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Katharine3628
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
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yuhe0920: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2014-09-30 17:03:37
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yuhe0920: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2014-09-30 17:03:37
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²éѯ½á¹û£º¹²²éµ½18¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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