamada, Nobuyoshi Nakajima,Hiroki Hamada Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (2R,3R)-3,4'-dihydroxy-7-methoxyflavan C16H16O4 ÏàËÆ¶È:62.5% Chemical & Pharmaceutical Bulletin 2009 57 1153-1157 Chemical Constituents of the Bulbs of Habranthus brachyandrus and Their Cytotoxic Activities Maki Jitsuno, Akihito Yokosuka, Hiroshi Sakagami and Yoshihiro Mimaki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 4-(4'-hydroxyphenyl)butan-2-one 4'-O-¦Â-D-glucopyranoside ÏàËÆ¶È:62.5% Phytochemistry 1990 29 3853-3858 Phenylbutan-2-one ¦Â-d-glucosides from raspberry fruit Anni Pabst,Denis Barron,Jacques Adda,Peter Schreier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . louisanin B ÏàËÆ¶È:62.5% Chinese Journal of Medicinal Chemistry 2009 19 375-378 Secondary metabolites from the broth of an alkalophilic streptomycete ZHENG Dan, JIANG Yi, LOU Kai, CHEN Yun, XU Li-hua, HAN Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 7-Methoxy-4-(4-methoxyphenyl)-2H-chromene ÏàËÆ¶È:62.5% European Journal of Organic Chemistry 2012 1603-1615 A One-Pot Three-Step Synthesis of Z-Trisubstituted Olefins from Arylalkynes and Their Cyclization into 4-Aryl-2H-chromenes Evelia Rasolofonjatovo, Bret Tr¨¦guier, Olivier Provot, Abdallah Hamze, Jean-Daniel Brion and Mouad Alami Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 3'-deoxysappanol ÏàËÆ¶È:62.5% Phytochemical Analysis 2012 23 228-231 Separation of Four Homoisoflavonoids from Caesalpinia sappan by High-speed Counter-current Chromatography Pingping Xu, Shuhong Guan, Ruihong Feng, Renneng Tang and Dean Guo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 4-methoxy-2,6-bis[4-(pent-4-enyloxy)phenylmethyloxymethyl]pyridine C32H39NO5 ÏàËÆ¶È:62.5% European Journal of Organic Chemistry 2010 4932-4940 27- to 39-Membered Pyridine Macrocycles Ulrich L¨¹ning, Ellen Mak, Melanie Zindler, Britta Hartkopf and Rainer Herges Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . sappanene C16H14O3 ÏàËÆ¶È:62.5% Journal of Medicinal Chemistry 2008 51 4419-4429 Naturally Occurring Homoisoflavonoids Function as Potent Protein Tyrosine Kinase Inhibitors by c-Src-Based High-Throughput Screening Li-Gen Lin, Hua Xie, Hong-Lin Li, Lin-Jiang Tong, Chun-Ping Tang, Chang-Qiang Ke, Qun-Fang Liu, Li-Ping Lin, Mei-Yu Geng, Hualiang Jiang, Wei-Min Zhao, Jian Ding and Yang Ye Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . N-[(1,1-dimethylethoxy)carbonyl]-O-[(2-methoxyethoxy)methyl]-(Z)-2,3-methano-m-tyrosine C19H27O7N ÏàËÆ¶È:62.5% Journal of Medicinal Chemistry 1992 35 1410-1417 Inhibition of pig kidney L-aromatic amino acid decarboxylase by 2,3-methano-m-tyrosines Saeed Ahmad, Robert S. Phillips, Charles H. Stammer Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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