| ²é¿´: 318 | »Ø¸´: 1 | |||
IMB001½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| »¯Ñ§Î»ÒÆ£º17.5, 17.9, 19.6, 19.7, 20.5, 21.3, 21.6, 22.2, 22.5, 23.5, 23.8, 23.8, 28.4, 29.1, 29.8, 30.0, 30.6, 31.2, 32.0, 32.1, 32.8, 33.2, 33.6, 33.9, 35.1, 37.3, 37.4, 39.7, 46.3, 47.0, 48.0, 48.5, 49.5, 50.0, 51.1, 53.9, 55.0, 55.9, 57.1, 58.1, 58.7, 61.5, 63.1, 68.5, 114.6, 115.0, 115.1, 115.2, 125.8, 126.3, 126.4, 127.2, 127.3, 127.6, 127.7, 128.3, 129.5, 129.7, 129.8, 129.9, 130.2, 130.3, 137.6, 137.8, 155.5, 155.6, 156.1, 156.2, 166.8, 167.2, 167.4, 167.9, 168.7, 169.4, 170.1, 170.1, 170.4, 170.6, 171.0, 171.4, 171.6, 173.8¡£ |
» ²ÂÄãϲ»¶
353Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
²ÄÁÏ»¯¹¤306·ÖÕÒºÏÊʵ÷¼Á
ÒѾÓÐ11È˻ظ´
µ÷¼Á
ÒѾÓÐ8È˻ظ´
¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸±±¾©2£¬²ÄÁÏÓ뻯¹¤308Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
0817»¯Ñ§¹¤³ÌÓë¼¼ÊõÇóµ÷¼Á£¬Ò»Ö¾Ô¸Öк£Ñó319
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸µç×ӿƼ¼´óѧ085600²ÄÁÏÓ뻯¹¤ 329·ÖÇóµ÷¼Á
ÒѾÓÐ6È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
IMB001: ½ð±Ò+18, ¡ï¡ï¡ïºÜÓаïÖú 2015-02-04 22:28:32
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
IMB001: ½ð±Ò+18, ¡ï¡ï¡ïºÜÓаïÖú 2015-02-04 22:28:32
|
1 . microviridin G C88H111O25N17 ÏàËÆ¶È:65.8% Phytochemistry 1997 45 1197-1202 Microviridins, elastase inhibitors from the cyanobacterium Nostoc minutum (NIES-26) Masahiro Murakami, Qi Sun, Keishi Ishida, Hisashi Matsuda, Tatsufumi Okino, Katsumi Yamaguchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . cyclo[O-[[[N-[(2S,3S,4S)-4-[(1S,2S)-3-amino-2-methoxy-cyclohexanecarbonyl]oxy]-3-oxo-2,5-dimethylhexanoyl]-L-leucyl]-L-prolyl]-N,O-dimethyl-L-tyrosyl]-L-threonyl] hydrochloride C42H64N5O11Cl ÏàËÆ¶È:64.6% The Journal of Organic Chemistry 1996 61 1655-1664 Synthetic Routes to a Constrained Ring Analog of Didemnin B Scott C. Mayer, Amy J. Pfizenmayer, and Madeleine M. Joulli¨¦ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-alanyl-N-methylleucyl-N-methylleucyl-N-methylvalyl-N-methyl-leucylnorvalylsarcosyl-N-methylleucylvalyl-N-meth-ylleucylalanine benzyl ester C82H127N11O14 ÏàËÆ¶È:61.6% The Journal of Organic Chemistry 2000 65 2951-2958 Total Synthesis of Cyclosporin O Both in Solution and in the Solid Phase Using Novel Thiazolium-, Immonium-, and Pyridinium-Type Coupling Reagents: BEMT, BDMP, and BEP1 Peng Li and Jie Cheng Xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . microviridin H C89H115O26N17 ÏàËÆ¶È:60.2% Phytochemistry 1997 45 1197-1202 Microviridins, elastase inhibitors from the cyanobacterium Nostoc minutum (NIES-26) Masahiro Murakami, Qi Sun, Keishi Ishida, Hisashi Matsuda, Tatsufumi Okino, Katsumi Yamaguchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 22 ÏàËÆ¶È:59.7% Journal of the American Chemical Society 2007 129 4175-4177 Total Synthesis of Plusbacin A3: A Depsipeptide Antibiotic Active Against Vancomycin-Resistant Bacteria Aaron Wohlrab, Ryan Lamer, and Michael S. VanNieuwenhze Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . pahayokolide A C72H105N13O20 ÏàËÆ¶È:58.5% Journal of Natural Products 2007 70 730-735 Structures of Pahayokolides A and B, Cyclic Peptides from a Lyngbya sp. Tianying An,Thallapuranam Krishnaswamy Suresh Kumar,Minglei Wang,Li Liu, Jackson O. Lay, Jr.,Rohana Liyanage, John Berry, Miroslav Gantar, Vered Marks,Robert E. Gawley,and Kathleen S. Rein Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . microviridin D C84H107N17O26S ÏàËÆ¶È:58.5% Tetrahedron 1996 52 8159-8168 Microviridins D-F, serine protease inhibitors from the cyanobacterium Oscillatoria agardhii (NIES-204) Hee Jae Shin, Masahiro Murakami, Hisashi Matsuda, Katsumi Yamaguchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 23 ÏàËÆ¶È:58.5% Journal of the American Chemical Society 2007 129 4175-4177 Total Synthesis of Plusbacin A3: A Depsipeptide Antibiotic Active Against Vancomycin-Resistant Bacteria Aaron Wohlrab, Ryan Lamer, and Michael S. VanNieuwenhze Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . apratoxin S8 C45H71N5O8S ÏàËÆ¶È:58.5% Journal of Medicinal Chemistry 2014 57 3011-3029 Improved Total Synthesis and Biological Evaluation of Potent Apratoxin S4 Based Anticancer Agents with Differential Stability and Further Enhanced Activity Qi-Yin Chen, Yanxia Liu, Weijing Cai, and Hendrik Luesch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . apratoxin E C43H66N5O7S ÏàËÆ¶È:57.3% Journal of Natural Products 2008 71(6) 1113-1116 Apratoxin E, a Cytotoxic Peptolide from a Guamanian Collection of the Marine Cyanobacterium Lyngbya bouillonii Susan Matthew, Peter J. Schupp, and Hendrik Luesch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 20 ÏàËÆ¶È:57.3% Journal of the American Chemical Society 2007 129 4175-4177 Total Synthesis of Plusbacin A3: A Depsipeptide Antibiotic Active Against Vancomycin-Resistant Bacteria Aaron Wohlrab, Ryan Lamer, and Michael S. VanNieuwenhze Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 19 ÏàËÆ¶È:56.4% Journal of the American Chemical Society 2007 129 4175-4177 Total Synthesis of Plusbacin A3: A Depsipeptide Antibiotic Active Against Vancomycin-Resistant Bacteria Aaron Wohlrab, Ryan Lamer, and Michael S. VanNieuwenhze Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methylleucyl-norvalylsarcosyl-N-methylleucylvalyl-N-methylleucyl-alanine benzyl ester C59H85N7O10 ÏàËÆ¶È:56.0% The Journal of Organic Chemistry 2000 65 2951-2958 Total Synthesis of Cyclosporin O Both in Solution and in the Solid Phase Using Novel Thiazolium-, Immonium-, and Pyridinium-Type Coupling Reagents: BEMT, BDMP, and BEP1 Peng Li and Jie Cheng Xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . apratoxin S9 C44H69N5O8S ÏàËÆ¶È:56.0% Journal of Medicinal Chemistry 2014 57 3011-3029 Improved Total Synthesis and Biological Evaluation of Potent Apratoxin S4 Based Anticancer Agents with Differential Stability and Further Enhanced Activity Qi-Yin Chen, Yanxia Liu, Weijing Cai, and Hendrik Luesch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . malevamide C C79H125N13O16 ÏàËÆ¶È:54.8% Journal of Natural Products 2000 63 461-467 Malevamides A-C, New Depsipeptides from the Marine Cyanobacterium Symploca laete-viridis F. David Horgen, Wesley Y. Yoshida, and Paul J. Scheuer Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . vioprolide A C40H62N8O11S ÏàËÆ¶È:54.8% European Journal of Organic Chemistry 1996 1996 971-978 Antibiotics from Gliding Bacteria, LXXVI. Vioprolides: New Antifungal and Cytotoxic Peptolides from Cystobacter violaceus Dietmar Schummer, Gerhard Höfle, Edgar Forche, Hans Reichenbach, Victor Wray and Tobias Domke Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Szentiamide C45H55N7O9 ÏàËÆ¶È:53.6% Natural Product Communications 2011 Vol. 6, No. 9 1247-1250 Szentiamide, an N-formylated Cyclic Depsipeptide from Xenorhabdus szentirmaii DSM 16338T Birgit Ohlendorf, Sven Simon, Jutta Wiese and Johannes F. Imhoff Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . Kendarimide A C83H134N14O15S2 ÏàËÆ¶È:53.6% Tetrahedron 2004 60 7053-7059 Kendarimide A, a novel peptide reversing P-glycoprotein-mediated multidrug resistance in tumor cells, from a marine sponge of Haliclona sp. Shunji Aoki, Liwei Cao, Kouhei Matsui, Rachmaniar Rachmat, Shin-ichi Akiyama, Motomasa Kobayashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-02-04 21:13:31














»Ø¸´´ËÂ¥