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²éѯ½á¹û£º¹²²éµ½12087¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . aspochracin ÏàËÆ¶È:95.6% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . JBIR-15 C22H34N4O4 ÏàËÆ¶È:90.9% Bioscience, Biotechnology, and Biochemistry 2009 73 1898-1900 JBIR-15, a New Aspochracin Derivative, Isolated from a Sponge-Derived Fungus, Aspergillus sclerotiorum Huber Sp080903f04 Keiichiro MOTOHASHI, Shigeki INABA, Motoki TAKAGI and Kazuo SHIN-YA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . sclerotiotide C C24H38N4O4 ÏàËÆ¶È:86.9% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . sclerotiotide E C23H36N4O4 ÏàËÆ¶È:86.9% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . sclerotiotide I C23H38N4O6 ÏàËÆ¶È:86.9% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . sclerotiotide K C23H38N4O6 ÏàËÆ¶È:86.9% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . sclerotiotide B C21H34N4O4 ÏàËÆ¶È:86.3% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . sclerotiotide D C22H34N4O4 ÏàËÆ¶È:86.3% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . sclerotiotide G C23H36N4O6 ÏàËÆ¶È:82.6% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . sclerotiotide H C23H38N4O6 ÏàËÆ¶È:82.6% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . sclerotiotide J C23H38N4O6 ÏàËÆ¶È:82.6% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . sclerotiotide A C22H34N4O4 ÏàËÆ¶È:81.8% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Sclerotiotide F C21H33N4O5 ÏàËÆ¶È:77.2% Phytochemistry Letters 2012 5 114-117 Unraveling the numerous biosynthetic products of the marine sediment-derived fungus,Aspergillus insulicola Q.X. Wu,X.J. Jin,M. Draskovic,M.S. Crews,K. Tenney,F.A. Valeriote,X.J. Yao,P. Crews Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 12q C25H31ClN2O4S ÏàËÆ¶È:73.9% The Journal of Organic Chemistry 2012 77 7435-7470 Assembly of Four Diverse Heterocyclic Libraries Enabled by Prins Cyclization, Au-Catalyzed Enyne Cycloisomerization, and Automated Amide Synthesis Jiayue Cui, David I. Chai, Christopher Miller, Jason Hao, Christopher Thomas, JingQi Wang, Karl A. Scheidt, and Sergey A. Kozmin Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . sclerotiotide F C21H32N4O5 ÏàËÆ¶È:72.7% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . N-{[2'-(1H-Tetrazol-5-yl)biphenyl-4-yl]methyl}-N-methyl-1-pentanoylpyrrolidine-2-carboxamide C25H30N6O2 ÏàËÆ¶È:72.7% Archiv der Pharmazie 2011 344 617-626 1-Pentanoyl-N-{[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-pyrrolidine-2-carboxamide: Investigation of Structural Variations Alessia Catalano, Alessia Carocci, Antonia Di Mola, Claudio Bruno, Patrick M. L. Vanderheyden,and Carlo Franchini Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Pre-sclerotiotide C20H30N4O5 ÏàËÆ¶È:72.7% Phytochemistry Letters 2012 5 114-117 Unraveling the numerous biosynthetic products of the marine sediment-derived fungus,Aspergillus insulicola Q.X. Wu,X.J. Jin,M. Draskovic,M.S. Crews,K. Tenney,F.A. Valeriote,X.J. Yao,P. Crews Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (2'E)-1,4-diacetoxy-2-(3',7'-dimethylocta-2',6'-dienyl)-6-methylbenzene C21H28O4 ÏàËÆ¶È:72.7% Phytochemistry 1981 20 2598-2600 Isoprenoid dihydroquinones from a brown alga, Cystophora sp. Robert J. Capon, Emilio L. Ghisalberti, Phillip R. Jefferies Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (3R,4S,5S,6S)-4-{(1E)-1,5-dimethylhexa-1,4-dien-1-yl}-5,6-diacetoxy-11-oxaspiro[2.5]octane C19H28O5 ÏàËÆ¶È:72.7% Tetrahedron 1999 55 2205-2224 Chiral and stereoselective total synthesis of novel immunosuppressant FR65814 from d-glucose Seiji Amano, Noriko Ogawa, Masami Ohtsuka, Noritaka Chida Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . gibberosene F C24H36O5 ÏàËÆ¶È:70.8% Journal of Natural Products 2008 71(2) 179-185 Oxygenated Cembranoids from a Formosan Soft Coral Sinularia gibberosa Atallah F. Ahmed, Zhi-Hong Wen, Jui-Hsin Su, Ya-Ting Hsieh, Yang-Chang Wu, Wan-Ping Hu, and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (1R*,5S*,6S*)-5-(acetyloxy)-6-[3-(acetyloxy)-1,5-dimethylhex-4-enyl]-3-methylcyclohex-2-en-4-on-1-yl (2Z)-2-methyl-but-2-enoate C24H34O7 ÏàËÆ¶È:70.8% Natural Product Communications 2010 5 667-668 A new Bisabolane Derivative of Leontopodium andersonii Stefan Schwaiger, Stefanie Hehenberger, Ernst P. Ellmerer and Hermann Stuppner Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . andrimid C27H33N3O5 ÏàËÆ¶È:70.8% Journal of the American Chemical Society 1987 109 4409-4411 Andrimid, a new peptide antibiotic produced by an intracellular bacterial symbiont isolated from a brown planthopper Andreas Fredenhagen, Susan Y. Tamura, Peter T. M. Kenny, Hajime Komura, Yoko Naya, Koji Nakanishi, Koushi Nishiyama, Miyoji Sugiura, Hiroshi Kita Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . helenalin-[(2-hydroxyethyl-3-methyl)acrylate] C20H24O6 ÏàËÆ¶È:69.5% Journal of Natural Products 2005 68 800-803 Pseudoguanolide Sesquiterpene Lactones from Vernoniopsis caudata and Their in Vitro Antiplasmodial Activities Voahangy Ramanandraibe, Marie-Thrse Martin, Dina L. Rakotondramanana, Lengo Mambu, David Ramanitrahasimbola, Medhi Labaed, Philippe Grellier, Philippe Rasoanaivo, and Franois Frappier Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . segetalin G C25H38O6N6 ÏàËÆ¶È:69.5% Journal of Natural Products 1997 60 216-218 Cyclic Peptides from Higher Plants. 34.1 Segetalins G and H, Structures and Estrogen-like Activity of Cyclic Pentapeptides from Vaccaria segetalis Young Sook Yun, Hiroshi Morita, Koichi Takeya, and Hideji Itokawa Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . Aripiprazole contaminant ÏàËÆ¶È:69.5% Bioorganic & Medicinal Chemistry Letters 2003 13 65-68 Synthetic study on the unique dimeric arylpiperazine: access to the minor contaminant of aripiprazole Yasuhiro Torisawa, Koichi Shinhama, Takao Nishi, Jun-ichi Minamikawa Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-09-18 15:32:59
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²éѯ½á¹û£º¹²²éµ½379¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . aspochracin ÏàËÆ¶È:95.6% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . sclerotiotide C C24H38N4O4 ÏàËÆ¶È:82.6% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . sclerotiotide H C23H38N4O6 ÏàËÆ¶È:82.6% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . sclerotiotide I C23H38N4O6 ÏàËÆ¶È:82.6% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . sclerotiotide J C23H38N4O6 ÏàËÆ¶È:82.6% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . sclerotiotide K C23H38N4O6 ÏàËÆ¶È:82.6% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . sclerotiotide E C23H36N4O4 ÏàËÆ¶È:78.2% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . sclerotiotide B C21H34N4O4 ÏàËÆ¶È:77.2% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . sclerotiotide D C22H34N4O4 ÏàËÆ¶È:72.7% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . sclerotiotide F C21H32N4O5 ÏàËÆ¶È:72.7% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . sclerotiotide G C23H36N4O6 ÏàËÆ¶È:69.5% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 4¦Â-acetoxy-3¦Â-angeloyloxy-11-hydroxy-6,7-dehydroeudesman-8-one ÏàËÆ¶È:68.1% Phytochemistry 1996 43 417-421 Eudesmane derivatives from Pluchea quitoc Giselle M. S. P. Guilhon, Adolfo H. M¨¹ller Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . Pre-sclerotiotide C20H30N4O5 ÏàËÆ¶È:63.6% Phytochemistry Letters 2012 5 114-117 Unraveling the numerous biosynthetic products of the marine sediment-derived fungus,Aspergillus insulicola Q.X. Wu,X.J. Jin,M. Draskovic,M.S. Crews,K. Tenney,F.A. Valeriote,X.J. Yao,P. Crews Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . JBIR-15 C22H34N4O4 ÏàËÆ¶È:63.6% Bioscience, Biotechnology, and Biochemistry 2009 73 1898-1900 JBIR-15, a New Aspochracin Derivative, Isolated from a Sponge-Derived Fungus, Aspergillus sclerotiorum Huber Sp080903f04 Keiichiro MOTOHASHI, Shigeki INABA, Motoki TAKAGI and Kazuo SHIN-YA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . andrimid C27H33N3O5 ÏàËÆ¶È:62.5% Journal of the American Chemical Society 1987 109 4409-4411 Andrimid, a new peptide antibiotic produced by an intracellular bacterial symbiont isolated from a brown planthopper Andreas Fredenhagen, Susan Y. Tamura, Peter T. M. Kenny, Hajime Komura, Yoko Naya, Koji Nakanishi, Koushi Nishiyama, Miyoji Sugiura, Hiroshi Kita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (1R*,2E,4R*,6E,8S*,10S*,11*,21R *)-8,18-Diacetoxy-10-hydroxy-2,6-dolabelladiene C24H38O5 ÏàËÆ¶È:62.5% The Journal of Organic Chemistry 1977 42 3157-3162 Diterpenes from Dolabella californica Chris Ireland, D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . sinulaflexiolide J C22H32O5 ÏàËÆ¶È:59.0% Journal of Natural Products 2008 71(7) 1133-1140 Sinulaflexiolides A#K, Cembrane-Type Diterpenoids from the Chinese Soft Coral Sinularia flexibilis Ting Wen, Yi Ding, Zhiwei Deng, Leen van Ofwegen, Peter Proksch, and Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 8¦Á-O-(4-acetoxy-5-hydroxyangeloyl)-11¦Â,13-dihydrocnicin C22H30O9 ÏàËÆ¶È:59.0% Journal of Natural Products 2007 70 1796-1799 Minor Sesquiterpene Lactones from Centaurea pullata and Their Antimicrobial Activity Samah Djeddi, Anastasia Karioti,Marina Sokovic, Dejan Stojkovic, Ratiba Seridi, and Helen Skaltsa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 8b-(4'-acetoxy-5'-hydroxytigloyloxy)-costunolide ÏàËÆ¶È:59.0% Phytochemistry 1999 51 79-82 Sesquiterpene lactones from Stevia alpina var. glutinosa Zaida N.J.de Herna ndez, Cesar A.N. Catalan, Luis R. Hernandez, Diana Guerra-Ramirez, Pedro Joseph!Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . sclerotiotide A C22H34N4O4 ÏàËÆ¶È:59.0% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . Sclerotiotide F C21H33N4O5 ÏàËÆ¶È:59.0% Phytochemistry Letters 2012 5 114-117 Unraveling the numerous biosynthetic products of the marine sediment-derived fungus,Aspergillus insulicola Q.X. Wu,X.J. Jin,M. Draskovic,M.S. Crews,K. Tenney,F.A. Valeriote,X.J. Yao,P. Crews Structure 13C NMR ̼Æ×Ä£Äâͼ |
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