| ²é¿´: 183 | »Ø¸´: 1 | ||
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| 12.8, 14.1, 17.8, 25.2, 39.5, 41.8, 45.2, 49.0, 49.6, 57.2, 61.8, 67.4, 68.0, 69.1, 70.5, 73.8, 74.6, 74.7, 75.0, 79.6, 99.0, 99.1, 123.0, 130.5, 132.4, 132.9, 133.4, 134.3, 134.6, 136.4, 137.7, 150.2, 167.3 |
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²éѯ½á¹û£º¹²²éµ½25¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . chaxalactin C C29H42O5 ÏàËÆ¶È:60.6% Journal of Natural Products 2011 74 1965-1971 Diverse Metabolic Profiles of a Streptomyces Strain Isolated from a Hyper-arid Environment Mostafa E. Rateb, Wael E. Houssen, William T. A. Harrison, Hai Deng, Chinyere K. Okoro, Juan A. Asenjo, Barbara A. Andrews, Alan T. Bull, Michael Goodfellow, Rainer Ebel, and Marcel Jaspars Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Roimatacene methyl ester C31H46O7 ÏàËÆ¶È:57.5% Chemistry-A European Journal 2011 17 7875-7881 Roimatacene: An Antibiotic against Gram-Negative Bacteria Isolated from Cystobacter ferrugineus Cb G35 (Myxobacteria) Wiebke Zander, Dr. Klaus Gerth, Dr. Kathrin I. Mohr, Dipl.-Ing. Wolfgang Kessler, Dr. Rolf Jansen and Prof. Dr. Rolf M¨¹ller Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1',14-dihydroxyisochainin C33H54O12 ÏàËÆ¶È:57.5% The Journal of Antibiotics 1989 42 577-584 PRODUCTION OF NEW POLYENE ANTIBIOTICS BY STREPTOMYCES CELLULOSAE AFTER ADDITION OF ETHYL (Z)-16-PHENYLHEXADEC-9-ENOATE ZHE LI, BERNARD J. RAWLINGS, PAUL H. HARRISON, JOHN C. VEDERAS Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . fungichromin ÏàËÆ¶È:57.1% Antonie van Leeuwenhoek 2013 103 1107-111 A new nematicidal compound produced by Streptomyces albogriseolus HA10002 Qingfei Zeng, Huiqin Huang, Jun Zhu, Zhe Fang, Qianguang Sun, Shixiang Bao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . fungichromin B C36H60O12 ÏàËÆ¶È:55.5% Antonie van Leeuwenhoek 2013 103 1107-111 A new nematicidal compound produced by Streptomyces albogriseolus HA10002 Qingfei Zeng, Huiqin Huang, Jun Zhu, Zhe Fang, Qianguang Sun, Shixiang Bao Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . elansolid B2 C38H52O7 ÏàËÆ¶È:55.5% Angewandte Chemie International Edition 2010 49 532-536 Elansolid A, a Unique Macrolide Antibiotic from Chitinophaga sancti Isolated as Two Stable Atropisomers Heinrich Steinmetz, Klaus Gerth, Rolf Jansen, Nadin Schl ger, Richard Dehn, Silke Reinecke, Andreas Kirschning, * and Rolf M ller* Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 14-hydroxyisochainin C33H54O11 ÏàËÆ¶È:54.5% The Journal of Antibiotics 1989 42 577-584 PRODUCTION OF NEW POLYENE ANTIBIOTICS BY STREPTOMYCES CELLULOSAE AFTER ADDITION OF ETHYL (Z)-16-PHENYLHEXADEC-9-ENOATE ZHE LI, BERNARD J. RAWLINGS, PAUL H. HARRISON, JOHN C. VEDERAS Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . N-acetylpimaricin C35H49NO14 ÏàËÆ¶È:54.2% The Journal of Antibiotics 2000 53 623-626 AB-400, a New Tetraene Macrolide Isolated from Streptomyces costae LIBRADA M. CAÑEDO,LUIS COSTA,LUIS M. CRIADO,JOS¨¦ L. FERN¨¢NDEZ PUENTES,MIGUEL A. MORENO and KENNETH L. RINEHART Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . fungichromin ÏàËÆ¶È:54.2% The Journal of Antibiotics 1989 42 577-584 PRODUCTION OF NEW POLYENE ANTIBIOTICS BY STREPTOMYCES CELLULOSAE AFTER ADDITION OF ETHYL (Z)-16-PHENYLHEXADEC-9-ENOATE ZHE LI, BERNARD J. RAWLINGS, PAUL H. HARRISON, JOHN C. VEDERAS Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . fungichromin ÏàËÆ¶È:54.2% Journal of the American Chemical Society 1988 110 2938-2945 Biosynthesis and full NMR assignment of fungichromin, a polyene antibiotic from Streptomyces cellulose Hiroshi. Noguchi, Paul H. Harrison, Kunizo. Arai, Thomas T. Nakashima, Laird A. Trimble, John C. Vederas Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . JBIR-13 C35H51NO13 ÏàËÆ¶È:54.2% Applied Microbiology and Biotechnology 2009 83 127-133 Discovery of a pimaricin analog JBIR-13, from Streptomyces bicolor NBRC 12746 as predicted by sequence analysis of type I polyketide synthase gene Hisayuki Komaki, Miho Izumikawa, Jun-ya Ueda, Takuji Nakashima, Shams Tabrez Khan, Motoki Takagi, Kazuo Shin-ya Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . rubroside C C42H54Cl2N2O16 ÏàËÆ¶È:52.9% The Journal of Organic Chemistry 1999 64 2331-2339 Rubrosides A−H, New Bioactive Tetramic Acid Glycosides from the Marine Sponge Siliquariaspongia japonica1 Noriko U. Sata, Shun-ichi Wada, Shigeki Matsunaga, Shugo Watabe, Rob W. M. van Soest, and Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Roimatacene C34H42O7 ÏàËÆ¶È:52.7% Chemistry-A European Journal 2011 17 7875-7881 Roimatacene: An Antibiotic against Gram-Negative Bacteria Isolated from Cystobacter ferrugineus Cb G35 (Myxobacteria) Wiebke Zander, Dr. Klaus Gerth, Dr. Kathrin I. Mohr, Dipl.-Ing. Wolfgang Kessler, Dr. Rolf Jansen and Prof. Dr. Rolf M¨¹ller Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 5 ÏàËÆ¶È:52.7% The Journal of Organic Chemistry 2009 74 675-684 Marinisporolides, Polyene-Polyol Macrolides from a Marine Actinomycete of the New Genus Marinispora Hak Cheol Kwon, Christopher A. Kauffman, Paul R. Jensen and William Fenical Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . marinisporolide A C38H58O10 ÏàËÆ¶È:52.6% The Journal of Organic Chemistry 2009 74 675-684 Marinisporolides, Polyene-Polyol Macrolides from a Marine Actinomycete of the New Genus Marinispora Hak Cheol Kwon, Christopher A. Kauffman, Paul R. Jensen and William Fenical Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . woodwardine C C33H52O7 ÏàËÆ¶È:51.5% Phytochemistry 2003 63 931-937 Two cyclohexenone glycosides from the North American fern Woodwardia virginica (L.) Smith Tom¨¢š Řezanka,Valery M. Dembitskyb,Lum¨ªr O. Hanuš Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . topsentisterol E1 C28H42O2 ÏàËÆ¶È:51.5% Journal of Natural Products 2006 69 1760-1768 26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp. Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . chaxalactin B C28H40O5 ÏàËÆ¶È:51.5% Journal of Natural Products 2011 74 1965-1971 Diverse Metabolic Profiles of a Streptomyces Strain Isolated from a Hyper-arid Environment Mostafa E. Rateb, Wael E. Houssen, William T. A. Harrison, Hai Deng, Chinyere K. Okoro, Juan A. Asenjo, Barbara A. Andrews, Alan T. Bull, Michael Goodfellow, Rainer Ebel, and Marcel Jaspars Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3-(1',2'-ethandiol)-24-methylcholest-8(9),22E-diene-3¦Â,5¦Á,6¦Á,7¦Á,11¦Á-pentaol C30H50O6 ÏàËÆ¶È:51.5% Magnetic Resonance in Chemistry 2007 45 1088-1091 Complete 1H and 13C NMR assignments of three new polyhydroxylated sterols from the South China Sea gorgonian Subergorgia suberosa (pages 1088¨C1091) Shu-Hua Qi, Si Zhang, Yi-Fei Wang and Ming-Yi Li Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (5R,7R,8R,13R)-8-(tert-Butyldimethylsilanyloxy)-5,13-dimethoxy-7-(4-methoxy-benzyloxy)-10-methyl-3-oxo-16-trimethylsilanyl)-hexadeca-di-(9E,11E)-en-15-ynoic acid ethyl ester C38H62O8Si2 ÏàËÆ¶È:51.5% Organic & Biomolecular Chemistry 2003 1 4173-4208 Total synthesis of (+)-phorboxazole A, a potent cytostatic agent from the sponge Phorbas sp. Gerald Pattenden, Miguel A. Gonz¨¢lez, Paul B. Little, David S. Millan, Alleyn T. Plowright, James A. Tornos and Tao Ye Structure 13C NMR ̼Æ×Ä£Äâͼ |
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