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daphniphyllum

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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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daphniphyllum

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daphniphyllum: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, thanks 2013-05-22 20:33:33
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
¼èÄÑÀ§¿à£¬ÓñÈêÓڳɡ£
3Â¥2013-05-22 18:59:43
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