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daphniphyllumľ³æ (ÕýʽдÊÖ)
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΢Æ×ÇóÖú
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| 13C NMR (CDCl3): 204.4, 164.3, 162.8, 158.5, 153.5, 153.4, 140.4, 126.7, 123.3, 102.8, 97.6, 97.3, 79.9, 79.0, 76.1, 60.9, 56.3, 56.2, 56.1, 42.6, 28.7, 27.9, 25.7, 25,5, 23.9, 23.8, 21.8. |
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- ×¢²á: 2007-08-26
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2Â¥2013-05-22 18:36:58
wm0629
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- Ìû×Ó: 1962
- ÔÚÏß: 77.9Сʱ
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- ×¢²á: 2013-01-01
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²éѯ½á¹û£º¹²²éµ½18¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . territrem B C29H34O10 ÏàËÆ¶È:96.1% Journal of Natural Products 1997 60 842-843 Structure and Anti-Acetylcholinesterase Activity of 4¦Á-(Hydroxymethyl)-4¦Á-demethylterritrem B Fu-Chuo Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . terreulactone D C30H36O10 ÏàËÆ¶È:80% The Journal of Antibiotics 2003 56 351-357 Terreulactones A, B, C, and D: Novel Acetylcholinesterase Inhibitors Produced by Aspergillus terreus II. Physico-chemical Properties and Structure Determination WON-GON KIM,KYUNG-MI CHO,CHONG-KIL LEE and ICK-DONG YOO Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 4¦Â-iodomethyl-4¦Â-demethyl territrem B C29H34O9 ÏàËÆ¶È:79.3% Journal of Natural Products 1995 Vol 58 857-862 Acetylcholinesterase Inhibition by Territrem B Derivatives Fu-Chuo Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2,3-epoxyterritrem B C29H34O10 ÏàËÆ¶È:75.8% Journal of Natural Products 1995 Vol 58 857-862 Acetylcholinesterase Inhibition by Territrem B Derivatives Fu-Chuo Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 4¦Â-hydroxymethyl-4¦Â-demethylterritrem B-succinate ÏàËÆ¶È:75% Journal of Agricultural and Food Chemistry 2004 52 3360-3365 Production of Polyclonal Antibodies against Territrem B and Detection of Territrem B in the Conidia of Aspergillus terreus 23-1 by Immunoelectron Microscopy Fu-Chuo Peng, Chiung-Hsiang Cheng, Jen-Cheng Liu, Ming-Fang Wu, Su-Huei Lee, and Huei-Ju Pan Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 4¦Á-(hydroxymethyl)-4¦Á-demethylterritrem B C29H34O10 ÏàËÆ¶È:73.0% Journal of Natural Products 1997 60 842-843 Structure and Anti-Acetylcholinesterase Activity of 4¦Á-(Hydroxymethyl)-4¦Á-demethylterritrem B Fu-Chuo Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . mesylate of 4¦Â-hydroxymethyl-4¦Â-demethylterritrem B ÏàËÆ¶È:73.0% Journal of Natural Products 1995 Vol 58 857-862 Acetylcholinesterase Inhibition by Territrem B Derivatives Fu-Chuo Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 10 ÏàËÆ¶È:73.0% The Journal of Antibiotics 2001 54 386-391 Determination of Absolute Stereochemistries of Arisugacin F and Territrem B, Novel Acetylcholinesterase Inhibitors MASAKI HANDA,TOSHIAKI SUNAZUKA,KENICHIRO NAGAI,RYOUKO KIMURA,KAZUHIKO OTOGURO,YOSHIHIRO HARIGAYA and SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 11 ÏàËÆ¶È:73.0% The Journal of Antibiotics 2001 54 386-391 Determination of Absolute Stereochemistries of Arisugacin F and Territrem B, Novel Acetylcholinesterase Inhibitors MASAKI HANDA,TOSHIAKI SUNAZUKA,KENICHIRO NAGAI,RYOUKO KIMURA,KAZUHIKO OTOGURO,YOSHIHIRO HARIGAYA and SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2,3-dihydroterritrem B C29H36O9 ÏàËÆ¶È:68.9% Journal of Natural Products 1995 Vol 58 857-862 Acetylcholinesterase Inhibition by Territrem B Derivatives Fu-Chuo Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . arisugacin D C29H36O8 ÏàËÆ¶È:55.1% The Journal of Antibiotics 2000 53 50-57 Arisugacins C and D, Novel Acetylcholinesterase Inhibitors and Their Related Novel Metabolites Produced by Penicillium sp. FO-4259-11 KAZUHIKO OTOGURO,KAZURO SHIOMI,YUUICHI YAMAGUCHI,NORIKO ARAI,TOSHIAKI SUNAZUKA,ROKURO MASUMA,YUZURU IWAI and SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . arisugacin H C29H36O9 ÏàËÆ¶È:55.1% The Journal of Antibiotics 2000 53 50-57 Arisugacins C and D, Novel Acetylcholinesterase Inhibitors and Their Related Novel Metabolites Produced by Penicillium sp. FO-4259-11 KAZUHIKO OTOGURO,KAZURO SHIOMI,YUUICHI YAMAGUCHI,NORIKO ARAI,TOSHIAKI SUNAZUKA,ROKURO MASUMA,YUZURU IWAI and SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . lecanindole C C30H39NO7 ÏàËÆ¶È:50% Journal of Natural Products 2009 72 1944-1948 The Lecanindoles, Nonsteroidal Progestins from the Terrestrial Fungus Verticillium lecanii 6144 Deborah M. Roll,Laurel R. Barbieri, Ramunas Bigelis, Leonard A. McDonald, Daniel A. Arias, Li-Ping Chang,Maya P. Singh, Scott W. Luckman,Thomas J. Berrodin, and Matthew R. Yudt Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 1 C52H62N6O10S2 ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 3669-3671 A free ligand for the asymmetric dihydroxylation of olefins utilizing one-phase catalysis and two-phase separation Yong-Qing Kuang, Sheng-Yong Zhang, Ru Jiang, Ling-Ling Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 4-(Dimethylamino)pyridinium 5-methoxy-3-(phenoxycarbonyl)-1-(piperidin-1-ylcarbonyl)-1H-indol-2-olate C29H32N4O5 ÏàËÆ¶È:50% Tetrahedron 2012 68 1427-1435 Convenient synthesis of 3-unsubstituted oxindole-1-carboxamides M¨¢rta Porcs-Makkay, Bal¨¢zs Volk, Eszter K¨®kai, Gyula Simig Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . isobicyclomangostin 5-methyl ether C25H28O6 ÏàËÆ¶È:50% Australian Journal of Chemistry 1998 51 249-254 Bicyclomangostin: a New Acid-Catalysed Cyclization Product from Mangostin Wilawan Mahabusarakam, Chaveng Pakawatchai, Pichaet Wiriyachitra, Walter C. Taylor, Brian W. Skelton and Allan H. White Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 5-hydroxy-7,3',5'-trimethoxy-4'-(3,3-dimethyl-allyloxy)flavone ÏàËÆ¶È:50% Journal of the Brazilian Chemical Society 2001 12 538-541 Flavones from the Leaves of Ficus gomelleira. Daniel F. Amaral, Mara S. P. Arruda, Alberto C. Arruda, Adolfo H. M¨¹ller, Luna L. J. Pantoja and Tânia M. da S. Lima Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Territrems B ÏàËÆ¶È:50% Mycosystema 2011 30 636-643 The bioactive metabolites of Aspergillus versicolor F62 isolated from Haliclona simulans DONG Shi-Hao GONG Ting ZHU Ping Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2013-05-22 18:59:43














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