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1 .     aspochalasin K
C25H39NO5     ÏàËÆ¶È:80%
Journal of Natural Products          2004          67          328-332
Aspochalasins I, J, and K: Three New Cytotoxic Cytochalasans of Aspergillus flavipes from the Rhizosphere of Ericameria laricifolia of the Sonoran Desert
Guang-Xiong Zhou, E. M. Kithsiri Wijeratne, Donna Bigelow,Leland S. Pierson, Hans D. VanEtten, and A. A. Leslie Gunatilaka

2 .     aspochalasin D
C24H35NO4     ÏàËÆ¶È:66.6%
The Journal of Antibiotics          2001          54          379-381
Selective Cytotoxicity and Stereochemistry of Aspochalasin D
TAIJIRO TOMIKAWA,KAZUO SHIN-YA,TAISEI KINOSHITA,ATSUSHI MIYAJIMA,HARUO SETO and YOICHI HAYAKAWA
3 .     aspochalasin H
C24H35NO5     ÏàËÆ¶È:62.5%
The Journal of Antibiotics          2002          55          666-668
Structure of Aspochalasin H, a New Member of the Aspochalasin Family
TAIJIRO TOMIKAWA,KAZUO SHIN-YA,HARUO SETO,NORIYUKI OKUSA,TAKAYUKI KAJIURA and YOICHI HAYAKAWA
4 .     methyl (1S,4aS,5R,6R,8aS)-5-[2-(3-furyl)ethyl]-1,4a-dimethyl-6-methylaminoperhydronaphthalene-1-carboxylate [methyl (8R)-15,16-epoxy-8-methylamino-17-norlabda-13(16),14-dien-18-oate]
    ÏàËÆ¶È:61.9%
Russian Journal of Organic Chemistry          2005          41          535-545
Synthetic Transformations of Higher Terpenoids: IX. Nitrogen-Containing Heterocyclic Compounds on the Basis of Lambertianic Acid
S. V. Chernov, E. E. Shul¡¯ts, M. M. Shakirov, I. Yu. Bagryanskaya and Yu. V. Gatilov, et al

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3Â¥2012-04-17 10:52:44
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1 .     14,17-diacetoxy-20-isopropyl-5,9-dimethylpentacyclo[10.6.2(1,10).0(4,9).0(13,18)]icos-19-ene-5-yl-methyl acetate
C32H48O6     ÏàËÆ¶È:50%
Russian Journal of Organic Chemistry          2008          44          1598-1605
Synthesis, structure, and acylation of dihydroquinopimaric acid hydroxy derivatives
I. E. Smirnova, E. V. Tret¡¯yakova, O. B. Flekhter, L. V. Spirikhin and F. Z. Galin, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------
4Â¥2012-04-18 08:44:44
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nju123456: ½ð±Ò+5 2012-04-18 09:10:27
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1 .     aspochalasin K
C25H39NO5     ÏàËÆ¶È:80%
Journal of Natural Products          2004          67          328-332
Aspochalasins I, J, and K: Three New Cytotoxic Cytochalasans of Aspergillus flavipes from the Rhizosphere of Ericameria laricifolia of the Sonoran Desert
Guang-Xiong Zhou, E. M. Kithsiri Wijeratne, Donna Bigelow,Leland S. Pierson, Hans D. VanEtten, and A. A. Leslie Gunatilaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

2 .     aspochalasin D
C24H35NO4     ÏàËÆ¶È:66.6%
The Journal of Antibiotics          2001          54          379-381
Selective Cytotoxicity and Stereochemistry of Aspochalasin D
TAIJIRO TOMIKAWA,KAZUO SHIN-YA,TAISEI KINOSHITA,ATSUSHI MIYAJIMA,HARUO SETO and YOICHI HAYAKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

3 .     aspochalasin H
C24H35NO5     ÏàËÆ¶È:62.5%
The Journal of Antibiotics          2002          55          666-668
Structure of Aspochalasin H, a New Member of the Aspochalasin Family
TAIJIRO TOMIKAWA,KAZUO SHIN-YA,HARUO SETO,NORIYUKI OKUSA,TAKAYUKI KAJIURA and YOICHI HAYAKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     methyl (1S,4aS,5R,6R,8aS)-5-[2-(3-furyl)ethyl]-1,4a-dimethyl-6-methylaminoperhydronaphthalene-1-carboxylate [methyl (8R)-15,16-epoxy-8-methylamino-17-norlabda-13(16),14-dien-18-oate]
    ÏàËÆ¶È:61.9%
Russian Journal of Organic Chemistry          2005          41          535-545
Synthetic Transformations of Higher Terpenoids: IX. Nitrogen-Containing Heterocyclic Compounds on the Basis of Lambertianic Acid
S. V. Chernov, E. E. Shul¡¯ts, M. M. Shakirov, I. Yu. Bagryanskaya and Yu. V. Gatilov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     3¦Â,17-dihydroxycleistantha-12,15-dien-2-one
C20H30O3     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2006          Vol. 89          2841
A Rare New Cleistanthane Diterpene from the Pericarp of Trewia nudiflora
Zhi-Zhi Du and Yue-Mao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

6 .     labd-7-en-15,18-dioic acid
    ÏàËÆ¶È:60%
Natural Product Research          2002          16          223-228
Labdane Diterpenes from Haplopappus Illinitus
Francesca Faini; Cecilia Labb¨¦; Ren¨¦ Torres; Giuliano Delle Monache; Franco Delle Monache
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     dihydrosteviol A
    ÏàËÆ¶È:60%
Journal of Natural Products          1987          Vol 50          434
Characterization and Feeding Deterrent Effects on the Aphid, Schizaphis graminum, of Some Derivatives of the Sweet Compounds, Stevioside and Rebaudioside A
N. P. D. Nanayakkara, J. A. Klocke, C. M. Compadre, R. A. Hussain, J. M. Pezzuto, A. D. Kinghorn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     ent-7-acetoxy-16,19-dihydroxygibberellan-20-oic acid 20,19-lactone
C22H32O5     ÏàËÆ¶È:60%
Phytochemistry          1993          34          693-696
Bio-transformation of gibberellin 20,19-lactones by Rhizopus stolonifer
Braulio M. Fraga, J.Clemente Diaz Gomez, M.Shaiq Ali, James R. Hanson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     compound 9b
    ÏàËÆ¶È:60%
Tetrahedron Letters          2001          42          4163-4165
Efforts towards the synthesis of jatrapholane diterpenes: a biomimetic transannular reaction approach
Tomoo Matsuura, Yukimasa Terada, Shosuke Yamamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     methyl (1S,4aS,5R,8aS)-5-[2-(3-furyl)ethyl]-1,4a-dimethyl-6-oxoperhydronaphthalene-1-carboxylate [methyl 15,16-epoxy-17-nor-8-oxolabda-13(16),14-dien-18-oate]
    ÏàËÆ¶È:60%
Russian Journal of Organic Chemistry          2005          41          535-545
Synthetic Transformations of Higher Terpenoids: IX. Nitrogen-Containing Heterocyclic Compounds on the Basis of Lambertianic Acid
S. V. Chernov, E. E. Shul¡¯ts, M. M. Shakirov, I. Yu. Bagryanskaya and Yu. V. Gatilov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

11 .     (1S,2E,4R,6R,7E,11S,12S)-6-acetoxy-2,7-cembradiene-4,,11,12-triol
    ÏàËÆ¶È:59.0%
Acta Chemica Scandinavica          1986          40          123-134
Tobacco Chemistry. 66. (5R,6S,7E,9S)-7-Megastigmene-5,6,9-triol, a New Constituent of Greek Tobacco.
Wahlberg, Inger; Eklund, Ann-Marie; Enzell, Curt R.; Berg, Jan-Eric
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

12 .     aspochalasin T
C24H35NO5     ÏàËÆ¶È:58.3%
Chinese Chemical Letters          2010          21          824-826
Three new aspochalasin derivatives from the marine-derived fungus Spicaria elegans
Zhen Jian Lin; Tian Jiao Zhu; Li Chen; Qian Qun Gu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     methyl havardate C
    ÏàËÆ¶È:57.1%
Phytochemistry          1987          26          483-489
Havardic acids A-F and havardiol,labdane diterpenoids from Grindelia havardii
Shivanand D. Jolad,Barbara N. Timmermann,Joseph J. Hoffmann,Robert B. Bates,Teruna J. Siahaan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     4¦Â-hydroxy-10¦Á-methoxy-15-(3-methyl-2-butenyl)aromadendrane
C21H36O2     ÏàËÆ¶È:57.1%
Tetrahedron          1997          53          9301-9312
Rare aromadendrane diterpenoids from a new soft coral species of Sinularia genus of the Indian Ocean
Ammanamanchi S.R. Anjaneyulu, Moturu V.R. Krishnamurthy, Gottumukkala V. Rao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     methyl ent-12¦Â-acetoxy-15¦Â,16¦Â-epoxykauran-19-oate
C23H34O5     ÏàËÆ¶È:56.5%
Journal of Natural Products          2004          67          614-621
Further Labdane and Kaurane Diterpenoids and Other Constituents from Plectranthus fruticosus
Cristina Gaspar-Marques, M. Ftima Simes, and Benjamn Rodrguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     aspochalasin R
    ÏàËÆ¶È:56%
Chinese Chemical Letters          2010          21          824-826
Three new aspochalasin derivatives from the marine-derived fungus Spicaria elegans
Zhen Jian Lin; Tian Jiao Zhu; Li Chen; Qian Qun Gu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     1¦Á,2¦Á,3¦Á,4a -Diepoxy-8¦Á-angeloyloxy-10¦Â-hydroxy-6¦ÂH,7¦ÁH,11¦ÂH-12,6¦Á-guaianolide
C22H29NO7     ÏàËÆ¶È:55%
Phytochemistry          2006          67          764-770
Sesquiterpene lactones from Achillea collina J. Becker ex Reichenb
Antoaneta Trendafilova, Milka Todorova, Bozhanka Mikhova, Antonina Vitkova, Helmut Duddeck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     2¦Á,3¦Â,13(S),16¦Á-tetrahydroxystemodane
C20H34O2     ÏàËÆ¶È:55%
Phytochemistry          2004          65          701-710
Investigation of the importance of the C-2 oxygen function in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145
Glenroy D.A. Martin, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     cussovantonin A
C20H32O5     ÏàËÆ¶È:55%
Phytochemistry          2002          61          367-372
ent-Kaurane diterpenoid glycosides from a Malagasy endemic plant, Cussonia vantsilana
Liva Harinantenaina, Ryoji Kasai, Kazuo Yamasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     pulioplopanone B
C15H26O3     ÏàËÆ¶È:55%
Journal of Natural Products          2005          68          523-531
Sesquiterpenoids from Pulicaria canariensis and Their Cytotoxic Activities
Jorge Triana, Mariana Lpez, Francisco J. Prez, Javier Gonzlez-Platas,Jos Quintana, Francisco Estvez, Francisco Len, and Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     compound 1
C20H33BrO2     ÏàËÆ¶È:55%
Journal of Natural Products          2003          66          1225-1228
New Brominated Labdane Diterpenes from the Red Alga Laurencia obtusa
Dimitra Iliopoulou,Nikos Mihopoulos, Vassilios Roussis,and Constantinos Vagias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     ent-16-ketobeyeran-19-oic acid
    ÏàËÆ¶È:55%
Journal of Natural Products          2002          65          273-277
Microbial Transformations of Isosteviol
Feng-Lin Hsu, Chia-Chung Hou, Li-Ming Yang, Juei-Tang Cheng, Tzong-Cherng Chi, Pang-Chun Liu, and Shwu-Jiuan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     (-)-16¦Á-hydroxykauran-19-oic acid
    ÏàËÆ¶È:55%
Journal of Natural Products          1999          62          1522-1525
Immunosuppressive Diterpenoids from Tripterygium wilfordii
Hongquan Duan, Yoshihisa Takaishi, Hiroshi Momota, Yasukazu Ohmoto, Takao, Taki, Yongfeng Jia, and Duan Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     isosteviol
    ÏàËÆ¶È:55%
Planta Medica          2007          73          1581-1587
Novel ent-Beyeran-19-oic Acids from Biotransformations of Isosteviol Metabolites by Mortierella isabellina
Che-Ling Lin1,Shwu-Jiuan Lin,Wei-Jan Huang,Yuan-Ling Ku,Tung-Hu Tsai,Feng-Lin Hsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     11¦Á,13-dihydro-2-O-tigloylflorilenalin
C20H28O5     ÏàËÆ¶È:55%
Planta Medica          2005          71          1044-1052
New Sesquiterpene Lactones from Arnica Tincture Prepared from Fresh Flowerheads of Arnica montana
Olha Kos,Maja T. Lindenmeyer,Aurelia Tubaro,Silvio Sosa,Irmgard Merfort
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     8¦Á,13S-epoxylabdane-14S,15-diol
C20H36O3     ÏàËÆ¶È:55%
Planta Medica          2000          66          734-739
Phytotoxic Compounds from Xanthocephalum gymnospermoides var.eradiatum
Isabel Rivero-Cruz,Jos¨¦ Luis Trejo,Mar¨ªa Isabel Aguilar,Robert Bye,Rachel Mata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     P4
C19H28ClNO5S     ÏàËÆ¶È:55%
Chemical & Pharmaceutical Bulletin          1996          44          273-279
Michael-Type Addition of Illudin S, a Toxic Substance from Lampteromyces japonicus, with Cysteine and Cysteine-Containing Peptides in Vitro
Ken TANAKA,Takako INOUE,Yasuhiro TEZUKA and Tohru KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     saussureamine A
C20H29O4N     ÏàËÆ¶È:55%
Chemical & Pharmaceutical Bulletin          1993          41          214-216
SAUSSUREAMINES A, B, C, D, AND E, NEW ANTI-ULCER PRINCIPLES FROM CHINESE SAUSSUREAE RADIX
Masayuki YOSHIKAWA,Shoko HATAKEYAMA,Yasuhiro INOUE and Johji YAMAHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     16¦Á-hydroxy-ent-kauran-19-oic acid
C20H32O3     ÏàËÆ¶È:55%
Chemical & Pharmaceutical Bulletin          1984          32          4620-4624
Chemical and Chemotaxonomical Studies on Filices. LI. Chemical Studies on the Constituents of Costa Rican Ferns. (3)
TOSHIKO SATAKE,TAKAO MURAKAMI,YASUHISA SAIKI,CHIUMING CHEN and LUIS D. GOMEZ P.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     3-Methylhydroxyestra-1,3,5(10)-trien-17-one
    ÏàËÆ¶È:55%
Chemistry of Natural Compounds          2004          40          50-53
SYNTHESIS OF NEW ESTRONE DERIVATIVES USING EXCESS OXALYL CHLORIDE
L. Nahar, S. D. Sarker,P. K. Li,and A. B. Turner1
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5Â¥2012-04-18 08:46:24
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