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1 .     cyclo-(L-isoleucyl-L-prolyl-L-leucyl-L-prolyl)
C22H36N4O4     ÏàËÆ¶È:58.3%
Journal of Natural Products          2003          66          883-884
A New Cyclic Peptide from a Marine-Derived Bacterium of the Genus Nocardiopsis
Jongheon Shin, Youngwan Seo, Hyi-Seung Lee,Jung-Rae Rho, and Sang Jun Mo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     barbilycopodin
    ÏàËÆ¶È:58.3%
Journal of the Chemical Society, Perkin Transactions 1          1986                   809-814
Dolabellane diterpenoids from the liverworts Barbilophozia floerkei, B. lycopodioides, and B. attenuata: spectroscopic and X-ray studies of structure, stereochemistry, and conformation. X-Ray molecular structure of 3S,4S;7S,8S-diepoxy-10R,18-dihydroxydoll
Siegfried Huneck, George A. Baxter, A. Forbes Cameron, Joseph D. Connolly, Leslie J. Harrison, William R. Phillips, David S. Rycroft and George A. Sim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     MKN-349A
    ÏàËÆ¶È:58.3%
Helvetica Chimica Acta          2014          97          1564-1570
A New Cyclic Peptide and a New Steroid from the Fungus Penicillium sp. GD6 Isolated from the Mangrove Bruguiera gymnorrhiza
Zhen-Fang Zhou, Xiao-Hong Yang, Hai-Li Liu, Yu-Cheng Gu, Bo-Ping Ye and Yue-Wei Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     tenacibactin C
C23H42N4O8     ÏàËÆ¶È:54.1%
Journal of Natural Products          2007          70          563-566
Tenacibactins A-D, Hydroxamate Siderophores from a Marine-Derived Bacterium, Tenacibaculum sp. A4K-17
Jae-Hyuk Jang,Kaneo Kanoh, Kyoko Adachi, Satoru Matsuda, and Yoshikazu Shizuri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (22R,23R)-3¦Â-Acetoxy-5¦Á,22,23-trihydroxystigmastan-6-one
C31H52O6     ÏàËÆ¶È:54.1%
Steroids          2000          65          329-337
Synthesis and bioactivity evaluation of brassinosteroid analogs
Javier A. Ram¨ªrez, Osvaldo M. Teme Centuri¨®n, Eduardo G. Gros, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     teucrolin D
C22H30O9     ÏàËÆ¶È:54.1%
Journal of Natural Products          1993          Vol 56          830
Neocleordane Diterpenoids and Their Artifacts from Teucrium olivarianum
Mohammed A. Al-Yahya, Ilias Muhammad, Humayun H. Mirza, Farouk S. El-Feraly, Andrew T. McPhail
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     10R,18-diacetoxydolabella-3E,7E-diene
C24H38O4     ÏàËÆ¶È:54.1%
Journal of the Chemical Society, Perkin Transactions 1          1986                   809-814
Dolabellane diterpenoids from the liverworts Barbilophozia floerkei, B. lycopodioides, and B. attenuata: spectroscopic and X-ray studies of structure, stereochemistry, and conformation. X-Ray molecular structure of 3S,4S;7S,8S-diepoxy-10R,18-dihydroxydoll
Siegfried Huneck, George A. Baxter, A. Forbes Cameron, Joseph D. Connolly, Leslie J. Harrison, William R. Phillips, David S. Rycroft and George A. Sim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3¦Â,8¦Á,9¦Â-triacetoxy-4¦Á-hydroxy-7-epi-eudesmane
C21H34O7     ÏàËÆ¶È:54.1%
The Journal of Organic Chemistry          2005          70          338-341
Enzyme-Catalyzed Rearrangement of a Diepoxy-germacrane Compound into New 7-epi-Eudesmane Derivatives
Andr¨¦s Garc¨ªa-Granados, Mar¨ªa C. Guti¨¦rrez, Antonio Mart¨ªnez, and Francisco Rivas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (+)-(1R,2R,4S,4aS,8aS)-4-(acetyloxy)-1-(2-(acetyloxy)ethyl)-2,5,5,8a-tetramethyldecahydro-2-naphthalenyl acetate
C22H36O6     ÏàËÆ¶È:54.1%
Tetrahedron          2001          57          5663-5679
The synthesis of Ambrox®-like compounds starting from (+)-larixol
Marjon G Bolster, Ben J.M Jansen, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (+)-(1R,2R,4S,4aS,8aS)-4-(acetyloxy)-1-(2-(acetyloxy)ethyl)-2,5,5,8a-tetramethyldecahydro-2-naphthalenyl acetate
C22H36O6     ÏàËÆ¶È:54.1%
Tetrahedron          2001          57          8369-8379
The synthesis of Ambrox®-like compounds starting from (+)-larixol. Part 2
Marjon G Bolster, B¨¦atrice M.F Lagnel, Ben J.M Jansen, Christophe Morin, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     22-½µ-3¦Â-ÒÒõ£Ñõ»ù¶¹çÞ-6-ͪ-22-È©
    ÏàËÆ¶È:54.1%
Chinese Journal of Organic Chemistry          2014          34          1816-1828
Synthesis and Antiproliferative Evaluation of Some Steroidal Oxime Ether
Huang, Yanmin Su, Shaoyang Jia, Linyi Gan, Chunfang Lin, Qifu Kong, Erbin Cui, Jianguo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (+)-(1R,2R,4S,4aS,8aS)-4-(acetyloxy)-1-((3E)-5-(acetyloxy)-3-methyl-3-pentenyl)-2,5,5,8a-tetramethyl-decahydro-2-naphthalenyl acetate
C24H38O4     ÏàËÆ¶È:53.8%
Tetrahedron          2001          57          5663-5679
The synthesis of Ambrox®-like compounds starting from (+)-larixol
Marjon G Bolster, Ben J.M Jansen, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (+)-(1R,2R,4S,4aS,8aS)-4-(acetyloxy)-1-((3E)-5-(acetyloxy)-3-methyl-3-pentenyl)-2,5,5,8a-tetramethyl-decahydro-2-naphthalenyl acetate
C24H38O4     ÏàËÆ¶È:53.8%
Tetrahedron          2001          57          8369-8379
The synthesis of Ambrox®-like compounds starting from (+)-larixol. Part 2
Marjon G Bolster, B¨¦atrice M.F Lagnel, Ben J.M Jansen, Christophe Morin, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ent-18,3¦Â,7¦Á,17-Tetracetoxy-15¦Â,16bepoxykaurane
28H40O9     ÏàËÆ¶È:53.5%
Phytochemistry          2005          66          1492-1498
ent-Kauranoid derivatives from Sideritis moorei
Hanae Ghoumari, Mohamed-Hassan Benajiba, Amina Azmani,Andr¨¦s Garc¨ªa-Granados, Antonio Mart¨ªnez, Andr¨¦s Parra,Francisco Rivas, Oswaldo Socorro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     cyclo(L-Val-D-Ile-L-Leu-L-pro-D-Leu)
C28H49N5O5     ÏàËÆ¶È:53.5%
Journal of Natural Products          2011          74          1303-1308
Isolation and Structural Elucidation of Proline-Containing Cyclopentapeptides from an Endolichenic Xylaria sp.
Wen Wu, Huanqin Dai, Li Bao, Biao Ren, Jingcai Lu, Yuanming Luo, Liangdong Guo, Lixin Zhang, and Hongwei Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     6¦Á-hydroxyhop-21¦ÂH-22(29)-en
C30H50O     ÏàËÆ¶È:52%
Pharmaceutical Biology          2006          44          217-220
Chemistry and Bioactivity of Physciaceae Lichens Pyxine consocians. and Heterodermia leucomelos.
Selvaluxmy Kathirgamanathar, W.D. Ratnasooriya, Peter Baekstrom, Raymond J. Andersen, Veranja Karunaratne
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     krempfielin J
C23H38O5     ÏàËÆ¶È:52%
Marine Drugs          2013          11          2741-2750
Krempfielins J-M, New Eunicellin-Based Diterpenoids from the Soft Coral Cladiella krempfi
Yan-Ning Lee, Chi-Jen Tai, Tsong-Long Hwang and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3¦Á-acetoxi-22(R),23-epoxi-24-nor-5¦Â-colan-12-ona
C25H38O4     ÏàËÆ¶È:52%
Journal of the Chilean Chemical Society          2002          47          511-516
SINTESIS Y ACTIVIDAD BIOLOGICA DE ANALOGOS DE BRASINOESTEROIDES
LUIS ESPINOZA C Y MANUEL CORTES M*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     3¦Á,11¦Á,20-Triacetoxy-1¦Â-iodo-5¦Â-pregnane
C27H41IO6     ÏàËÆ¶È:51.8%
Steroids          2011          76          1458-1464
Microwave assisted preparation of C(1)-C(11) oxygen-bridged pregnanes
Lautaro D. Alvarez, Juan M. Sonego, Adriana S. Veleiro, Gerardo Burton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     compound 37
C29H48O3     ÏàËÆ¶È:51.7%
Journal of the American Chemical Society          2010          132          5300-5308
Biomimetic Syntheses from Squalene-Like Precursors: Synthesis of ent-Abudinol B and Reassessment of the Structure of Muzitone
Matthew A. Boone, Rongbiao Tong, Frank E. McDonald, Sheri Lense, Rui Cao and Kenneth I. Hardcastle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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