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yhjiqimao: ½ð±Ò+30 2012-12-23 10:44:05
1 .     zonarol
C21H30O2     ÏàËÆ¶È:66.6%
Tetrahedron Letters          2000          41          5469-5473
Total synthesis of the marine sesquiterpene hydroquinones zonarol and isozonarol and the sesquiterpene quinones zonarone and isozonarone
Jörg Schröder, Christine Magg, Karlheinz Seifert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (+)-copalol
C20H34NO     ÏàËÆ¶È:65%
Journal of Natural Products          2006          69(3)          381-386
(+)-Agelasine D: Improved Synthesis and Evaluation of Antibacterial and Cytotoxic Activities
Anders Vik, Erik Hedner, Colin Charnock, rjan Samuelsen,Rolf Larsson, Lise-Lotte Gundersen, and Lars Bohlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (E)15-nor-16-oxo-8 (17),12-labdadiene
C19H30O     ÏàËÆ¶È:65%
Journal of Asian Natural Products Research          2004          6          199-204
CHEMICAL CONSTITUENTS FROM ALPINIA TONKINENSIS
JIAN ZHANG and LING-YI KONG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     12(S)-15,16-epoxy-13(16),14-labdaiene-8,12-diol
C20H30O2     ÏàËÆ¶È:65%
Acta Chemica Scandinavica          1978          32          203-215
Tobacco Chemistry. 50. (3S,5R,8S,9xi)-5,8-Epoxy-6-megastigmene-3,9-diol and (3S*,5R*,6R*,7E,9xi)-3,6-Epoxy-7-megastigmene-5,9-diol. Two New Nor-carotenoids of Greek Tobacco.
Behr, Dan; Wahlberg, Inger; Nishida, Toshiaki; Enzell, Curt R.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     hydroxybutenolide
C20H30O4     ÏàËÆ¶È:65%
Journal of Chemical Research          2007          31          342-346
Facile access to labdane-type diterpenes: synthesis of coronarin C, zerumin B, labda-8(17), 13(14)-dien-15,16-olide and derivatives from (+)-manool
Villamizar, JosÉ E.; Juncosa, JosÉ; Pittelaud, Jean; Hern¨¢ndez, Madeleyn; Canudas, Nieves; Tropper, Eleonora; Salaza, Franklin; Fuentes, Juan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     petrosaspongiolide L
C24H35O2N     ÏàËÆ¶È:62.5%
Tetrahedron          1997          53          10451-10458
New cytotoxic sesterterpenes from the New Caledonian marine sponge Petrosaspongia nigra (Bergquist)
Luigi Gomez Paloma, Antonio Randazzo, Luigi Minale, C¨¦cile Debitus, Christos Roussakis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     cryptoporic acid H
    ÏàËÆ¶È:61.9%
Phytochemistry          2002          61          25-30
Identification of the major glucosinolate (4-mercaptobutyl glucosinolate) in leaves of Eruca sativa L. (salad rocket)
Richard N. Bennett, Fred A. Mellon, Nigel P. Botting, John Eagles,Eduardo A.S. Rosa, Gary Williamson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     labd-8(17)-en-15-oic acid
    ÏàËÆ¶È:60%
Phytochemistry          1999          50          443-447
A bis-labdenic diterpene from Moldenhawera nutans
Juceni P. David, Jorge M. David, Shu-Wei Yang, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     Labda-8(17),12Z,14-triene
    ÏàËÆ¶È:60%
Phytochemistry          1992          31          615-620
Diterpenoids and cyclolanostanolides from Abies marocana
Alejandro F. Barrero, Juan F. Sanchez, Enrique J. Alvarez-Manzaneda, Manuel Muñoz, Ali Haïdour
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     steviol
    ÏàËÆ¶È:60%
Phytochemistry          1992          31          1553-1559
Minor diterpene glycosides from sweet leaves of Rubus suavissimus
Kazuhiro Ohtani, Yoko Aikawa, Ryoji Kasai, Wen-Hua Chou, Kazuo Yamasaki, Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Compound 4
    ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry Letters          1997          7          2485-2490
Design and synthesis of an ¦Á-mannosyl terpenoid as selective inhibitor of P-selectin
Tsuyoshi Ikeda, Tetsuya Kajimoto, Hirosato Kondo, Chi-Huey Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     8(17),14-Labdadien-13-ol
    ÏàËÆ¶È:60%
Molecules          2011          16          10653-10667
Resin Diterpenes from Austrocedrus chilensis
Ver¨®nica Rachel Olate, Olatz Goikoetxeaundia Usandizaga and Guillermo Schmeda-Hirschmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 24a
    ÏàËÆ¶È:60%
Organic & Biomolecular Chemistry          2011          9          2156-2165
Substrate specificity of Rv3378c, an enzyme from Mycobacterium tuberculosis, and the inhibitory activity of the bicyclic diterpenoids against macrophage phagocytosis
Tsutomu Hoshino, Chiaki Nakano, Takahiro Ootsuka, Yosuke Shinohara and Takashi Hara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 24b
    ÏàËÆ¶È:60%
Organic & Biomolecular Chemistry          2011          9          2156-2165
Substrate specificity of Rv3378c, an enzyme from Mycobacterium tuberculosis, and the inhibitory activity of the bicyclic diterpenoids against macrophage phagocytosis
Tsutomu Hoshino, Chiaki Nakano, Takahiro Ootsuka, Yosuke Shinohara and Takashi Hara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     compound 26a+b
    ÏàËÆ¶È:60%
Organic & Biomolecular Chemistry          2011          9          2156-2165
Substrate specificity of Rv3378c, an enzyme from Mycobacterium tuberculosis, and the inhibitory activity of the bicyclic diterpenoids against macrophage phagocytosis
Tsutomu Hoshino, Chiaki Nakano, Takahiro Ootsuka, Yosuke Shinohara and Takashi Hara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     (+)-zerumin B
    ÏàËÆ¶È:60%
The Journal of Organic Chemistry          2006          71          6670-6673
Synthesis and Stereochemistry of the Antitumor Diterpenoid (+)-Zerumin B
John Boukouvalas, Jian-Xin Wang, Olivier Marion, and Bruno Ndzi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     copalyl diphosphate
C20H35O7P2Na     ÏàËÆ¶È:60%
The Journal of Antibiotics          2004          57          739-747
Presence of Copalyl Diphosphate Synthase Gene in an Actinomycete Possessing the Mevalonate Pathway
TAKASHI KAWASAKI,TOMOHISA KUZUYAMA,YUKO KUWAMORI,NOBUYASU MATSUURA,NOBUYA ITOH,KAZUO FURIHATA,HARUO SETO and TOHRU DAIRI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     zerumin B
C20H30O4     ÏàËÆ¶È:60%
Journal of Chemical Research          2007          31          342-346
Facile access to labdane-type diterpenes: synthesis of coronarin C, zerumin B, labda-8(17), 13(14)-dien-15,16-olide and derivatives from (+)-manool
Villamizar, JosÉ E.; Juncosa, JosÉ; Pittelaud, Jean; Hern¨¢ndez, Madeleyn; Canudas, Nieves; Tropper, Eleonora; Salaza, Franklin; Fuentes, Juan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     16-aza-ent-trachylobane
    ÏàËÆ¶È:60%
Journal of the American Chemical Society          2007          129          12453-12460
16-Aza-ent-beyerane and 16-Aza-ent-trachylobane:  Potent Mechanism-Based Inhibitors of Recombinant ent-Kaurene Synthase from Arabidopsis thaliana
Arnab Roy, Frank G. Roberts, P. Ross Wilderman, Ke Zhou, Reuben J. Peters, and Robert M. Coates
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     ent-beyeran-16¦Â-ol
    ÏàËÆ¶È:60%
Journal of the American Chemical Society          2007          129          12453-12460
16-Aza-ent-beyerane and 16-Aza-ent-trachylobane:  Potent Mechanism-Based Inhibitors of Recombinant ent-Kaurene Synthase from Arabidopsis thaliana
Arnab Roy, Frank G. Roberts, P. Ross Wilderman, Ke Zhou, Reuben J. Peters, and Robert M. Coates
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     tagalsin O
C20H28O     ÏàËÆ¶È:60%
Natural Product Communications          2010          5          9-12
A New Dolabrane-type Diterpene from Ceriops tagal
Xiao-Wei Ouyang, Xia-Chang Wang, Qing-Xi Yue and Li-Hong Hu*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     8,14-labdadien-13-ol
C20H34O     ÏàËÆ¶È:60%
Archives of Pharmacal Research          2011          34          913-917
Inhibition of Nitric Oxide Production in RAW 264.7 Macrophages by Diterpenoids from Phellinus pini
Hyun Jin Jang and Ki-Sook Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     isocoronarin-D
C20H30O3     ÏàËÆ¶È:60%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2004          43(5)          58-60
Studies on the Chemical Constituents of Hedychium forrestii Diels.
LIU Li-juan, GUO Wan-cheng, PENG Qin-long, YAN Su-jun, SU Jing-yu, ZENGLong-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     compound 12
C20H32O3     ÏàËÆ¶È:60%
Phytochemistry          2012          75          90-98
Oxygenated compounds from the bioconversion of isostevic acid and their inhibition of TNF-¦Á and COX-2 expressions in LPS-stimulated RAW 264.7 cells
Li-Ming Yang, Shwu-Fen Chang, Wen-Kuang Lin, Bo-Hon Chou, Li-Hsuan Wang, Pan-Chun Liu, Shwu-Jiuan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     2''-Omethyl cryptoporic acid H
C22H34O7     ÏàËÆ¶È:59.0%
Phytochemistry          2002          61          25-30
Identification of the major glucosinolate (4-mercaptobutyl glucosinolate) in leaves of Eruca sativa L. (salad rocket)
Richard N. Bennett, Fred A. Mellon, Nigel P. Botting, John Eagles,Eduardo A.S. Rosa, Gary Williamson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-12-23 09:57:15
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