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²éѯ½á¹û£º¹²²éµ½466¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 3b-linoleyloxyergost-7-ene ÏàËÆ¶È:64.5% Phytochemistry 2000 54 603-610 Constituents of various wood-rotting basidiomycetes Joachim Rösecke, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate ÏàËÆ¶È:62.5% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3b-linoleyloxyergosta-7,22-diene ÏàËÆ¶È:62.5% Phytochemistry 2000 54 603-610 Constituents of various wood-rotting basidiomycetes Joachim Rösecke, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . pentacetylfusapyrone ÏàËÆ¶È:62.5% Natural Toxins 1994 2 4-13 Fusapyrone and deoxyfusapyrone, two antifungal ¦Á-Pyrones From Fusarium semitectum Antonio Evidente, Luigi Conti, Claudio Altomare, Antonio Bottalico, Giovanni Sindona, Anna Laura Segre and Antonio Logrieco Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid C45H78O4 ÏàËÆ¶È:62.5% Life Sciences 2013 92 202-210 Antiulcer and antioxidant activities of a new steroid from Morus alba Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (1S,2R,3R,4aR,6aS,7R,8R,10aR,10bR,12aR)-Benzyl-3-acetoxy-2-((S)-2-(((benzyloxy)carbonyl)(methyl)amino)-2,3-dimethylbutoxy)-1,6a,8,10a-tetramethyl-8-((R)-3-methylbutan-2-yl)-2,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-1,4a-(methanooxymethano)ch C54H77NO8 ÏàËÆ¶È:61.2% The Journal of Organic Chemistry 2012 77 3297-3310 Synthesis of Antifungal Glucan Synthase Inhibitors from Enfumafungin Yong-Li Zhong, Donald R. Gauthier, Jr., Yao-Jun Shi, Mark McLaughlin, John Y. L. Chung, Philippe Dagneau, Benjamin Marcune, Shane W. Krska, Richard G. Ball, Robert A. Reamer, and Nobuyoshi Yasuda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (3¦Â,5¦Á,6¦Á,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate C46H76O4 ÏàËÆ¶È:60.4% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . georgamide C46H69O10N5 ÏàËÆ¶È:60.4% Journal of Natural Products 2001 64 143-146 Georgamide, a New Cyclic Depsipeptide with an Alkynoic Acid Residue from an Australian Cyanobacterium Feng Wan and Karen L. Erickson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . xanthanthusin B C44H52O12 ÏàËÆ¶È:60.4% Acta Botanica Yunnanica 1993 15(4) 403-407 DITERPENOID QUINONES FROM COLEUS XANTHANTHUS LIChao-Ming, LIN Zhong-Wen. TAOGuo-Da, SUN Han-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 7¦Â-tert-Butyldimethylsilyloxysitosteryl oleate C53H96O3Si ÏàËÆ¶È:60.4% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . iristectorene A monoacetate ÏàËÆ¶È:60.4% Phytochemistry 1994 36 425-431 Iristectorenes A and C-G, monocyclic triterpene esters from Iris tectorum Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3-O-(4'-benzhydryloxy-3',3'-dimethylsuccinyl)-28-O-glutarylbetulin C54H74O8 ÏàËÆ¶È:60.4% Bioorganic & Medicinal Chemistry 2010 18 6451-6469 Conjugates of betulin derivatives with AZT as potent anti-HIV agents Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3-O-(5'-benzhydryloxygluta-ryl)-28-O-(2'',2''-dimethylsuccinyl)dihydrobetulin C54H76O8 ÏàËÆ¶È:60.4% Bioorganic & Medicinal Chemistry 2010 18 6451-6469 Conjugates of betulin derivatives with AZT as potent anti-HIV agents Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 3-O-(5'-benzhydryloxyglutaryl)-28-O-glutaryldihydro-betulin C53H74O8 ÏàËÆ¶È:60.4% Bioorganic & Medicinal Chemistry 2010 18 6451-6469 Conjugates of betulin derivatives with AZT as potent anti-HIV agents Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 6'-linoleic-¦Â-daucosterol C30H50O ÏàËÆ¶È:60.4% Natural Product Research and Development 2009 21 776-778 Chemical Constituents of the Roots of Ligularia fischeri DENG Mei-cai; JIAO Wei; DONG Wei-wei; LU Run-hua Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (1S,2R,3R,4aR,6aS,7R,8R,10aR,10bR,12aR)-Benzyl3-acetoxy-2-((S)-2,3-dimethyl-2-(methylamino)butoxy)-1,6a,8,10a-tetramethyl-8-((R)-3-methylbutan-2-yl)-2,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-1,4a-(methanooxymethano)chrysene-7-carboxylate C46H71NO6 ÏàËÆ¶È:60.4% The Journal of Organic Chemistry 2012 77 3297-3310 Synthesis of Antifungal Glucan Synthase Inhibitors from Enfumafungin Yong-Li Zhong, Donald R. Gauthier, Jr., Yao-Jun Shi, Mark McLaughlin, John Y. L. Chung, Philippe Dagneau, Benjamin Marcune, Shane W. Krska, Richard G. Ball, Robert A. Reamer, and Nobuyoshi Yasuda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (1S,2R,3R,4aR,6aS,7R,8R,10aR,10bR,12aR)-3-Acetoxy-2-((S)-2-(((benzyloxy)carbonyl)(methyl)amino)-2,3-dimethylbutoxy)-1,6a,8,10a-tetramethyl-8-((R)-3-methylbutan-2-yl)-2,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-1,4a-(methanooxymethano)chrysene- C47H71NO8 ÏàËÆ¶È:60.4% The Journal of Organic Chemistry 2012 77 3297-3310 Synthesis of Antifungal Glucan Synthase Inhibitors from Enfumafungin Yong-Li Zhong, Donald R. Gauthier, Jr., Yao-Jun Shi, Mark McLaughlin, John Y. L. Chung, Philippe Dagneau, Benjamin Marcune, Shane W. Krska, Richard G. Ball, Robert A. Reamer, and Nobuyoshi Yasuda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . compound 23 C52H86N8O12 ÏàËÆ¶È:60% Journal of Natural Products 2003 66 1356-1363 Isolation and Structure Determination of Lyngbyastatin 3, a Lyngbyastatin 1 Homologue from the Marine Cyanobacterium Lyngbya majuscula.Determination of the Configuration of the 4-Amino-2,2-dimethyl-3-oxopentanoic Acid Unit in Majusculamide C, Dolastatin 1 Philip G. Williams,Richard E. Moore,and Valerie J. Paul Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . leucinostatin A hydrochloride C62H111N11O13 ÏàËÆ¶È:58.8% The Journal of Antibiotics 1983 36 1606-1612 STUDIES ON PEPTIDE ANTIBIOTICS, LEUCINOSTATINS I. SEPARATION, PHYSICO-CHEMICAL PROPERTIES AND BIOLOGICAL ACTIVITIES OF LEUCINOSTATINS A AND B KAZUTAKA FUKUSHIMA, TADASHI ARAI, YUJI MORI, MAKOTO TSUBOI, MAKOTO SUZUKI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . Benzyl oleanolate 3-O-2,3,4,6-tetra-O-acetyl-¦Á-D-mannopyranoside C51H72O8 ÏàËÆ¶È:58.8% Molecules 2011 16 1113-1128 Synthesis and Anti-Fungal Activity of Seven Oleanolic Acid Glycosides Hanqing Zhao, Guanghui Zong, Jianjun Zhang, Daoquan Wang and Xiaomei Liang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-oleate ÏàËÆ¶È:58.3% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . homodolastatin 16 C48H72N6O10 ÏàËÆ¶È:58.3% Journal of Natural Products 2003 66 712-715 Isolation of Homodolastatin 16, a New Cyclic Depsipeptide from a Kenyan Collection of Lyngbya majuscula Michael T. Davies-Coleman, Thomas M. Dzeha, Christopher A. Gray, Sonja Hess, Lewis K. Pannell, Denver T. Hendricks, and Catherine E. Arendse Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . compound 27 C50H82N8O11 ÏàËÆ¶È:58.3% Journal of Natural Products 2003 66 1356-1363 Isolation and Structure Determination of Lyngbyastatin 3, a Lyngbyastatin 1 Homologue from the Marine Cyanobacterium Lyngbya majuscula.Determination of the Configuration of the 4-Amino-2,2-dimethyl-3-oxopentanoic Acid Unit in Majusculamide C, Dolastatin 1 Philip G. Williams,Richard E. Moore,and Valerie J. Paul Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . gymnasterone A C45H67NO5 ÏàËÆ¶È:58.3% Journal of Natural Products 2007 70 1731-1740 Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source Taro Amagata,Makoto Tanaka,Takeshi Yamada, Mitsunobu Doi, Katsuhiko Minoura, Hirofumi Ohishi,Takao Yamori, and Atsushi Numata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 3-O-tetradecanoyl-16-O-acetylisoiridogermanal C46H78O6 ÏàËÆ¶È:58.3% Journal of Natural Products 1999 62 89-93 Iridal-Type Triterpenoids with Ichthyotoxic Activity from Belamcanda chinensis Hideyuki Ito, Satomi Onoue, Yoko Miyake, and Takashi Yoshida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . xanthanthusin C C44H52O12 ÏàËÆ¶È:58.3% Acta Botanica Yunnanica 1993 15(4) 403-407 DITERPENOID QUINONES FROM COLEUS XANTHANTHUS LIChao-Ming, LIN Zhong-Wen. TAOGuo-Da, SUN Han-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . 3¦Â-Acetoxy-7¦Â-tert-butyldimethylsilyloxystigma-5-ene C37H66O3Si ÏàËÆ¶È:58.3% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . Iristectorene B monoacetate C46H78O6 ÏàËÆ¶È:58.3% Phytochemistry 1994 36 433-438 Iristectorene B, a monocyclic triterpene ester from Iris tectorum Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . BRM-14 C46H70BO15 ÏàËÆ¶È:58.3% Heterocycles 2010 82 289-295 Boromycin Derivatives: Synthesis and Antimalarial Activity in vitro and in vivo Ayumi Tsutsui, Yujiro Furuya, Tomoyasu Hirose, Riyon Kim, Rokurou Masuma, Atsuko Matsumoto, Yoko Takahashi, Aki Ishiyama, Miyuki Namatame, Kazuhiko Otoguro, Satoshi ¨mura, and Toshiaki Sunazuka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . Compound 7 C33H37N4O3F ÏàËÆ¶È:58.3% Bioorganic & Medicinal Chemistry Letters 1997 7 799-804 Synthesis and evaluation of halogenated dibenzodiazepines as muscarinic receptor ligands Michael Kassiou, Roger W. Read, Xue-qin Shi Structure 13C NMR ̼Æ×Ä£Äâͼ |
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½1043¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3b-linoleyloxyergost-7-ene ÏàËÆ¶È:64.5% Phytochemistry 2000 54 603-610 Constituents of various wood-rotting basidiomycetes Joachim Rösecke, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-O-[6'-O-n-acyl-¦Â-D-glucosyl]-22-dehydroclerosterol ÏàËÆ¶È:64.5% Phytochemistry 1994 36 167-170 Acylglucosylsterols from two Aegiphila species Suzana G. Leitão, Maria Auxiliadora C. Kaplan, Franco Delle Monache Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate ÏàËÆ¶È:62.5% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3b-linoleyloxyergosta-7,22-diene ÏàËÆ¶È:62.5% Phytochemistry 2000 54 603-610 Constituents of various wood-rotting basidiomycetes Joachim Rösecke, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . pentacetylfusapyrone ÏàËÆ¶È:62.5% Natural Toxins 1994 2 4-13 Fusapyrone and deoxyfusapyrone, two antifungal ¦Á-Pyrones From Fusarium semitectum Antonio Evidente, Luigi Conti, Claudio Altomare, Antonio Bottalico, Giovanni Sindona, Anna Laura Segre and Antonio Logrieco Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid C45H78O4 ÏàËÆ¶È:62.5% Life Sciences 2013 92 202-210 Antiulcer and antioxidant activities of a new steroid from Morus alba Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (1S,2R,3R,4aR,6aS,7R,8R,10aR,10bR,12aR)-Benzyl-3-acetoxy-2-((S)-2-(((benzyloxy)carbonyl)(methyl)amino)-2,3-dimethylbutoxy)-1,6a,8,10a-tetramethyl-8-((R)-3-methylbutan-2-yl)-2,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-1,4a-(methanooxymethano)ch C54H77NO8 ÏàËÆ¶È:61.2% The Journal of Organic Chemistry 2012 77 3297-3310 Synthesis of Antifungal Glucan Synthase Inhibitors from Enfumafungin Yong-Li Zhong, Donald R. Gauthier, Jr., Yao-Jun Shi, Mark McLaughlin, John Y. L. Chung, Philippe Dagneau, Benjamin Marcune, Shane W. Krska, Richard G. Ball, Robert A. Reamer, and Nobuyoshi Yasuda Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2014-08-04 15:38:21
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²éѯ½á¹û£º¹²²éµ½466¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3b-linoleyloxyergost-7-ene ÏàËÆ¶È:64.5% Phytochemistry 2000 54 603-610 Constituents of various wood-rotting basidiomycetes Joachim Rösecke, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate ÏàËÆ¶È:62.5% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3b-linoleyloxyergosta-7,22-diene ÏàËÆ¶È:62.5% Phytochemistry 2000 54 603-610 Constituents of various wood-rotting basidiomycetes Joachim Rösecke, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . pentacetylfusapyrone ÏàËÆ¶È:62.5% Natural Toxins 1994 2 4-13 Fusapyrone and deoxyfusapyrone, two antifungal ¦Á-Pyrones From Fusarium semitectum Antonio Evidente, Luigi Conti, Claudio Altomare, Antonio Bottalico, Giovanni Sindona, Anna Laura Segre and Antonio Logrieco Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid C45H78O4 ÏàËÆ¶È:62.5% Life Sciences 2013 92 202-210 Antiulcer and antioxidant activities of a new steroid from Morus alba Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (1S,2R,3R,4aR,6aS,7R,8R,10aR,10bR,12aR)-Benzyl-3-acetoxy-2-((S)-2-(((benzyloxy)carbonyl)(methyl)amino)-2,3-dimethylbutoxy)-1,6a,8,10a-tetramethyl-8-((R)-3-methylbutan-2-yl)-2,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-1,4a-(methanooxymethano)ch C54H77NO8 ÏàËÆ¶È:61.2% The Journal of Organic Chemistry 2012 77 3297-3310 Synthesis of Antifungal Glucan Synthase Inhibitors from Enfumafungin Yong-Li Zhong, Donald R. Gauthier, Jr., Yao-Jun Shi, Mark McLaughlin, John Y. L. Chung, Philippe Dagneau, Benjamin Marcune, Shane W. Krska, Richard G. Ball, Robert A. Reamer, and Nobuyoshi Yasuda Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (3¦Â,5¦Á,6¦Á,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate C46H76O4 ÏàËÆ¶È:60.4% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . georgamide C46H69O10N5 ÏàËÆ¶È:60.4% Journal of Natural Products 2001 64 143-146 Georgamide, a New Cyclic Depsipeptide with an Alkynoic Acid Residue from an Australian Cyanobacterium Feng Wan and Karen L. Erickson Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . xanthanthusin B C44H52O12 ÏàËÆ¶È:60.4% Acta Botanica Yunnanica 1993 15(4) 403-407 DITERPENOID QUINONES FROM COLEUS XANTHANTHUS LIChao-Ming, LIN Zhong-Wen. TAOGuo-Da, SUN Han-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 7¦Â-tert-Butyldimethylsilyloxysitosteryl oleate C53H96O3Si ÏàËÆ¶È:60.4% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . iristectorene A monoacetate ÏàËÆ¶È:60.4% Phytochemistry 1994 36 425-431 Iristectorenes A and C-G, monocyclic triterpene esters from Iris tectorum Katsura Seki, Toshiya Tomihari, Kazuo Haga, Ryohei Kaneko Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3-O-(4'-benzhydryloxy-3',3'-dimethylsuccinyl)-28-O-glutarylbetulin C54H74O8 ÏàËÆ¶È:60.4% Bioorganic & Medicinal Chemistry 2010 18 6451-6469 Conjugates of betulin derivatives with AZT as potent anti-HIV agents Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-O-(5'-benzhydryloxygluta-ryl)-28-O-(2'',2''-dimethylsuccinyl)dihydrobetulin C54H76O8 ÏàËÆ¶È:60.4% Bioorganic & Medicinal Chemistry 2010 18 6451-6469 Conjugates of betulin derivatives with AZT as potent anti-HIV agents Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2014-08-05 09:20:46













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