| ²é¿´: 259 | »Ø¸´: 1 | ||
×óÐýVCľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö£¬Ð»Ð» ÒÑÓÐ1È˲ÎÓë
|
|
̼Æ×Êý¾ÝÈçÏ£º 11.7,14.5,18.0,23.8,26.1,33.0,36.3,39.6,41.2,44.3,45.2,45.4,60.5,70.3,71.5,72.5,73.2,73.4,74.0,74.2,74.3,75.3,78.3,80.5,129.1,130.0,132.0,133.7,134.2,134.3,134.4, 135.0,135.5,138.6,173.0 лл£¡ |
» ²ÂÄãϲ»¶
294Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
324Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
Ò»Ö¾Ô¸ÉϺ£´óѧÉúÎïѧ346
ÒѾÓÐ3È˻ظ´
322Çóµ÷¼Á£ºÒ»Ö¾Ô¸ºþÄÏ´óѧ ²ÄÁÏÓ뻯¹¤£¨085600£©£¬ÒѹýÁù¼¶¡£
ÒѾÓÐ16È˻ظ´
µ÷¼Á
ÒѾÓÐ10È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
0703µ÷¼Á
ÒѾÓÐ6È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ6È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¡¼±£¡Ð»Ð»£¡
ÒѾÓÐ5È˻ظ´
European Journal of Wood and Wood Products
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬¿É·ñÓÐÈËÖ¸µã»òÔõÑù²éµ½´øÓÐÒÑÖªµ¥ÌåµÄºË´ÅÆ×Êý¾ÝÎÄÏ×
ÒѾÓÐ4È˻ظ´
¼±Çó£¡Î¢ÆÕÇóÖú£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
¡¾·ÖÏí¡¿Ãâ·ÑµÄ20¸öÆ×ͼÊý¾Ý¿â
ÒѾÓÐ13È˻ظ´
Ãâ·ÑµÄÆ×ͼÊý¾Ý¿â20¸ö
ÒѾÓÐ42È˻ظ´
¡¾Ô´´·ÖÏí¡¿»¹ÇóÖúô£ºÃâ·ÑµÄÆ×ͼÊý¾Ý¿â20¸ö£¨Ç××Ô²âÊÔ£¬È«²¿ÓÐЧ£©¡¾ÎÞÖØ¸´¡¿
ÒѾÓÐ190È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
×óÐýVC: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-09-12 20:16:02
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
×óÐýVC: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-09-12 20:16:02
|
²éѯ½á¹û£º¹²²éµ½82¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
2Â¥2014-09-12 11:20:45














»Ø¸´´ËÂ¥