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1 .     fungichromin
    ÏàËÆ¶È:100%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     fungichromin
    ÏàËÆ¶È:100%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     fungichromin
    ÏàËÆ¶È:100%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     fungichromin B
C36H60O12     ÏàËÆ¶È:88.8%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     1',14-dihydroxyisochainin
C33H54O12     ÏàËÆ¶È:88.5%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     14-hydroxyisochainin
C33H54O11     ÏàËÆ¶È:80%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     1'-hydroxyisochainin
C33H54O11     ÏàËÆ¶È:77.1%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     Antifungalmycin
C35H60O14     ÏàËÆ¶È:68.5%
Natural Products and Bioprospecting          2012          2          41-45
Antifungalmycin, an antifungal macrolide from Streptomyces padanus 702
Yi-Fen Wang, Sai-Jin Wei, Zhi-Ping Zhang, Tong-He Zhan, Guo-Quan Tu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     TPU-0043
C33H54O10     ÏàËÆ¶È:65.7%
The Journal of Antibiotics          2005          58          523-525
Absolute Configuration of TPU-0043, a Pentaene Macrolide from Streptomyces sp. FREE
Yasuhiro Igarashi, Yasuko In, Toshimasa Ishida, Tsuyoshi Fujita, Takashi Yamakawa, Hiroyasu Onaka and Tamotsu Furumai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     isochainin
C33H54O10     ÏàËÆ¶È:65.7%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     paenimacrolidin
C33H50O6     ÏàËÆ¶È:60%
Microbial Biotechnology          2011          4          491-502
Paenimacrolidin, a novel macrolide antibiotic from Paenibacillus sp. F6-B70 active against methicillin-resistant Staphylococcus aureus
Xue-Chang Wu, Chao-Dong Qian, Hai-Huan Fang,Yan-Ping Wen, Jian-Ying Zhou, Zha-Jun Zhan,Rui Ding, Ou Li and Haichun Gao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     7-acetyl-10-deacetyltaxol
C47H51NO14     ÏàËÆ¶È:57.1%
Journal of Natural Products          2001          64          450-455
New Taxane Analogues from the Needles of Taxus canadensis
Junzeng Zhang,Francoise Sauriol,Orval Mamer,Xiao-Li You,Moulay A. Alaoui-Jamali,Gerald Batist,and Lolita O. Zamir
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     YM-32890 A
C33H48O6     ÏàËÆ¶È:57.1%
The Journal of Antibiotics          1997          50          556-561
YM-32890 A and B, New Types of Macrolide Antibiotics Produced by Cytophaga sp.
KAZUMA KAMIGIRI, TATSUHIRO TOKUNAGA, TAKEO SUGAWARA, KOJI NAGAI, MITSUYOSHI SHIBAZAKI, BOENJAMIN SETIAWAN, RANTIA MURNI RANTIATMODJO, MOTOO MORIOKA, KENICHI SUZUKI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     YM-32890 B
C33H48O6     ÏàËÆ¶È:57.1%
The Journal of Antibiotics          1997          50          556-561
YM-32890 A and B, New Types of Macrolide Antibiotics Produced by Cytophaga sp.
KAZUMA KAMIGIRI, TATSUHIRO TOKUNAGA, TAKEO SUGAWARA, KOJI NAGAI, MITSUYOSHI SHIBAZAKI, BOENJAMIN SETIAWAN, RANTIA MURNI RANTIATMODJO, MOTOO MORIOKA, KENICHI SUZUKI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     compound 46
C51H78O11Si     ÏàËÆ¶È:56.7%
Heterocycles          2012          86          565-598
ASSEMBLY OF THE SOUTHERN MACROCYCLIC HALF OF (+)-SPIRASTRELLOLIDE A THROUGH CYCLIC ACETAL TETHERED RING-CLOSING METATHESIS AND 1,3-ANTI-MUKAIYAMA-ALDOL
Yu Tang,* Jin-Haek Yang, Jia Liu, Chao-Chao Wang, Ming-Can Lv, Yi-Biao Wu, Xue-Liang Yu, Changhong Ko, and Richard Hsung
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     strevertene A
C31H48O10     ÏàËÆ¶È:54.2%
Tetrahedron          1999          55          5977-5990
Strevertenes, antifungal pentaene macrolides produced by Streptoverticillcum LL-30F848
Gerhard Schlingmann, Lisa Milne, Donald B. Borders, Guy T. Carter
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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