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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 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . caryolane-1,9¦Â-Diol ÏàËÆ¶È:100% Chinese Traditional and Herbal Drugs 2012 43 51-54 Chemical constituents in stems and leaves of Illicium simonsii LIU Ji-feng; ZHANG Xue-mei; SHI Yao; ZHANG Quan; MA Yun-bao; CHEN Ji-jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . caryolane-1,9¦Â-Diol ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2012 37 3426-3429 Sesquiterpenes from stem of Schisandra glaucescens ZHANG Pei-pei; GAO Sha-sha; ZHANG Tian-tian; CHEN Jia-chun; DUAN Hong-quan; FANG Jin-bo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . caryolane-1,9¦Â-diol ÏàËÆ¶È:100% Journal of Chinese Medicinal Materials 2013 36 223-225 Study on the Chemical Constituents in the Fruit of Harrisonia perforata YAN Xiao-xia, LIANG Zheng-fen, WANG Mao-yuan, WANG Jian-rong, WANG Zhu-nian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (-)-caryophyllene ¦Â-oxide ÏàËÆ¶È:93.3% 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 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-caryophyllene alcohol ÏàËÆ¶È:73.3% Flavour and Fragrance Journal 2013 28 2-9 Volatile constituents of the fruit of Garcinia atroviridis and their antibacterial and anti-inflammatory activities Wen-Nee Tan, Keng-Chong Wong, Melati Khairuddean, Ibrahim M. Eldeen, Mohd. Zaini Asmawi and Baharuddin Sulaiman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 5 ÏàËÆ¶È:73.3% Australian Journal of Chemistry 1988 41 1755-1761 Sesquiterpenes From a New Zealand Sponge of the Genus Eurypon CJ Barrow, JW Blunt and MHG Munro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (4R,8R,9R)-8-methoxyisocaryolane-9,15-diol C16H28O3 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 9¦Á-hydroxy-1¦Â-methoxycaryolanol ÏàËÆ¶È:68.7% Chinese Traditional and Herbal Drugs 2013 44 2195-2199 Chemical constituents in stems of Zhuang Medicine Alsophila spinulosa LU Ru-mei, CAO Min, LIAO Peng-ying, WEI Jian-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . (1S,4R,5R,8S,9S)-clovane-5,9,12-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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . (()-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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 1 C15H26O2 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . (¡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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . compound 4 C15H20O4 ÏàËÆ¶È:66.6% Journal of Natural Products 1988 Vol 51 1006 Structure of Cyperanic Acid, a New Sesquiterpene from Dittrichia viscosa Paolo Ceccherelli, Massimo Curini, Maria Carla Marcotullio, Alessandro Menghini Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . (-)-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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 1 C15H26O ÏàËÆ¶È:66.6% Phytochemistry 1992 31 2153-2154 A sesquiterpene alcohol from Litsea amara S.A. Achmad, E.L. Ghisalberti, E.H. Hakim, L. Makmur, M. Manurung Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 27 . (+)-cycloisolongifol-5¦Â-ol C15H24O ÏàËÆ¶È:66.6% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 28 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 29 . (-)-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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 30 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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-Caryophyllene Oxide and Its Derivatives