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1 .     caryolane-1,9¦Â-diol
    ÏàËÆ¶È:100%
China Journal of Chinese Materia Medica          2009          34          2765-2767
Bioactive constituents from whole herbs of Vernonia cinerea (¢ò)
ZHU Huaxu, TANG Yuping, MIN Zhida, GONG Zhunan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     compound 17
    ÏàËÆ¶È:100%
Phytochemistry          1990          29          757-763
Rearranged caryophyllenes by biotransformation with Chaetomium cochliodes
Wolf-Rainer Abraham,Ludger Ernst,Hans-Adolf Arfmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (-)-caryophyllene ¦Â-oxide
    ÏàËÆ¶È:100%
Tetrahedron          1992          48          377-392
Neurotrophic sesquiterpene-neolignans from magnolia obovata: structure and neurotrophic activity
Yoshiyasu Fukuyama, Yukio Otoshi, Kumi Miyoshi, Kazuhiko Nakamura, Mitsuaki Kodama, Masakazu Nagasawa, Takashi Hasegawa, Hiroshi Okazaki, Michiharu Sugawara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     (1S,4R,5R,8S,9S)-clovane-5,9,12-triol
C15H26O3     ÏàËÆ¶È:73.3%
Journal of Natural Products          2006          69(10)          1429-1434
Microbial Transformation and Butyrylcholinesterase Inhibitory Activity of (−-Caryophyllene Oxide and Its Derivatives
Muhammad Iqbal Choudhary, Zafar A. Siddiqui, Sarfraz A. Nawaz, and Atta-ur-Rahman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     compound 1
C15H26O2     ÏàËÆ¶È:73.3%
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

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6 .     (+)-cycloisolongifol-5¦Â-ol
C15H24O     ÏàËÆ¶È:73.3%
Zeitschrift f¨¹r Naturforschung B          2006          61b          1035-1038
Microbial Metabolism of (+)-Cycloisolongifol-5¦Â-ol
Muhammad Iqbal Choudhary, Waseem Kausar, Zafar Ali Siddiqui, and Atta-ur-Rahman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     compound 21
    ÏàËÆ¶È:73.3%
Phytochemistry          1981          20          469-472
Sesquiterpenes from three Senecio species
Ferdinand Bohlmann, J¨¹rgen Ziesche
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     1¦Á,7¦Á-dihydroxyconfertifolin
C15H22O4     ÏàËÆ¶È:73.3%
Journal of Asian Natural Products Research          2012          14          577-580
Metabolites from endophytic fungus A12 of Dracaena cambodiana
Dong-Dong Chang, Wen-Jian Zuo, Wen-Li Mei & Hao-Fu Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     9¦Á-hydroxy-1¦Â-methoxycaryolanol
C16H28O2     ÏàËÆ¶È:68.7%
Helvetica Chimica Acta          2008          Vol. 91          1894
Four New Compounds from Sinacalia tangutica
Ying Zhu, Yan Zhao, Guo-Du Huang, and Wang-Suo Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (8R,9R)-8-methoxyisocaryolan-9-ol
    ÏàËÆ¶È:68.7%
Journal of Natural Products          2011          74          1707-1712
Biotransformation of Bioactive Isocaryolanes by Botrytis cinerea
Jociani Ascari, Maria Am elia Diamantino Boaventura, Jacqueline Aparecida Takahashi, Rosa Dur an-Patr on, Rosario Hern andez-Gal an, Antonio J. Mac¨ªas-S anchez, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     15-hydroxyallo-cedrol
C15H26O2     ÏàËÆ¶È:66.6%
Phytochemistry          2007          68          2409-2414
Sesquiterpenes from the wood of Juniperus lucayana
Yarelis Ort¨ªz Nuñez, Iraida Spengler Salabarria, Isidro G. Collado,Rosario Hern¨¢ndez-Gal¨¢n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     (1R,4R,5R,8S,9S,13S)-caryolane-5,8,13-triol
C15H26O3     ÏàËÆ¶È:66.6%
Journal of Natural Products          2006          69(10)          1429-1434
Microbial Transformation and Butyrylcholinesterase Inhibitory Activity of (−-Caryophyllene Oxide and Its Derivatives
Muhammad Iqbal Choudhary, Zafar A. Siddiqui, Sarfraz A. Nawaz, and Atta-ur-Rahman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     sativene epoxide
C15H24O3     ÏàËÆ¶È:66.6%
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 .     (()-3,7,11-trimethyl-1,7,11-dodecanetriol
C15H32LiO3     ÏàËÆ¶È:66.6%
Journal of Natural Products          2002          65          1319-1322
African Elephant Sesquiterpenes. II. Identification and Synthesis of New Derivatives of 2,3-Dihydrofarnesol
Thomas E. Goodwin,Felisia D. Brown, Richard W. Counts, Nichole C. Dowdy, Patrick L. Fraley,Randall A. Hughes, Daniel Z. Liu, Courtney D. Mashburn, Josh D. Rankin, Russell S. Roberson, Katie D. Wooley, Elizabeth L. Rasmussen, Scott W. Riddle, Heidi S. Ridd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     compound 3
C15H24O2     ÏàËÆ¶È:66.6%
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

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16 .     1R,3S,6S,7R,10S-7-Isopropyl-4,10-dimethylbicyclo[4.4.0]dec-4-en-3,10-diol
C15H26O2     ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          2002          38          154-160
SYNTHESIS OF THE ELEUTHESIDE CORE FROM (+)-d-CADINOL:CONSTRUCTION OF SIDE CHAINS ON THE MENTHANE RING
I. P. Tsypysheva, A. M. Kunakova, O. V. Shitikova,L. V. Spirikhin, F. A. Valeev, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     4,5-dioxo-10-epi-4,5-seco-¦Ã-eudesmol
    ÏàËÆ¶È:66.6%
Chinese Chemical Letters          2005          16          569-571
Total Synthesis of Two 4, 5-Dioxo-seco-eudesmane Sesquiterpenes
Li Jing FANG, Chen Xi ZHANG, Jin Chun CHEN, Guo Jun ZHENG, Yu Lin LI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     5¦Á-Hydroxy-¦Â-eudesmol
C15H26O2     ÏàËÆ¶È:66.6%
Molecules          2003          8          670-677
Sesquiterpenes from Cymbopogon proximus
Hesham I. El-Askary, Meselhy R. Meselhy and Ahmed M. Galal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     compound 2
C15H26O3     ÏàËÆ¶È:66.6%
Journal of Asian Natural Products Research          2009          11          539-547
Constituents from the seeds of Brucea javanica with inhibitory activity of Tobacco mosaic virus
Qi-Jian Chena, Ming-An Ouyangab, Qing-Wei Tanb, Zheng-Kun Zhanga,Zu-Jian Wua and Qi-Ying Lina
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     cubebol
    ÏàËÆ¶È:66.6%
Natural Product Research          1993          2          231-236
Aduncamide, a Cytotoxic and Antibacterial b-Phenylethylamine-Derived Amide from Piper aduncum
Jimmy Orjala; Anthony D. Wright; Topul Rali; Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     (¡À)-[1S-(1¦Â,4¦Â,4a¦Â,6¦Á,8a¦Á)]-1,6-Dimethyl-4-(1-methylethyl)-1,2,3,4,4a,5,6,7,8,8a-decahydro-1,6-naphthalenediol
    ÏàËÆ¶È:66.6%
Phytochemistry          1996          42          1097-1103
Three new oxygenated cadinanes from Baccharis species
Carmen L. Queiroga, Vera L. Ferracini, A. J. Marsaioli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     (-)-5¦ÂH-eudesmane-4¦Â,11-diol
C15H28O2     ÏàËÆ¶È:66.6%
Journal of Natural Products          1994          Vol 57          1189
Synthetic Studies of Sesquiterpenes with a cis-Fused Decalin System, 4. Synthesis of (+)-5¦ÂH-Eudesma-3,11-diene, (-)-5¦ÂH-Eudesmane-4¦Â,11-diol, and (+)-5¦ÂH-Eudesmane-4¦Á,11-diol, and Structure Revision of a Natural Eudesmane-4,11-diol Isolated from Pluchea
Masayoshi Ando, Koji Arai, Kazuhira Kikuchi, Koji Isogai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     ricciocarpin B
C15H20O4     ÏàËÆ¶È:66.6%
Phytochemistry          1990          29          2565-2568
Sesquiterpenoids from the liverwort Ricciocarpos natans
Gerald Wurzel,Hans Becker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     compound 17
    ÏàËÆ¶È:66.6%
Phytochemistry          1981          20          469-472
Sesquiterpenes from three Senecio species
Ferdinand Bohlmann, J¨¹rgen Ziesche
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     bromocyclococanol
C15H25BrO     ÏàËÆ¶È:66.6%
Tetrahedron Letters          2002          43          2551-2553
Bromocyclococanol, a halogenated sesquiterpene with a novel carbon skeleton from the red alga Laurencia obtusa
Inmaculada Brito, Mercedes Cueto, Enrique Dorta, Jos¨¦ Darias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     6¦Á-Hydroxyginsenol
C15H26O2     ÏàËÆ¶È:66.6%
Journal of the Chemical Society, Perkin Transactions 1          1999                   727-730
Biotransformation of the fungistatic sesquiterpenoid ginsenol by Botrytis cinerea
Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, James R. Hanson, Peter B. Hitchcock and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     (-)-cubebol
    ÏàËÆ¶È:66.6%
Bioscience, Biotechnology, and Biochemistry          2008          72          611-614
Antifeedants against Locusta migratoria from the Japanese Cedar, Cryptomeria japonica II
Bin WU, Takehiro KASHIWAGI, Ikuhiro KURODA, Xiao Hui CHEN, Shin-ich TEBAYASHI and Chul-Sa KIM
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     compound 11
C14H20O     ÏàËÆ¶È:66.6%
Bulletin of the Chemical Society of Japan          1993          66          2694-2699
Synthetic Photochemistry. LXI. A Total Synthesis of (¡À)-Valeranone, a cis-Decalone Sesquiterpenoid from Valeriana officinalis, via an Intramolecular Photocycloaddition
Hitoshi Takeshita, Ying-She Cui, Nobuo Kato, Akira Mori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     4,5-epicryptomeridiol
    ÏàËÆ¶È:66.6%
Heterocycles          2001          54          765-776
Intramolecular Photocycloaddition of 2-Cycloalkenyl-1,3-dioxin-4-one. Stereoselective Synthesis of cis-Eudesmane-4,11-diols
Toshihide Hatsui,* Ka Li, Akira Mori,* and Hitoshi Takeshita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     10¦ÂH-8¦Á,12-epidioxyeremophil-7(11)-en-8¦Â-ol
C15H24O2     ÏàËÆ¶È:66.6%
Tetrahedron          2011          67          2220-2231
Overlapping chemical and genetic diversity in Ligularia lamarum and Ligularia subspicata. Isolation of ten new eremophilanes and a new seco-bakkane compound
Yoshinori Saito, Masato Hattori, Yuko Iwamoto, Yuriko Takashima, Kanako Mihara, Yoko Sasaki, Miho Fujiwara, Misato Sakaoku, Anna Shimizu, Xun Chao, Chiaki Kuroda, Xun Gong, Ryo Hanai, Motoo Tori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     15-nor-cadinan-4¦Á-ol
C14H26O     ÏàËÆ¶È:66.6%
Tetrahedron          1999          55          15109-15126
Autoxidation of 4-amorphen-11-ol and the biogenesis of nor- and seco-amorphane sesquiterpenes from fabiana imbricata
Koon-Sin Ngo, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     cadinane-4¦Â,5¦Á,10¦Á-triol
C15H28O3     ÏàËÆ¶È:66.6%
Planta Medica          2012          78          1010-1014
Sesquiterpenoids from the Rhizomes of Homalomena occulta
Xie, Xiao-Yu; Wang, Rui; Shi, Yan-Ping:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     Ishwarane
    ÏàËÆ¶È:66.6%
Journal of Natural Medicines          2011          65          206-211
A bioactive sesquiterpene from Bixa orellana
Dennis D. Raga ,Rafael A. Espiritu ,Chien-Chang Shen ,Consolacion Y. Ragasa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     compound 7
    ÏàËÆ¶È:66.6%
Journal of Agricultural and Food Chemistry          1997          45          221-226
Syntheses of Sesquiterpene Epoxides and Alcohols from ¦Ã-Gurjunene
Isabelle Bombarda, Emile M. Gaydou, Robert Faure, and Jacqueline Smadja
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     CCDC-256464
C20H38O4     ÏàËÆ¶È:65%
Tetrahedron Letters          2005          46          1623-1626
Oxidative cyclization of a seco-cladiellane diterpenoid
Manuel Friedel, Gregor Golz, Peter Mayer, Thomas Lindel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     (9R)-9-acetoxypatchoulol
C17H28O3     ÏàËÆ¶È:64.7%
Journal of Natural Products          1999          62          437-440
Biotransformation of the Fungistatic Sesquiterpenoid Patchoulol by Botrytis cinerea
Josefina Aleu, James R. Hanson, Rosario Hern¨¢ndez Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     3¦Â-hydroxy-5¦Á,13¦Á-androstane
C21H33O2Cl     ÏàËÆ¶È:63.1%
Phytochemistry          1997          45          951-956
The hydroxylation of some 13¦Á-methylsteroids by Cephalosporium aphidicola
Juliette Boynton, James R. Hanson, A. Christy Hunter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     compound 9
    ÏàËÆ¶È:63.1%
Organic Magnetic Resonance          1984          22          736-738
Carbon-13 nuclear magnetic resonance spectra of some heterocyclic D-homoandrostanes
Deanna Marcano, Jeannette De M¨¦ndez, Ana C. Ortiz and Mirna Salinas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     1¦Á,3¦Â-dihydroxyambrox
C16H28O3     ÏàËÆ¶È:62.5%
Journal of Natural Products          2006          69(6)          957-959
Biotransformation of (−-Ambrox by Cell Suspension Cultures of Actinidia deliciosa
Asma Nasib, Syed Ghulam Musharraf, Sajjad Hussain, Saifullah Khan,Shazia Anjum, Shamsher Ali, Atta-ur-Rahman, and M. Iqbal Choudhary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     9-thiocyanatopupukeanane
C16H25SN     ÏàËÆ¶È:62.5%
Journal of Natural Products          2003          66          1512-1514
New 9-Thiocyanatopupukeanane Sesquiterpenes from the Nudibranch Phyllidia varicosa and Its Sponge-Prey Axinyssa aculeata
Yasman, Ru Angelie Edrada,Victor Wray, and Peter Proksch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     1¦Á,3¦Â-dihydroxysclareolide
C16H26O4     ÏàËÆ¶È:62.5%
Journal of Natural Products          1997          60          1038-1040
Microbial Transformation of Sclareolide
Atta-ur-Rahman, Afgan Farooq, and M. Iqbal Choudhary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     compound 16b
    ÏàËÆ¶È:62.5%
Journal of Natural Products          1984          Vol 47          592-599
Cmr Spectroscopy of Labdanic Diterpenes and Related Substances
Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     acetylginsenol
    ÏàËÆ¶È:62.5%
Journal of Natural Products          1994          Vol 57          738
Inhibition of Botrytis cinerea by New Sesquiterpenoid Compounds Obtained from the Rearrangement of Isocaryophyllene
Isidro G. Collado, Josefina Aleu, Antonio J. Mac¨ªas-S¨¢nchez, Rosario Hern¨¢ndez-Gal¨¢n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     (4R,8R,9R)-8-methoxyisocaryolane-9,15-diol
C16H28O3     ÏàËÆ¶È:62.5%
Journal of Natural Products          2011          74          1707-1712
Biotransformation of Bioactive Isocaryolanes by Botrytis cinerea
Jociani Ascari, Maria Am elia Diamantino Boaventura, Jacqueline Aparecida Takahashi, Rosa Dur an-Patr on, Rosario Hern andez-Gal an, Antonio J. Mac¨ªas-S anchez, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     Norambreinolide
C16H26O2     ÏàËÆ¶È:62.5%
Chemistry of Natural Compounds          2011          Vol. 47, No. 4          574-578
ENANTIOSELECTIVE SYNTHESIS OF 11-HOMODRIM-7-EN-9¦Á,12,13-TRIOL
P. F. Vlad, K. G. Edu, M. N. Koltsa, A. G. Chokyrlan,A. Nikolescu, and K. Delyanu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     (8aS,1R,2R)-1-(2-Hydroxyethyl)-2,5,5,8a-tetramethyl-perhydro-2-naphthalenol
    ÏàËÆ¶È:62.5%
The Journal of Organic Chemistry          2001          66          7263-7269
Total Synthesis and Determination of the Absolute Configuration of Coscinosulfate. A New Selective Inhibitor of Cdc25 Protein Phosphatase
St¨¦phane Poigny, Samia Nouri, Ang¨¨le Chiaroni, Mich¨¨le Guyot, and Mohammad Samadi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     (-)-(1R,2R,4aS,8aS)-1-(2-hydroxyethyl)-2,5,5,8a-tetramethyldecahydro-2-naphthalenol
C16H30O2     ÏàËÆ¶È:62.5%
Tetrahedron          2001          57          5657-5662
The synthesis of (−-Ambrox® starting from labdanolic acid
Marjon G Bolster, Ben J.M Jansen, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     compound 4
    ÏàËÆ¶È:61.1%
Natural Product Research          1993          2          215-220
Synthesis and Mass Spectral Confirmation of the Identity of Two New Tricyclic Terpanes Found in Chinese Bituminous Sandstones
Teodoro S. Kaufman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     T-Muurolol
C15H26O     ÏàËÆ¶È:60%
Journal of Natural Products          2009          72          99-101
T-Muurolol Sesquiterpenes from the Marine Streptomyces sp. M491 and Revision of the Configuration of Previously Reported Amorphanes
Ling Ding, Roland Pfoh, Stephan Ruhl, Song Qin,and Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     rulepidadiol
C15H22O3     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2000          Vol. 83          3191
New Terpenoids from Basidiomycetes Russula lepida
Tan Jian-Wen, Dong Ze-Jun, and Liu Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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