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9.4,18.9,21.6,22.4,24.0,29.9,34.5,35.6,38.6,40.4,42.7,45.6,48.8,50.3,106.0,129.6,153.5,170.9,207.2
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yhjiqimao: ½ð±Ò+50, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-07-15 16:26:40
1 .     17-epioxandrolone
C19H32O3     ÏàËÆ¶È:68.4%
Steroids          1992          57          306-312
Studies on anabolic steroids. 9. Tertiary sulfates of anabolic 17¦Á-methyl steroids: synthesis and rearrangement
Honggang Bi, Robert Mass¨¦, George Just
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     17-Epioxandrolone
    ÏàËÆ¶È:68.4%
Steroids          1992          57          537-550
17-Epimerization of 17¦Á-methyl anabolic steroids in humans: metabolism and synthesis of 17¦Á-hydroxy-17¦Â-methyl steroids
Willi Schänzer, Georg Opfermann, Manfred Donike
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     8¦Â-Methoxyeremophil-7(11)- ene-12,8¦Á(4¦Â,6¦Á)-diolide
    ÏàËÆ¶È:63.1%
Chemistry of Natural Compounds          2007          43          746-748
EREMOPHILANE SESQUITERPENE LACTONES FROM Ligularia intermedia NAKAI OF SHANXI
Xue Huiqing, Ma Xuemei, Xing Xuelei, and Wang Hanqing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     2¦Â−acetoxy-14,15,17-trinor-ent-labdane-8-oxa-9-oxo-12-one
    ÏàËÆ¶È:63.1%
Molecules          2007          12          2605-2620
Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part II
Luis E. Catal¨¢n, Karen C. Mar¨ªn, H¨¦ctor C. Altamirano, Mauricio C. Fritis and Mar¨ªa C. Chamy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     Oxandrolone
C19H30O3     ÏàËÆ¶È:63.1%
Steroids          2009          74          1040-1044
New oxandrolone derivatives by biotransformation using Rhizopus stolonifer
M. Iqbal Choudhary, Mohammad Yasin Mohammad, Syed Ghulam Musharraf, Masood Parvez, Amal Al-Aboudi, Atta-ur-Rahman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     8¦Â-methoxyeremophil-7(11)-ene-12,8¦Á(4¦Â,6¦Á)-diolide
    ÏàËÆ¶È:63.1%
China Journal of Chinese Materia Medica          2007          32          1044-1047
Study on chemical constituents from Ligularia intermedia of Shanxi
XUE Huiqing, MA Xuemei, WEI Xiaoning, WU Suixian, WANG Hanqing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     8¦Â-methoxyeremophil-7(11)-en-6¦Á,15;8¦Á,12-diolide
C16H20O5     ÏàËÆ¶È:63.1%
Journal of Natural Products          1995          Vol 58          1358-1364
Eight New Eremophilane Derivatives from the Roots of Ligularia przewalskii
Yu Zhao, Zhongjian Jia, Hairuo Peng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     compound 13
    ÏàËÆ¶È:63.1%
Steroids          1992          57          306-312
Studies on anabolic steroids. 9. Tertiary sulfates of anabolic 17¦Á-methyl steroids: synthesis and rearrangement
Honggang Bi, Robert Mass¨¦, George Just
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     oxandrolone
    ÏàËÆ¶È:63.1%
Steroids          1992          57          537-550
17-Epimerization of 17¦Á-methyl anabolic steroids in humans: metabolism and synthesis of 17¦Á-hydroxy-17¦Â-methyl steroids
Willi Schänzer, Georg Opfermann, Manfred Donike
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     2¦Â-hydroxy-13-methylene-stemarane
    ÏàËÆ¶È:60%
Phytochemistry          1995          40          1751-1754
Diterpenoids from calceolaria dentata
M. C. Chamy, M. Piovano, J. A. Garbarino, C. Vargas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     6¦Á-acetoxy-9,13¦Â-epoxy-13¦Â-methylpodocarpane
C20H32O3     ÏàËÆ¶È:60%
Tetrahedron          2006          62          8489-8497
Photodegradation of some 14,15-bisnorlabdene-13-ones, derived from larixol. Synthesis of drimanic dienes with functional groups at C-6
Pavel F. Vlad, Alexandru G. Ciocarlan, Mihai N. Coltsa, Calin Deleanu, Oana Costan, Yurii A. Simonov, Victor Ch. Kravtsov, Janusz Lipkowski, Tadeusz Lis, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     (1S*,3E,5R*,7Z,11S*,12S*)-5-acetoxy-12-hydroxydrolabella-3,7-dien-9-one
C22H32O3     ÏàËÆ¶È:59.0%
Phytochemistry          1994          37          509-513
Diterpenes from the brown alga Dictyota bartayresiana
Ch.Bheemasankara Rao, G. Trimurtulu, Ch. Sreedhara, D.Venkata Rao, Steven C. Bobzin, D.John Faulkner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     drechslerine D
C15H22O3     ÏàËÆ¶È:57.8%
Journal of Natural Products          2002          65          306-313
Rare Sesquiterpenes from the Algicolous Fungus Drechslera dematioidea
Claudia Osterhage, Gabriele M. König, Ulrich Höller, and Anthony D. Wright
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     (4R*,5R*,7S*,10R*)-4-isocyanatoeudesm-11-ene
C16H25N     ÏàËÆ¶È:57.8%
Journal of Natural Products          2002          65          851-855
New Nitrogenous Eudesmane-Type Compounds Isolated from the Caribbean Sponge Axinyssa ambrosia
Natalia V. Petrichtcheva,Carmenza Duque, Adriana Dueñas, Sven Zea, Noriyuki Hara,and Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     strychnistenolide A acetyl methyl
    ÏàËÆ¶È:57.8%
Journal of Natural Products          2001          64          286-288
New Eudesmane Sesquiterpenes from the Root of Lindera strychnifolia
Isao Kouno,Asuka Hirai,Akiko Fukushige, Zhi-Hong Jiang, and Takashi Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     11¦Á,13-dihydro-6-deoxychamissonolide
    ÏàËÆ¶È:57.8%
Planta Medica          1995          61          544-550
Sesquiterpene Lactones and Inositol Esters from Arnica angustfolial
Thomas J. Schmidt, G¨¹nter Willuhn. Alois Steigel, andDetlefWendisch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     laggerone A
C15H26O3     ÏàËÆ¶È:57.8%
Chinese Chemical Letters          1996          7          1093-1094
EUDESMANES AND EUDESMANOIC GLUCOSIDES FROM LAGGERA PETERODONTA
YU ZHAO,JIAN MIN YUE,JING KAI DING,ZHONG WEN LIN AND HAN DONG SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (4S,8S,9S,13S,1R,5R,12R)-11-[2-((4S,8S,9S,13S,1R,5R,12R)-11-aza-1,5,9-trimethyl-14,15-dioxa-10-oxotetracyclo [10.2.1.0<4,13>.0<8,13>]pentadec-11-yl)ethyl]-11-aza-1,5,9-trimethyl-14,15-dioxatetracyclo [10.2.1.0<4,13>.0<8,13>]pentadecan-10-one
C32H49N2O6     ÏàËÆ¶È:57.8%
Molecules          2003          8          901-909
New Bioactive Azaartemisinin Derivatives
Mai M. Al-Oqail, Ahmed M. Galal, Mohamed S. Ahmad, Ahlam M. Al-Fishawi and Farouk S. El-Feraly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     3¦Â-Hydroxy-5-methyl-19-nor-5¦Â,9¦Á,10¦Á-androstan-17-one
    ÏàËÆ¶È:57.8%
Steroids          2002          67          57-70
Analogues of androgen hormones with inverted configuration at carbons 5, 9, and 10
Alexander Kasal, Miloš Budĕš¨ªnský, Pavel Drašar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     (13S)-13,14-Seco-androst-4-en-3,17-dione
    ÏàËÆ¶È:57.8%
Steroids          2004          69          501-509
Synthesis of 13,14-secotestosterone derivatives
Vladimir A. Khripach, Vladimir N. Zhabinskii, Anna I. Kuchto, Yuliya Y. Zhiburtovich, Galina P. Fando, Alexander S. Lyakhov, Alla A. Govorova, Marinus B. Groen, Jaap van der Louw, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     4¦Â,5¦Â-Epoxy-17-hydroxy-A-homo-4-oxaandrostan-3-one
C20H30O4     ÏàËÆ¶È:57.8%
Steroids          2006          71          116-119
Steroidal seven-membered A-ring epoxy lactones by oxidation of the corresponding ¦¤4-3-ketosteroids
Maria L. Di Gioia, Antonella Leggio, Adolfo Le Pera, Francesca Perri, Andrea F. Pitrelli, Angelo Liguori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     6¦Á-hydroxyoxandrolone
C19H30O4     ÏàËÆ¶È:57.8%
Steroids          2009          74          1040-1044
New oxandrolone derivatives by biotransformation using Rhizopus stolonifer
M. Iqbal Choudhary, Mohammad Yasin Mohammad, Syed Ghulam Musharraf, Masood Parvez, Amal Al-Aboudi, Atta-ur-Rahman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     4¦Â,11-dihydroxyenantioeudesmane-1-one
C15H26O3     ÏàËÆ¶È:57.8%
Phytochemistry          1997          44          459-464
Eudesmane sesquiterpenes from Laggera pterodonta
Yu Zhao, Jianmin Yue, Zhongwen Lin, Jingkai Ding, Handong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     19-norabieta-7,13-dien-4-ol
C19H30O     ÏàËÆ¶È:57.8%
Phytochemistry          1995          39          391-394
Norditerpenes from Juniperus chinensis
Ching-Kuo Lee, Jim-Min Fang, Yu-Shia Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     7-Isocyanoamphilecta-11(20),15-diene
    ÏàËÆ¶È:57.8%
Canadian Journal of Chemistry          2009          87          612-618
8-Isocyanoamphilecta-11(20),15-diene, a new antimalarial isonitrile diterpene from the sponge Ciocalapata sp.
Chatchai Wattanapiromsakul, Naphatson Chanthathamrongsiri,Somchai Bussarawit, Supreeya Yuenyongsawad, Anuchit Plubrukarn, and Khanit Suwanborirux
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     (4R,5S,7R,10S)-eudesm-11-en-4-ol acetate
    ÏàËÆ¶È:57.8%
Phytochemistry          1990          29          3207-3211
Eudesmane glycosides from Carthamus lanatus
Arturo San Feliciano,Manuel Medarde,Benedicto Del Rey,Jose M. Miguel Del Corral,Alejandro F. Barrero
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     4¦Â,5¦Â-Epoxyandrostane-6,17-dione
    ÏàËÆ¶È:57.8%
Steroids          1995          60          499-505
Competing pathway involved in allylic acetoxylation of androst-5-en-17-one, and oxidation of allylic alcohols with chromium oxides
Mitsuteru Numazawa, Mii Tachibana, Miyako Kamiza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     Oxandrolone 17¦Â-sulfate pyridinium salt
C19H30O6S     ÏàËÆ¶È:57.8%
Steroids          1992          57          306-312
Studies on anabolic steroids. 9. Tertiary sulfates of anabolic 17¦Á-methyl steroids: synthesis and rearrangement
Honggang Bi, Robert Mass¨¦, George Just
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     14,15-dinor-8-labdene-7,13-dione
    ÏàËÆ¶È:57.8%
Acta Chemica Scandinavica          1988          42          708-716
Tobacco Chemistry. 71. Structure Determination and Biomimetic Studies of Five New Tobacco Cembranoids.
Arndt, Rolf; Berg, Jan-Eric; Wahlberg, Inger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     8¦Â-(acetoxy)-des-A,B-21-norcholestane-18-nitrile
C19H31NO2     ÏàËÆ¶È:57.8%
Bioorganic & Medicinal Chemistry          2009          17          7658-7669
Removal of the 20-methyl group from 2-methylene-19-nor-(20S)-1¦Á,25-dihydroxyvitamin D3 (2MD) selectively eliminates bone calcium mobilization activity
Rafal Barycki, Rafal R. Sicinski, Lori A. Plum, Pawel Grzywacz, Margaret Clagett-Dame, Hector F. DeLuca
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     (3aR,4aS,8aR,9aR,E)-8a-methyl-5-methylidene-3-(4-chlorobenzylidene)decahydronaphtho[2,3-b]-furan-2(3H)-one
C21H23O2Cl     ÏàËÆ¶È:57.8%
Russian Journal of Organic Chemistry          2010          46          1719-1734
Synthetic transformations of methylenelactones of eudesmanic type. Behavior of isoalantolactone under the conitions of heck reaction
A. V. Belovodskii, E. E. Shults, M. M. Shakirov, I. Yu. Bagryanskaya and Yu. V. Gatilov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     (¡À)-12-methoxy-13-hydroxymethylpodocarpane-8,11,13-trene
C19H28O2     ÏàËÆ¶È:57.8%
Journal of the Chinese Chemical Society          2004          51          505-508
Facile Total Synthesis of (¡À)-Nimbiol
Zhen-Ting Dua, Guo-Ren Yue, An-Pai Li,Jun-Ying Ma, Tong-Xing Wu,Xue-Gong She and Xin-Fu Pan*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     methyl 7,8(¦Á)epoxy-15-hydroxylabdan-17-oate
C21H36O4     ÏàËÆ¶È:57.1%
Molecules          2004          9          300-322
From Labdanes to Drimanes. Degradation of the Side Chain of Dihydrozamoranic Acid.
Jes¨²s M. Rodilla, D. D¨ªez, J. G. Urones and Pedro M. Rocha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     compound 5
    ÏàËÆ¶È:57.1%
Steroids          2002          67          621-626
13C-NMR study of 4-azasteroids in solution and solid state
Jacek W. Morzycki, Iwona Wawer, Agnieszka Gryszkiewicz, Jadwiga Maj, Leszek Siergiejczyk, Alicja Zaworska
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     (13S)-5¦Â,9¦Â,10¦Á-8(20)-labden-15-saure-methylester
    ÏàËÆ¶È:57.1%
Helvetica Chimica Acta          1978          61          1004-1010
Über die Herstellung von Äther der enantio-14, 15-Dinorlabdan-Reihe aus Eperusure
Ashesh Kumar Dey and Hans Richard Wolf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     (1S,3aR,3a1S,4S,6S,6aS,9aR)-1-isocyano-1,4-dimethyl-7-methylene-6-(2-methylprop-1-enyl)-dodecahydro-1H-phenalene
C21H31N     ÏàËÆ¶È:57.1%
Journal of Natural Products          2011          74          2299-2303
Evaluation of the Antiproliferative Activity of Diterpene Isonitriles from the Sponge Pseudoaxinella flava in Apoptosis-Sensitive and Apoptosis-Resistant Cancer Cell Lines
Delphine Lamoral-Theys,Ernesto Fattorusso, Alfonso Mangoni, Cristina Perinu, Robert Kiss, and Valeria Costantino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     cis-T2
C42H61O4     ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry Letters          2010          20          2078-2081
First synthesis of separable isomeric testosterone dimers showing differential activities on prostate cancer cells
Dominic Bastien, Val¨¦rie Leblanc, Éric Asselin, Gervais B¨¦rub¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     compound 7
C21H31N     ÏàËÆ¶È:57.1%
Tetrahedron          1999          55          12629-12636
Structures and absolute stereochemistry of isocyanide and isothiocyanate amphilectenes from the Caribbean sponge Cribochalina sp.
Maria Letizia Ciavatta, Angelo Fontana, Raffaella Puliti, Gennaro Scognamiglio, Guido Cimino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     compound 8
C21H33NO2     ÏàËÆ¶È:57.1%
European Journal of Organic Chemistry          2012                   1202-1208
Studies on the Diastereoselective Intramolecular Pauson¨CKhand Reaction on Regioisomeric Chiral Perhydrobenzoxazines Derived from (¨C)-8-Aminomenthol
Alicia Maestro, Rafael Pedrosa, Alfonso P¨¦rez-Encabo and Juan J. P¨¦rez-Rueda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     ent-12¦Â-acetoxykaur-16-en-19-oic acid
C23H34O4     ÏàËÆ¶È:56.5%
Phytochemistry          1983          22          875-881
Diterpene acids from Helianthus species and their microbiological conversion by Gibberella fujikuroi, mutant B1-41a
Michael H. Beale, John R. Bearder, Jake Macmillan, Akihiko Matsuo, Bernard O. Phinney
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     cis-(1S*,3S*,4R*,7S*,8S*,12S*,13S*)-7-formamidoamphilecta-11(20),15-diene
C21H33NO     ÏàËÆ¶È:55%
Journal of Natural Products          2009          72          492-495
Diterpene Formamides from the Tropical Marine Sponge Cymbastela hooperi and Their Antimalarial Activity in Vitro
Anthony D. Wright, and Naomi Lang-Unnasch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     1S-hydroxy-1,2-dihydrosphaerococcenol-A
C20H31BrO3     ÏàËÆ¶È:55%
Journal of Natural Products          2008          71(8)          1386-1392
Brominated Diterpenes with Antibacterial Activity from the Red Alga Sphaerococcus coronopifolius
Vangelis Smyrniotopoulos, Constantinos Vagias, M.Mukhlesur Rahman, Simon Gibbons, and Vassilios Roussis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     agallochin H
C20H30O3     ÏàËÆ¶È:55%
Journal of Natural Products          2002          65          382-385
ent-Kaurane and Beyerane Diterpenoids from Excoecaria agallocha1
Ammanamanchi S. R. Anjaneyulu, Vadali Lakshmana Rao, and Karanam Sreedhar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     (6E)-2¦Á,9¦Á-epoxyeunicella-6,11(12)-dien-3¦Â-ol
C20H32O2     ÏàËÆ¶È:55%
Journal of Natural Products          1999          62          1322-1324
New Fish Feeding Deterrents, Including a Novel Sesquiterpenoid Heterogorgiolide, from the Brazilian Gorgonian Heterogorgia uatumani (Octocorallia, Gorgonacea)
Lenize F. Maia, Rosaˆngela de A. Epifanio, Tegan Eve, and William Fenical
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     farblose nadeln
C20H34O3     ÏàËÆ¶È:55%
Chemical & Pharmaceutical Bulletin          1983          31          4409-4416
Chemische und Chemotaxonomische Untersuchungen der Pterophyten. XLIV. Chemische Untersuchungen der Inhaltsstoffe von Microlepia marginata (PANZER) C. CHR. (2)
TADAYUKI KURAISHI,TAKAO TANIGUCHI,KAZUYUKI HORI,TAKAO MURAKAMI,NOBUTOSHI TANAKA,YASUHISA SAIKI and CHIUMING CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     pinifodiol
    ÏàËÆ¶È:55%
Chemistry of Natural Compounds          1981          17          408-410
A STUDY OF THE PROPERTIES AND 13C NMR SPECTRA OF PINIFOLIC ACID AND ITS DERIVATIVES
I. I. Bardyshev, A. S. Degtyarenko, T. I. Pekhk, and S. A. Makhnach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     9,13-epi-ent-Pimara-7,15-diene
C20H32     ÏàËÆ¶È:55%
Phytochemistry Letters          2009          2          201-203
Microbiological transformation of an ent-pimaradiene hydrocarbon by Gibberella fujikuroi
Braulio M. Fraga, Pedro Gonz¨¢lez, Melchor G. Hern¨¢ndez, Mar¨ªa C. Chamy, Juan A. Garbarino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     1,3,5,15-valparatetraene
C20H28     ÏàËÆ¶È:55%
Natural Product Research          2001          15          401-09
BI- and Tricyclic Diterpenoids from Halimium viscosum
Jes¨¹s M. L. Rodilla; Dina I. De Mendonça; M. Isabel; G. Ismael; J. Albertino Figueiredo; Maria L¨¹cia A. Silva; Elisabete Lopes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




49 .     ent-2¦Á-hydroxy-8(14),15-pimaradiene
C20H32O     ÏàËÆ¶È:55%
Natural Product Research          2002          16          33-37
Diterpenes from Sideritis Trojana
G¨¹laçti Topçu; Ahmet Gören; Turgut Kılİç; Y. Kemal YıLdız; G¨¹lendam T¨¹men
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     labd-8(17)-en-15-oic acid
    ÏàËÆ¶È:55%
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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51 .     flavidusin A
C20H34O2     ÏàËÆ¶È:55%
Phytochemistry          1998          48          1025-1029
Diterpenoids from Isodon flavidus
Qin-Shi Zhao, Tian Jun, Jian-Min Yue, Shao-Nong Chen, Zhong-Wen Lin, Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




52 .     isolushinin A
C20H28O3     ÏàËÆ¶È:55%
Journal of Natural Products          2010          73          1112-1116
Cytotoxic ent-Kaurane Diterpenoids from Isodon rubescens var. lushiensis
Cytotoxic ent-Kaurane Diterpenoids from Isodon rubescens var. lushiensis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




53 .     ent-5¦Á-dolabr-4(18)-ene-15S,16-diol
    ÏàËÆ¶È:55%
Acta Pharmaceutica Sinica          2005          Vol 40          935-939
Chemical constituents from the mangrove plant Ceriops tagal
ZHANG Yan; DENG Zhi-wei; GAO Tian-xiang; FU Hong-zheng; LIN Wen-han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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54 .     13-epi-homoverrucosan-6¦Â-ol-5-one
C20H32O2     ÏàËÆ¶È:55%
Phytochemistry          1995          40          199-203
13-Epi-homoverrucosane derivatives and other diterpenes from Plagiochila (hepaticae)
Susanne Valcic, Volker Huch, Michael Veith, Hans Becker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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55 .     compound 5
C26H32O     ÏàËÆ¶È:55%
Phytochemistry          1991          30          589-592
Diterpenoids from Calceolaria thyrsiflora
M. C. Chamy, M. Piovano, J. A. Garbarino, C. Miranda, V. Gambaro, M. L. Rodr¨ªguez, C. Ruiz-P¨¦rez, I. Brito
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




56 .     (13S)-5¦Â,9¦Â,10¦Á-8(20)-labden-15-saure(eperusaure)
    ÏàËÆ¶È:55%
Helvetica Chimica Acta          1978          61          1004-1010
Über die Herstellung von Äther der enantio-14, 15-Dinorlabdan-Reihe aus Eperusure
Ashesh Kumar Dey and Hans Richard Wolf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




57 .     9-epi-ent-7,15-isopimaradiene
C20H32     ÏàËÆ¶È:55%
Phytochemistry          1988          27          1145-1149
18-Malonyloxy-9-epi-ent-isopimarol,a diterpene from Calceolaria glandulosa
Marisa Piovano,Vicente Gambaro,Mar¨ªa C. Chamy,Juan A. Garbarino,Marcello Nicoletti,Jean Guilhem,Claudine Pascard
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




58 .     11,12-dihydroxy-8,11,13-icetexatrien-1-one
C20H28O3     ÏàËÆ¶È:55%
Planta Medica          2010          76          629-632
The Corrected Structure of Rosmaridiphenol, a Bioactive Diterpene from Rosmarinus officinalis
Pertino, Mariano Walter; Schmeda-Hirschmann, Guillermo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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59 .     Compound 9
    ÏàËÆ¶È:55%
Magnetic Resonance in Chmesitry          2001          39          414-416
Assignment of 1H and 13C NMR data for (−-methyl thyrsiflorin A and some scopadulan precursors
Manuel Arn¨®, Miguel A. Gonz¨¢lez, M. Luisa Mar¨ªn and Ram¨®n J. Zaragoz¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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60 .     compound 1
    ÏàËÆ¶È:55%
Phytochemistry          1985          24          977-979
Diterpenoid hydrocarbons in the sea grass Amphibolis antartica
Robert W. Dunlop
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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61 .     17¦Á-hydroxy-17¦Â-methyl-5¦Â-androstan-3-one
    ÏàËÆ¶È:55%
Steroids          1983          41          493-500
Metabolism of 17¦Á-methyl-5¦Â-dihydrotestosterone in the rabbit
John F. Templeton, Chung-Ja Choi Jackson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




62 .     15S,16-dihydroxy-3-oxoisopimar-9(11)-ene
C20H32O3     ÏàËÆ¶È:55%
Phytochemistry          2010          71          804-809
Sesquiterpenes and diterpenes from Ambrosia arborescens
Marinella De Leo, Mariela Beatriz Vera Saltos, Blanca Fabiola Naranjo Puente, Nunziatina De Tommasi, Alessandra Braca
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




63 .     prevezol D
C20H33O3Br     ÏàËÆ¶È:55%
The Journal of Organic Chemistry          2003          68          7667-7674
Novel Cytotoxic Brominated Diterpenes from the Red Alga Laurencia obtusa
Dimitra Iliopoulou, Nikos Mihopoulos, Constantinos Vagias, Panagiota Papazafiri, and Vassilios Roussis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




64 .     prevezol E
C20H33O3Br     ÏàËÆ¶È:55%
The Journal of Organic Chemistry          2003          68          7667-7674
Novel Cytotoxic Brominated Diterpenes from the Red Alga Laurencia obtusa
Dimitra Iliopoulou, Nikos Mihopoulos, Constantinos Vagias, Panagiota Papazafiri, and Vassilios Roussis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




65 .     aphidicol-16-ene
C20H32     ÏàËÆ¶È:55%
Tetrahedron          1999          55          7541-7554
Biosynthesis of diterpenoid aphidicolin: Isolation of intermediates from P-450 inhibitor treated mycelia of Phoma betae
Hideaki Oikawa, Satoshi Ohashi, Akitami Ichihara, Sadao Sakamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




66 .     (+)-(1S,4S,4aS,8aR)-4-(4-acetoxy-octahydro-5,5,8a-trimethyl-spiro[naphtalene-2(1H),2'-oxiran]-yl)-2-butanone
C18H28O2     ÏàËÆ¶È:55%
Tetrahedron          2001          57          5663-5679
The synthesis of Ambrox®-like compounds starting from (+)-larixol
Marjon G Bolster, Ben J.M Jansen, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




67 .     compound 92
    ÏàËÆ¶È:55%
Natural Product Communications          2008          3          399-412
Structural Elucidation of Pimarane and IsopimaraneDiterpenoids: The 13C NMR Contribution
Ana M. L. Seca, Diana C. G. A. Pinto and Artur M. S. Silva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




68 .     compound 125
    ÏàËÆ¶È:55%
Natural Product Communications          2008          3          399-412
Structural Elucidation of Pimarane and IsopimaraneDiterpenoids: The 13C NMR Contribution
Ana M. L. Seca, Diana C. G. A. Pinto and Artur M. S. Silva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




69 .     2¦Â,16¦Á -dihydroxy-entkaurane
    ÏàËÆ¶È:55%
Records of Natural Products          2011          5          247-251
Ent-Kaurane Diterpenoids from Euphorbia hirta
Shijun Yan, Dawei Ye, Yi Wang, Yan Zhao, Jianxin Pu, Xue Du, Lei Luo and Yong Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




70 .     12-bromostemod-12-en-2-one
C20H29BrO     ÏàËÆ¶È:55%
Phytochemistry          2011          72          2361-2368
Stemodin-derived analogues with lipid peroxidation, cyclooxygenase enzymes and human tumour cell proliferation inhibitory activities
Floyd A. Russell, Vanisree Mulabagal, Dwayne R. Thompson, Marvadeen A. Singh-Wilmot, William F. Reynolds, Muraleedharan G. Nair, Vratislav Langer, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




71 .     13¦Â-hydroxy-15(8¡ú9)abeo,14(13¡ú16)abeo-8¦Â(H)-stach-15-en-2-one
C20H30O2     ÏàËÆ¶È:55%
Phytochemistry          2011          72          2361-2368
Stemodin-derived analogues with lipid peroxidation, cyclooxygenase enzymes and human tumour cell proliferation inhibitory activities
Floyd A. Russell, Vanisree Mulabagal, Dwayne R. Thompson, Marvadeen A. Singh-Wilmot, William F. Reynolds, Muraleedharan G. Nair, Vratislav Langer, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




72 .     19-(N,N-dimethylcarbamoxy)-2¦Â,13-dihydroxystemarane
C23H39NO4     ÏàËÆ¶È:54.5%
Phytochemistry          2006          67          1088-1093
Bioconversion of Stemodia maritima diterpenes and derivatives by Cunninghamella echinulata var. elegans and Phanerochaete chrysosporium
Andrew S. Lamm, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




73 .     melissoidesin P
C22H34O6     ÏàËÆ¶È:54.5%
Journal of Natural Products          2004          67          1441-1444
Diterpenoids from Isodon melissoides
Ai-Hua Zhao, Quan-Bin Han, Rong-Tao Li, Sheng-Hong Li, Chen Qing,Yan-Li Zhang, Qin-Shi Zhao, Fu-Sheng Wang, and Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




74 .     3¦Â-Acetoxy-5¦Á,6¦Á-epoxy-20-hydroxyiminopregnan-20-one
    ÏàËÆ¶È:54.5%
Molecules          2009          14          4655-4668
Synthesis of Pregnane Derivatives, Their Cytotoxicity on LNCap and PC-3 Cells, and Screening on 5¦Á-Reductase Inhibitory Activity
Sujeong Kim and Eunsook Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




75 .     longirabdolide G
C22H30O6     ÏàËÆ¶È:54.5%
Phytochemistry          1997          45          785-789
Longirabdolides E, F and G, 6, 7-seco-ent-kaurenoids from Rabdosia longituba
Yoshio Takeda, Yukako Futatsuishi, Takashi Matsumoto, Toshiya Masuda, Hiroshi Terada, Hideaki Otsuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




76 .     rotundeic acid B
C23H32O4     ÏàËÆ¶È:54.5%
Phytochemistry          1997          44          653-657
Ent-kaurane-type diterpenoids from the liverwort Jungermannia rotundata
Fumihiro Nagashima, Hironao Tanaka, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




77 .     compound 5
    ÏàËÆ¶È:54.5%
Journal of Natural Products          1990          Vol 53          1374
An Acid-Catalyzed Isomerization of Isoatisine
Haridutt K. Desai, Qingping Jiang, S. William Pelletier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




78 .     2¦Â-acetoxy-13-methylene-stemarane
    ÏàËÆ¶È:54.5%
Phytochemistry          1995          40          1751-1754
Diterpenoids from calceolaria dentata
M. C. Chamy, M. Piovano, J. A. Garbarino, C. Vargas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




79 .     15-acetoxy-7-labden-17-oic acid
    ÏàËÆ¶È:54.5%
Phytochemistry          1987          26          3037-3040
Labdane diterpenoids from Halimium viscosum and H. verticilatum
Julio G. Urones,Isidro S¨¢nchez Marcos,David Diez Martin,F.M.S.Brito Palma,Jes¨²s M. Rodilla
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




80 .     28-acetoxy-15¦Á-hydroxymansumbinone
C24H3604     ÏàËÆ¶È:54.1%
Phytochemistry          2002          59          399-403
Two octanordammarane triterpenes from Commiphora kua
Aman Dekebo, Ermias Dagne, Lars K. Hansen, Odd R. Gautun, Arne J. Aasen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




81 .     melissoidesin Q
C24H36O7     ÏàËÆ¶È:54.1%
Journal of Natural Products          2004          67          1441-1444
Diterpenoids from Isodon melissoides
Ai-Hua Zhao, Quan-Bin Han, Rong-Tao Li, Sheng-Hong Li, Chen Qing,Yan-Li Zhang, Qin-Shi Zhao, Fu-Sheng Wang, and Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




82 .     [(3aR,6aR,7S,9aS,9bR)-3a,4,6a,7,8,9,9a,9b-Octahydro-2,2,9a-trimethyl-7-(1-methylethyl)azuleno[4, 5-d][1,3]dioxol-5-yl]methanol
C18H30O3     ÏàËÆ¶È:52.6%
Helvetica Chimica Acta          2006          Vol. 89          16
Uncommon Sesquiterpenoids and New Triterpenoids from Jatropha neopauciflora (Euphorbiaceae)
Abraham Garc¨ªa and Guillermo Delgado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




83 .     (6¦Â,8¦Â)-6-(acetyloxy)-8-chloroeremophil-7(11)-en-12,8-olide
    ÏàËÆ¶È:52.6%
Helvetica Chimica Acta          2006          Vol. 89          915
Terpenoids from the Roots of Ligularia muliensis
Qiu-Hong Wu, Chun-Mei Liu, Yan-Jun Chen, and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




84 .     methyl ent-2,4-seco-15,16-epoxy-4-oxo-3,19- dinorbeyer-15-en-2-oate
C19H28O4     ÏàËÆ¶È:52.6%
Phytochemistry          2007          68          546-553
ent-Beyerane diterpenoids from the heartwood of Excoecaria parvifolia
Mary H. Grace, Juan A. Faraldos, Mary Ann Lila, Robert M. Coates
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




85 .     11¦Â,17¦Â-dihydroxyandrost-4-en-3-one
C19H28O3     ÏàËÆ¶È:52.6%
Phytochemistry          2004          65          2205-2209
Biotransformation of hydrocortisone by a natural isolate of Nostoc muscorum
Mojtaba Tabatabaei Yazdi, Homeira Arabi, Mohammad Ali Faramarzi,Younes Ghasemi, Mohsen Amini, Shadman Shokravi, Farzaneh Aziz Mohseni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




86 .     compound 6
C18H28O3     ÏàËÆ¶È:52.6%
Journal of Natural Products          2008          71(11)          1806-1811
Meroditerpenoids and Derivatives from the Brown Alga Cystoseira baccata and Their Antifouling Properties
Redouane Mokrini, Mohammed Ben Mesaoud, Mohammed Daoudi, Claire Hellio, Jean-Philippe Mar¨¦chal, Mohamed El Hattab, Annick Ortalo-Magn¨¦, Louis Piovetti, and G¨¦rald Culioli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




87 .     ethylenedithioketal
C19H28S4     ÏàËÆ¶È:52.6%
Journal of Natural Products          2004          67          189-193
Preparation of Moreliane-Derived Volatile Sesquiterpenes
Carlos M. Cerda-Garca-Rojas, Mara A. Bucio, Luisa U. Romn, Juan D. Hernndez, and Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




88 .     diketone
C19H24O2     ÏàËÆ¶È:52.6%
Journal of Natural Products          2007          70          910-917
Vasorelaxant Activity of Diterpenes from Croton zambesicus and Synthetic Trachylobanes and Their Structure-Activity Relationships
Chiara Baccelli,Ismael Navarro, S¨¦bastien Block, Antonio Abad, Nicole Morel, and Joëlle Quetin-Leclercq
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




89 .     horiolide
C19H22O5     ÏàËÆ¶È:52.6%
Journal of Natural Products          2002          65          737-739
Horiolide, a Novel Norditerpenoid from Indian Ocean Soft Coral of the Genus Sinularia
Parvataneni Radhika, Potluri V. Subba Rao, Vallurupalli Anjaneyulu, Ratnakar N. Asolkar, and Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




90 .     (1S,4aS,8aS)-N-methoxy-N-methyl1-(2,5,5,8a-tetramethyl-1,4,4a,5,6,7,8-octahydronaphthalenyl)acetamide
C18H31NO2     ÏàËÆ¶È:52.6%
Journal of Natural Products          2002          65          661-668
An Approach to Furolabdanes and Their Photooxidation Derivatives from R-(+)-Sclareolide
Mar¨ªa C. de la Torre,Isabel Garc¨ªa, and Miguel A. Sierra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




91 .     junceol A
C17H28O3     ÏàËÆ¶È:52.6%
Journal of Natural Products          2001          64          1241-1242
Junceol A, a New Sesquiterpenoid from the Sea Pen Virgularia juncea
Shin-Pin Chen,Ping-Jyun Sung,Chang-Yih Duh,Chang-Feng Dai, and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




92 .     11-hydroxyplectranthone
C19H28O6     ÏàËÆ¶È:52.6%
Journal of Natural Products          2000          63          1709-1711
Microbial Transformation of the Eudesmane Sesquiterpene Plectranthone
Khaled Y. Orabi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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93 .     3¦Â-acetoxy-10¦Â-hydroxy-6¦Â,8¦Â-dimethoxyeremophil-7(11)-en-8¦Á,12-olide
C19H28O7     ÏàËÆ¶È:52.6%
Planta Medica          2009          75          635-640
Eremophilane-Type Sesquiterpene Derivatives from Ligularia hodgsonii
Wen-Xian Li, Ming Lei, Dong-Qing Fei, Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




94 .     6¦Â,8¦Â-dimethoxy-10¦Â-hydroxyeremophil-7(11)-en-12,8¦Á-olide
C17H26O5     ÏàËÆ¶È:52.6%
Planta Medica          2003          69          356-360
Eremophilenolides and Other Constituents from the Eremophilenolides and Other Constituents from the
Xu-Qin Li,Kun Gao,Zhong-Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




95 .     compound 4
C15H26O     ÏàËÆ¶È:52.6%
Chemical & Pharmaceutical Bulletin          1990          38          1405-1407
Studies on the Sesquiterpenoids of Panax ginseng C. A. MEYER. IV
Hisakatsu IWABUCHI,Nobuo KATO and Masahiro YOSHIKURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




96 .     synthesizing
C15H23N     ÏàËÆ¶È:52.6%
Chemistry of Natural Compounds          2009          45          367-370
SYNTHESIS OF 11-AMINODRIM-7-ENE FROM DRIMENOL
K. I. Kuchkova, A. N. Arycu, and P. F. Vlad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




97 .     (1S,4R,13S)-Ethoxycembra-2(E),7(E),11(E)-trien-4-ol
C20H36O2     ÏàËÆ¶È:52.6%
Chemistry of Natural Compounds          2007          43          143-148
SYNTHESIS OF N-METHYL UROCANATES OF HYDROXYDERIVATIVES OF ISOCEMBROL
F. A. Valeev,1 Sh. M. Salikhov,O. Yu. Krasnoslobodtseva,B. T. Sharipov L. V. Spirikhin, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




98 .     (1S,4S,7R)-4,8,8-Trimethyl-2-methylen-4-vinylbicyclo[5.2.0]nonane
    ÏàËÆ¶È:52.6%
Chemistry of Natural Compounds          2006          42          304-306
ABSOLUTE CONFIGURATION OF BIRKENAL, A nor-SESQUITERPENE ALDEHYDE FROM ESSENTIAL OIL OF Betula pubescens BUDS
D. V. Domrachev and A. V. Tkachev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




99 .     2¦Â-acetoxy-11¦ÂH-eudesma-4-en-12,8¦Á-olide
C17H24O4     ÏàËÆ¶È:52.6%
Chinese Chemical Letters          2002          13          855-856
A New Eudesmanoilde from Carpesium macrocephalum
Chao YANG, Cheng Shan YUAN, Yi Feng HAN, Zhong Jian JIA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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100 .     6¦Á,8¦Á-dimethoxy-10¦Á-hydroxy-eremophil-7(11)-en-12,8¦Â-olide
C17H26O5     ÏàËÆ¶È:52.6%
Chinese Chemical Letters          2002          13          963-964
Two New Eremophilenolides from Ligularia sagitta

Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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