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²éѯ½á¹û£º¹²²éµ½15¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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