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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½700¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . haliclamide C26H40N2O5 ÏàËÆ¶È:66.6% Tetrahedron 2001 57 4443-4446 Haliclamide, a novel cyclic metabolite from the Vanuatu marine sponge Haliclona sp. Antonio Randazzo, C¨¦cile Debitus, Luigi Gomez-Paloma Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . monacolin X C24H34O6 ÏàËÆ¶È:66.6% The Journal of Antibiotics 1985 38 321-327 DIHYDROMONACOLIN L AND MONACOLIN X, NEW METABOLITES THOSE INHIBIT CHOLESTEROL BIOSYNTHESIS AKIRA ENDO, KEIJI HASUMI, TSUNEO NAKAMURA, MAMORU KUNISHIMA, MINORU MASUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . monacolin K ÏàËÆ¶È:66.6% The Journal of Antibiotics 1985 38 444-448 BIOSYNTHESIS OF ML-236B (COMPACTIN) AND MONACOLIN K AKIRA ENDO, YOSHINORI NEGISHI, TAKASHI IWASHITA, KOSEI MIZUKAWA, MASAHIRO HIRAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ethyl 2-(3-(2-cyclohexylethoxy)-4-phenethoxybenzylidene) hexanoate ÏàËÆ¶È:62.9% Bioorganic & Medicinal Chemistry 2011 19 5372-5382 SAR studies of acidic dual ¦Ã-secretase/PPAR¦Ã modulators Martina Hieke, Julia Ness, Ramona Steri, Christine Greiner, Oliver Werz, Manfred Schubert-Zsilavecz, Sascha Weggen, Heiko Zettl Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound ÏàËÆ¶È:62.5% Zeitschrift f¨¹r Naturforschung C 2003 58 62-64 Production and Purification of Statins from Pleurotus ostreatus (Basidiomycetes) Strains J. Alarc¨®n, S. ¨¢guila, P. Arancibia-Avila, O. Fuentes, E. Zamorano-Ponce, and M. Hern¨¢ndez Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Âå·¥ËûÍ¡ ÏàËÆ¶È:62.5% Mycosystema 2011 30 636-643 The bioactive metabolites of Aspergillus versicolor F62 isolated from Haliclona simulans DONG Shi-Hao GONG Ting ZHU Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (3'R)-3'-Hydroxy-lovastatin ÏàËÆ¶È:62.5% Acta Pharmaceutica Sinica B 2012 2 300-305 Microbial transformation of lovastatin by Beauveria bassiana Lirui Qiao, Dan Xie, Quan Liu, Jianhua Zou, Zhufang Shen, Jungui Dai Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-[1-Hydroxy-1-(4-chlorophenyl)methyl]-4-methylcyclohexan-1-one ÏàËÆ¶È:62.5% Indian Journal of Chemistry Section B 2013 52 1202-1209 Pyrrolidine catalyzed diastereoselective direct aldol reaction in water: A green approach Singh, Sarbjit; Chimni, Swapandeep Singh Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 6-Desmethyl-16-hydroxymethyl epothilone C C25H37NO6S ÏàËÆ¶È:60% Natural Product Research 2011 25 1707-1712 New epothilone congeners from Sorangium cellulosum strain So0157-2 Ji-Dong Wang, Nan Jiang, Hui Zhang, Lin-Ping Ying, Chuan-Xi Wang, Wen-Sheng Xiang, BoWu, Hai-Bin Wang and Hua Bai Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . lactone ring-opened monacolin K ÏàËÆ¶È:60% Mycosystema 2011 30 636-643 The bioactive metabolites of Aspergillus versicolor F62 isolated from Haliclona simulans DONG Shi-Hao GONG Ting ZHU Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (1S,2S,2'S,6R,8S,8aR,11R,13R)-(1,2,6,7,8,8A-Hexahydro-11,13-dihydroxy-2,6-dimethyl-8-(2-methylbutyryl)oxy-1-naphthaleneheptanoicacidmethylester ÏàËÆ¶È:60% Acta Pharmaceutica Sinica B 2012 2 300-305 Microbial transformation of lovastatin by Beauveria bassiana Lirui Qiao, Dan Xie, Quan Liu, Jianhua Zou, Zhufang Shen, Jungui Dai Structure 13C NMR ̼Æ×Ä£Äâͼ |

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