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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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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-12-09 10:36:31
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