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13c nmr CDCL3
14.5,16.8,20.3,21.8,29.2,32.7,35.0,35.2,36.2,41.5,47.4,50.5,54.0,66.3,111.6,112.5,118.8,120.1,122.6,122.8,127.0,127.2,128.5,129.8,130.8,132.9,
133.1,136.8,140.0,146.7,174.4,197.7
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1 .     chaetoglobosin S
C32H38N2O3     ÏàËÆ¶È:87.5%
Journal of Natural Products          2004          67          1722-1725
Chaetoglobosins Q, R, and T, Three Further New Metabolites from Chaetomium globosum
Wenxu Jiao, Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     chaetoglobosin A
    ÏàËÆ¶È:65.6%
Chemical & Pharmaceutical Bulletin          1983          31          490-498
Chaetoglobosins, Cytotoxic 10-(Indol-3-yl)-[13] cytochalasans from Chaetomium spp. IV. 13C-Nuclear Magnetic Resonance Spectra and Their Application to a Biosynthetic Study
SETSUKO SEKITA,KUNITOSHI YOSHIHIRA and SHINSAKU NATORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     chaetoglobosin O
C32H38N2O5     ÏàËÆ¶È:62.5%
Bioscience, Biotechnology, and Biochemistry          1996          60          360-361
Chaetoglobosin O and Other Phytotoxic Metabolites from Cylindrocladium floridanum, a Causal Fungus of Alfalfa Black Rot Disease
Akitami ICHIHARA, Kinya KATAYAMA, Hiroshi TESHIMA, Hideaki OIKAWA, SADAO SAKAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     chaetoglobosin P
C33H38N2O5     ÏàËÆ¶È:60.6%
Natural Product Research          1997          10          39-42
Uncommon Glycoconjugates of 2-Phenylethanol from Rose Flowers and Riesling Wine
Naoharu Watanabe; Monika Messerer; Peter Winterhalter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     chaetoglobosin R
C32H38N2O6     ÏàËÆ¶È:59.3%
Journal of Natural Products          2004          67          1722-1725
Chaetoglobosins Q, R, and T, Three Further New Metabolites from Chaetomium globosum
Wenxu Jiao, Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Chaetoglobosin V
C32H38N2O3     ÏàËÆ¶È:59.3%
Archives of Pharmacal Research          2010          33          1135-1141
Cytotoxic 10-(indol-3-yl)-[13]cytochalasans from the fungus Chaetomium elatum ChE01
Santi Thohinung, Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Veerapol Kukongviriyapan and Ornanong Tusskorn, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Penochalasin A
C32H35N3O3     ÏàËÆ¶È:59.3%
Journal of the Chemical Society, Perkin Transactions 1          1996                   239-245
Penochalasins, a novel class of cytotoxic cytochalasans from a Penicillium species separated from a marine alga: structure determination and solution conformation
Atsushi Numata, Chika Takahashi, Yoshinori Ito, Katsuhiko Minoura, Takeshi Yamada, Chitose Matsuda and Kyosuke Nomoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Penochalasin C
C32H35N3O3     ÏàËÆ¶È:59.3%
Journal of the Chemical Society, Perkin Transactions 1          1996                   239-245
Penochalasins, a novel class of cytotoxic cytochalasans from a Penicillium species separated from a marine alga: structure determination and solution conformation
Atsushi Numata, Chika Takahashi, Yoshinori Ito, Katsuhiko Minoura, Takeshi Yamada, Chitose Matsuda and Kyosuke Nomoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     penochalasin E
C32H38N2O5     ÏàËÆ¶È:59.3%
Tetrahedron          2001          57          2997-3004
Cytotoxic cytochalasans from a Penicillium species separated from a marine alga
Chika Iwamoto, Takeshi Yamada, Yoshinori Ito, Katsuhiko Minoura, Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Manzamine J
C36H46N4O     ÏàËÆ¶È:59.3%
The Journal of Organic Chemistry          1992          57          2480-2483
Ircinals A and B from the Okinawan marine sponge Ircinia sp.: plausible biogenetic precursors of manzamine alkaloids
Kazuhiko Kondo, Hideyuki Shigemori, Yumiko Kikuchi, Masami Ishibashi, Takuma Sasaki, Junichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     chaetoglobosin-540
C34H40N2O4     ÏàËÆ¶È:58.8%
Journal of Natural Products          2005          68          1592-1597
Using Jasplakinolide to Turn on Pathways that Enable the Isolation of New Chaetoglobosins from Phomospis asparagi
Omar E. Christian, Jennifer Compton, Keisha R. Christian,Susan L. Mooberry, Fredrick A.Valeriote,and Phillip Crews
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     chaetoglobosin K
    ÏàËÆ¶È:58.8%
Natural Product Research          1997          10          39-42
Uncommon Glycoconjugates of 2-Phenylethanol from Rose Flowers and Riesling Wine
Naoharu Watanabe; Monika Messerer; Peter Winterhalter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Chaetoglobosin K
    ÏàËÆ¶È:58.8%
Helvetica Chimica Acta          1988          71          1881-1884
Chaetoglobosin M, a New Metabolite of a Mutant of Diplodia macrospora, belonging to the family of (1H-indol-3-yl)-substituted 10,11-diethyl-10,11-dinorcytochalasans
Christoph Spöndlin and Christoph Tamm
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     cytochalasin Y
C29H36N2O5     ÏàËÆ¶È:57.5%
Journal of Natural Products          2002          65          1274-1277
Three Novel Cytochalasins X, Y, and Z from Pseudeurotium zonatum
Yunjiang Feng,John W. Blunt, Anthony L. J. Cole,and Murray H. G. Munro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Metacridamide B
C35H53NO5     ÏàËÆ¶È:57.5%
Journal of Natural Products          2012          75          175−180
Metacridamides A and B,Macrocycles from Conidia of the Entomopathogenic Fungus Metarhizium acridum
Stuart B. Krasnoff,Ulrich Englich,Paula G. Miller,Michael L. Shuler,Raymond P. Glahn,Bruno G. G. Donzelli,and Donna M. Gibson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (rel)-2-oxozuelanin-6¦Â-cinnamate
    ÏàËÆ¶È:57.5%
Phytochemistry          1990          29          1609-1614
Diterpenes from Zuelania guidonia
Mamunur R. Khan,Alexander I. Gray,David R. Reed,Ian H. Sadler,Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (3¦Á,5¦Á)-3-{[trans-2,5-Dimethyl-4-{[2-(trifluoromethyl)-phenyl]sulfonyl}piperazin-1-yl]methyl}-3-hydroxyandrostan-17-one
C33H47F3N2O4S     ÏàËÆ¶È:57.5%
Bioorganic & Medicinal Chemistry          2011          19          4652-4668
Development of 3-substituted-androsterone derivatives as potent inhibitors of 17¦Â-hydroxysteroid dehydrogenase type 3
Ren¨¦ Maltais, Michelle-Audrey Fournier, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     hemsine A
C32H40N5O4     ÏàËÆ¶È:56.2%
Helvetica Chimica Acta          2003          Vol. 86          127
14-Membered Cyclopeptides from Paliurus ramosissimus and P. hemsleyanus
Hui-yi Lin, Chung-Hsiung Chen, Karin C. S. Chen Liu, and Shoei-Sheng Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     cytochalasin D
    ÏàËÆ¶È:56.2%
Helvetica Chimica Acta          2002          Vol. 85          1439
Neoengleromycin, a Novel Compound from Engleromyces goetzii
Liu Jikai, Tan Jianwen, Dong Zejun, Ding Zhihui, Wang Xianghua, and Liu Peigui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     chaetoglobosin Q
C32H38N2O6     ÏàËÆ¶È:56.2%
Journal of Natural Products          2004          67          1722-1725
Chaetoglobosins Q, R, and T, Three Further New Metabolites from Chaetomium globosum
Wenxu Jiao, Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     chaetoglobosin G
    ÏàËÆ¶È:56.2%
Chemical & Pharmaceutical Bulletin          1983          31          490-498
Chaetoglobosins, Cytotoxic 10-(Indol-3-yl)-[13] cytochalasans from Chaetomium spp. IV. 13C-Nuclear Magnetic Resonance Spectra and Their Application to a Biosynthetic Study
SETSUKO SEKITA,KUNITOSHI YOSHIHIRA and SHINSAKU NATORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (13E,17E)-12-phenylsulfonylbicyclogeranylfarnesol
    ÏàËÆ¶È:56.2%
Chemistry of Natural Compounds          2007          43          268-273
SUPERACID CYCLIZATION OF(2E,6E,10E,14E)-8- PHENYLSULFONYLGERANYLFARNESOL TETRAHYDROPYRANYL ETHER
V. Kulcitki, M. Grin'ko, A. Barba,N. Ungur, and P. F. Vlad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     chaetoglobosin A
    ÏàËÆ¶È:56.2%
Helvetica Chimica Acta          1981          64          2056-2064
19-O-Acetylchaetoglobosin B and 19-O-Acetylchaetoglobosin D, Two New Metabolites of Chaetomium globosum
Alessandro Probst, Christoph Tamm
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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