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»¯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¡£
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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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
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