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1 .     aspochracin
    ÏàËÆ¶È:95.6%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     JBIR-15
C22H34N4O4     ÏàËÆ¶È:90.9%
Bioscience, Biotechnology, and Biochemistry          2009          73          1898-1900
JBIR-15, a New Aspochracin Derivative, Isolated from a Sponge-Derived Fungus, Aspergillus sclerotiorum Huber Sp080903f04
Keiichiro MOTOHASHI, Shigeki INABA, Motoki TAKAGI and Kazuo SHIN-YA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     sclerotiotide C
C24H38N4O4     ÏàËÆ¶È:86.9%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     sclerotiotide E
C23H36N4O4     ÏàËÆ¶È:86.9%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     sclerotiotide I
C23H38N4O6     ÏàËÆ¶È:86.9%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     sclerotiotide K
C23H38N4O6     ÏàËÆ¶È:86.9%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     sclerotiotide B
C21H34N4O4     ÏàËÆ¶È:86.3%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     sclerotiotide D
C22H34N4O4     ÏàËÆ¶È:86.3%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     sclerotiotide G
C23H36N4O6     ÏàËÆ¶È:82.6%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     sclerotiotide H
C23H38N4O6     ÏàËÆ¶È:82.6%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     sclerotiotide J
C23H38N4O6     ÏàËÆ¶È:82.6%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     sclerotiotide A
C22H34N4O4     ÏàËÆ¶È:81.8%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Sclerotiotide F
C21H33N4O5     ÏàËÆ¶È:77.2%
Phytochemistry Letters          2012          5          114-117
Unraveling the numerous biosynthetic products of the marine sediment-derived fungus,Aspergillus insulicola
Q.X. Wu,X.J. Jin,M. Draskovic,M.S. Crews,K. Tenney,F.A. Valeriote,X.J. Yao,P. Crews
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 12q
C25H31ClN2O4S     ÏàËÆ¶È:73.9%
The Journal of Organic Chemistry          2012          77          7435-7470
Assembly of Four Diverse Heterocyclic Libraries Enabled by Prins Cyclization, Au-Catalyzed Enyne Cycloisomerization, and Automated Amide Synthesis
Jiayue Cui, David I. Chai, Christopher Miller, Jason Hao, Christopher Thomas, JingQi Wang, Karl A. Scheidt, and Sergey A. Kozmin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     sclerotiotide F
C21H32N4O5     ÏàËÆ¶È:72.7%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     N-{[2'-(1H-Tetrazol-5-yl)biphenyl-4-yl]methyl}-N-methyl-1-pentanoylpyrrolidine-2-carboxamide
C25H30N6O2     ÏàËÆ¶È:72.7%
Archiv der Pharmazie          2011          344          617-626
1-Pentanoyl-N-{[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-pyrrolidine-2-carboxamide: Investigation of Structural Variations
Alessia Catalano, Alessia Carocci, Antonia Di Mola, Claudio Bruno, Patrick M. L. Vanderheyden,and Carlo Franchini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Pre-sclerotiotide
C20H30N4O5     ÏàËÆ¶È:72.7%
Phytochemistry Letters          2012          5          114-117
Unraveling the numerous biosynthetic products of the marine sediment-derived fungus,Aspergillus insulicola
Q.X. Wu,X.J. Jin,M. Draskovic,M.S. Crews,K. Tenney,F.A. Valeriote,X.J. Yao,P. Crews
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (2'E)-1,4-diacetoxy-2-(3',7'-dimethylocta-2',6'-dienyl)-6-methylbenzene
C21H28O4     ÏàËÆ¶È:72.7%
Phytochemistry          1981          20          2598-2600
Isoprenoid dihydroquinones from a brown alga, Cystophora sp.
Robert J. Capon, Emilio L. Ghisalberti, Phillip R. Jefferies
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     (3R,4S,5S,6S)-4-{(1E)-1,5-dimethylhexa-1,4-dien-1-yl}-5,6-diacetoxy-11-oxaspiro[2.5]octane
C19H28O5     ÏàËÆ¶È:72.7%
Tetrahedron          1999          55          2205-2224
Chiral and stereoselective total synthesis of novel immunosuppressant FR65814 from d-glucose
Seiji Amano, Noriko Ogawa, Masami Ohtsuka, Noritaka Chida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     gibberosene F
C24H36O5     ÏàËÆ¶È:70.8%
Journal of Natural Products          2008          71(2)          179-185
Oxygenated Cembranoids from a Formosan Soft Coral Sinularia gibberosa
Atallah F. Ahmed, Zhi-Hong Wen, Jui-Hsin Su, Ya-Ting Hsieh, Yang-Chang Wu, Wan-Ping Hu, and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (1R*,5S*,6S*)-5-(acetyloxy)-6-[3-(acetyloxy)-1,5-dimethylhex-4-enyl]-3-methylcyclohex-2-en-4-on-1-yl (2Z)-2-methyl-but-2-enoate
C24H34O7     ÏàËÆ¶È:70.8%
Natural Product Communications          2010          5          667-668
A new Bisabolane Derivative of Leontopodium andersonii
Stefan Schwaiger, Stefanie Hehenberger, Ernst P. Ellmerer and Hermann Stuppner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     andrimid
C27H33N3O5     ÏàËÆ¶È:70.8%
Journal of the American Chemical Society          1987          109          4409-4411
Andrimid, a new peptide antibiotic produced by an intracellular bacterial symbiont isolated from a brown planthopper
Andreas Fredenhagen, Susan Y. Tamura, Peter T. M. Kenny, Hajime Komura, Yoko Naya, Koji Nakanishi, Koushi Nishiyama, Miyoji Sugiura, Hiroshi Kita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     helenalin-[(2-hydroxyethyl-3-methyl)acrylate]
C20H24O6     ÏàËÆ¶È:69.5%
Journal of Natural Products          2005          68          800-803
Pseudoguanolide Sesquiterpene Lactones from Vernoniopsis caudata and Their in Vitro Antiplasmodial Activities
Voahangy Ramanandraibe, Marie-Thrse Martin, Dina L. Rakotondramanana, Lengo Mambu, David Ramanitrahasimbola, Medhi Labaed, Philippe Grellier, Philippe Rasoanaivo, and Franois Frappier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     segetalin G
C25H38O6N6     ÏàËÆ¶È:69.5%
Journal of Natural Products          1997          60          216-218
Cyclic Peptides from Higher Plants. 34.1 Segetalins G and H, Structures and Estrogen-like Activity of Cyclic Pentapeptides from Vaccaria segetalis
Young Sook Yun, Hiroshi Morita, Koichi Takeya, and Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     Aripiprazole contaminant
    ÏàËÆ¶È:69.5%
Bioorganic & Medicinal Chemistry Letters          2003          13          65-68
Synthetic study on the unique dimeric arylpiperazine: access to the minor contaminant of aripiprazole
Yasuhiro Torisawa, Koichi Shinhama, Takao Nishi, Jun-ichi Minamikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-18 15:32:59
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gaochang1989

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1 .     aspochracin
    ÏàËÆ¶È:95.6%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     sclerotiotide C
C24H38N4O4     ÏàËÆ¶È:82.6%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     sclerotiotide H
C23H38N4O6     ÏàËÆ¶È:82.6%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     sclerotiotide I
C23H38N4O6     ÏàËÆ¶È:82.6%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     sclerotiotide J
C23H38N4O6     ÏàËÆ¶È:82.6%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     sclerotiotide K
C23H38N4O6     ÏàËÆ¶È:82.6%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

7 .     sclerotiotide E
C23H36N4O4     ÏàËÆ¶È:78.2%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

8 .     sclerotiotide B
C21H34N4O4     ÏàËÆ¶È:77.2%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

9 .     sclerotiotide D
C22H34N4O4     ÏàËÆ¶È:72.7%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

10 .     sclerotiotide F
C21H32N4O5     ÏàËÆ¶È:72.7%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

11 .     sclerotiotide G
C23H36N4O6     ÏàËÆ¶È:69.5%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

12 .     4¦Â-acetoxy-3¦Â-angeloyloxy-11-hydroxy-6,7-dehydroeudesman-8-one
    ÏàËÆ¶È:68.1%
Phytochemistry          1996          43          417-421
Eudesmane derivatives from Pluchea quitoc
Giselle M. S. P. Guilhon, Adolfo H. M¨¹ller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

13 .     Pre-sclerotiotide
C20H30N4O5     ÏàËÆ¶È:63.6%
Phytochemistry Letters          2012          5          114-117
Unraveling the numerous biosynthetic products of the marine sediment-derived fungus,Aspergillus insulicola
Q.X. Wu,X.J. Jin,M. Draskovic,M.S. Crews,K. Tenney,F.A. Valeriote,X.J. Yao,P. Crews
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

14 .     JBIR-15
C22H34N4O4     ÏàËÆ¶È:63.6%
Bioscience, Biotechnology, and Biochemistry          2009          73          1898-1900
JBIR-15, a New Aspochracin Derivative, Isolated from a Sponge-Derived Fungus, Aspergillus sclerotiorum Huber Sp080903f04
Keiichiro MOTOHASHI, Shigeki INABA, Motoki TAKAGI and Kazuo SHIN-YA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

15 .     andrimid
C27H33N3O5     ÏàËÆ¶È:62.5%
Journal of the American Chemical Society          1987          109          4409-4411
Andrimid, a new peptide antibiotic produced by an intracellular bacterial symbiont isolated from a brown planthopper
Andreas Fredenhagen, Susan Y. Tamura, Peter T. M. Kenny, Hajime Komura, Yoko Naya, Koji Nakanishi, Koushi Nishiyama, Miyoji Sugiura, Hiroshi Kita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

16 .     (1R*,2E,4R*,6E,8S*,10S*,11*,21R *)-8,18-Diacetoxy-10-hydroxy-2,6-dolabelladiene
C24H38O5     ÏàËÆ¶È:62.5%
The Journal of Organic Chemistry          1977          42          3157-3162
Diterpenes from Dolabella californica
Chris Ireland, D. John Faulkner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

17 .     sinulaflexiolide J
C22H32O5     ÏàËÆ¶È:59.0%
Journal of Natural Products          2008          71(7)          1133-1140
Sinulaflexiolides A#K, Cembrane-Type Diterpenoids from the Chinese Soft Coral Sinularia flexibilis
Ting Wen, Yi Ding, Zhiwei Deng, Leen van Ofwegen, Peter Proksch, and Wenhan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

18 .     8¦Á-O-(4-acetoxy-5-hydroxyangeloyl)-11¦Â,13-dihydrocnicin
C22H30O9     ÏàËÆ¶È:59.0%
Journal of Natural Products          2007          70          1796-1799
Minor Sesquiterpene Lactones from Centaurea pullata and Their Antimicrobial Activity
Samah Djeddi, Anastasia Karioti,Marina Sokovic, Dejan Stojkovic, Ratiba Seridi, and Helen Skaltsa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

19 .     8b-(4'-acetoxy-5'-hydroxytigloyloxy)-costunolide
    ÏàËÆ¶È:59.0%
Phytochemistry          1999          51          79-82
Sesquiterpene lactones from Stevia alpina var. glutinosa
Zaida N.J.de Herna ndez, Cesar A.N. Catalan, Luis R. Hernandez, Diana Guerra-Ramirez, Pedro Joseph!Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

20 .     sclerotiotide A
C22H34N4O4     ÏàËÆ¶È:59.0%
Journal of Natural Products          2010          73          1133-1137
Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1
Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

21 .     Sclerotiotide F
C21H33N4O5     ÏàËÆ¶È:59.0%
Phytochemistry Letters          2012          5          114-117
Unraveling the numerous biosynthetic products of the marine sediment-derived fungus,Aspergillus insulicola
Q.X. Wu,X.J. Jin,M. Draskovic,M.S. Crews,K. Tenney,F.A. Valeriote,X.J. Yao,P. Crews
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-09-18 16:06:34
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