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1 . nigramide K C29H42N2O4 ÏàËÆ¶È:55.1% The Journal of Organic Chemistry 2005 70 1164-1176 Nigramides A−S, Dimeric Amide Alkaloids from the Roots of Piper nigrum Kun Wei, Wei Li, Kazuo Koike, Yingjie Chen, and Tamotsu Nikaido Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . viteagnusin B ÏàËÆ¶È:53.8% Chemical & Pharmaceutical Bulletin 2008 56(11) 1621-1624 Five New Diterpenoids, Viteagnusins A¡ªE, from the Fruit of Vitex agnus-castus Masateru ONO,Toru YAMASAKI,Masatarou KONOSHITA,Tsuyoshi IKEDA,Masafumi OKAWA,Junei KINJO,Hitoshi YOSHIMITSU,and Toshihiro NOHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . amphiacrolide O C25H3608 ÏàËÆ¶È:53.8% Journal of Natural Products 1996 59 5-14 cis-Clerodane Diterpene Lactones from Amphiachyris dracunculoides. Fathalla M. Harraz, Michael J. Pcolinski, and Raymond W. Doskotch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 7¦Â-hydroxycholesterol C27H46O2 ÏàËÆ¶È:53.8% Steroids 2005 70 907-912 Synthesis and antifungal activity of oxygenated cholesterol derivatives Jean Michel Brunel, C¨¦line Loncle, Nicolas Vidal, Michel Dherbomez, Yves Letourneux Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 5,16¦Á,17¦Á-Trihydroxy-3¦Â-tosyloxy-5¦Á-pregna-6,20-dione C28H38O8S ÏàËÆ¶È:53.8% Canadian Journal of Chemistry 2005 83 1084-1092 Synthesis and preliminary bioactivity evaluation of new pregnane brassinosteroid-like compounds Daniel G. Rivera and Francisco Coll Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . N,N,N-Trimethyl-3-(5-(2-dodecanoyloxazol-5-yl)pentylsulfonyl)-propan-1-ammonium iodide C26H49N2O4S ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2012 20 1100-1112 Design, synthesis and evaluation of polar head group containing 2-keto-oxazole inhibitors of FAAH Marion Rusch,Stefan Zahov,Ingrid R. Vetter, Matthias Lehr, Christian Hedberg Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Dimethyl 18-succinyloxygrindelate C26H40O7 ÏàËÆ¶È:53.8% Phytochemistry 1980 19 2689-2693 Grindelane diterpenoids from Chrysothamnus nauseosus Allan F. Rose Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Dimethyl 18-succinyloxygrindelate C26H40O7 ÏàËÆ¶È:53.8% Phytochemistry 1980 19 2689-2693 Grindelane diterpenoids from Chrysothamnus nauseosus Allan F. Rose Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 7 C25H32NO5Cl ÏàËÆ¶È:53.8% The Journal of Antibiotics 2002 55 165-171 Stachyflin and Acetylstachyflin, Novel Anti-influenza A Virus Substances, Produced by Stachybotrys sp. RF-7260 II. Synthesis and Preliminary Structure-Activity Relationships of Stachyflin Derivatives KAZUYUKI MINAGAWA,SHUICHI KOUZUKI and TOSHIYUKI KAMIGAUCHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . striatal C C25H34O7 ÏàËÆ¶È:53.8% Zeitschrift f¨¹r Naturforschung C 2002 57 263-271 Studies on the Biosynthesis of Striatal-Type Diterpenoids and the Biological Activity of Herical T. Anke, U. Rabe, P. Schu, T. Eizenhöfer, M. Schrage, and W. Steglich Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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