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1 .     cupresol
C19H26O4     ÏàËÆ¶È:80%
Journal of Natural Products          1984          Vol 47          983-987
A New Diterpene From Cupressus goveniana var. Abramasiana: 5¦Â-Hydroxy-6-Oxasugiol (Cupresol)
Shivanand D. Jolad, Joseph J. Hoffmann, Karl H. Schram, Jack R. Cole, Robert B. Bates, Michael S. Tempesta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (¡À)-N1-[2-(1-Cyclohexenyl)ethyl]-N3-(3,7-dimethyloctyl)guanidine hydrochloride
C19H38N3Cl     ÏàËÆ¶È:80%
Archiv der Pharmazie          2002          335          535-546
Novel High Energy Intermediate Analogues with Triazasterol-Related Structures as Inhibitors of Ergosterol Biosynthesis Part I: Synthesis and Antifungal Activity of N-alkyl-N'-(phenethyl-and cyclohexenylethyl)guanidines and N2-Substituted 2-Imidazolinamin฀
Edith Gößnitzer, Roland Malli, Silvia Schuster, Bertrand Favre and Neil S. Ryder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (9S, 10S)-ent-9,10-epoxyverticillol
C20H34O2     ÏàËÆ¶È:75%
Phytochemistry          2005          66          1662-1670
ent-Verticillane-type diterpenoids from the Japanese liverwort Jackiella javanica
Fumihiro Nagashima , Katsuhiro Kishi, Yuko Hamada,Shigeru Takaoka, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     phytenal
    ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2009          40          1198-1201
Chemical constituents of Lobelia chinensis
DENG Ke-zhong; XIONG Ying; GAO Wen-yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 2
C20H32O     ÏàËÆ¶È:75%
Bulletin of the Chemical Society of Japan          2002          75          131-136
New Dolabellane-Type Diterpenoids from the Okinawan Soft Coral of the Genus Clavularia
Kazuo Iguchi, Hisako Sawai, Hiroto Nishimura, Minako Fujita, Takao Yamori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (4S,8S)-4-hydroxy-1(14),17-dolastadiene
    ÏàËÆ¶È:75%
Tetrahedron          2008          64          3975-3979
Dolastanes from the brown alga Dilophus spiralis: absolute stereochemistry and evaluation of cytotoxicity
Efstathia Ioannou, Antonio Quesada, Constantinos Vagias, Vassilios Roussis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     xanthoperol
C20H26O3     ÏàËÆ¶È:75%
Journal of Chemical Ecology          2009          35          635-642
Antitermitic Activities of Abietane-type Diterpenes from Taxodium distichum Cones
Norihisa Kusumoto, Tatsuya Ashitani, Yuichi Hayasaka, Tetsuya Murayama and Koichi Ogiyama, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     xanthoperol
C20H26O3     ÏàËÆ¶È:75%
Journal of Chemical Ecology          2009          35          635-642
Antitermitic Activities of Abietane-type Diterpenes from Taxodium distichum Cones
Norihisa Kusumoto, Tatsuya Ashitani, Yuichi Hayasaka, Tetsuya Murayama, Koichi Ogiyama, Koetsu Takahashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     cassa13(14),15-dien-19-oic acid
C20H30O2     ÏàËÆ¶È:70%
Chemical & Pharmaceutical Bulletin          2003          51(2)          207-208
Diterpenoids from Amazonian Crude Drug of Fabaceae
Tadashi KIDO, Masahiko TANIGUCHI, and Kimiye BABA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (13S,14S)-Ent-13,14-epoxy-5-epi-verticillol
C20H34O2     ÏàËÆ¶È:70%
Phytochemistry          2005          66          1662-1670
ent-Verticillane-type diterpenoids from the Japanese liverwort Jackiella javanica
Fumihiro Nagashima , Katsuhiro Kishi, Yuko Hamada,Shigeru Takaoka, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (1S,3Z,7E,11S,12S)-(+)-verticilla-3,7-dien-12,20-diol
C20H34O2     ÏàËÆ¶È:70%
Journal of Natural Products          2005          68          1598-1602
Verticillane Derivatives from Bursera suntui and Bursera kerberi
Juan D. Hernndez-Hernndez, Luisa U. Romn-Marn, Carlos M. Cerda-Garca-Rojas, and Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (1S,3Z,7E,11S,12S)-(+)-verticilla-3,7-dien-12,20-diol 20-acetate
C22H36O3     ÏàËÆ¶È:70%
Journal of Natural Products          2005          68          1598-1602
Verticillane Derivatives from Bursera suntui and Bursera kerberi
Juan D. Hernndez-Hernndez, Luisa U. Romn-Marn, Carlos M. Cerda-Garca-Rojas, and Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     biflora-4,9,15-triene
    ÏàËÆ¶È:70%
Journal of Natural Products          2007          70          901-905
Lemnalosides A-D, Decalin-Type Bicyclic Diterpene Glycosides from the Marine Soft Coral Lemnalia sp.
Guangmin Yao, Nicholas B. Vidor, Adam P. Foss, and Leng Chee Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3¦Â-hydroxygrindelic acid
    ÏàËÆ¶È:70%
Journal of Natural Products          2001          64          1365-1367
Manoyl Oxide r-Arabinopyranoside and Grindelic Acid Diterpenoids from Grindelia integrifolia
Ahmed A. Ahmed,Ahmed A. Mahmoud, Usama M. Ahmed, Ashraf A. El-Bassuony, Mohamed H. Abd El-Razk,Paul W. Pare, and Joe Karchesy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     mulin-9(10),12(13)-diene
    ÏàËÆ¶È:70%
Journal of Natural Products          1998          61          965-968
A New Antitubercular Mulinane Diterpenoid from Azorella madreporica Clos
Gerald A. Wächter, Scott G. Franzblau, Gloria Montenegro, Enrique Suarez, Ren¨¦e H. Fortunato, Edgardo Saavedra, and Barbara N. Timmermann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     15-oxolabda-8(17),13Z-dien-19-oic acid
C20H30O3     ÏàËÆ¶È:70%
Planta Medica          2003          69          69-72
Potential Antitumor Promoting Diterpenoids from the Stem Bark of Thuja standishii
Manabu Iwamoto,Toshifumi Minami, Harukuni Tokuda,Hironori Ohtsu,Reiko Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Cespihypotone
C20H28O4     ÏàËÆ¶È:70%
Helvetica Chimica Acta          2009          92          2146-2154
Verticillane and Norverticillane Diterpenoids from the Formosan Soft Coral Cespitularia hypotentaculata
Jiun-Yang Chang, Mohamed H. Abd El-Razek, Ya-Ching Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     phytenal
    ÏàËÆ¶È:70%
China Journal of Chinese Materia Medica          2006          31          1787-1790
Chemical constituents from red alga Corallina pilulifera
YUAN Zhaohui, HAN Lijun, FAN Xiao, LI Shuai, SHI Dayong, SUN Jie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     5¦Â-hydroxy-epi-neoverrucosane
    ÏàËÆ¶È:70%
Phytochemistry          1997          44          1495-1502
Epi-neoverrucosane- and epi-homoverrucosane-type diterpenoids from Fossombronia alaskana
Carola Grammes, Gunther Burkhardt, Michael Veith, Volker Huch, Hans Becker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (+)-13-epi-neoverrucosan-5¦Â-ol
    ÏàËÆ¶È:70%
Phytochemistry          1996          43          1057-1064
Terpenoid constituents of the new zealand liverwort Jamesoniella tasmanica
Masao Toyota, Eri Nakaishi, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     3-hydroxygrin-delic acid
    ÏàËÆ¶È:70%
Journal of Natural Products          1988          Vol 51          125
Bioconversion of Grindelic Acid into 3¦Á-Hydroxygrindelic Acid
Joseph J. Hoffmann, Hunsa Punnapayak, Shivanand D. Jolad, Robert B. Bates, Fernando A. Camou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (11R*,2E,4R*,7E,11S*,12R*)-18-Hydroxy-2,7-dolabelladiene
C20H34O     ÏàËÆ¶È:70%
Phytochemistry          1991          30          3679-3682
Diterpenes from the brown algaDictyota divaricata
Gabriele M. Ko¡§nig, Anthony D. Wright, Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     (¨C)-Solenopodin C
C20H34O2     ÏàËÆ¶È:70%
Marine drugs          2011          9          934-943
Discovery of New Eunicellins from an Indonesian Octocoral Cladiella sp.
Yung-Husan Chen,Chia-Ying Tai,Yin-Di Su,Yu-Chia Chang,Mei-Chin Lu,Ching-Feng Weng,Jui-Hsin Su,Tsong-Long Hwang,Yang-Chang Wu and Ping-Jyun Sung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     solenopodin C
    ÏàËÆ¶È:70%
Marine drugs          2011          9          934-943
Discovery of New Eunicellins from an Indonesian Octocoral Cladiella sp.
Yung-Husan Chen,Chia-Ying Tai,Yin-Di Su,Yu-Chia Chang,Mei-Chin Lu,Ching-Feng Weng,Jui-Hsin Su,Tsong-Long Hwang,Yang-Chang Wu and Ping-Jyun Sung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-08-07 17:21:21
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1 .     cupresol
C19H26O4     ÏàËÆ¶È:75%
Journal of Natural Products          1984          Vol 47          983-987
A New Diterpene From Cupressus goveniana var. Abramasiana: 5¦Â-Hydroxy-6-Oxasugiol (Cupresol)
Shivanand D. Jolad, Joseph J. Hoffmann, Karl H. Schram, Jack R. Cole, Robert B. Bates, Michael S. Tempesta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     8-methoxyserrulatane
    ÏàËÆ¶È:65%
Phytochemistry          1986          25          1377-1383
Serrulatane diterpenes from Eremophila spp. Original
Peter G. Forster, Emilio L. Ghisalberti, Phillip R. Jefferies, Virginia M. Poletti, Nola J. Whiteside
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (¡À)-N1-[2-(1-Cyclohexenyl)ethyl]-N3-(3,7-dimethyloctyl)guanidine hydrochloride
C19H38N3Cl     ÏàËÆ¶È:65%
Archiv der Pharmazie          2002          335          535-546
Novel High Energy Intermediate Analogues with Triazasterol-Related Structures as Inhibitors of Ergosterol Biosynthesis Part I: Synthesis and Antifungal Activity of N-alkyl-N'-(phenethyl-and cyclohexenylethyl)guanidines and N2-Substituted 2-Imidazolinamin฀
Edith Gößnitzer, Roland Malli, Silvia Schuster, Bertrand Favre and Neil S. Ryder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 12
    ÏàËÆ¶È:61.9%
Tetrahedron Letters          2003          44          4233-4237
Guanacastepene-A total synthesis: construction of the tricyclic iso-guanacastepane, epi-guanacastepane and guanacastepane frameworks
Goverdhan Mehta, Jayant D. Umarye, Kalidindi Srinivas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     mopaneol B
C20H36O3     ÏàËÆ¶È:60%
Journal of Natural Products          2003          66          30-33
Diterpenes from Colophospermum mopane: ¡°Missing Links¡± in the Biogenesis of 9,13-Epoxylabdanes
Emily Reiter, Edward Treadwell, Ericka Cederstrom, Paul B. Reichardt, and Thomas P. Clausen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     viguiepinone
C20H30O     ÏàËÆ¶È:60%
Journal of Natural Products          2007          70          1712-1717
Studies on Terpenoids Produced by Actinomycetes: Oxaloterpins A, B, C, D, and E, Diterpenes from Streptomyces sp. KO-3988
Keiichiro Motohashi, Ryoko Ueno, Masayuki Sue, Kazuo Furihata, Takuo Matsumoto, Tohru Dairi, Satoshi Omura, and Haruo Seto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     clavirolide D
C20H28O3     ÏàËÆ¶È:60%
Journal of Natural Products          1991          Vol 54          380
Four Novel Diterpenoids: Clavirolides B, C, D, and E from the Chinese Soft Coral Clavularia viridis
Jingyu Su, Yongli Zhong, Longmei Zeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 37
C18H25O2F     ÏàËÆ¶È:60%
Canadian Journal of Chemistry          2006          84          29-48
Total synthesis of 14¦Â-fluorosteroids via a transannular Diels-Alder reaction
Sylvie Beaubien and Pierre Deslongchamps
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     hinokiol
    ÏàËÆ¶È:60%
Phytochemistry          1987          26          1211-1212
18-Oxoferruginol from the leaf of Torreya nucifera
Leslie J. Harrison,Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (¡À)-N1-(3,7-Dimethyloctyl)-N3-phenethylguanidine hydrochloride
C19H34N3Cl     ÏàËÆ¶È:60%
Archiv der Pharmazie          2002          335          535-546
Novel High Energy Intermediate Analogues with Triazasterol-Related Structures as Inhibitors of Ergosterol Biosynthesis Part I: Synthesis and Antifungal Activity of N-alkyl-N'-(phenethyl-and cyclohexenylethyl)guanidines and N2-Substituted 2-Imidazolinamin฀
Edith Gößnitzer, Roland Malli, Silvia Schuster, Bertrand Favre and Neil S. Ryder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 2
C20H32O     ÏàËÆ¶È:60%
Bulletin of the Chemical Society of Japan          2002          75          131-136
New Dolabellane-Type Diterpenoids from the Okinawan Soft Coral of the Genus Clavularia
Kazuo Iguchi, Hisako Sawai, Hiroto Nishimura, Minako Fujita, Takao Yamori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     clavirolide D
    ÏàËÆ¶È:60%
Chinese Journal of Chemistry          1992          10          155-160
Two new diterpenoids from the marine soft coral Clavularia viridis
Jing-Yu Su, Yong-Li Zhong and Long-Mei Zeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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3Â¥2013-08-07 17:25:06
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