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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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