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yuhe0920

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1 .     8¦Â-acetoxy-12¦Â-hydroxy-epidihydrolycopodine
C18H29NO4     ÏàËÆ¶È:66.6%
Journal of Asian Natural Products Research          2014          16          574-580
New Lycopodium alkaloids from Phlegmariurus squarrosus
Fei Liu, Liao-Bin Dong, Xiu Gao, Xing-De Wu, Juan He, Li-Yan Peng, Xiao Cheng & Qin-Shi Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     valinomycin
C54H90N6O18     ÏàËÆ¶È:55.5%
Natural Product Sciences          2007          13          144-147
Antifungal Activity of Valinomycin, a Cyclodepsipeptide from Streptomyces padanus TH-04
Lim, Tae-Heon; Oh, Hyun-Cheol; Kwon, Soon-Youl; Kim, Jin-Ho; Seo, Hyo-Won; Lee, Jeong-Hun; Kim, Jin-Cheol; Lim, Chi-Hwan; Cha, Byeong-Jin; Min, Byung-Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     6¦Á,11¦Á-epoxyryanodane-1¦Á,5¦Â,7¦Â,11¦Â,13¦Â,14¦Á-hexaol
C20H3207     ÏàËÆ¶È:55%
Phytochemistry          2007          68          1735-1739
Ryanodane diterpenes from two Erythroxylum species
Marizeth L. Barreiros, Juceni P. David, Jorge M. David,Lucia M. Xavier Lopes, Matheus S. de Sab, JoseF.O. Costa, Mara Z. Almeida,Luciano P. de Queiroz, Antonio E.G. Sant¡¯Ana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     N-[N'-(16-acetoxyhexadecyl)thiocarbamoyl]-1,6-anhydro-L-idonojirimycin
C25H46N2O6S     ÏàËÆ¶È:55%
ChemBioChem          2013          14          943-949
Bicyclic Derivatives of L-Idonojirimycin as Pharmacological Chaperones for Neuronopathic Forms of Gaucher Disease (pages 943¨C949)
Dr. Pilar Alfonso, Dr. Vanesa Andreu, Dr. Almudena Pino-Angeles, Dr. Aurelio A. Moya-Garc¨ªa, Dr. M. Isabel Garc¨ªa-Moreno, Prof. Jos¨¦ C. Rodr¨ªguez-Rey, Prof. Francisca S¨¢nchez-Jim¨¦nez, Prof. Miguel Pocov¨ª, Prof. Carmen Ortiz Mellet, Prof. Jose M. Garc¨ªa Fe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (1S)-1-C-[4-(adamant-1-ylmethoxy)butyl]-N-butyl-1-deoxynojirimycin
C25H45NO5     ÏàËÆ¶È:52.6%
European Journal of Organic Chemistry          2010                   1258-1283
Synthesis and Evaluation of Lipophilic Aza-C-glycosides as Inhibitors of Glucosylceramide Metabolism
Tom Wennekes, Richard J. B. H. N. van den Berg, Thomas J. Boltje, Wilma E. Donker-Koopman, Bastiaan Kuijper, Gijsbert A. van der Marel, Anneke Strijland, Carlo P. Verhagen, Johannes M. F. G. Aerts and Herman S. Overkleeft
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     rosiridoside C
C18H30O8     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2008          56(5)          695-700
Reinvestigation of Absolute Stereostructure of (-)-Rosiridol: Structures of Monoterpene Glycosides, Rosiridin, Rosiridosides A, B, and C, from Rhodiola sachalinensis
Masayuki YOSHIKAWA,Seikou NAKAMURA, Xuezheng LI, and Hisashi MATSUDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     canusesnol C
C15H24O4     ÏàËÆ¶È:50%
Journal of Natural Products          2004          67          1893-1896
New Sesquiterpenes from Capsicum annuum
Yousuke Kawaguchi, Toshimasa Ochi, Yoshihisa Takaishi, Kazuyoshi Kawazoe, and Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (S)-N-methyl-tert-leucyl-(S)-tert-leucyl-(2e,4S)-N-methyl-4-amino-2,5-dimethylhex-2-enoic acid
C18H31N3O4     ÏàËÆ¶È:50%
Journal of Natural Products          2003          66          183-199
Synthesis and Antimitotic/Cytotoxic Activity of Hemiasterlin Analogues
James A. Nieman, John E. Coleman, Debra J. Wallace, Edward Piers, Lynette Y. Lim, Michel Roberge, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     15,16,17-trihydroxy-7-oxopima¦Á-8(9)-ene
C20H32O4     ÏàËÆ¶È:50%
Journal of Natural Products          2002          65          1742-1745
Structure and Absolute Configuration of New Diterpenes from Lavandula multifida
Matteo Politi,Nunziatina De Tommasi, Gennaro Pescitelli, Lorenzo Di Bari, Ivano Morelli, and Alessandra Braca
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Compound 3d
C27H54NO6     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry Letters          2007          17          6643-6646
Synthesis of novel phytosphingosine derivatives and their preliminary biological evaluation for enhancing radiation therapy
Byung Seok Moon, Moon-Taek Park, Jeong Hoon Park, Sang Wook Kim, Kyo Chul Lee, Gwang Il An, Seung Dae Yang, Dae Yoon Chi, Gi Jeong Cheon, Su-Jae Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Penazetidine A
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry Letters          1994          4          2447-2450
Penazetidine A, an alkaloid inhibitor of protein kinase C
Khisal A. Alvi, Marcel Jaspars, Phillip Crews, Berta Strulovici, Edwin Oto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     sorbitol1,2,5,6-tetradecanoate
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          1994          2          707-713
Regioselectivity and fatty acid specificity of Chromobacterium viscosum lipase
Ra¨²l J. Barros, Pedro G.V. Moura-Pinto, Maurice C.R. Franssen, de Groot Aede, Anja E.M. Janssen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Cernuine N-oxide
C16H26N2O2     ÏàËÆ¶È:50%
Tetrahedron          2004          60          7015-7023
New phlegmarane-type, cernuane-type, and quinolizidine alkaloids from two species of Lycopodium
Hiroshi Morita, Yusuke Hirasawa, Takakazu Shinzato, Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     cernuine
    ÏàËÆ¶È:50%
Tetrahedron          2004          60          7015-7023
New phlegmarane-type, cernuane-type, and quinolizidine alkaloids from two species of Lycopodium
Hiroshi Morita, Yusuke Hirasawa, Takakazu Shinzato, Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (2S,3R,4S)-4-acetamido-2-tetradecyltetrahydrofuran-3-yl acetate
C22H41NO4     ÏàËÆ¶È:50%
Tetrahedron          2013          69          8228-8244
A common approach to the total synthesis of l-arabino-, l-ribo-C18-phytosphingosines, ent-2-epi-jaspine B and 3-epi-jaspine B from d-mannose
Miroslava Martinkov¨¢, Kvetoslava Pomikalov¨¢, Jozef Gonda, M¨¢ria Vilkov¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (2S,3R,4R)-4-acetamido-2-tetradecyltetrahydrofuran-3-yl acetate
C22H41NO4     ÏàËÆ¶È:50%
Tetrahedron          2013          69          8228-8244
A common approach to the total synthesis of l-arabino-, l-ribo-C18-phytosphingosines, ent-2-epi-jaspine B and 3-epi-jaspine B from d-mannose
Miroslava Martinkov¨¢, Kvetoslava Pomikalov¨¢, Jozef Gonda, M¨¢ria Vilkov¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (2S,3R,4S)-Penazetidine A
C23H47O2N     ÏàËÆ¶È:50%
European Journal of Organic Chemistry          1996          1996          1083-1089
Synthesis of Sphingosine Relatives, XVIII!. Synthesis of Penazetidine A, an Alkaloid Inhibitor of Protein Kinase C Isolated from the Marine Sponge Penares sollasi
Arata Yajima, Hirosato Takikawa and Kenji Mori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     compound (12'S)-1a
C23H47O2N     ÏàËÆ¶È:50%
European Journal of Organic Chemistry          1996          1996          1083-1089
Synthesis of Sphingosine Relatives, XVIII!. Synthesis of Penazetidine A, an Alkaloid Inhibitor of Protein Kinase C Isolated from the Marine Sponge Penares sollasi
Arata Yajima, Hirosato Takikawa and Kenji Mori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2014-09-30 16:26:22
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