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²éѯ½á¹û£º¹²²éµ½1086¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 DerivativesMuhammad Iqbal Choudhary, Zafar A. Siddiqui, Sarfraz A. Nawaz, and Atta-ur-Rahman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 DerivativesMuhammad Iqbal Choudhary, Zafar A. Siddiqui, Sarfraz A. Nawaz, and Atta-ur-Rahman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 deliciosaAsma Nasib, Syed Ghulam Musharraf, Sajjad Hussain, Saifullah Khan,Shazia Anjum, Shamsher Ali, Atta-ur-Rahman, and M. Iqbal Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 acidMarjon G Bolster, Ben J.M Jansen, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |

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-Caryophyllene Oxide and Its Derivatives