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²éѯ½á¹û£º¹²²éµ½33¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Rubralactone C14H12O6 ÏàËÆ¶È:86.6% Bioscience, Biotechnology, and Biochemistry 2007 71 1896-1901 Rubralactone, Rubralides A, B and C, and Rubramin Produced by Penicillium rubrum Yasuo KIMURA, Takashi YOSHINARI, Hiroyuki KOSHINO, Shozo FUJIOKA, Katsuhide OKADA and Atsumi SHIMADA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . altenuene ÏàËÆ¶È:66.6% Phytochemistry 1994 35 665-669 5¡ä-epialtenuene and neoaltenuene, dibenzo-¦Á-pyrones from Alternaria alternata cultured on rice Nigel Bradburn, Raymond D. Coker, Gerald Blunden, Christopher H. Turner, Trevor A. Crabb Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . altenuene ÏàËÆ¶È:66.6% Journal of Agricultural and Food Chemistry 2014 62 3584−3590 Secondary Metabolites from the Endophytic Botryosphaeria dothidea of Melia azedarach and Their Antifungal, Antibacterial, Antioxidant,and Cytotoxic Activities Jian Xiao, Qiang Zhang, Yu-Qi Gao, Jiang-Jiang Tang, An-Ling Zhang, and Jin-Ming Gao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . altenuene C15H16O6 ÏàËÆ¶È:66.6% Fitoterapia 2012 83 1087-1091 Heptaketides with antiviral activity from three endolichenic fungal strains Nigrospora sp., Alternaria sp. and Phialophora sp. Jun-Wei He, Guo-Dong Chen, Hao Gao, Fan Yang, Xiao-Xia Li, Tao Peng, Liang-Dong Guo, Xin-Sheng Yao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . isoaltenuene C15H16O6 ÏàËÆ¶È:66.6% Fitoterapia 2012 83 1087-1091 Heptaketides with antiviral activity from three endolichenic fungal strains Nigrospora sp., Alternaria sp. and Phialophora sp. Jun-Wei He, Guo-Dong Chen, Hao Gao, Fan Yang, Xiao-Xia Li, Tao Peng, Liang-Dong Guo, Xin-Sheng Yao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . isoaltenuene C15H16O6 ÏàËÆ¶È:66.6% Acta Pharmaceutica Sinica 2013 48 891-895 A new sesquiterpenoid from fungus Colletotrichum sp. and its cytotoxicity YANG Zhi-jun, YANG Tian, LUO Min-yu, XIA Xing, CHEN Dai-jie, QIAN Xiu-ping Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 1-[1-oxo-3(3,4-methylenedioxy-5-methoxyphenyl)-2Z-propenyl]piperidine C16H19NO4 ÏàËÆ¶È:62.5% Journal of Natural Products 2004 67 1005-1009 New Amide Alkaloids from the Roots of Piper nigrum Kun Wei, Wei Li, Kazuo Koike, Yuping Pei, Yingjie Chen, and Tamotsu Nikaido Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . thunberginol E C16H14O6 ÏàËÆ¶È:62.5% Chemical & Pharmaceutical Bulletin 1996 44 1440-1447 Development of Bioactive Functions in Hydrangeae Dulcis Folium. V. On the Antiallergic and Antimicrobial Principles of Hydrangeae Dulcis Folium. (2). Thunberginols C, D, and E, Thunberginol G 3'-O-Glucoside, (-)-Hydrangenol10'-O-Glucoside, and (+)-Hydran Masayuki YOSHIKAWA,Hisashi MATSUDA,Hiroshi SHIMODA,Hiromi SHIMADA,Emiko HARADA,Yoshikazu NAITOH,Akiko MIKI,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . thunberginol E C16H14O6 ÏàËÆ¶È:62.5% Chemical & Pharmaceutical Bulletin 1992 40 3352-3354 THUNBERGINOLS C, D, AND E, NEW ANTIALLERGIC AND ANTIMICROBIAL DIHYDROISOCOUMARINS, AND THUNBERGINOL G 3'-O-GLUCOSIDE AND (-)-HYDRANGENOL 4'-O-GLUCOSIDE, NEW DIHYDROISOCOUMARIN GLYCOSIDES, FROM HYDRANGEAE DULCIS FOLIUM Masayuki TOSHIKAWA,Emiko UCHIDA,Nobuyasu CHATANI,Hiromi KOBAYASHI,Yoshikazu NAITOH,Yasuhiro OKUNO,Hisashi MATSUDA,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . botrallin C16H14O7 ÏàËÆ¶È:62.5% Zeitschrift f¨¹r Naturforschung C 2005 60 11-21 Metabolites from Microsphaeropsis olivacea an Endophytic Fungus of Pilgerodendron uviferum E. Hormazabal, G. Schmeda-Hirschmann, L. Astudillo, J. Rodr¨ªguez, and C. Theoduloz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 11 ÏàËÆ¶È:62.5% Food Science and Biotechnology 2013 22 1547-1557 Isolation and Identification of Antioxidative Compounds and Their Activities from Suaeda japonica Jeong-Yong Cho, Xing Yang, Kyung-Hee Park, Hye Jin Park, Sun-Young Park, Jae-Hak Moon, and Kyung-Sik Ham Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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