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»¯ºÏÎï1 1 . aspochalasin D C24H35NO4 ÏàËÆ¶È:96% The Journal of Antibiotics 2001 54 379-381 Selective Cytotoxicity and Stereochemistry of Aspochalasin D TAIJIRO TOMIKAWA,KAZUO SHIN-YA,TAISEI KINOSHITA,ATSUSHI MIYAJIMA,HARUO SETO and YOICHI HAYAKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . aspochalasin Z C24H35NO2 ÏàËÆ¶È:88% The Journal of Antibiotics 2004 57 715-720 Aspochalamins A-D and Aspochalasin Z Produced by the Endosymbiotic Fungus Aspergillus niveus LU 9575 II. Structure Elucidation ALEXANDRA HÖLTZEL,DIETMAR G. SCHMID,GRAEME J. NICHOLSON,PHILIPP KRASTEL,AXEL ZEECK,KLAUS GEBHARDT,HANS-PETER FIEDLER and GÜNTHER JUNG Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 17,18-di-O-acetyl aspochalasin D ÏàËÆ¶È:82.1% The Journal of Organic Chemistry 1997 62 2148-2151 Phomacins: Three Novel Antitumor Cytochalasan Constituents Produced by a Phoma sp. Khisal A. Alvi, Bipin Nair, Henry Pu, Rocky Ursino, Cathy Gallo, and Ursula Mocek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . aspochalasin H C24H35NO5 ÏàËÆ¶È:76% The Journal of Antibiotics 2002 55 666-668 Structure of Aspochalasin H, a New Member of the Aspochalasin Family TAIJIRO TOMIKAWA,KAZUO SHIN-YA,HARUO SETO,NORIYUKI OKUSA,TAKAYUKI KAJIURA and YOICHI HAYAKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . scutebarbatine H C26H31NO7 ÏàËÆ¶È:73.0% Chemical & Pharmaceutical Bulletin 2007 55(8) 1218-1221 Five New neo-Clerodane Diterpenoid Alkaloids from Scutellaria barbata with Cytotoxic Activities Sheng-Jun DAI,Gong-Fu WANG, Meng CHEN, Ke LIU, and Li SHEN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 2 C26H38O9 ÏàËÆ¶È:73.0% Natural Product Communications 2010 5 669-674 Eudesmanolides and Methyl Ester Derivatives fromDimerostemma arnottii S¨¦rgio Ricardo Ambrosio, Ricardo Stefani, Vladimir Constantino Gomes Heleno,M¨¢rcio Antônio de Menezes, Antonio Gilberto Ferreira, Paulo Gustavo BarboniDantas Nascimento , Mara Angelina Galvão Magenta and Fernando Batista Da Costa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . aspochalasin K C25H39NO5 ÏàËÆ¶È:72% Journal of Natural Products 2004 67 328-332 Aspochalasins I, J, and K: Three New Cytotoxic Cytochalasans of Aspergillus flavipes from the Rhizosphere of Ericameria laricifolia of the Sonoran Desert Guang-Xiong Zhou, E. M. Kithsiri Wijeratne, Donna Bigelow,Leland S. Pierson, Hans D. VanEtten, and A. A. Leslie Gunatilaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . aspochalasin R ÏàËÆ¶È:72% Chinese Chemical Letters 2010 21 824-826 Three new aspochalasin derivatives from the marine-derived fungus Spicaria elegans Zhen Jian Lin; Tian Jiao Zhu; Li Chen; Qian Qun Gu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . aspochalasin T C24H35NO5 ÏàËÆ¶È:72% Chinese Chemical Letters 2010 21 824-826 Three new aspochalasin derivatives from the marine-derived fungus Spicaria elegans Zhen Jian Lin; Tian Jiao Zhu; Li Chen; Qian Qun Gu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 14a C24H37NO4 ÏàËÆ¶È:72% Tetrahedron 2012 68 159-165 Construction of A/E/F ring systems of C19-diterpenoid alkaloids with both C-1 and C-6 oxygen functions Zhi-Gang Liu, Liang Xu, Qiao-Hong Chen, Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . phomacin A C25H37NO5 ÏàËÆ¶È:72% The Journal of Organic Chemistry 1997 62 2148-2151 Phomacins: Three Novel Antitumor Cytochalasan Constituents Produced by a Phoma sp. Khisal A. Alvi, Bipin Nair, Henry Pu, Rocky Ursino, Cathy Gallo, and Ursula Mocek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . phomacin C C25H37NO4 ÏàËÆ¶È:72% The Journal of Organic Chemistry 1997 62 2148-2151 Phomacins: Three Novel Antitumor Cytochalasan Constituents Produced by a Phoma sp. Khisal A. Alvi, Bipin Nair, Henry Pu, Rocky Ursino, Cathy Gallo, and Ursula Mocek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (3S,6R,7R,8R)-3,14-dihydroxy-8-(2'-methylbutyroyloxy)-helianga-1(10),4,11(13)-trien-6,12-olide C22H30O7 ÏàËÆ¶È:72% Bioorganic & Medicinal Chemistry 2009 17 3189-3197 Inhibitory effects of sesquiterpene lactones isolated from Eupatorium chinense L. on IgE-mediated degranulation in rat basophilic leukemia RBL-2H3 cells and passive cutaneous anaphylaxis reaction in mice Tomohiro Itoh, Masayoshi Oyama, Norihiko Takimoto, Chihiro Kato, Yoshinori Nozawa, Yukihiro Akao, Munekazu Iinuma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |

2Â¥2012-04-01 22:30:35
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»¯ºÏÎï2 1 . dehydrocurvularin ÏàËÆ¶È:88.2% Journal of Natural Products 1993 Vol 56 2175 6-Chlorodehydrocurvularin, a New Metabolite from Cochliobolus spicifer Emilio L. Ghisalberti, Catherine Y. Rowland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . dehydrocurvularin ÏàËÆ¶È:82.3% The Journal of Antibiotics 2004 57 341-344 A New Anthraquinone and Cytotoxic Curvularins of a Penicillium sp. from the Rhizosphere of Fallugia paradoxa of the Sonoran Desert JIXUN ZHAN,E. M. KITHSIRI WIJERATNE,CHRISTOPHER J. SELIGA,JUN ZHANG,ELIZABETH E. PIERSON,LELAND S. PIERSON III,HANS D. VANETTEN and A. A. LESLIE GUNATILAKA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . E-6-chloro-10,11-dehydrocurvularin ÏàËÆ¶È:76.4% Journal of Natural Products 1993 Vol 56 2175 6-Chlorodehydrocurvularin, a New Metabolite from Cochliobolus spicifer Emilio L. Ghisalberti, Catherine Y. Rowland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (3R ),(5R )-5-hydroxy-de-O-methyllasiodiplodin C16H22O5 ÏàËÆ¶È:70.5% Phytochemistry 2000 54 489-494 Potato micro-tuber inducing hydroxylasiodiplodins from Lasiodiplodia theobromae Qing Yang, Maki Asai, Hideyuki Matsuura, Teruhiko Yoshihara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . trans-dehydrocurvularin C16H18O5 ÏàËÆ¶È:70.5% Natural Product Research and Development 2005 17 677-680 Isolation of Secondary Metabolites of 9F Series Marine Fungi and Their Bioactivities against Pyricularia oryzae ZHAO Ling-ling; ZHANG Hui-ping Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . xestospongiene Z3/Z4 C17H23Br3O3 ÏàËÆ¶È:70.5% Tetrahedron 2011 67 58-68 Brominated polyunsaturated lipids and their stereochemistry from the Chinese marine sponge Xestospongia testudinaria Wei Jiang, Dong Liu, Zhiwei Deng, Nicole J. de Voogd, Peter Proksch, Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2012-04-01 22:35:18
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4Â¥2012-04-01 22:46:41
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5Â¥2012-04-05 19:10:55













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