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ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½215¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Phosphatidyl-nerol ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry Letters 2008 18 4044-4046 Synthesis of phosphatidylated-monoterpene alcohols catalyzed by phospholipase D and their antiproliferative effects on human cancer cells Yukihiro Yamamoto, Masashi Hosokawa, Hideyuki Kurihara, Takashi Maoka, Kazuo Miyashita Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1-[(11S)-3¦Â-hydroxyeudesma-4,6-dien-12-oyl]-piperidine C20H31NO2 ÏàËÆ¶È:60% Tetrahedron 1996 52 10507-10518 Ring-opening aminolysis of sesquiterpene lactones: An easy entry to bioactive sesquiterpene derivatives. Synthesis of (+)-¦Â-cyperone and (− -eudesma-3,5-diene from santoninGonzalo Blay, Luz Cardona, Begoña Garc¨ªa, Cristina L. Garc¨ªa, Jos¨¦R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . triptinin-A C21H28O3 ÏàËÆ¶È:57.1% Phytochemistry 1997 44 1511-1514 Triptinins A and B, two leukotriene D4 antagonistic 19(4¡ú3)-abeo-abietanes from Tripterygium wilfordii Jingya Xu, Tetsuro Ikekawa, Masanori Ohkawa, Itsuro Yokota, Noriyuki Hara, Yoshinori Fujimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . viscida-3,9,14-triene ÏàËÆ¶È:55% Phytochemistry 2005 66 941-949 Composition of the essential oil of the liverwort Radula perrottetii of Japanese origin Hailemichael Tesso, Wilfried A. König, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . eiseniachloride C C20H29ClO3 ÏàËÆ¶È:55% Journal of Natural Products 2003 66 1318-1323 Novel Oxylipin Metabolites from the Brown Alga Eisenia bicyclis Kenji Kousaka, Nobuyuki Ogi, Yasutomo Akazawa,Makiko Fujieda, Yuzo Yamamoto, Yuuki Takada, and Junji Kimura Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . acalycixeniolide F C20H30O3 ÏàËÆ¶È:55% Journal of Natural Products 2000 63 254-257 New Xenicane Diterpenoids from the Gorgonian Acalycigorgia inermis Jung-Rae Rho, Hyi-Seung Lee, Youngwan Seo, Ki Woong Cho, and Jongheon Shin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (2E,4E,8Z,11E)-2'-hydroxy-N-isobutyl-2,4,8,11-tetradecatetraenamide C18H29NO2 ÏàËÆ¶È:55% Chemical & Pharmaceutical Bulletin 1988 36 2362-2365 Amides from Huajiao, Pericarps of Zanthoxylum bungeanum MAXIM. KENJI MIZUTANI,YUICHIRO FUKUNAGA,OSAMU TANAKA,NAOYUKI TAKASUGI,YUH-ICHIROU SARUWATARI,TOHRU FUWA,TATSUO YAMAUCHI,JIAN WANG,MING-RU JIA,FANG-YAO LI and YI-KUI LING Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 11 ÏàËÆ¶È:55% Chemistry of Natural Compounds 1988 24 241-246 1H and 13C NMR SPECTRA OF BIOLOGICALLY ACTIVE COMPOUNDS.III. DIASTEREOMERS OF (¡À)-7-THIA- AND 13-THIA-16-ARYLOXY ANALOGS OF II-DEOXYPROSTAGLANDINS OF THE E l SERIES L. M. Khalluov, A. A. Panasenko E. V. Vasil'eva, N. A. Danilova,Ya. L. Vel'der, and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . isobungeanool ÏàËÆ¶È:55% Phytochemistry 1997 46 1123-1126 Alkylamides from pericarps of Zanthoxylum bungeanum Quanbo Xiong, Dawen Shi, Hirofumi Yamamoto, Mizuo Mizuno Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Bis[(3¦Â-(3,4-dichlorophenyl)-8-methyl-8-azabicyclo[3.2.1]octan-2¦Â-yl)]methyl octanedioate C38H48Cl4N2O4 ÏàËÆ¶È:55% |

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