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¹û¹û½ÇÂä½ð³æ (СÓÐÃûÆø)
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[ÇóÖú]
΢Æ×Êý¾ÝÇóÖú
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13c nmr CDCL3 14.5,16.8,20.3,21.8,29.2,32.7,35.0,35.2,36.2,41.5,47.4,50.5,54.0,66.3,111.6,112.5,118.8,120.1,122.6,122.8,127.0,127.2,128.5,129.8,130.8,132.9, 133.1,136.8,140.0,146.7,174.4,197.7 |
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²éѯ½á¹û£º¹²²éµ½357¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . chaetoglobosin S C32H38N2O3 ÏàËÆ¶È:87.5% Journal of Natural Products 2004 67 1722-1725 Chaetoglobosins Q, R, and T, Three Further New Metabolites from Chaetomium globosum Wenxu Jiao, Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . chaetoglobosin A ÏàËÆ¶È:65.6% Chemical & Pharmaceutical Bulletin 1983 31 490-498 Chaetoglobosins, Cytotoxic 10-(Indol-3-yl)-[13] cytochalasans from Chaetomium spp. IV. 13C-Nuclear Magnetic Resonance Spectra and Their Application to a Biosynthetic Study SETSUKO SEKITA,KUNITOSHI YOSHIHIRA and SHINSAKU NATORI Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . chaetoglobosin O C32H38N2O5 ÏàËÆ¶È:62.5% Bioscience, Biotechnology, and Biochemistry 1996 60 360-361 Chaetoglobosin O and Other Phytotoxic Metabolites from Cylindrocladium floridanum, a Causal Fungus of Alfalfa Black Rot Disease Akitami ICHIHARA, Kinya KATAYAMA, Hiroshi TESHIMA, Hideaki OIKAWA, SADAO SAKAMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . chaetoglobosin P C33H38N2O5 ÏàËÆ¶È:60.6% Natural Product Research 1997 10 39-42 Uncommon Glycoconjugates of 2-Phenylethanol from Rose Flowers and Riesling Wine Naoharu Watanabe; Monika Messerer; Peter Winterhalter Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . chaetoglobosin R C32H38N2O6 ÏàËÆ¶È:59.3% Journal of Natural Products 2004 67 1722-1725 Chaetoglobosins Q, R, and T, Three Further New Metabolites from Chaetomium globosum Wenxu Jiao, Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Chaetoglobosin V C32H38N2O3 ÏàËÆ¶È:59.3% Archives of Pharmacal Research 2010 33 1135-1141 Cytotoxic 10-(indol-3-yl)-[13]cytochalasans from the fungus Chaetomium elatum ChE01 Santi Thohinung, Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Veerapol Kukongviriyapan and Ornanong Tusskorn, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Penochalasin A C32H35N3O3 ÏàËÆ¶È:59.3% Journal of the Chemical Society, Perkin Transactions 1 1996 239-245 Penochalasins, a novel class of cytotoxic cytochalasans from a Penicillium species separated from a marine alga: structure determination and solution conformation Atsushi Numata, Chika Takahashi, Yoshinori Ito, Katsuhiko Minoura, Takeshi Yamada, Chitose Matsuda and Kyosuke Nomoto Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Penochalasin C C32H35N3O3 ÏàËÆ¶È:59.3% Journal of the Chemical Society, Perkin Transactions 1 1996 239-245 Penochalasins, a novel class of cytotoxic cytochalasans from a Penicillium species separated from a marine alga: structure determination and solution conformation Atsushi Numata, Chika Takahashi, Yoshinori Ito, Katsuhiko Minoura, Takeshi Yamada, Chitose Matsuda and Kyosuke Nomoto Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . penochalasin E C32H38N2O5 ÏàËÆ¶È:59.3% Tetrahedron 2001 57 2997-3004 Cytotoxic cytochalasans from a Penicillium species separated from a marine alga Chika Iwamoto, Takeshi Yamada, Yoshinori Ito, Katsuhiko Minoura, Atsushi Numata Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Manzamine J C36H46N4O ÏàËÆ¶È:59.3% The Journal of Organic Chemistry 1992 57 2480-2483 Ircinals A and B from the Okinawan marine sponge Ircinia sp.: plausible biogenetic precursors of manzamine alkaloids Kazuhiko Kondo, Hideyuki Shigemori, Yumiko Kikuchi, Masami Ishibashi, Takuma Sasaki, Junichi Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . chaetoglobosin-540 C34H40N2O4 ÏàËÆ¶È:58.8% Journal of Natural Products 2005 68 1592-1597 Using Jasplakinolide to Turn on Pathways that Enable the Isolation of New Chaetoglobosins from Phomospis asparagi Omar E. Christian, Jennifer Compton, Keisha R. Christian,Susan L. Mooberry, Fredrick A.Valeriote,and Phillip Crews Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . chaetoglobosin K ÏàËÆ¶È:58.8% Natural Product Research 1997 10 39-42 Uncommon Glycoconjugates of 2-Phenylethanol from Rose Flowers and Riesling Wine Naoharu Watanabe; Monika Messerer; Peter Winterhalter Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Chaetoglobosin K ÏàËÆ¶È:58.8% Helvetica Chimica Acta 1988 71 1881-1884 Chaetoglobosin M, a New Metabolite of a Mutant of Diplodia macrospora, belonging to the family of (1H-indol-3-yl)-substituted 10,11-diethyl-10,11-dinorcytochalasans Christoph Spöndlin and Christoph Tamm Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . cytochalasin Y C29H36N2O5 ÏàËÆ¶È:57.5% Journal of Natural Products 2002 65 1274-1277 Three Novel Cytochalasins X, Y, and Z from Pseudeurotium zonatum Yunjiang Feng,John W. Blunt, Anthony L. J. Cole,and Murray H. G. Munro Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Metacridamide B C35H53NO5 ÏàËÆ¶È:57.5% Journal of Natural Products 2012 75 175−180 Metacridamides A and B,Macrocycles from Conidia of the Entomopathogenic Fungus Metarhizium acridum Stuart B. Krasnoff,Ulrich Englich,Paula G. Miller,Michael L. Shuler,Raymond P. Glahn,Bruno G. G. Donzelli,and Donna M. Gibson Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (rel)-2-oxozuelanin-6¦Â-cinnamate ÏàËÆ¶È:57.5% Phytochemistry 1990 29 1609-1614 Diterpenes from Zuelania guidonia Mamunur R. Khan,Alexander I. Gray,David R. Reed,Ian H. Sadler,Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (3¦Á,5¦Á)-3-{[trans-2,5-Dimethyl-4-{[2-(trifluoromethyl)-phenyl]sulfonyl}piperazin-1-yl]methyl}-3-hydroxyandrostan-17-one C33H47F3N2O4S ÏàËÆ¶È:57.5% Bioorganic & Medicinal Chemistry 2011 19 4652-4668 Development of 3-substituted-androsterone derivatives as potent inhibitors of 17¦Â-hydroxysteroid dehydrogenase type 3 Ren¨¦ Maltais, Michelle-Audrey Fournier, Donald Poirier Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . hemsine A C32H40N5O4 ÏàËÆ¶È:56.2% Helvetica Chimica Acta 2003 Vol. 86 127 14-Membered Cyclopeptides from Paliurus ramosissimus and P. hemsleyanus Hui-yi Lin, Chung-Hsiung Chen, Karin C. S. Chen Liu, and Shoei-Sheng Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . cytochalasin D ÏàËÆ¶È:56.2% Helvetica Chimica Acta 2002 Vol. 85 1439 Neoengleromycin, a Novel Compound from Engleromyces goetzii Liu Jikai, Tan Jianwen, Dong Zejun, Ding Zhihui, Wang Xianghua, and Liu Peigui Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . chaetoglobosin Q C32H38N2O6 ÏàËÆ¶È:56.2% Journal of Natural Products 2004 67 1722-1725 Chaetoglobosins Q, R, and T, Three Further New Metabolites from Chaetomium globosum Wenxu Jiao, Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . chaetoglobosin G ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 1983 31 490-498 Chaetoglobosins, Cytotoxic 10-(Indol-3-yl)-[13] cytochalasans from Chaetomium spp. IV. 13C-Nuclear Magnetic Resonance Spectra and Their Application to a Biosynthetic Study SETSUKO SEKITA,KUNITOSHI YOSHIHIRA and SHINSAKU NATORI Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (13E,17E)-12-phenylsulfonylbicyclogeranylfarnesol ÏàËÆ¶È:56.2% Chemistry of Natural Compounds 2007 43 268-273 SUPERACID CYCLIZATION OF(2E,6E,10E,14E)-8- PHENYLSULFONYLGERANYLFARNESOL TETRAHYDROPYRANYL ETHER V. Kulcitki, M. Grin'ko, A. Barba,N. Ungur, and P. F. Vlad Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . chaetoglobosin A ÏàËÆ¶È:56.2% Helvetica Chimica Acta 1981 64 2056-2064 19-O-Acetylchaetoglobosin B and 19-O-Acetylchaetoglobosin D, Two New Metabolites of Chaetomium globosum Alessandro Probst, Christoph Tamm Structure 13C NMR ̼Æ×Ä£Äâͼ |

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