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(2S,3R,2 R,4E,8E)-N-(2-hydroxyeicosanosyl)-9-methyl-1,3-dihydroxy-2-amino-4,8-nonadecadiene ÏàËÆ¶È:80% Acta Scientiarum Naturalium Universitatis Sunyatseni 2007 46(4) 116-118 The Secondary Metabolite of the Soft Coral Cespitularia cocerulea May(¢ò) HE Xi-xin, YAN Su-jun, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . menthalactone C23H41NO3 ÏàËÆ¶È:78.2% Zeitschrift f¨¹r Naturforschung C 2009 64 809-812 Menthalactone, a New Analgesic from Mentha cordifolia Opiz. Leaves I. M. Villaseñor and A. C. Sanchez Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . N-(2-Hydroxyhexadecanoyl)-4-sphingenine ÏàËÆ¶È:77.2% Helvetica Chimica Acta 2004 Vol. 87 1912 Vibratilicin: a Novel Compound from the Basidiomycete Cortinarius vibratilis Fei Wang, Jian-Wen Tan, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (2S,3R,2'R,4E)-2'-hydroxy-C6-ceramide C24H47NO4 ÏàËÆ¶È:77.2% Bioorganic & Medicinal Chemistry 2010 18 7565-7579 Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (2S,3R,2'S,4E)-2'-hydroxy-C6-ceramide C24H47NO4 ÏàËÆ¶È:77.2% Bioorganic & Medicinal Chemistry 2010 18 7565-7579 Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (2S,3R,2'R,4E)-2'-hydroxy-C16-ceramide C34H67NO4 ÏàËÆ¶È:77.2% Bioorganic & Medicinal Chemistry 2010 18 7565-7579 Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (2S,3R,2'S,4E)-2'-hydroxy-C16-ceramides ÏàËÆ¶È:77.2% Bioorganic & Medicinal Chemistry 2010 18 7565-7579 Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦¤4,5(E),¦¤8,9(E)-sphingol-n-hexadecamide ÏàËÆ¶È:77.2% Acta Scientiarum Naturalium Universitatis Sunyatseni 2007 46(4) 116-118 The Secondary Metabolite of the Soft Coral Cespitularia cocerulea May(¢ò) HE Xi-xin, YAN Su-jun, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (24S)-ergost-5-ene-3¦Â,7¦Á-diol ÏàËÆ¶È:77.2% Acta Scientiarum Naturalium Universitatis Sunyatseni 2005 44(5) 113-115 Studies on the Secondary Metabolite of the Soft Coral Lobophytum sp. (¢ò) HE Xi-xin, YAN Su-jun, ZENG Long-mei, SU Jing-yu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ¡÷4,5(E),¡÷8,9(E)-sphingol-n-hexanecamide ÏàËÆ¶È:77.2% Acta Scientiarum Naturalium Universitatis Sunyatseni 2002 41(6) 38-41 Studies on the Secondary Metabolites of the Soft Coral Sinularia grayi Tix.-Dur. MA Xiang-quan, ZHANG Guang-wen, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ¡÷4,5(E),¡÷8,9(E)-sphingol-n-hexanecamide ÏàËÆ¶È:77.2% Acta Scientiarum Naturalium Universitatis Sunyatseni 2002 41(2) 114-116 Studies on Chemical Constitutions of the Soft Coral Sinularia cervicornis Tix.-Dur. HE Xi-xin, YANG Ruo-lin, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (2S,2'R,3R,4E,8E)-N-2'-Hydroxyhexadecanoyl-2-amino-9-methyl-4,8-octadecadiene-1,3-diol C35H67NO4 ÏàËÆ¶È:73.9% Chemical & Pharmaceutical Bulletin 2002 50(5) 681-684 Ceramide Constituents from Five Mushrooms Yasunori YAOITA, Rie KOHATA, Rie KAKUDA, Koichi MACHIDA, and Masao KIKUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 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²éѯ½á¹û£º¹²²éµ½3011¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . natural (2'R)-2'-hydroxy-C18-ceramide C42H82NO4 ÏàËÆ¶È:86.3% Bioorganic & Medicinal Chemistry 2010 18 7565-7579 Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 2 C42H84NO4 ÏàËÆ¶È:81.8% Natural Product Research 2009 23 44-50 Isolation and structure determination of the biologically active sphingolipids from marine sponge Haliclona species Seif-Eldin N. Ayyad; Saleh Omar S. Bahaffi; Nadia E. Hashish Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (2S,3R,2 R,4E,8E)-N-(2-hydroxyeicosanosyl)-9-methyl-1,3-dihydroxy-2-amino-4,8-nonadecadiene ÏàËÆ¶È:80% Acta Scientiarum Naturalium Universitatis Sunyatseni 2007 46(4) 116-118 The Secondary Metabolite of the Soft Coral Cespitularia cocerulea May(¢ò) HE Xi-xin, YAN Su-jun, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . menthalactone C23H41NO3 ÏàËÆ¶È:78.2% Zeitschrift f¨¹r Naturforschung C 2009 64 809-812 Menthalactone, a New Analgesic from Mentha cordifolia Opiz. Leaves I. M. Villaseñor and A. C. Sanchez Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . N-(2-Hydroxyhexadecanoyl)-4-sphingenine ÏàËÆ¶È:77.2% Helvetica Chimica Acta 2004 Vol. 87 1912 Vibratilicin: a Novel Compound from the Basidiomycete Cortinarius vibratilis Fei Wang, Jian-Wen Tan, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (2S,3R,2'R,4E)-2'-hydroxy-C6-ceramide C24H47NO4 ÏàËÆ¶È:77.2% Bioorganic & Medicinal Chemistry 2010 18 7565-7579 Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (2S,3R,2'S,4E)-2'-hydroxy-C6-ceramide C24H47NO4 ÏàËÆ¶È:77.2% Bioorganic & Medicinal Chemistry 2010 18 7565-7579 Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (2S,3R,2'R,4E)-2'-hydroxy-C16-ceramide C34H67NO4 ÏàËÆ¶È:77.2% Bioorganic & Medicinal Chemistry 2010 18 7565-7579 Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (2S,3R,2'S,4E)-2'-hydroxy-C16-ceramides ÏàËÆ¶È:77.2% Bioorganic & Medicinal Chemistry 2010 18 7565-7579 Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦¤4,5(E),¦¤8,9(E)-sphingol-n-hexadecamide ÏàËÆ¶È:77.2% Acta Scientiarum Naturalium Universitatis Sunyatseni 2007 46(4) 116-118 The Secondary Metabolite of the Soft Coral Cespitularia cocerulea May(¢ò) HE Xi-xin, YAN Su-jun, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (24S)-ergost-5-ene-3¦Â,7¦Á-diol ÏàËÆ¶È:77.2% Acta Scientiarum Naturalium Universitatis Sunyatseni 2005 44(5) 113-115 Studies on the Secondary Metabolite of the Soft Coral Lobophytum sp. (¢ò) HE Xi-xin, YAN Su-jun, ZENG Long-mei, SU Jing-yu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ¡÷4,5(E),¡÷8,9(E)-sphingol-n-hexanecamide ÏàËÆ¶È:77.2% Acta Scientiarum Naturalium Universitatis Sunyatseni 2002 41(6) 38-41 Studies on the Secondary Metabolites of the Soft Coral Sinularia grayi Tix.-Dur. MA Xiang-quan, ZHANG Guang-wen, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ¡÷4,5(E),¡÷8,9(E)-sphingol-n-hexanecamide ÏàËÆ¶È:77.2% Acta Scientiarum Naturalium Universitatis Sunyatseni 2002 41(2) 114-116 Studies on Chemical Constitutions of the Soft Coral Sinularia cervicornis Tix.-Dur. HE Xi-xin, YANG Ruo-lin, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (2S,2'R,3R,4E,8E)-N-2'-Hydroxyhexadecanoyl-2-amino-9-methyl-4,8-octadecadiene-1,3-diol C35H67NO4 ÏàËÆ¶È:73.9% Chemical & Pharmaceutical Bulletin 2002 50(5) 681-684 Ceramide Constituents from Five Mushrooms Yasunori YAOITA, Rie KOHATA, Rie KAKUDA, Koichi MACHIDA, and Masao KIKUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (2S,3S,4R,10E)-2-[(2R)-2-hydroxytetracosanoylamino]10-octadecene-1,3,4-triol ÏàËÆ¶È:73.9% Natural Product Research and Development 2006 18 411-414 Phytochemical Study on Zehneria maysorensis LI Hong-juan;LUO Ying-gang; HE Zhi-heng; ZHANG Guo-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1,4-dideoxy-5-O-[(9Z,12Z)-octadeca-9,12-dien-1-yl]-1,4-imino-D-ribitol C23H43NO3 ÏàËÆ¶È:73.9% Bioorganic & Medicinal Chemistry 2011 19 7720-7727 Anti-cancer activity of 5-O-alkyl 1,4-imino-1,4-dideoxyribitols Claudia Bello, Giovanna Dal Bello, Michele Cea, Aimable Nahimana, Dominique Aubry, Anna Garuti, Giulia Motta, Eva Moran, Floriana Fruscione, Paolo Pronzato, Francesco Grossi, Franco Patrone, Alberto Ballestrero, Marc Dupuis, Bernard Sordat, Kaspar Zimmermann, Jacqueline Loretan, Markus Wartmann, Michel A. Duchosal, Alessio Nencioni, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (2S,3R)-1-O-(¦Á-D-galactopyranosyl)-2-[N-(R)-2-hydroxytetracosanoyl)amino]-1,3-octadecanediol C48H95NO9 ÏàËÆ¶È:73.9% Journal of Medicinal Chemistry 1995 38 2176-2187 Structure-Activity Relationship of .alpha.-Galactosylceramides against B16-Bearing Mice Masahiro Morita, Kazuhiro Motoki, Kohji Akimoto, Takenori Natori, Teruyuki Sakai, Eiji Sawa, Kazuo Yamaji, Yasuhiko Koezuka, Eiichi Kobayashi, Hideaki Fukushima Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . N-1-ôÇ»ù¼×»ù-2-ôÇ»ù-(E,E)-3,7-Ê®Æß̼¶þÏ©»ùÊ®ÁùÖ¬·¾õ£°· C34H65NO3 ÏàËÆ¶È:73.9% Journal of Chinese Medicinal Materials 1999 22 75-77 Studies on the Chemical Constituents of Soft Coral Sarcophyton elegans Suo Qiliang, Zhang Min Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (3R)-hydroxy-14-methyldocos-(4E)-en-1-yne C23H42O ÏàËÆ¶È:72.7% Journal of Natural Products 1992 Vol 55 1275 Further Bioactive Acetylenic Compounds from the Caribbean Sponge Cribrochalina vasculum Anna Aiello, Ernesto Fattorusso, Marialuisa Menna, Maurizio Pansini Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (2S,3S,4R,9Z)-2-[(R)-2-acetoxypentadecanoylamino]-9-docosen-1,3,4-triol C39H75NO6 ÏàËÆ¶È:72.7% Bulletin of the Chemical Society of Japan 1998 71 259-272 Total Synthesis of Acanthacerebroside A and Astrocerebroside A via a Chiral Epoxide Intermediate Derived from L-Quebrachitol Noritaka Chida, Noboru Sakata, Katsuyuki Murai, Takahiko Tobe, Toshihiko Nagase, Seiichiro Ogawa Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 1,2-di-O-linoleoylglycerol C39H68O5 ÏàËÆ¶È:72.7% Natural Product Communications 2012 7 917-918 Search for Bioactive Compounds from Cantharellus cibarius Włodzimierz Maria Daniewskia, Witold Danikiewiczb , W. Marek Gołębiewskic,* Mirosław Gucmac,Agnieszka Łysikc, Jacek Grodnerc and Elżbieta Przybyszc Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ¡÷4,5(E),¡÷8,9(E)-sphingol-n-hexadecamide C34H65NO3 ÏàËÆ¶È:72.7% Academic Journal of Second Military Medical University 2002 23 250-253 Chemical constituents of marine sea anemone Anthopleura pacific(¢ñ) ZHANG Shu Yu, YI Yang Hua, TANG Hai Feng, XU Qiang Zhi, ZOU Zheng Rong, LI Ling Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 1 C34H65NO3 ÏàËÆ¶È:72.7% Indian Journal of Chemistry Section B 1996 35B 578-580 New spingosines from two soft corals of the Andaman & Nicobar Islands C Subrahmanyam, R Kulatheeswaran & C Venkateswara Rao Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (15S,16S)-15-methoxy-16-methyl-tetratriacontan-1-ol C36H74O2 ÏàËÆ¶È:72.7% Tetrahedron 2013 69 6285-6296 The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird Structure 13C NMR ̼Æ×Ä£Äâͼ |
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