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1 .     jolkinol A'
    ÏàËÆ¶È:64%
Planta Medica          2004          70          244-249
Euphopubescenol and Euphopubescene, Two New Jatrophane Polyesters, and Lathyrane-type Diterpenes from Euphorbia pubescens
Valente, Cl¨¢udia; Pedro, Madalena; Ascenso, Jos¨¦ R.; Abreu, Pedro M.; Nascimento, Maria São Jos¨¦; Ferreira, Maria-Jos¨¦ U.Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     scabronine H
C27H36O5     ÏàËÆ¶È:56%
Helvetica Chimica Acta          2004          Vol. 87          2877
Isolation and Characterization of New Bitter Diterpenoids from the Basidiomycete Sarcodon scabrosus
Bing-Ji Ma, Hua-Jie Zhu, and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 8
C27H38N4O6     ÏàËÆ¶È:56%
Journal of the American Chemical Society          2007          129          3007-3012
Molecular Insights into Azumamide E Histone Deacetylases Inhibitory Activity
Nakia Maulucci, Maria Giovanna Chini, Simone Di Micco, Irene Izzo, Emiddio Cafaro, Adele Russo, Paola Gallinari, Chantal Paolini, Maria Chiara Nardi, Agostino Casapullo, Raffaele Riccio, Giuseppe Bifulco, and Francesco De Riccardis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     jolkinol A
    ÏàËÆ¶È:55.5%
Planta Medica          2004          70          244-249
Euphopubescenol and Euphopubescene, Two New Jatrophane Polyesters, and Lathyrane-type Diterpenes from Euphorbia pubescens
Valente, Cl¨¢udia; Pedro, Madalena; Ascenso, Jos¨¦ R.; Abreu, Pedro M.; Nascimento, Maria São Jos¨¦; Ferreira, Maria-Jos¨¦ U.Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (20S,22S)-3¦Â,22-dihydroxycucurbita-5(10),24-diene-26,29-dioic acid ¦Ä-lactone
C30H44O5     ÏàËÆ¶È:53.5%
Natural Product Research          2002          16          261-266
New Triterpenoids from the Leaves of Abrus Precatorius
Nam-Cheol Kim; Darrick Kim; A. Douglas Kinghorn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3¦Â-hydroxy-5¦Á,8¦Á-epidioxyergosta-6,22-diene
C28H44O3     ÏàËÆ¶È:53.5%
Mycosystema          2011          30          263-267
Metabolites of endophytic fungus Pestalotiopsis clavispora isolated from the stem of Bruguiera sexangula
DENG Hui-Ying XING Jian-Guang LUO Du-Qiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     gelliusterol A
C25H38O2     ÏàËÆ¶È:52%
Journal of Natural Products          2001          64          741-744
Gelliusterols A-D, New Acetylenic Sterols from a Sponge, Gellius Species
Winklet A. Gallimore, Michelle Kelly, and Paul J. Scheuer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (-)-(1R,2R,3R,4R,5R)-3-Azidomethyl-2-tert-butoxy-1-(tertbutyl-diphenyl-silanyloxymethyl)-4-(6-chloro-purin-9-yl)-bicyclo[3.1.0]hexan-3-ol
C33H40ClN7O3Si     ÏàËÆ¶È:52%
Tetrahedron          2012          68          1253-1261
Stereoselective synthesis and anti-HCV activity of conformationally restricted 2'-C-substituted carbanucleosides
Won Jun Choi, Yun Jung Ko, Girish Chandra, Hyuk Woo Lee, Hea Ok Kim, Hyo Jung Koh, Hyung Ryong Moon, Young Hoon Jung, Lak Shin Jeong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 24
C29H42N4O6     ÏàËÆ¶È:52%
Journal of the American Chemical Society          2007          129          3007-3012
Molecular Insights into Azumamide E Histone Deacetylases Inhibitory Activity
Nakia Maulucci, Maria Giovanna Chini, Simone Di Micco, Irene Izzo, Emiddio Cafaro, Adele Russo, Paola Gallinari, Chantal Paolini, Maria Chiara Nardi, Agostino Casapullo, Raffaele Riccio, Giuseppe Bifulco, and Francesco De Riccardis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (+)-(1R,2R,3R,4R,5R)-(Acetic acid 2-tert-butoxy-1-(tert-butyldiphenyl-silanyloxymethyl)-4-(6-chloro-purin-9-yl)-3-hydroxy-bicyclo[3.1.0]hex-3-ylmethyl ester
C35H43ClN4O5Si     ÏàËÆ¶È:51.8%
Tetrahedron          2012          68          1253-1261
Stereoselective synthesis and anti-HCV activity of conformationally restricted 2'-C-substituted carbanucleosides
Won Jun Choi, Yun Jung Ko, Girish Chandra, Hyuk Woo Lee, Hea Ok Kim, Hyo Jung Koh, Hyung Ryong Moon, Young Hoon Jung, Lak Shin Jeong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Ent-7¦Á-cinnamoyloxy-l5¦Â-hydroxy-kaur- 16-en- 19-oic acid
    ÏàËÆ¶È:51.7%
Phytochemistry          1998          49          805-809
Kaurene diterpenes from Mikania vitifolia
G. O. Lobitz, G. Tamayo-Castillo, L. Poved¦Á, I. Merfort
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Ent- 15¦Â-cinnamoyloxy-7¦Á-hydroxy-kaur- 16-en- 19-oic acid
    ÏàËÆ¶È:51.7%
Phytochemistry          1998          49          805-809
Kaurene diterpenes from Mikania vitifolia
G. O. Lobitz, G. Tamayo-Castillo, L. Poved¦Á, I. Merfort
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     topsentisterol E1
C28H42O2     ÏàËÆ¶È:50%
Journal of Natural Products          2006          69          1760-1768
26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp.
Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     eurysponiol B3
C28H48O7     ÏàËÆ¶È:50%
Tetrahedron          1994          50          3813-3828
Euryspongiols: Ten new highly hydroxylated 9,11-secosteroids with antihistaminic activity from the sponge euryspongia sp. Stereochemistry and reduction.
Jos¨¦ Dopeso, Emilio Quiño¨¢, Ricardo Riguera, C¨¦cile Debitus, Patricia R. Bergquist
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     eurysponiol B4
C28H48O7     ÏàËÆ¶È:50%
Tetrahedron          1994          50          3813-3828
Euryspongiols: Ten new highly hydroxylated 9,11-secosteroids with antihistaminic activity from the sponge euryspongia sp. Stereochemistry and reduction.
Jos¨¦ Dopeso, Emilio Quiño¨¢, Ricardo Riguera, C¨¦cile Debitus, Patricia R. Bergquist
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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